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非洲爪蟾作为一种模式生物,用于研究神经嵴集体细胞迁移过程中的异源三聚体G蛋白信号通路。

Xenopus as a model organism to study heterotrimeric G-protein pathway during collective cell migration of neural crest.

作者信息

Toro-Tapia G, Villaseca S, Leal J I, Beyer A, Fuentealba J, Torrejón M

机构信息

Departamento de Bioquímica y Biología Molecular, Facultad de Ciencias Biológicas, Universidad de Concepción, Casilla 160-C, Concepción, Chile.

出版信息

Genesis. 2017 Jan;55(1-2). doi: 10.1002/dvg.23008.

Abstract

Collective cell migration is essential in many fundamental aspects of normal development, like morphogenesis, organ formation, wound healing, and immune responses, as well as in the etiology of severe pathologies, like cancer metastasis. In spite of the huge amount of data accumulated on cell migration, such a complex process involves many molecular actors, some of which still remain to be functionally characterized. One of these signals is the heterotrimeric G-protein pathway that has been studied mainly in gastrulation movements. Recently we have reported that Ric-8A, a GEF for Gα proteins, plays an important role in neural crest migration in Xenopus development. Xenopus neural crest cells, a highly migratory embryonic cell population induced at the border of the neural plate that migrates extensively in order to differentiate in other tissues during development, have become a good model to understand the dynamics that regulate cell migration. In this review, we aim to provide sufficient evidence supporting how useful Xenopus model with its different tools, such as explants and transplants, paired with improved in vivo imaging techniques, will allow us to tackle the multiple signaling mechanisms involved in neural crest cell migration.

摘要

集体细胞迁移在正常发育的许多基本方面都至关重要,如形态发生、器官形成、伤口愈合和免疫反应,以及在严重病理状况(如癌症转移)的病因学中。尽管在细胞迁移方面积累了大量数据,但这样一个复杂的过程涉及许多分子参与者,其中一些仍有待进行功能表征。这些信号之一是异源三聚体G蛋白途径,该途径主要在原肠胚形成运动中得到研究。最近我们报道,Ric-8A,一种Gα蛋白的鸟苷酸交换因子,在非洲爪蟾发育过程中的神经嵴迁移中发挥重要作用。非洲爪蟾神经嵴细胞是一种高度迁移的胚胎细胞群体,在神经板边缘诱导产生,在发育过程中广泛迁移以便在其他组织中分化,已成为理解调节细胞迁移动态的良好模型。在这篇综述中,我们旨在提供充分的证据,支持非洲爪蟾模型及其不同工具(如外植体和移植),与改进的体内成像技术相结合,将如何使我们能够解决神经嵴细胞迁移中涉及的多种信号机制。

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