成纤维细胞生长因子8促进主干神经嵴细胞的软骨形成:一个可能的基因调控网络。

Raphaella Josino, Saloe Bispo, Bernardo Bonilauri, Bruno Dallagiovanna, Giordano Wosgrau Calloni
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引用次数: 0

摘要

神经嵴(NC)是一种具有高度迁移能力的胚胎细胞群。它有助于形成几个器官和组织,如颅面骨骼和脊椎动物的周围神经系统。迁移前和迁移后的NC细胞都具有可塑性,通过响应不同的诱导环境信号而采取多种分化路径。头神经嵴细胞(CNCCs)产生了头部的大部分软骨和骨组织。另一方面,干神经嵴细胞(tncc)的间充质电位在一些动物群体中很少检测到。tncc的间充质潜能可以通过特定的NC培养环境条件来揭示。在这项研究中,我们提出证据表明,FGF8治疗可以促进tncc的软骨分化,特别是在迁移阶段的治疗期间。此外,我们对tncc的迁移后阶段进行了转录组学分析,注意到外源性FGF8信号可以维持多能状态,并且可能同时维持一个促软骨调节基因网络。我们的研究结果为tncc的软骨分化机制提供了更全面的理解。
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Fibroblast Growth Factor 8 enhances the chondrogenesis of trunk neural crest cells: a possible gene regulatory network.

The neural crest (NC) is an embryonic cell population with high migratory capacity. It contributes to forming several organs and tissues, such as the craniofacial skeleton and the peripheral nervous system of vertebrates. Both pre-migratory and post-migratory NC cells are plastic, adopting multiple differentiation paths by responding to different inductive environmental signals. Cephalic neural crest cells (CNCCs) give rise to most of the cartilage and bone tissues in the head. On the other hand, the mesenchymal potential of trunk neural crest cells (TNCCs) is sparsely detected in some animal groups. The mesenchymal potential of TNCCs can be unveiled through specific environmental conditions of NC cultures. In this study, we present evidence that FGF8 treatment can foster increased chondrogenic differentiation of TNCCs, particularly during treatment at the migratory stage. Additionally, we conducted a transcriptomic analysis of TNCCs in the post-migratory stage, noting that exogenous FGF8 signaling can sustain multipotent status and, possibly, at the same time, a pro-cartilage regulatory gene network. Our results provide a more comprehensive understanding of the mechanisms underlying chondrogenic differentiation from TNCCs.

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