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体内和体外形态发生的发育潜能。

Developmental potential for morphogenesis in vivo and in vitro.

作者信息

Kaneko Kunihiko, Sato Katsuhiko, Michiue Tatsuo, Okabayashi Koji, Ohnuma Kiyoshi, Danno Hiroki, Asashima Makoto

机构信息

Department of Basic Science, The University of Tokyo, Tokyo, Japan.

出版信息

J Exp Zool B Mol Dev Evol. 2008 Sep 15;310(6):492-503. doi: 10.1002/jez.b.21222.

Abstract

Development is a complex process that involves differentiation into a variety of cell types. In spite of its complexity, the macroscopic pattern and cell types are robust to environmental and developmental perturbations. Even in vitro far from normal developmental conditions, ten normal tissues have been generated from Xenopus animal caps by successive treatment with activin and retinoic acid (RA). To describe both normal development and in vitro organogenesis, we introduce developmental potential following the pioneering study by Waddington. This potential value represents changeability of a cellular state, which decreases toward a local minimum through development. The attraction to a particular cell type through development is described as a process to decrease the potential value to its local minimum. By choosing an explicit potential form as a function of the concentrations of treated activin and RA, the concentration dependence of in vitro organogenesis is reproduced. The potential landscape is shown to have several local minima, each of which represents a stable cell type. This potential also explains why the induction of given tissues requires more treatment of activin at later stages. The consequences of the developmental potential hypothesis encompass the robustness of each tissue generation, the loss of competence through development, and the order of tissues in induction by tissues, which we have confirmed experimentally for in vitro organogenesis. The developmental potential hypothesis for a global description of early development is crucial to understanding the robustness of morphogenesis and explains the achievement of in vitro organogenesis using few molecules as well.

摘要

发育是一个复杂的过程,涉及分化为多种细胞类型。尽管其过程复杂,但宏观模式和细胞类型对环境和发育扰动具有稳健性。即使在远离正常发育条件的体外环境中,通过用激活素和视黄酸(RA)连续处理,非洲爪蟾动物帽也已产生了十种正常组织。为了描述正常发育和体外器官发生,我们继沃丁顿的开创性研究之后引入了发育潜能。这种潜能值代表细胞状态的可变性,其在发育过程中朝着局部最小值降低。通过发育对特定细胞类型的吸引被描述为将潜能值降低到其局部最小值的过程。通过选择作为处理过的激活素和RA浓度函数的显式潜能形式,再现了体外器官发生的浓度依赖性。潜能景观显示有几个局部最小值,每个最小值代表一种稳定的细胞类型。这种潜能还解释了为什么在后期诱导特定组织需要更多的激活素处理。发育潜能假说的结果包括每种组织生成的稳健性、发育过程中能力的丧失以及组织诱导中组织的顺序,我们已通过体外器官发生的实验得到证实。用于早期发育全局描述的发育潜能假说对于理解形态发生的稳健性至关重要,并且也解释了使用少量分子实现体外器官发生的原因。

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