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Model based dynamics analysis in live cell microtubule images
BMC Cell Biology volume 8, Article number: S4 (2007)
Abstract
Background
The dynamic growing and shortening behaviors of microtubules are central to the fundamental roles played by microtubules in essentially all eukaryotic cells. Traditionally, microtubule behavior is quantified by manually tracking individual microtubules in timelapse images under various experimental conditions. Manual analysis is laborious, approximate, and often offers limited analytical capability in extracting potentially valuable information from the data.
Results
In this work, we present computer vision and machinelearning based methods for extracting novel dynamics information from timelapse images. Using actual microtubule data, we estimate statistical models of microtubule behavior that are highly effective in identifying common and distinct characteristics of microtubule dynamic behavior.
Conclusion
Computational methods provide powerful analytical capabilities in addition to traditional analysis methods for studying microtubule dynamic behavior. Novel capabilities, such as building and querying microtubule image databases, are introduced to quantify and analyze microtubule dynamic behavior.
Background
Microtubules (MTs) are filamentous cytoskeletal structures composed of tubulin protein subunits. These subunits can associate with, or dissociate from, existing tubulin polymers rapidly, making MTs highly dynamic. Through these dynamic behaviors, MTs are critically involved in many essential cellular functions. MT dynamics are finely regulated in the cell, [1]. It has been hypothesized that inadequate regulation of neuronal MT dynamics may underlie neuronal cell death in Alzheimer's and related dementias, [2]. Additionally, drug induced modulation of MT dynamics underlies the effectiveness of various anticancer drugs, such as Taxol, [3]. For these and a host of basic biology issues, the regulation of MT dynamics is a very active area of research in modern cell biology.
A key tool of MT dynamics research is to track the growing and shortening behaviors of individual MT tips from timelapse images (Fig. 1), and quantitatively describe MT behavior under different experimental conditions. Traditional MT dynamics parameters consist of statistics derived from the growth and shortening events between consecutive frames. In general, tracking is a largely manual and laborious task, [4]. Furthermore, it is approximate (Fig. 2), variable between users and labs, and potentially biased for more dynamic MTs, [5]. The resulting quantification and analysis capabilities are limited with manual feasibility. For example, while MT deformations may contain valuable information in studying neuronal growthcone path finding, it is impractical to manually collect relevant data, e.g. curvature or orientation, from many MTs. Additionally, due to the laborious nature of manual data collection, a limited sample for each experimental condition must represent all MTs collected in that condition. While different subsets of MTs undertake distinct tasks in the cell, and therefore can exhibit distinct dynamic characteristics, generally there are limited means of observing such dynamics in isolation through manual methods. Analysis of dynamic behavior is further limited by pairwise comparisons of behavioral features between control and treated conditions. Therefore, computational methods could make an immediate contribution to MT dynamics research.
In this work, we propose a powerful approach for analyzing MT dynamic behavior. Briefly, we use an automated tracking method for measuring MT dynamics, which are then modeled as MT behavior patterns by Hidden Markov Models. The proposed methods go beyond the traditional analysis capabilities and offer new insights in investigating MT dynamic behavior.
Microtubule structure and function
The cytoskeleton of a eukaryotic cell consists of a network of fibers. MTs are one of the three principal types of cytoskeletal fibers. They are hollow cylindrical structures, 25 nm in diameter and up to several μ m in length, consisting of noncovalently bound tubulin protein subunits. MTs are constantly assembled and disassembled, making the cytoskeleton a dynamic system. MTs are critically involved in a number of essential cellular functions, such as chromosome segregation at mitosis and intracellular cargo transport. Additional background information on MT structure and function can be found in [1].
The growing and shortening dynamics of MTs are finely regulated, for example, by the action of MTassociated proteins (MAP) and MTtargeted drugs (MTD). A large body of evidence, reviewed by Feinstein and Wilson [2], suggest that cell viability requires that MT dynamics be properly regulated within a narrow range. Common conjecture is that certain diseases such as Alzheimers and cancer are at least correlated with the regulatory abnormalities in MT dynamics, [6–8]. Consequently, gaining a detailed mechanistic understanding of the regulatory activities of MAPs, [5, 6, 9], and MTDs, [3, 10], is a major focus of current research. A major challenge is assessing the activities of the large number of MAPs and their many isoforms, as well as the large number of MTDs and their many derivatives. For instance, the MAP tau consists of 441 amino acids, more than 25 of which can be phosphorylated in various combinatorial patterns. Whereas phosphorylation normally serves to regulate tau activity, excessive and abnormal phosphorylation correlates with cell death and dementia. Thus, to fully understand normal and pathological tau action, the regulatory effects of the many different combinational phosphorylation patterns of tau must be understood.
Current analysis method
MTs are polar structures, possessing biochemically distinct minus and plus ends. Conventionally, the minus end of a MT is assumed to be fixed at the MT organizing center near the nucleus, and the other end the plus end or the tip is the dynamic end that is observed in most MT dynamics studies. Typically, in live cell studies, minus ends of the MTs are not visible because of the high density of MTs converging on the organizing center. Thus, in calculating the MT length, a point on the MT body is selected as a reference point, origin, after an initial observation of all frames in the timelapse images, (Fig. 2).
Traditionally, timelapse images of MT populations are collected following treatment with MTDs or MAPs. Dynamics parameters are then manually calculated from image sequences as follows. The positions of MT plus ends are manually tracked individually across all frames, (Fig. 1). MT lengths are approximated as the (Euclidean) distance between tracked tip positions and the origin, producing MT life histories or tracks, (Fig. 2). The change in MT length is computed between consecutive frames, and growth and shortening statistics are tabulated. Length changes below a threshold are marked as attenuation or pause, signifying undetectable change. Other biologically significant events are the conversion of a MT from a growing state to rapid disassembly, designated as a catastrophe, and a subsequent potential recovery from shortening to attenuation or growth, called rescue. To estimate the effects of a regulatory agent upon MT dynamics, these statistics are aggregated over a number of MTs from the same experimental condition. Resulting statistics of each condition are compared with the control behavior to quantify the effects of the examined agent on dynamics parameters.
In this fashion, regulatory effects of each individual agent are studied through a laborious set of tasks. Quantifying sufficient image data to achieve statistical significance and limited comparative capabilities in the presence of innumerous possible agents pose an enormous challenge to researchers. Example studies are [3, 5, 9–12].
Statistics obtained from the growth and shortening events treat these events independently, rather than as being part of a behavior pattern. For instance, a certain growth measurement is counted as the same event regardless of where it occurs in relation to preceding or subsequent events. Furthermore, studying event correlations between neighboring MTs are generally infeasible, despite potential biological significance.
There are no established nonmanual methods for examining the similarities and differences in particular dynamic behaviors imposed by various agents. Furthermore, studying combined effects of multiple regulatory agents is difficult, due to the limitations imposed by the pairwise comparisons between experimental conditions. For example, consider a hypothetical MTD AB, derived from MTDs A and B. In order to understand the contributions of A and B, multiple individual experiments must be conducted. Therefore, quantifying behavioral similarities across experimental conditions may provide essential guidance in constructing hypotheses.
In this work, we propose an automated tracking and analysis method to address the limitations mentioned above. The tracking component provides behavioral features for subsequent analysis. We define the MT dynamic behavior as a sequence of changes in MT length over equal time intervals. Experimental conditions may exhibit a number of behavioral patterns, which are estimated in parametric form by a mixture of Hidden Markov Models. By using a modelbased clustering technique, we propose to analyze the constituent parts of MT behavior in each experimental condition. Thus, each experimental condition can be described as a mixture of behaviors exhibited by different MT populations. Through estimated average behavior patterns, we introduce a probabilistic behavioral distance measure between experimental conditions. Furthermore, parameters of individual models may present significant information about the properties of corresponding behavioral patterns. We describe how modelbased analysis can be effective in addressing the above limitations (see Discussion).
Results
We present statistical models of MT behavior that are estimated using automatically tracked MT dynamics data. As a comparison, we provide models of manually collected MT tracks. We describe the results of automated tracking using visual samples and associated errors.
Quantifying microtubule dynamics by automated tracking
For quantifying MT growth and shortening, we used the tracking method proposed in [13]. In the spatiotemporal graph matching (see Methods), up to three missing frames between tips of the same MT track were allowed. The computation of the geodesics, the distances for the weights on the graph, and the selection of a fixed point on the MT body were carried out using the Fast Marching algorithm, [14]. Visual tracking results are shown in (Fig. 3, 4, 5, 6, 7).
Quantitative results of MT tracking were given in [13]. Evaluations against manually tracked data shows that the mean and the standard deviation of tracking error are 2.85 and 4.36 pixels, respectively. This error level is acceptable for biological studies. Recall that the MT width is 25 nm (see Background), which appears as curves that are 3 pixels in width. Thus, a growth or shortening event that is less than 3 pixels would correspond to an event that is too small to quantify reliably, and is considered as attenuation.
We note that the tracking performance is sensitive to the accuracy of initial tip detection step. Furthermore, the proposed approach requires multiple tips to be detected for reliable extraction of MT tracks by design. In other words, the tracking performance may be adversely affected in tracking MTs individually, which may limit the ability to track a particular MT in a cell. Finally, intersecting MTs may steal the body trace, as the geodesic distance will favor higher intensity levels, (Fig. 3d – 3f). This issue could be addressed with further constraints on the MT orientation and curvature. However, in this work, we limit the behavioral features to the observed change of length in the MT plus end, which only requires consistent estimation of the MT body.
While tracking performance may be improved as a consequence of higher image quality and suitable algorithms targeting frequent intersections, deformations, and intensity variations. In its current state, automated tracking can track and quantify 10 times more MT tracks per image sequence than manual methods. With this increase in analyzable data volume, we are able to estimate behavior models for different experimental conditions. Estimated statistical models of MT dynamic behaviors are presented in the next section.
Statistical models of microtubule behavior
In this work, we used MT timelapse live cell images from [10]. The authors of [10] investigate the hypothesis that resistance to Taxol may involve altered sensitivity to different tubulin isotypes. Chinese hamster ovary (CHO) cells were microinjected with rhodaminelabeled tubulin. A total of 111 sequences were acquired using fluorescence microscopy with a 100× objective lens (1000× magnification). 25 frames per sequence were captured at 4 second intervals, from five different conditions.
Growth and shortening rates were computed as the differences of a MT lengths between consecutive frames, measured in pixels. Thus, each track consists of an observation sequence composed of 25 points in time. Resulting observation sequences were in the range [13.03, 11.22] pixels, where () and (+) denoting shortening and growth rates, respectively.
The study in [10] analyzes the potential for Taxol (a cancer therapeutic) resistance in cells expressing different tubulin isoforms. Five experimental conditions were recorded, Table 1. Results in [10] show that two groups of EC exhibit different dynamics: {EC_{1}, EC_{2}, EC_{4}} vs. {EC_{3}, EC_{5}}, where the MTs in the first group are more dynamic than the ones in the second group. It is also reported that EC_{4} is more dynamic than EC_{5}. In this work, we evaluated our modeling approach using both automatically (3068 tracks) and manually (210 tracks) tracked MTs, Table 1.
The first experiment was designed to confirm biological results. A classification score between EC_{4} and EC_{5}, denoted by EX:A, and between condition groups {EC_{3}, EC_{5}} and {EC_{1}, EC_{2}, EC_{4}}, denoted by EX:B, were computed with a 3way crossvalidation, Table 2. Well defined separations between the two groups and between Taxoltreated and control tracks agree with established biological findings. A third test, denoted by EX:C, was aimed to separate EC_{3} from EC_{5}. Biological results indicate that these experimental conditions exhibit highly similar dynamics. A maximum separation of much less than EX:A and EX:B verify this finding.
The same set of experiments were repeated with manually tracked MT data. Separation results are shown in Table 2. Similar classification rates with the automatically tracked experiments confirm the automated tracking as well as the applicability of model based analysis.
Our HMM implementation was derived from [15]. Experimentation with both leftright and fully connected HMMs revealed that fully connected models were better suited for the modeling task, in line with biological input. Growth and shortening rates were assumed to be drawn from Gaussian emissions. It should be noted that the number of larger growth and shortening events decrease exponentially as the length of the event increases. Therefore, using exponential emission distributions may be appropriate. However, detection of events measuring less than 3 pixels may be unreliable for both manual and automated tracking (see Current analysis method). Since good initialization values are essential with continuous emission distributions, we derived statistics from observation vectors for initializing emissions. Transition and state priors were initialized randomly, and the number of clusters was determined experimentally, Table 3.
Ultimately, statistics collected by the model parameters are more significant in biological studies than the classification scores. To that end, we examine the models of each EC. Table 4 shows emission distributions of selected component models used in EX:A. The models were estimated by using automatically tracked MTs. Table 5 shows the corresponding models estimated with manual tracks. The first rows in each model correspond to the mean length change captured by that model state (q_{ i }), where negatives indicate shortening. Nearly all states of λ_{4} show stable distributions, while states in λ_{5} show significantly more dynamic behavior. Both models have states exhibiting stable growth and shortening, indicating that the main discriminating factor between the two behavior patterns are the large growth and shortening events occurring occasionally. Naturally, the average growth and shortening rates captured in model states are direct results of the observations, and they confirm that Taxoltreated MTs show suppressed dynamics with β Itubulin than nontreated MTs.
Discussion
Estimated models can provide more descriptive information about the behavior patterns than what is available through manual methods: (i) typical growth and shortening states of the modified behavior, and (ii) the transition probabilities between these states. For example, as a direct comparison with manual methods, besides the traditional catastrophe and rescue frequencies, transitions from small to larger events of the same type can be quantified. In essence, characteristics of behavior patterns are parametrically encoded in models, which can then be used in generating these behaviors. We describe further modelbased analysis capabilities in the next section.
Novel analytical capabilities
The proposed approach provides a number of novel analytical capabilities (see Background). The most important aspect of this approach is using entire MT life histories as opposed to parsing the events into predefined categories. Therefore, events are evaluated for their contribution in different behavior patterns. With the introduction of this method, it becomes possible to compare effects of regulatory agents at different levels: (i) the constituent parts of behavioral characteristics through examining representative model parameters, and (ii) by quantifying the overall behavioral dissimilarity. Distance measures between behavior patterns w, and between experimental conditions EC, can be defined as model distances. One possible measure between models λ_{w 1}and λ_{w 2}, for a set of observations O_{w 1}and O_{w 2}can be defined as
where L(w_{1}, w_{2}) is given by
By quantifying behavioral comparisons between regulatory agents, studying combined effects of multiple regulatory agents may be guided with enhanced predictions. We envision a repository of MT dynamics data that can be probabilistically queried for behavioral similarities for a new regulatory agent, an isotype, or a combination. This can be done by evaluating p(OEC) for an experimental condition EC, or evaluating p(Ow) for behavioral pattern w. Assuming that the tracking and modeling tasks were undertaken, a MT image database would contain a collection of individual MT tracks and model parameters representing w, in addition to original image sequences. Model based content retrieval provides additional advantages in query design. Hypothesized behaviors can be created and queried by manually selecting model parameters. Alternatively, query models can be estimated from a subset of MT tracks in the database.
To study spatial relationships between MTs behaviorally, tracks can be grouped and visualized based on their behavior characteristics. For example, (Fig. 8) shows frames from EC_{5}, with overlaid tracks. All tracks were evaluated for their similarity to conditions EC_{4} and EC_{5}. In (Fig. 8), values of p(trackEC_{5}) were quantized into four categories, indicated by four different shades of red channel, and were superimposed on MTs for illustration purposes. Darker shades indicate lower probability, e.g. behavioral association between the condition and the track.
This analysis provides the researcher with visual cues about regional dynamics within a cell. This may be especially important in studies of polarized cell types, such as neurons, where specific regional regulation of dynamics is critical to processes such as outgrowth and transport. Behavioral comparisons in adjacent populations may provide insight to the inner workings of flux between the soluble and polymeric tubulin fractions within the cytoplasm. The ratio between these two functionally distinct, but codependent phases may indicate cellautonomous or druginfluenced regulation.
Conclusion
MT dynamics research seeks to understand the complex mechanisms that underlie cytoskeletal responses to changes in environmental conditions. A clear understanding of the regulation of MT dynamic behavior may elucidate causal factors in various diseases and may reveal new therapeutic targets and strategies. In this work, we introduce novel data collection and analysis capabilities based on computer vision and machine learning tools. With the proposed methods, researchers can study MT dynamics with improved spatial and temporal quantification.
The most notable contribution of the proposed method is the novel analysis capabilities that are beyond the current stateoftheart. Other contributions are the improvements over the manual data collection methods, such as higher accuracy (length along the MT vs Euclidean estimate), increased number of analyzable MT tracks, and objective consideration of all MT tracks at a fraction of the normally required time. Our preliminary results support manually established findings, and show that automated analysis of spatial and temporal patterns offers previously unattainable insights. Most notably, the standardization of data collection and analysis facilitates a comparative platform for future biological research.
As the volume and number of dynamics datasets has increased in recent years, similarities between the behavioral influence of MAPs and MTDs upon dynamics have emerged, leading to speculation of similar mechanisms. Dynamics models may facilitate the union of previously isolated MAP and MTD datasets, furthering our understanding of regulatory mechanisms of MTs.
Despite the difficulties inherent in fluorescence imaging, the proposed approach confirms manual findings in both track computation and in analysis. For example, due to photobleaching, observation durations were generally limited to only a few minutes with very low signaltonoise ratios in images. With emerging techniques in microscopy and probes, such as the tipbinding proteins (EB1), much longer acquisition times will be possible with superior image quality. Our goal is to track all MTs in live cell images at longer durations. In this direction, the tracking method can be improved by reliably identifying all MTs individually. The nature of live cell MT images requires that frequent intersections, abrupt intensity variations on a single MT body, and focusing issues must be addressed adequately.
Methods
The proposed analysis system evaluates MT dynamic behavior as a function of entire MT life histories through estimating statistical models from observations. A number of MT tracks per experimental condition is necessary for reliable estimates of model parameters. Thus, an automated tracking procedure was used in data collection.
Automated tracking
To achieve reliable models of MT behavior, numerous observations (MT tracks) are needed. Automated MT tracking provides a significant increase in analyzable data volume. The MT tracking problem has a short history in the literature, since live cell MT imaging has only been a mainstream research tool for about a decade. However, similar problems, such as the tracing of curvilinear structures in images, were previously addressed on neurons, blood vessels, roads, and so on. The most notable difference in MT images is the use of fluorescence, which presents additional difficulties in image analysis. For example, photobleaching, the gradual decay of fluorescence, causes illumination variations. Another issue is the additive nature of fluorescence. Overlapping MTs result in brighter regions in images, causing frequent over saturation. In (Fig. 9), such saturation is visible in lower regions of frames. Additionally, sample fluorescence exacerbates offfocus blur, which produces great challenges in detecting MT tips moving in and out of focus.
Previous work on automated MT detection and tracking include [16–18]. In [13, 19], we described our tracking approach for live cell images and introduced the idea of model based analysis. In [16], the authors extract MT plus ends using a MT body and a tip model in a multiscale operation. In [17] and [18], MTs are traced in segments from initially selected points and subsequently tracked. In [17], MTs are searched in a constrained space for tracking in subsequent frames.
In this work, we used the tracking method from [13]. Conceptually, the proposed approach consists of three components, (Fig. 10). First, MT tip candidates are extracted in every frame of the image sequence. Then, tip correspondences between frames are established into MT tip tracks. Finally, the MT bodies are traced from the tips to extract dynamics information.
An automated MT tracking method should address the following: (i) highly variable tubule shapes, (ii) accurate estimation of the MT length considering the nonlinear shape, (iii) frequent occlusions and intersections from surrounding MTs, and (iv) low signaltonoise ratios with spatial and temporal variations in illumination.
To address these issues, we consider MTs as flexible open curves in the image plane, with a fixed minus end near the nucleus and a dynamic plus end. Formally, a single MT is modeled by the open curve C(s), where s ∈ [0, 1] is the curve parameter. The goal of the MT tracking task is to estimate the MT length by locating the tip and tracing the deformation of the MT body, in every frame.
Estimating microtubule tip positions
To address noise and illumination variations, we process the MT images with a line filter. Let I denote the intensity function in a frame, then the filter output is given by
where the derivative of the Gaussian is taken along orientations θ at position (x, y), and σ is chosen as the average MT width. The maximum filter response, I^{f}(x, y), is then binarized to generate a mask showing MT polymer mass. The binary mask is used for determining tip candidates in each frame. Example tip detection results from consecutive frames are shown in (Fig. 9).
Once the tip candidates are located in each frame, correspondences are established between frames by using a multiframe graph matching algorithm. The reasoning behind formulating the correspondence as a graph optimization problem is that by matching multiple tips at once, occasional spurious tips are removed. Furthermore, the graph matching algorithm provides the flexibility of skipping frames, which handles missing tips between frames.
Extracting microtubule tip tracks
Consider a MT timelapse image sequence with T frames. Let N_{ i }denote the number of tip candidates detected in frame i for 1 ≤ i ≤ T. Then, detected tips over the entire sequence can be individually denoted by {t}_{i}^{h} where h denotes the tip number in frame i, within the range 1 ≤ h ≤ N_{ i }. We construct a graph G = (V, E) whose vertices V are the detected tip positions in frames 1..T, and the edges E represent the similarity of tip positions between frames. Thus, we represent tracks of MT tips with paths over G, (Fig. 11). Edges between vertices in nonconsecutive frames are allowed, representing tracks with occasional missing tips.
To compute the similarity between tip positions in different frames, edge weights on G, we use the distance between tip positions constrained on a MT body. Note that the Euclidean distance cannot be used since different tips tend to move within close proximity of each other. Consider two tips {t}_{i}^{h} and {t}_{j}^{r} in two different frames f_{ i }and f_{ j }. The main idea is to check if {t}_{i}^{h} and {t}_{j}^{r} share a MT body between f_{ i }and f_{ j }. If {t}_{i}^{h} and {t}_{j}^{r} do not belong to the same MT, then their similarity is insignificant. If {t}_{i}^{h} and {t}_{j}^{r} belong to the same MT, then both growing and shortening cases should be considered between f_{ i }and f_{ j }. In the case of a growing MT, we project the position of {t}_{i}^{h} on f_{ i }to the same position on f_{ j }and compute the distance, d_{ g }({t}_{i}^{h}, {t}_{j}^{r}). We compute the shortening case, d_{ s }({t}_{i}^{h}, {t}_{j}^{r}), in the same way. Then, the weight on G between vertices {t}_{i}^{h} and {t}_{j}^{r} is computed as
Once G is constructed, we compute a maximum weight matching of G where paths correspond to MT tracks. In graph theory, a vertex disjoint path cover C is a covering of G where each vertex of G is in one and only one path of C. The weight of a path cover is defined as the sum of weights on its edges. Using the notion of path cover, the problem of finding the best MT tracks corresponds to finding the maximum weight path cover of G with the weights defined by the similarity in (4). Formally, a maximum weight path cover C(G) is a path cover which satisfies
where W(Ci)={\displaystyle {\sum}_{{e}_{uv}\in {C}_{i}}Sim({e}_{uv})} and u, v are two vertices in G for which the similarity is computed as in Eq.(4). Note that between two frames the best tracks can be computed as the maximum match of a bipartite graph. However, for multiple frames, the problem becomes NPhard. Here, we adopt the approximation proposed in [20].
The described method is sufficient to track MT tips between different frames. However, without tracing the MT body, the best estimates of MT growth and shortening would be limited to Euclidean approximations between tip positions, (see Current analysis method). Since in live cell images, the MT body is typically nonlinear, this approximation is a rough one in practice. Instead, we determine the MT body length in all frames.
Estimating microtubule body
In essence, we compute the MT body length along the body in each frame and determine the growth and shortening as consecutive length differences. Given the tip positions in each frame, we estimate the deformable curve constituting the MT body between these tips and a fixed point along the MT body. Note that the fixed point does not have to lie on the body of a specific MT for the purposes of computing the growth and shortening. In cases where the fixed point lies on another MT rather than the MT being measured, the resulting change in length is still a better estimate than the Euclidean case, so long as the fixed point taken consistently across frames. Details of fixing this point can be found in [13]. Due to the constant deformations, the fixed point location may exhibit small variations, (Fig. 5d – 5f). This is the major contributor of errors in length estimation between frames. Finally, based on the estimated plus and minus ends of the MT, the MT body is extracted using active contours with ridge features.
Model based analysis
A number of studies examined physical models for MT structure and dynamics. We refer the interested reader to [21–23], and the references therein, for a review of previous models of MT dynamic instability. For example, in [23], the authors use a simulation model to investigate the fluctuations in tubulin concentration in relation to MT dynamics. In contrast to previous dynamics models, we propose using machine learning methods for modeling various MT behavior patterns occurring in different experimental conditions.
MT behavior can be considered as a random process that evolves in time. For example, (Fig. 12) shows different behaviors of hypothetical MTs from different MT populations. MTs in the middle row exhibit a growth tendency, while MTs in the top row show several length excursions within the same amount of time. The bottom chart shows two different shortening MT groups for visual comparison of behavior patterns.
Automated tracking is sufficient to quantify traditional dynamics parameters. We propose an analysis approach targeting behavioral information beyond what is provided by the traditional parameters. We begin with including contextual information in time. In other words, as opposed to parsing the growth and shortening events out of MT tracks (life histories), we keep the MT tracks intact. Therefore, each MT track is treated as an observation from some behavior pattern. For example, the tracks in (Fig. 12, top row and middle row) are observation instances from different behavior patterns. Thus, if g denotes a small, and G denotes a large growth events, then the observed tracks, ggggGGGG and ggGGggGG should be treated as different behaviors even if the average growth rates may be equal. This definition of a MT behavior pattern leads to new analysis capabilities. Each behavior pattern can be described by a model. Subsequently, estimated models are used in analyzing MT dynamic behavior; for instance, in evaluating dynamic similarities between MT populations.
In modeling the MT dynamic behavior, biological insights provide essential guidance. Similar behavior patterns are known to be shared between different experimental conditions, while MT populations within a cell may exhibit dissimilar patterns. Thus, modeling design should handle expected variations of behavior within each experimental condition, and similarities between different experimental conditions.
Formally, we denote each experimental condition by EC, consisting of groups of behavior patterns, w. All experimental conditions have a known label, while patterns making up a condition are unknown. The problem is to estimate a model λ for each pattern w, such that differences between EC_{ i }and EC_{ j }, i ≠ j, are emphasized, while each pattern may occur in different experimental conditions, w ∈ EC_{ i }and w ∈ EC_{ j }. Note that our formulation calls for a discriminative approach between EC, while descriptive models of w is the goal across different EC's.
A well known class of models used in representing activity is the Hidden Markov Models (HMMs). In the past, they have been used in numerous applications, most notably in speech recognition, [24], and in genomic sequence analysis, [25–28]. Particularly in activity context, HMMs were used in activity recognition [29], abnormal activity detection, gesture recognition, and American Sign Language recognition. In the next section we review the essentials of HMMs, while referring the reader to [24] for further details.
Hidden Markov models
HMMs are probabilistic generative models estimating the statistics of a process from observation sequences generated by that process. The modeled process is assumed to be not directly observable, thus hidden states capture statistics of the process, subject to stochastic constraints. In practice, hidden states generally correspond to certain physical characteristics of the process. Detailed information on modeling with HMMs can be found in [24, 28]. Concisely, HMMs, denoted by λ, are described by parameters λ = (π, A, B), where π is the state priors, A is the transition, and B is the emission probabilities. Given an observation sequence O = (o_{1}, o_{2},..., o_{ T }), where t = 1..T denotes time, and a model λ = (π, A, B), the quantity P(Oλ) can be computed efficiently. Given a set of observation sequences, estimating the parameters of λ is generally performed using maximum likelihood methods, while discriminative techniques were suggested in classification tasks, [30, 31].
Modeling microtubule dynamics by HMMs
From the biological perspective, classification of tracks to respective EC is not the end goal for dynamics analysis since labels of EC are known a priori. However, estimated behavior models, λ, provide novel analytical capabilities. Furthermore, model parameters may reveal further insights into MT dynamic behavior. Our formulation of the problem aims to extract behavior patterns through estimating λ, while discriminating between different EC. In doing so, we employ the classification score as our measure of model reliability. The problem description motivates us to use a model based clustering approach to estimate a λ for each w. HMM based clustering methods are discussed in [32].
After parameter estimation, each EC is represented by a mixture of λ where dynamics variations within each EC are modeled by the components of the mixture. In this sense, each λ models the (pseudo)center of a w, the component behavior patterns contributing to the resulting behavior in respective EC. The estimation of λ is primarily a modeling task, while discrimination between w is handled by clustering the observations, MT tracks, into behavior patterns represented by the respective w.
Model estimation
We define the quantity P(Oλ) as the similarity measure between the observation sequences O and the cluster center λ_{ w }of dynamics category w. Expected overall likelihood
is maximized through

Repartition

assign o to cluster C_{ w }such that

w = arg max_{ w' }log p(oλ_{ w' })

Reestimate models

train λ_{ w }on C_{ w }, w = 1..W

In each iteration of the algorithm, observation o is assigned to maximally likely cluster C_{ w }, whose center λ_{ w }is reestimated using the new members of C_{ w }. The iterations are terminated when no significant increase in the overall likelihood is observed.
Model evaluation
As mentioned, we utilize the classification accuracy between EC as our measure for overall model reliability. We compute the probability p(oEC) by
where P_{ w }is the relative number of cluster members, and estimate the separation by counting the number of correctly classified tracks o ∈ O using the decision rule
Note that the decision is conditional on λ_{ w }, EC, representing contributions of each member λ_{ w }of EC.
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Acknowledgements
We would like to thank to Motaz ElSaban and Emre Sargin for their contributions in the automated tracking of microtubules. This study was funded by Center for Bioimage Informatics under grants NSFITR 0331697(BSM, KR, LW, SCF), NIHROI NS35010(SCF), NIHROI NS13560(LW).
This article has been published as part of BMC Cell Biology Volume 8 Supplement 1, 2007: 2006 International Workshop on Multiscale Biological Imaging, Data Mining and Informatics. The full contents of the supplement are available online at http://www.biomedcentral.com/14712121/8?issue=S1
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Authors' contributions
AA carried out the quantification and modeling of dynamics. AJP and EK performed data collection and manual tracking of MTs. LW, SCF, BSM, KR participated in the design and coordination of the study, as well as critical reading of the manuscript.
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Altınok, A., Kiris, E., Peck, A.J. et al. Model based dynamics analysis in live cell microtubule images. BMC Cell Biol 8 (Suppl 1), S4 (2007). https://doi.org/10.1186/147121218S1S4
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DOI: https://doi.org/10.1186/147121218S1S4