首页> 美国卫生研究院文献>The Journal of Neuroscience >Spatiotemporal patterns of expression of NGF and the low-affinity NGF receptor in rat embryos suggest functional roles in tissue morphogenesis and myogenesis
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Spatiotemporal patterns of expression of NGF and the low-affinity NGF receptor in rat embryos suggest functional roles in tissue morphogenesis and myogenesis

机译:大鼠胚胎中NGF和低亲和力NGF受体表达的时空模式表明在组织形态发生和肌发生中的功能作用

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摘要

We show here that NGF and its low-affinity receptor (p75NGFR) are expressed during rat embryogenesis at sites that are known to have important roles in tissue morphogenesis and myogenesis. The developing skin of the maxilla, the mandible, and the limb showed very similar patterns of NGF and p75NGFR expression. However, NGF and p75NGFR expression in the developing limb initiated at the limb bud stage and was concentrated at proximal and distal developmental sites that have been reported to be involved in limb morphogenesis. Expression at the proximal/distal ends of the limb persisted throughout limb development, with some of the highest levels of expression occurring at the limb axillary sites, which were not highly innervated. We have also found p75NGFR expression at sites of mesenchymal/epithelial interactions in several developing organs that do not appear to have an adjacent source of NGF and may therefore be sites that bind and respond to the other members of the NGF family (brain-derived neurotrophic factor and neurotrophin-3). These organs include the lung, testes, and kidney, where expression of p75NGFR occurred during the morphogenesis of specific epithelial structures and was coexpressed with the cell adhesion molecule NCAM. In addition, we found that NGF and p75NGFR were expressed during myogenesis. p75NGFR was observed in myoblast cells expressing MyoD1, a myoblast differentiation marker, and NGF transcripts in cells just adjacent to the developing myoblasts. When the myoblasts differentiate into myotubes, p75NGFR and MyoD1 cease to be expressed and the adjacent cells concomitantly cease to be make NGF. However, NGF and p75NGFR were not present in the early muscle precursor cells of the myotome of the somites but were observed in the dermatome and sclerotome, respectively. These results suggest that NGF and p75NGFR have functional roles in developmental processes that affect morphogenesis and cell differentiation.
机译:我们在这里显示NGF及其低亲和力受体(p75NGFR)在大鼠胚胎发生期间在已知在组织形态发生和肌发生中具有重要作用的位点表达。上颌骨,下颌骨和四肢的发育中皮肤显示出非常相似的NGF和p75NGFR表达模式。然而,NGF和p75NGFR在发育中的肢体中的表达始于肢体芽期,并集中在据报道与肢体形态发生有关的近端和远端发育部位。在肢体的整个发育过程中,肢体近端/远端的表达一直持续存在,其中一些最高水平的表达发生在肢体腋窝部位,而这些部位并没有高度被神经支配。我们还发现p75NGFR在几个发育器官中的间充质/上皮相互作用位点表达,这些器官似乎没有相邻的NGF来源,因此可能是结合并响应NGF家族其他成员的位点(脑源性神经营养性因子和Neurotrophin-3)。这些器官包括肺,睾丸和肾脏,其中p75NGFR的表达在特定上皮结构的形态发生期间发生,并与细胞粘附分子NCAM共表达。另外,我们发现NGF和p75NGFR在肌发生过程中表达。在表达成肌细胞分化标记MyoD1的成肌细胞中观察到p75NGFR,并且在与发育中的成肌细胞相邻的细胞中观察到NGF转录本。当成肌细胞分化成肌管时,p75NGFR和MyoD1不再表达,相邻细胞也随之停止生成NGF。然而,NGF和p75NGFR不存在于体节的子宫肌节的早期肌肉前体细胞中,但分别在皮刀和菌核组中观察到。这些结果表明,NGF和p75NGFR在影响形态发生和细胞分化的发育过程中具有功能性作用。

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