- Research article
- Open Access
Cell adhesion and signaling on the fibronectin 1st type III repeat; requisite roles for cell surface proteoglycans and integrins
BMC Cell Biology volume 2, Article number: 18 (2001)
The first type III repeat of fibronectin is known to be involved in fibronectin matrix assembly, and recombinant proteins from this type III repeat can inhibit cell proliferation, tumor metastasis and angiogenesis. We have analyzed the way rat aortic smooth muscle cells (RASMCs) interact with a recombinant protein encompassing a C-terminal portion of the first type III repeat of fibronectin (protein III1-C).
Cells are able to adhere to and spread on III1-C coated on a dish. Both β1 integrins and cell surface heparan sulfate proteoglycans serve as receptors for III1-C. For example, cell attachment to III1-C is partially inhibited by agents that block β1 integrins or by heparin. Complete inhibition of cell attachment is seen only when integrin blocking agents are combined with heparin. Affinity chromatography revealed the binding of proteins that likely represent the integrin β1 and α5 submits to a III1-C column. Cell adhesion to III1-C results in robust ERK1/2 activation that is blocked by integrin-blocking agents. In addition, cell adhesion to III1-C and ERK1/2 activation by III1-C are both inhibited by heparan sulfate but not by chondroitin sulfate. Moreover, heparitinase treatment, but not chondroitinase treatment of RASMCs results in reduced cell adhesion and ERK1/2 activation. Affinity chromatography experiments demonstrated that 35SO4-labeled cell surface heparan sulfate proteoglycans bound specifically to III1-C.
The results suggest that the 1st type III repeat of fibronectin contains a previously unrecognized cell adhesion domain that stimulates robust ERK1/2 activation in RASMCs. Cells interact with this domain through cell surface heparan sulfate proteoglycans and integrins, and both classes of receptors are required for optimal cell adhesion and ERK1/2 activation.
Fibronectin can control many aspects of cell behavior, including cell growth, migration and differentiation . Fibronectin exists in the blood as a dimer, but in tissues it is in the form of an insoluble fibrillar matrix. The fibrillar form of fibronectin is thought to be the most relevant form in vivo because this is the form with which most cells interact . Various lines of evidence suggest that the fibrillar matrix form of fibronectin exerts effects on cells that are not duplicated by the dimeric form of fibronectin. For example, high concentrations of dimeric fibronectin enhance cell migration whereas high concentrations of fibrillar fibronectin reduce cell migration . Also, inhibition of fibronectin matrix assembly has been shown to inhibit cell growth in various systems [3–5]. These findings suggest that fibrillar fibronectin may stimulate signal transduction pathways in cells that are either not stimulated, or only marginally stimulated, by dimeric fibronectin.
Fibronectin matrix assembly is a cell-mediated process that requires the activity of integrins [1, 6–8]. The integrin that is primarily responsible for assembling fibronectin into the matrix is α5β1, although αvβ3, αllbβ3 and α4β1 can also function in this capacity [9–14]. In addition to integrins, fibronectin matrix assembly also depends on self-association sites within fibronectin. For example, the N-terminal 70 kDa region, the 1st type III repeat and the 10th type III repeat are thought to be important for the proper alignment of fibronectin molecules during matrix assembly [15–22]. We and others have shown that a recombinant protein representing a portion of the first type III repeat (protein III1-C) can affect fibronectin matrix assembly and cell growth [2–4, 16]. Moreover, a mutant recombinant fibronectin molecule that is lacking the first seven type III repeats has been shown to lead to defective fibronectin matrix assembly in cell culture and in vivo, and to inhibition of cell proliferation [23, 24]. Although the matrix produced with fibronectin lacking the first seven type III repeats was somewhat aberrant, this study does show that some matrix assembly can occur without the first type III repeat. Therefore, several approaches reveal that the fibronectin type III repeats, and especially the first type III repeat, play important roles in the regulation of fibronectin matrix assembly and cell growth.
III1-C is known to inhibit cell proliferation [3, 4]. Recently, III1-C (also known as anastellin) has been shown to inhibit angiogenesis, and tumor growth and metastasis . In the present study we examine how cells interact with and respond to III1-C, with a particular focus on signaling through the Ras/ERK pathway. We find that cells can adhere and spread on III1-C and that two classes of receptors function in cell adhesion to III1-C; integrins and cell-surface proteoglycans.
Cell attachment and spreading on the first type III repeat of fibronectin
III1-C is a recombinant fibronectin fragment that encompasses most of the first type III repeat, but is missing the A and B β-strands of the repeat . We had previously found that III1-C inhibited the growth of normal diploid smooth muscle cells (SMCs) in culture . During these experiments we noticed that the presence of III1-C in the culture medium affected the morphology of cells at early times after plating. As shown in Figure 1, cells plated onto fibronectin coated dishes attached and spread well, typically containing numerous lamellipodia per cell (Fig. 1A, panel FN). Cells seeded onto fibronectin coated dishes with III1-C in the culture medium spread more extensively and in a more circular pattern at early times after plating than cells plated on fibronectin in the absence of III1-C (Fig. 1A, panels FN and FN+C, and Fig. 1B). Cells cultured on fibronectin for 4 hours show approximately the same extent of spreading as cells on fibronectin plus III1-C (Fig. 1B), indicating that III1-C accelerated the rate of spreading of the cells but did not affect the eventual extent of spreading. The effect on cell morphology was specific for III1-C because the negative control protein III 11-C (a recombinant protein derived from the 11th type III repeat in fibronectin, which, similar to III1-C, is missing the A and B β-strands of this repeat) had no effect on the morphology of the cells (Fig. 1A, panel FN+11C, and Fig. 1B). Interestingly, the effect of III1-C on cell morphology was seen even when the plates had not been coated with fibronectin (Fig. 1A, panel C, and Fig. 1B), indicating that intact fibronectin was not required for cell attachment and spreading when III1-C was in the culture medium. Again, the negative control protein III 11-C had no effect on cell morphology; cells seeded onto uncoated plates with III 11-C in the culture medium remained rounded and did not appreciably spread over several hours (Fig. 1A, panel 11C, and Fig. 1B). These results indicated that III1-C had an effect on the morphology of freshly plated cells. Moreover, the plates did not need to be coated with any adhesive protein prior to seeding the cells with III1-C in the culture medium, indicating that III1-C may have adsorbed onto the tissue culture plastic and that cells then attached and spread on the adsorbed III1-C.
To directly test whether cells were able to bind to III1-C coated on a dish, various concentrations of either fibronectin, III1-C or III 11-C were coated onto dishes and cell attachment to these substrates was measured. As shown in Figure 2, cells attach well to fibronectin and to III1-C, but not to III 11-C coated on a dish. On a molar basis, III1-C was less effective at supporting cell attachment than fibronectin, however, it was clear that RASMCs do attach and spread well on III1-C coated on a dish. The morphology of the cells seeded onto the III1-C–coated wells was indistinguishable from the morphology shown in Fig. 1A, panel C.
Role of integrins in cell attachment to III1-C
The attachment of RASMCs to III1-C was analyzed further to determine the role played by integrins as potential adhesive receptors for III1-C. Various integrin-blocking reagents were tested for their ability to block RASMC attachment to III1-C and to fibronectin. The adhesion of SMCs to fibronectin is mediated through β1 integrins [1, 26]. We confirmed these previous findings for our RASMCs, by showing a complete block of cell attachment to fibronectin by EDTA (an agent that blocks all integrins), anti-β1 blocking mAb, and RGD peptide, but not by the negative control RAD peptide (Fig. 3A). Anti-fibronectin antibodies also effectively blocked RASMC attachment to fibronectin (Fig. 3A). Heparin did not inhibit cell attachment to fibronectin (Fig. 3A), however, it did modestly reduce cell spreading on fibronectin (15% inhibition of cell spreading, data not shown). These results indicate that RASMC adhesion to fibronectin is mediated by β1 integrins.
Blocking studies indicated that cell attachment to III1-C was partially mediated by β1 integrins. For example, RASMC attachment was partially blocked by EDTA, anti-β1 mAb, and RGD peptide (Fig. 3B), indicating the involvement of integrins. However, cell attachment was also partially blocked by heparin, which did not inhibit cell attachment to fibronectin (Fig. 3A and 3B, Hep samples), indicating that a non-integrin receptor also mediated cell attachment to III1-C. A complete block of cell attachment to III1-C was only observed when heparin was combined with integrin blocking agents; e.g., heparin + anti-β1 mAb or heparin + RGD peptide (Fig. 3B). Anti-fibronectin antibodies modestly inhibited cell attachment, but anti-III 1-C antibodies effectively blocked cell attachment to III1-C (Fig. 3B). These results demonstrate that cell attachment to III1-C was mediated through both β1 integrins and another class of receptors on RASMCs.
One way in which integrins were originally shown to be fibronectin receptors was by affinity chromatography of radioiodinated cell surface proteins on a fibronectin column [27, 28]. Consistent with these earlier studies, cell surface radioiodination of RASMCs followed by affinity chromatography on fibronectin Sepharose and elution with EDTA revealed the binding of two major bands at 120 kDa and 140 kDa (Fig. 4,E lane under FN). These sizes match those of the β1 and α5 integrin submits, respectively, that have been shown by affinity chromatography to bind to the cell binding domain (i.e., 10th type III repeat) of fibronectin [27–31]. Affinity chromatography on a III1-C Sepharose column revealed the binding of three major bands of sizes 120 kDa, 140 kDa and 150 kDa (Fig. 4,E lane under C). The 120 kDa and 140 kDa bands likely represent the β1 and α5 subunits (as above), while the 150 kDa band may represent either the α2 or α3 integrin subunits, which are known to be expressed by VSMCs . Affinity chromatography on the control III 11-C column yielded no radioiodinated proteins that were eluted from the column (Fig. 4,E lane under 11C). These results are consistent with the hypothesis that one or more pi integrins act as receptors for III1-C. Taken together with the integrin-blocking results described above, it is clear that RASMC adhesion to III1-C is partially mediated through β1 integrins.
Cell adhesion to III1-C activates ERK1/2
Integrins are known to activate signaling pathways in cells [32–35]. Among the most well-studied signaling pathways is the Ras/MAPK pathway leading to activation of ERK1 and ERK2 . We therefore decided to test the effect of cell adhesion to III1-C on ERK activation. As expected, treatment of RASMCs with PDGF resulted in activation of ERK1/2 (Fig. 5, PDGF lanes). Plating RASMCs onto a fibronectin coated dish in the absence of growth factors yielded moderate activation of ERK1/2, which peaked at 30 min then decreased somewhat over the next 30 min of the experiment (Fig. 5, bottom panel). However, plating cells onto a III1-C coated dish gave strong activation of ERK1/2, which peaked at 30 min and remained relatively constant for the subsequent 30 min (Fig. 5, top panel). The control protein III 11-C did not appreciably stimulate ERK1/2 phosphorylation (Fig. 5, 11C lanes, both panels). Thus, the adhesion of RASMCs to III1-C resulted in robust activation of ERK1/2 that was comparable to the activation obtained with PDGF.
ERK activation by III1-C is dependent on β1 integrins
As shown above, several agents that block β1 integrin function partially inhibit cell attachment to III1-C. We therefore tested the effects of these agents on ERK1/2 activation by III1-C. The results obtained with ERK1/2 activation closely paralleled the results obtained with cell attachment to III1-C, except that the individual blocking agents were relatively more efficient at inhibiting ERK1/2 activation. For example, heparin, EDTA, anti-β1 mAb and RGD peptide all significantly inhibited ERK1/2 activation by cell adhesion to III1-C (Fig. 6). Heparin was most effective and completely blocked ERK1/2 activation. (Fig. 6). In contrast, the negative control RAD peptide did not inhibit ERK1/2 activation by III1-C (Fig. 6, C+RAD lane). These results indicate that both integrins and the class of receptors inhibited by heparin were required for III1-C mediated activation of ERK1/2.
Role of heparan sulfate proteoglycans in cell adhesion to III1-C and ERK1/2 activation by III1-C
Because heparin was able to inhibit the attachment of cells to III1-C and the activation of ERK1/2 by III1-C, we tested the effect of other glycosaminoglycans on III1-C stimulated ERK1/2 activity. Heparin, heparan sulfate and dermatan sulfate blocked ERK1/2 activation by III1-C (Fig. 7), and cell adhesion to III1-C (not shown). In contrast, hyaluronic acid, chondroitin-4-sulfate and chondroitin-6-sulfate had no effect on the ability of III1-C to stimulate ERK1/2 activity (Fig. 7) or on the adhesion of cells to III1-C (not shown). It is possible that heparin, heparan sulfate and dermatan sulfate inhibit III1-C mediated cell adhesion and ERK1/2 activation due to common chemical features. For example, heparin, heparan sulfate, and dermatan sulfate all contain iduronic acid residues whereas chondroitin sulfate and hyaluronic acid do not. The results presented above indicate that a heparan sulfate proteoglycan (HSPG) or dermatan sulfate proteoglycan on the surface of RASMCs may serve as a receptor for III1-C.
To further explore the possibility that a cell surface proteoglycan serves as a receptor for III1-C, RASMCs were treated with the glycosaminoglycan-degrading enzymes seeded onto III1-C, and analyzed for the activation of ERK1/2. Heparitinase treatment, but not chondroitinase ABC treatment decreased the amount of ERK1/2 activation by III1-C (Fig. 8). Heparitinase treatment also inhibited cell adhesion by 25–40%, while chondroitinase ABC treatment did not inhibit cell adhesion to III1-C (not shown). This result is consistent with the idea that HSPGs but not chondroitin sulfate proteoglycans serve as signaling receptors for III1-C.
To identify the cell surface proteoglycans that may serve as receptors for III1-C, RASMCs were labeled with 35SO4 and cell lysates were applied to III1-C and III 11-C columns. The most highly labeled band, migrating in a smear at about 450 kDa, bound efficiently to the III1-C column (Fig. 9A, compare flow through and elution lanes). This proteoglycan resisted elution by 8 M urea but was eluted by boiling the Sepharose beads in SDS (Fig. 9A). This same proteoglycan did not bind appreciably to the III 11-C column (Fig. 9A). Heparitinase and chondroitinase ABC treatment of the 35SO4 labeled samples revealed that the 450 kDa proteoglycan was composed mostly of HSPGs (Fig. 9B). These results indicate that most of the cell surface HSPGs of RASMCs can bind to III1-C in affinity chromatography.
RASMC HSPGs were analyzed further by immunoblotting with the monoclonal antibody 3G10 which specifically recognizes desaturated uronates on the heparan sulfate stubs that remain associated with core proteins after heparitinase digestion . Complete digestion of RASMC lysates with heparitinase reveals major bands at 46 kDa and 70 kDa, indicating that these are the sizes of the major HSPG core proteins (not shown). RASMC lysates were subjected to partial heparitinase treatment (full digestion was not performed in order to allow some GAGs to remain associated with the core proteins) then applied to either III1-C or III 11-C Sepharose. As shown in Fig. 10, most of the 46 kDa and 70 kDa HSPGs bound to III1-C Sepharose but not to III 11-C Sepharose. In addition, the presence of heparin in the lysate inhibited the 46 kDa and 70 kDa HSPGs from binding to the III1-C column (Fig. 10, compare C and C•H lanes). The inhibition of 46 kDa and 70 kDa binding to III1-C by heparin suggests that these HSPGs may serve as receptors for III1-C in cell adhesion and ERK1/2 signaling.
We have found that cells can interact with a portion of the fibronectin first type III repeat, leading to cell adhesion and activation of ERK, and that this signaling requires both cell surface HSPGs and integrins. RASMCs are able to adhere to and spread on III1-C. Adhesion to III1-C results in robust activation of ERK; comparable to that seen with PDGF stimulation. Several independent lines of evidence indicate that cell surface HSPGs and β1 integrins act as receptors for III1-C and are required for cell adhesion and ERK activation by III1-C. For example, various β1 integrin blocking agents inhibit cell attachment to III1-C and ERK activation by III1-C. In addition, inhibition by heparin, heparan-sulfate, and heparitinase, but not by chondroitin sulfates or chondroitinase ABC all point to the importance of HSPGs as receptors. Affinity chromatography with 125I surface labeled proteins resulted in the binding of proteins of the appropriate sizes of β1 integrins to both FN and III1-C columns. Moreover, affinity chromatography with 35SO4-labeled cells suggests that HSPGs with core protein sizes of 46 kDa and 70 kDa serve as III1-C receptors. Taken together, these results indicate that the first type III repeat of fibronectin can serve as a cell binding domain and that both integrins and cell surface HSPGs function as receptors for this type III repeat.
Our results demonstrate that both integrins and cell surface HSPGs are required for robust ERK 1/2 activation when cells adhere to III1-C. These results are one of the first demonstrations that HSPGs can activate the ERK signaling pathway. Another example of this closely parallels our findings . The adhesion of Jurkat T cells to thrombospondin-1 has been shown to require the cooperation of three classes of receptors; β1 integrins, CD47 and HSPGs . Adhesion of the Jurkat T cells to thrombospondin-1 stimulates ERK1/2 activation and the binding of HSPGs to thrombospondin-1 is required for this signaling. The particular HSPGs that mediate ERK1/2 activation in Jurkat T cells have not been identified, however, the authors speculate that syndecans may participate in the adhesion and signaling in that system . This may also be the case in our system, as described below.
One major family of cell surface HSPGs is the syndecan family. There are 4 members in the syndecan family (syndecan-1 through-4) [39, 40]. Syndecan-1, -2 and -4 are known to bind to extracellular matrix proteins and syndecan-1 and -4 have been shown to support stress fiber formation in conjunction with integrins [41–45]. The HSPGs we have identified as III1-C receptors have core proteins that migrate at the approximate sizes of syndecan-1 (~69 kDa core protein) and syndecan-2 (~48 kDa core protein) . It is therefore possible that our 46 kDa and 70 kDa HSPGs represent syndecan family members. As described above, the syndecans may cooperate with β1 integrins and CD47 to activate the ERK signaling pathway in T cells . A similar mechanism may apply to the adhesion of RASMCs to III1-C. Future studies will determine the identity of the HSPGs that act as III1-C receptors.
The Ras/MAPK pathway is typically thought to be a part of a mitogenic pathway . However, we and others have shown that prolonged treatment with III1-C can inhibit cell proliferation [3, 4], and here we show that cell adhesion to III1-C can activate ERK1/2. One possible explanation for this apparent discrepancy is that although ERK1/2 are often involved in mitogenesis, in SMCs ERK activation can lead to inhibition of proliferation . This occurs through ERK-mediated stimulation of PGE2 production, which then inhibits the proliferation of SMCs . Further experiments will determine whether RASMCs produce PGE2 after treatment with III1-C. Another possibility is that III1-C stimulates other signaling pathways apart from the ERK pathway, and that one of the other signaling pathways inhibits proliferation of the cells. The relationship between ERK activation, stimulation of other signaling pathways and growth inhibition by III1-C will be elucidated by future experiments.
The III1-C protein has recently been shown to inhibit angiogenesis, tumor growth and metastasis . Those findings, along with our present findings reveal some intriguing parallels between III1-C and the angiogenesis inhibitor endostatin . For example, both III1-C and endostatin are fragments of matrix proteins and can inhibit angiogenesis and tumor growth. In addition, recent work has shown that cells interact with endostatin through two classes of receptors; integrins and glypicans (cell surface HSPGs) [48, 49]. This parallels our findings in this present report, that cells interact with III1-C through integrins and cell surface HSPGs. Therefore, III1-C and endostatin may inhibit angiogenesis through related mechanisms involving both integrins and HSPGs. Future work will determine the relative contributions of these two classes of receptors in the biological effects of III1-C.
We have found that cells can interact with the fibronectin first type III repeat, leading to cell adhesion and activation of ERK, and that this signaling requires both cell surface HSPGs and integrins. Results from various independent types of experiments indicate that the first type III repeat of fibronectin can serve as a cell binding domain and that both integrins and cell surface HSPGs function as receptors for this type III repeat.
Materials and Methods
DMEM and glutamine Pen-Strep were obtained from Life Technologies, Inc. FBS was purchased from HyClone Laboratories, Inc. Plasma fibronectin was purified from human plasma by gelatin-agarose affinity chromatography . 4–20% gradient SDS-PAGE gels were from Novex. Anti-phospho-p44/42 MAPK polyclonal antibody and anti-p44/42 ERK polyclonal antibody were purchased from New England Biolabs. Anti-β1 blocking antibody (Ha2/5) was from PharMingen. Peptides GRGDSP and GRADSP were purchased from Life Technologies, Inc. Texas red and FITC labeled secondary antibodies and 35SO4 were from ICN. Heparitinase, chondroitinase ABC and mAb 3G10 were from Seikagaku. Anti-FN antibodies were a gift of Dr. Erkki Ruoslahti (Burnham Institute). ECL plus reagent and Hyperfilm were obtained from Amersham. Complete™ protease inhibitor cocktail tablets were purchased from Boehringer Mannheim Biochemicals. The expression vector pQE-12 was obtained from Qiagen. Heparin and all other chemicals were obtained from Sigma.
The purified glycosaminoglycans used in this study were a generous gift of Dr. Nancy Schwartz (Univ. of Chicago). The glycosaminoglycans were produced under a contract from the National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIH) and serve as reference standards. The tissue sources of the glycosaminoglycans were as follows: hyaluronic acid, human umbilical cord; heparan sulfate, beef lung; dermatan sulfate, hog mucosa; chondroitin-4-sulfate, notochord from river sturgeon (S. platorhynchus), and chondroitin-6-sulfate, cranial cartilage of river sturgeon.
Primary rat aortic smooth muscle cells (RASMCs) were isolated from 12–16 week old Sprague-Dawley rats as described previously . RASMCs were cultured in DMEM supplemented with 10% FBS and glutamine Pen-Strep. RASMCs were typically between passages 2 and 7 for experiments.
Recombinant protein production
Proteins III1-C and III 11-C (previously called III11) were produced in bacteria and purified as described previously . III1-C encompasses fibronectin amino acids 600–674 (Asn-Ala-Pro-Gln-...Thr-Ser-Thr-Pro), and III 11-C amino acids 1,532–1,599 (Leu-Pro-Ser-Ser-...Thr-Ala-Val-Thr), according to the previously published numbering method . The recombinant proteins were expressed by the pQE-12 vector, which places a 6-His coding sequence at the C-terminus of each protein. The proteins were purified on Ni-agarose columns and were >98% pure as judged by SDS-PAGE and coomassie staining. Stock protein solutions were typically 700 μM for III1-C and 520 μM for III 11-C in PBS.
Anti-III1-C antibodies were produced by immunizing rabbits with III1-C. After one month the rabbits were boosted and serum samples were collected every two weeks. The rabbit serum was applied to an affinity column to purify the anti-III 1-C antibodies. In order to avoid purifying antibodies to the 6-His tag in III1-C, the affinity column was made with a GST fusion protein. The 1st type III repeat of fibronectin was expressed as a fusion protein coupled to GST, and this GST-3FN1 fusion protein was coupled to Sepharose and used in affinity purification. Bound antibodies were eluted with 100 mM triethylamine, pH 11.5 and the pH was neutralized with 1 M Tris, pH 8; (the antibody concentration was 0.4 mg/ml). BSA (0.5 mg/ml) was added to stabilize the antibody for subsequent handling. The antibody prep was dialyzed extensively against PBS before use.
Cell attachment and spreading assays
For the cell spreading assay shown in Fig. 1, fibronectin (20 μg/ml) was coated onto 24-well dishes for 1 hr at RT. The wells were washed 3 times with PBS before adding cells. Growing RASMCs were harvested by trypsinization and collected into DMEM + 0.5% BSA + soybean trypsin inhibitor. Cells were washed 3 times with DMEM + 0.5% BSA, then resuspended at 1 × 105 cells/ml in DMEM + 0.5% BSA, in the absence or presence of 25 μM III1-C or 25 μM III 11-C in the medium. Cells were seeded onto the wells (0.5 ml/well, ~30% confluence), placed in a 37°C incubator and allowed to adhere for either 7, 15, 30, 60, 120 or 240 min. Cells were then fixed with 3.7% paraformaldehyde, 60 mM sucrose in TBS, followed by staining with Coomassie Blue dye (1 mg/ml Coomassie Brilliant Blue, 45% MeOH, 10% acetic acid). Cells were destained with water, air-dried, then photographed with a Leica DM IRB phase microscope connected to a Polaroid CCD camera and an Apple Macintosh computer for capturing images. To quantitate the amount of spreading, each image was analyzed with the NIH Image 1.61 application to determine the total amount of area covered by cells and this number was divided by the total number of cells in the image to give an average area per cell (in pixels2/cell).
Cell attachment assays shown in Fig. 2 and 3 were done essentially as described previously . Briefly, fibronectin, III1-C or III 11-C at various concentrations were coated onto 96-well dishes for 1 hr at RT. The wells were then washed 3 times with PBS before adding cells. Growing RASMCs were harvested by trypsinization and collected into DMEM + 0.5% BSA + soybean trypsin inhibitor. Cells were washed 3 times with DMEM + 0.5% BSA, then resuspended at 4 × 105 cells/ml in DMEM + 0.5% BSA with or without inhibitors, as indicated in the figures. Cells were seeded onto the coated wells and allowed to adhere for 30 min at 37°C. The cells were then fixed with 3.7% paraformaldehyde, 60 mM sucrose in TBS, followed by 20% methanol, and staining in 0.5% crystal violet in 20% methanol. Stained cells were washed with water and the dye was solubilized with 0.1 M sodium citrate, pH 4.2, 50% ethanol. Attachment was quantitated by measuring the absorbance at 600 nm.
125I cell surface labeling and affinity chromatography
The procedure was a modification of the procedure used to isolate the fibronectin receptor and other integrins [27, 28]. The affinity resins were prepared by coupling fibronectin, III1-C or III 11-C to CNBr-activated Sepharose CL-4B according to the manufacturer's recommendations. The concentration of protein was typically 4–5 mg fibronectin/ml of resin, or 8–10 mg protein/ml of resin for III1-C and III 11-C. Ten 15-cm dishes of RASMCs were washed twice with PBS, then harvested by detachment of cells in PBS + 10 mM EDTA. The cells were washed twice more with PBS, then resuspended at 4 × 107 cells/ml in PBS. Cells were labeled with 1 mCi Na125I and lactoperoxidase-H2O2, as previously described . After labeling the cell pellet was washed with ice-cold PBS + NaN3, then lysed in 2 volumes of OG Lysis Buffer (200 mM octylglucoside, 1 mM CaCl2, 1 mM MgCl2, TBS, PMSF) at 4°C. The lysate was spun at 14,000 × g for 15 min at 4°C, and the supernatant was used for affinity chromatography. Lysate was applied to the affinity columns (0.2 ml lysate was applied to 0.1 ml affinity matrix bed volume), flow through fractions were collected and passed over the columns twice more. Columns were washed with 10 column volumes of Wash Buffer (40 mM octylglucoside, 1 mM CaCl2, 1 mM MgCl2, TBS), before elution of bound protein with 10 mM EDTA in Wash Buffer. Samples from the final wash and eluted samples were separated on 4–20% gradient Novex gels, the gels were dried and exposed to phosphorimager cassette and the radioactive signal was measured with a Storm phosphorimager instrument.
MAPK assay and immunoblotting
Wells of a 6-well plate were coated with either 20 μg/ml fibronectin, 25 μM III1-C or 25 μM III 11-C for 1 hr at RT. Wells were washed 3 times with PBS before adding cells. Growing RASMCs were harvested by trypsinization and collected into DMEM + 0.5% BSA + soybean trypsin inhibitor. Cells were washed 3 times with DMEM + 0.5% BSA, then resuspended at 3 × 105 cells/ml in DMEM + 0.5% BSA with or without integrin blocking agents or other additions, as described in the figure legends. Cells were either left in suspension (for suspended and PDGF stimulated samples) or were seeded onto the coated wells (1 ml per well) and allowed to adhere for 30 min at 37°C, or for the times indicated in the figure legend (Fig. 5). The cells stimulated with PDGF (2 ng/ml PDGF-BB) received the growth factor 10 min before collecting the cells for lysis, while the other samples received no growth factor or serum. After the adhesion period plates were placed on ice, unattached cells were collected and spun down, while cell monolayers were washed once with ice cold PBS then lysed with SDS-PAGE sample buffer (100 μl/well). Centrifuged pellets of unattached cells were combined with the appropriate monolayer lysate sample and the samples were heated to 100°C for 5 min. Samples were separated on 4–20% gradient Novex gels, transferred to Immobilon P membranes, blocked with 5% nonfat dry milk in TBS-Tween, then probed with anti-phospho-p44/42 MAPK antibody according to the manufacturer's recommendations. Blots were then stripped in Stripping Buffer (2% SDS, 100 mM β-mercaptoethanol, 62.5 mM Tris, pH 6.7) at 50°C for 30 min, washed 4 times with TBS-Tween, blocked with 5% nonfat dry milk in TBS-Tween, then probed with anti-p44/42 ERK antibody according to the manufacturer's recommendations. All blots were developed with the ECL plus reagent and exposed to Hyperfilm. For both antibodies the typical exposure times were under 5 min.
Heparitinase treatment of cells and lysates
6 well plates were coated with either fibronectin, III1-C or III 11-C as described above. Growing RASMCs were harvested by trypsinization and washed in DMEM + BSA as described above. For GAGase treatment of intact cells, the cells remained in suspension and received either no enzyme or 0.1 u/ml heparitinase or 0.1 u/ml chondroitinase ABC for 1 hr at 37°C with constant gentle rotation. Cells were then plated onto precoated dishes and processed for immunoblotting with anti-phospho-p44/42 MAPK antibody as described above. Alternatively, after heparitinase digestion cells were lysed directly in SDS sample buffer and analyzed by immunoblotting with the 3G10 mAb (essentially as described above for anti-phospho-p44/42 MAPK immunoblotting).
For GAGase treatment of cell lysates, cells were lysed on ice in NP40 Lysis buffer (1% Nonidet P 40, 150 mM NaCl, 50 mM Tris, pH 8.0) plus protease inhibitors (Complete™ protease inhibitor cocktail) at 2 × 106 cells/ml. Insoluble material was removed by centrifugation at 14,000 × g for 15 min at 4°C. Lysate was prepared for heparitinase treatment by adding CaCl2 to 10 μM final concentration. Heparitinase was added to 0.1 u/ml final concentration and the lysate was incubated at 37°C for 1 hr. The lysate was then applied to affinity chromatography columns as described below.
35SO4 labeling and affinity chromatography
Growing RASMCs labeled for 20 hr at 37°C with 200 μCi/ml 35S04 in DMEM + 10% dialyzed FCS + Pen-Strep. Cells were placed on ice, washed once with PBS, then lysed in NP40 Lysis buffer as described above. III1-C and III 11-C columns were produced as described above. Cell lysates were applied to III1-C or III 11-C columns (typically 500 μl lysate was applied to 250 μl affinity matrix bed volume), flow through fractions were collected and passed over the columns twice more. The final flow through fractions were then collected. Columns were washed with 10 column volumes of NP40 Lysis buffer, then bound material was removed by boiling the Sepharose beads in 2 column volumes of SDS sample buffer. Alternatively, the bound material was first eluted with 2 column volumes of 8 M urea buffer (8 M urea, 0.1 M NaH2PO4, 10 mM Tris, pH 8.0), followed by washing with 10 column volumes of NP40 Lysis buffer, and then removing any remaining bound material by boiling the Sepharose beads in SDS sample buffer. Samples were separated on 4–20% Novex SDS-PAGE gels, the gels were fixed and dried and the radioactive material was detected by using a phosphorimager.
Hynes RO: Fibronectins. New York: Springer-Verlag;. 1990
Morla A, Zhang Z, Ruoslahti E: Superfibronectin is a functionally distinct form of fibronectin. Nature. 1994, 367: 193-196. 10.1038/367193a0.
Bourdoulous S, Orend G, MacKenna DA, Pasqualini R, Ruoslahti E: Fibronectin matrix regulates activation of RHO and CDC42 GTPases and cell cycle progression. J Cell Biol. 1998, 143: 267-276. 10.1083/jcb.143.1.267.
Mercurius KO, Morla AO: Inhibition of vascular smooth muscle cell growth by inhibition of fibronectin matrix assembly. Circ Res. 1998, 82: 548-556.
Saulnier R, Bhardwaj B, Klassen J, Leopold D, Rahimi N, Tremblay E, Mosher D, Elliott B: Fibronectin fibrils and growth factors stimulate anchorage-independent growth of a murine mammary carcinoma. Exp Cell Res. 1996, 222: 360-369. 10.1006/excr.1996.0045.
McDonald JA: Extracellular matrix assembly. Annual Review of Cell Biology. 1988, 4: 183-207. 10.1146/annurev.cb.04.110188.001151.
Mosher DF, Sottile J, Wu C, McDonald JA: Assembly of extracellular matrix. Curr Opin Cell Biol. 1992, 4: 810-818.
Schwarzbauer JE, Sechler JL: Fibronectin fibrillogenesis: a paradigm for extracellular matrix assembly. Curr Opin Cell Biol. 1999, 11: 622-627. 10.1016/S0955-0674(99)00017-4.
Wu C, Hughes PE, Ginsberg MH, McDonald JA: Identification of a new biological function for the integrin alpha v beta 3: initiation of fibronectin matrix assembly. Cell Adhes Commun. 1996, 4: 149-158.
Wu C, Keivens VM, O'Toole TE, McDonald JA, Ginsberg MH: Integrin activation and cytoskeletal interaction are essential for the assembly of a fibronectin matrix. Cell. 1995, 83: 715-724.
Wennerberg K, Lohikangas L, Gullberg D, Pfaff M, Johansson S, Fassler R: Beta 1 integrin-dependent and -independent polymerization of fibronectin. J Cell Biol. 1996, 132: 227-238.
Wu C, Bauer JS, Juliano RL, McDonald JA: The alpha 5 beta 1 integrin fibronectin receptor, but not the alpha 5 cytoplasmic domain, functions in an early and essential step in fibronectin matrix assembly. J Biol Chem. 1993, 268: 21883-21888.
Ruoslahti E: Integrins. J clin Invest. 1991, 87: 1-5.
Sechler JL, Cumiskey AM, Gazzola DM, Schwarzbauer JE: A novel RGD-independent fibronectin assembly pathway initiated by alpha4 beta 1 integrin binding to the alternatively spliced V region. J Cell Sci. 2000, 113: 1491-1498.
Morla A, Ruoslahti E: A fibronectin self-assembly site involved in fibronectin matrix assembly: reconstruction in a synthetic peptide. J Cell Biol. 1992, 118: 421-429.
Hocking DC, Smith RK, McKeown-Longo PJ: A novel role for the integrin-binding III-10 module in fibronectin matrix assembly. J Cell Biol. 1996, 133: 431-444.
Hocking DC, Sottile J, McKeown-Longo PJ: Fibronectin's III-1 module contains a conformation-dependent binding site for the amino-terminal region of fibronectin. J Biol Chem. 1994, 269: 19183-19187.
Aguirre KM, McCormick RJ, Schwarzbauer JE: Fibronectin self-association is mediated by complementary sites within the amino-terminal one-third of the molecule. J Biol Chem. 1994, 269: 27863-27868.
Chernousov MA, Fogerty FJ, Koteliansky VE, Mosher DF: Role of the 1–9 and III-1 modules of fibronectin in formation of an extracellular fibronectin matrix. J Biol Chem. 1991, 266: 10851-10858.
McKeown-Longo PJ, Mosher DF: Interaction of the 70,000-mol-wt amino-terminal fragment of fibronectin with the matrix-assembly receptor of fibroblasts. J Cell Biol. 1985, 100: 364-374.
Quade BJ, McDonald JA: Fibronectin's amino-terminal matrix assembly site is located within the 29-kDa amino-terminal domain containing five type I repeats. J Biol Chem. 1988, 263: 19602-19609.
Schwarzbauer JE: Identification of the fibronectin sequences required for assembly of a fibrillar matrix. J Cell Biol. 1991, 113: 1463-1473.
Sechler JL, Schwarzbauer JE: Control of cell cycle progression by fibronectin matrix architecture. J Biol Chem. 1998, 273: 25533-25536. 10.1074/jbc.273.40.25533.
Darribere T, Schwarzbauer JE: Fibronectin matrix composition and organization can regulate cell migration during amphibian development. Mech Dev. 2000, 92: 239-250. 10.1016/S0925-4773(00)00245-8.
Yi M, Ruoslahti E: A fibronectin fragment inhibits tumor growth, angiogenesis, and metastasis. Proc NatI Acad Sci USA. 2001, 98: 620-624. 10.1073/pnas.98.2.620.
Glukhova MA, Koteliansky VE: Integrins, cytoskeletal and extracellular matrix proteins in developing smooth muscle cells of human aorta. San Diego: Academic Press Inc;. 1995
Pytela R, Pierschbacher MD, Ruoslahti E: Identification and isolation of a 140 kd cell surface glycoprotein with properties expected of a fibronectin receptor. Cell. 1985, 40: 191-198.
Pytela R, Pierschbacher MD, Argraves S, Suzuki S, Ruoslahti E: Arginine-glycine-aspartic acid adhesion receptors. Methods in Enzymology. 1987, 144: 475-489.
Argraves WS, Pytela R, Suzuki S, Millan JL, Pierschbacher MD, Ruoslahti E: cDNA sequences from the alpha subunit of the fibronectin receptor predict a transmembrane domain and a short cytoplasmic peptide. J Biol Chem. 1986, 261: 12922-12924.
Pierschbacher MD, Hayman EG, Ruoslahti E: Location of the cell-attachment site in fibronectin with monoclonal antibodies and proteolytic fragments of the molecule. Cell. 1981, 26: 259-267.
Pierschbacher MD, Ruoslahti E: Cell attachment activity of fibronectin can be duplicated by small synthetic fragments of the molecule. Nature. 1984, 309: 30-33.
Giancotti FG, Ruoslahti E: Integrin Signaling. Science. 1999, 285: 1028-1032. 10.1126/science.285.5430.1028.
Guan JL: Focal adhesion kinase in integrin signaling. Matrix Biol. 1997, 16: 195-200. 10.1016/S0945-053X(97)90008-1.
Hynes RO: Integrins: versatility, modulation, and signaling in cell adhesion. Cell. 1992, 69: 11-25.
Juliano RL, Haskill S: Signal transduction from the extracellular matrix. J Cell Biol. 1993, 120: 577-585.
Robinson MJ, Cobb MH: Mitogen-activated protein kinase pathways. Curr Opin Cell Biol. 1997, 9: 180-186. 10.1016/S0955-0674(97)80061-0.
David G, Bai XM, Van der Schueren B, Cassiman JJ, Van den Berghe H: Developmental changes in heparan sulfate expression: in situ detection with mAbs. J Cell Biol. 1992, 119: 961-975.
Wilson KE, Li Z, Kara M, Gardner KL, Roberts DD: Beta 1 integrin- and proteoglycan-mediated stimulation of T lymphoma cell adhesion and mitogen-activated protein kinase signaling by thrombospondin-1 and thrombospondin-1 peptides. J Immunol. 1999, 163: 3621-3628.
Carey DJ: Syndecans: multifunctional cell-surface co-receptors. Biochem J. 1997, 327: 1-16.
Bernfield M, Kokenyesi R, Kato M, Hinkes MT, Spring J, Gallo RL, Lose EJ: Biology of the syndecans: a family of transmembrane heparan sulfate proteoglycans. Annual Review of Cell Biology. 1992, 8: 365-393. 10.1146/annurev.cb.08.110192.002053.
Bloom L, Ingham KC, Hynes RO: Fibronectin regulates assembly of actin filaments and focal contacts in cultured cells via the heparin-binding site in repeat III13. Mol Biol Cell. 1999, 10: 1521-1536.
Saoncella S, Echtermeyer F, Denhez F, Nowlen JK, Mosher DF, Robinson SD, Hynes RO, Goetinck PF: Syndecan-4 signals cooperatively with integrins in a Rho-dependent manner in the assembly of focal adhesions and actin stress fibers. Proc NatI Acad Sci USA. 1999, 96: 2805-2810. 10.1073/pnas.96.6.2805.
Woods A, Couchman JR: Syndecan 4 heparan sulfate proteoglycan is a selectively enriched and widespread focal adhesion component. Mol Biol Cell. 1994, 5: 183-192.
Woods A, Oh ES, Couchman JR: Syndecan proteoglycans and cell adhesion. Matrix Biol. 1998, 17: 477-483. 10.1016/S0945-053X(98)90095-6.
Woods A, Couchman JR: Syndecans: synergistic activators of cell adhesion. Trends Cell Biol. 1998, 8: 189-192. 10.1016/S0962-8924(98)01244-6.
Bormfeldt KE, Campbell JS, Koyama H, Argast GM, Leslie CC, Raines EW, Krebs EG, Ross R: The mitogen-activated protein kinase pathway can mediate growth inhibition and proliferation in smooth muscle cells. Dependence on the availability of downstream targets. J Clin Invest. 1997, 100: 875-885.
O'Reilly MS, Boehm T, Shing Y, Fukai N, Vasios G, Lane WS, Flynn E, Birkhead JR, Olsen BR, Folkman J: Endostatin: an endogenous inhibitor of angiogenesis and tumor growth. Cell. 1997, 88: 277-285.
Karumanchi SA, Jha V, Ramchandran R, Karihaloo A, Tsiokas L, Chan B, Dhanabal M, Hanai JI, Venkataraman G, Shriver Z, Keiser N, Kalluri R, Zeng H, Mukhopadhyay D, Chen RL, Lander AD, Hagihara K, Yamaguchi Y, Sasisekharan R, Cantley L, Sukhatme VP: Cell surface glypicans are low-affinity endostatin receptors. Mol Cell. 2001, 7: 811-822. 10.1016/S1097-2765(01)00225-8.
Rehn M, Veikkola T, Kukk-Valdre E, Nakamura H, Ilmonen M, Lombardo C, Pihiajamemi T, Alitalo K, Vuori K: Interaction of endostatin with integrins implicated in angiogenesis. Proc Natl Acad Sci USA. 2001, 98: 1024-1029. 10.1073/pnas.031564998.
Engvall E, Ruoslahti E: Binding of soluble form of fibroblast surface protein, fibronectin, to collagen. International Journal of Cancer. 1977, 20: 1-5.
Blank RS, Thompson MM, Owens GK: Cell cycle versus density dependence of smooth muscle alpha actin expression in cultured rat aortic smooth muscle cells. J Cell Biol. 1988, 107: 299-306.
Kornblihtt AR, Umezawa K, Vibe-Pedersen K, Baralle FE: Primary structure of human fibronectin: differential splicing may generate at least 10 polypeptides from a single gene. Embo J. 1985, 4: 1755-1759.
We are grateful to Drs. Nancy Schwartz and Miriam Domowicz (Univ. of Chicago) for their generous gifts of glycosaminoglycans and for helpful discussions and comments on the manuscript. We also thank Tim Carlson and Patrick Cullinan for careful review of the manuscript. We wish to thank Dr. Erkki Ruoslahti (Burnham Institute) for anti-FN antibodies. This work was supported by grants R01 HL-59962 from the National Heart, Lung, and Blood Institute and by Grant-In-Aid #95014530 from the American Heart Association to AOM.
Authors’ original submitted files for images
Below are the links to the authors’ original submitted files for images.
About this article
Cite this article
Mercurius, K.O., Morla, A.O. Cell adhesion and signaling on the fibronectin 1st type III repeat; requisite roles for cell surface proteoglycans and integrins. BMC Cell Biol 2, 18 (2001). https://doi.org/10.1186/1471-2121-2-18
- Dermatan Sulfate
- NP40 Lysis Buffer
- Cell Binding Domain
- Cell Surface Proteoglycan
- Cell Surface Heparan Sulfate Proteoglycan