اشترك بالحزمة الذهبية واحصل على وصول غير محدود شمرا أكاديميا
تسجيل مستخدم جديدTransient Leadership and Collective Cell Movement in Early Diverged Multicellular Animals
93
0
0.0
(
0
)
اسأل ChatGPT حول البحث
ﻻ يوجد ملخص باللغة العربية
Collective motion of cells is critical to some of the most vital tasks including wound healing, development, and immune response [Friedl and Gilmour 2009; Tokarski et al. 2012; Lee et al. 2012; Beltman et al. 2009], and is common to many pathological processes including cancer cell invasion and teratogenesis [Khalil and Friedl 2010]. The extensive understanding of movement by single cells [R{o}rth 2011; Insall and Machesky 2011; Houk et al. 2012] is insufficient to predict the behavior of cellular groups [Theveneau et al. 2013; Trepat, X. and Fredberg 2011], and identifying underlying rules of coordination in collective cell migration is still evasive. Few of the supposed benefits of collective motion have ever been tested at the cellular scale. As an example, though collective sensing allows for larger groups to exhibit greater accuracy in navigation [Simons 2004; Berdahl et al. 2013] and group taxis is possible through the leadership of only a few individuals [Couzin et al. 2005], such effects have never been investigated in collective cell migration. We will investigate collective motion and decision-making in a primitive multicellular animal, Trichoplax adhaerens to understand how intercellular coordination affects animal behavior and how migration accuracy scales with cellular group size.
قيم البحث
اقرأ أيضاً
In this paper we develop mathematical models for collective cell motility. Initially we develop a model using a linear diffusion-advection type equation and fit the parameters to data from cell motility assays. This approach is helpful in classifying
the results of cell motility assay experiments. In particular, this model can determine degrees of directed versus undirected collective cell motility. Next we develop a model using a nonlinear diffusion term that is able capture in a unified way directed and undirected collective cell motility. Finally we apply the nonlinear diffusion approach to a problem in tumor cell invasion, noting that neither chemotaxis or haptotaxis are present in the system under consideration in this article.
The maintenance of the proliferative cell niche is critical to epithelial tissue morphology and function. In this paper we investigate how current modelling methods can result in the erroneous loss of proliferative cells from the proliferative cell n
iche. Using an established model of the inter-follicular epidermis we find there is a limit to the proliferative cell densities that can be maintained in the basal layer (the niche) if we do not include additional mechanisms to stop the loss of proliferative cells from the niche. We suggest a new methodology that enables maintenance of a desired homeostatic population of proliferative cells in the niche: a rotational force is applied to the two daughter cells during the mitotic phase of division to enforce a particular division direction. We demonstrate that this new methodology achieves this goal. This methodology reflects the regulation of the orientation of cell division.
Modeling cell interactions such as co-attraction and contact-inhibition of locomotion is essential for understanding collective cell migration. Here, we propose a novel deep reinforcement learning model for collective neural crest cell migration. We
apply the deep deterministic policy gradient algorithm in association with a particle dynamics simulation environment to train agents to determine the migration path. Because of the different migration mechanisms of leader and follower neural crest cells, we train two types of agents (leaders and followers) to learn the collective cell migration behavior. For a leader agent, we consider a linear combination of a global task, resulting in the shortest path to the target source, and a local task, resulting in a coordinated motion along the local chemoattractant gradient. For a follower agent, we consider only the local task. First, we show that the self-driven forces learned by the leader cell point approximately to the placode, which means that the agent is able to learn to follow the shortest path to the target. To validate our method, we compare the total time elapsed for agents to reach the placode computed using the proposed method and the time computed using an agent-based model. The distributions of the migration time intervals calculated using the two methods are shown to not differ significantly. We then study the effect of co-attraction and contact-inhibition of locomotion to the collective leader cell migration. We show that the overall leader cell migration for the case with co-attraction is slower because the co-attraction mitigates the source-driven effect. In addition, we find that the leader and follower agents learn to follow a similar migration behavior as in experimental observations. Overall, our proposed method provides useful insight on how to apply reinforcement learning techniques to simulate collective cell migration.
Massive single-cell profiling efforts have accelerated our discovery of the cellular composition of the human body, while at the same time raising the need to formalise this new knowledge. Here, we review current cell ontology efforts to harmonise an
d integrate different sources of annotations of cell types and states. We illustrate with examples how a unified ontology can consolidate and advance our understanding of cell types across scientific communities and biological domains.
We present a stochastic model which describes fronts of cells invading a wound. In the model cells can move, proliferate, and experience cell-cell adhesion. We find several qualitatively different regimes of front motion and analyze the transitions b
etween them. Above a critical value of adhesion and for small proliferation large isolated clusters are formed ahead of the front. This is mapped onto the well-known ferromagnetic phase transition in the Ising model. For large adhesion, and larger proliferation the clusters become connected (at some fixed time). For adhesion below the critical value the results are similar to our previous work which neglected adhesion. The results are compared with experiments, and possible directions of future work are proposed.
سجل دخول لتتمكن من نشر تعليقات
التعليقات
جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
