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      Relaxation-expansion model for self-driven retinal morphogenesis : A hypothesis from the perspective of biosystems dynamics at the multi-cellular level

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          Abstract

          The generation of complex organ structures such as the eye requires the intricate orchestration of multiple cellular interactions. In this paper, early retinal development is discussed with respect to the structure formation of the optic cup. Although recent studies have elucidated molecular mechanisms of retinal differentiation, little is known about how the unique shape of the optic cup is determined. A recent report has demonstrated that optic-cup morphogenesis spontaneously occurs in three-dimensional stem-cell culture without external forces, indicating a latent intrinsic order to generate the structure. Based on this self-organizing phenomenon, we introduce the “relaxation-expansion” model to mechanically interpret the tissue dynamics that enable the spontaneous invagination of the neural retina. This model involves three consecutive local rules (relaxation, apical constriction, and expansion), and its computer simulation recapitulates the optic-cup morphogenesis in silico.

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          Most cited references51

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          Phosphorylation and activation of myosin by Rho-associated kinase (Rho-kinase).

          The small GTPase Rho is implicated in physiological functions associated with actin-myosin filaments such as cytokinesis, cell motility, and smooth muscle contraction. We have recently identified and molecularly cloned Rho-associated serine/threonine kinase (Rho-kinase), which is activated by GTP Rho (Matsui, T., Amano, M., Yamamoto, T., Chihara, K., Nakafuku, M., Ito, M., Nakano, T., Okawa, K., Iwamatsu, A., and Kaibuchi, K. (1996) EMBO J. 15, 2208-2216). Here we found that Rho-kinase stoichiometrically phosphorylated myosin light chain (MLC). Peptide mapping and phosphoamino acid analyses revealed that the primary phosphorylation site of MLC by Rho-kinase was Ser-19, which is the site phosphorylated by MLC kinase. Rho-kinase phosphorylated recombinant MLC, whereas it failed to phosphorylate recombinant MLC, which contained Ala substituted for both Thr-18 and Ser-19. We also found that the phosphorylation of MLC by Rho-kinase resulted in the facilitation of the actin activation of myosin ATPase. Thus, it is likely that once Rho is activated, then it can interact with Rho-kinase and activate it. The activated Rho-kinase subsequently phosphorylates MLC. This may partly account for the mechanism by which Rho regulates cytokinesis, cell motility, or smooth muscle contraction.
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            Directed differentiation of telencephalic precursors from embryonic stem cells.

            We demonstrate directed differentiation of telencephalic precursors from mouse embryonic stem (ES) cells using optimized serum-free suspension culture (SFEB culture). Treatment with Wnt and Nodal antagonists (Dkk1 and LeftyA) during the first 5 d of SFEB culture causes nearly selective neural differentiation in ES cells ( approximately 90%). In the presence of Dkk1, with or without LeftyA, SFEB induces efficient generation ( approximately 35%) of cells expressing telencephalic marker Bf1. Wnt3a treatment during the late culture period increases the pallial telencephalic population (Pax6(+) cells yield up to 75% of Bf1(+) cells), whereas Shh promotes basal telencephalic differentiation (into Nkx2.1(+) and/or Islet1/2(+) cells) at the cost of pallial telencephalic differentiation. Thus, in the absence of caudalizing signals, floating aggregates of ES cells generate naive telencephalic precursors that acquire subregional identities by responding to extracellular patterning signals.
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              Vertebrate neural cell-fate determination: lessons from the retina.

              Postmitotic neurons are produced from a pool of cycling progenitors in an orderly fashion during development. Studies of cell-fate determination in the vertebrate retina have uncovered several fundamental principles by which this is achieved. Most notably, a model for vertebrate cell-fate determination has been proposed that combines findings on the relative roles of extrinsic and intrinsic regulators in controlling cell-fate choices. At the heart of the model is the proposal that progenitors pass through intrinsically determined competence states, during which they are capable of giving rise to a limited subset of cell types under the influence of extrinsic signals.
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                Author and article information

                Journal
                Bioessays
                bies
                Bioessays
                WILEY-VCH Verlag (Weinheim )
                0265-9247
                1521-1878
                January 2012
                : 34
                : 1
                : 17-25
                Affiliations
                [1) ]simpleOrganogenesis and Neurogenesis Group, RIKEN Center for Developmental Biology Kobe, Japan
                [2) ]simpleUnit for Four-Dimensional Tissue Analysis, RIKEN Center for Developmental Biology Kobe, Japan
                [3) ]simpleDepartment of Biomechanics, Institute for Frontier Medical Sciences, Kyoto University Kyoto, Japan
                [4) ]simpleComputational Cell Biomechanics Team, VCAD System Research Program RIKEN, Wako, Japan
                Author notes
                * Corresponding authors: Mototsugu Eiraku E-mail: eiraku@ 123456cdb.riken.jp Yoshiki Sasai E-mail: yoshikisasai@ 123456cdb.riken.jp
                Article
                10.1002/bies.201100070
                3266490
                22052700
                6ff3e063-6af4-4148-aba7-d3639606be3a
                Copyright © 2012 WILEY Periodicals, Inc.

                Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation.

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                Categories
                Insights & Perspectives

                Cell biology
                self-organization,es cells,optic cup,internal force,retina
                Cell biology
                self-organization, es cells, optic cup, internal force, retina

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