Schober A, Krieglstein K, Unsicker K
Neuroanatomy, University of Heidelberg, Germany.
Eur J Clin Invest. 2000 Dec;30 Suppl 3:87-90. doi: 10.1046/j.1365-2362.2000.0300s3087.x.
Based on recent evidence from in vitro and gene knockout/insertion studies, this short review summarizes the molecular scenario underlying the development of adrenal chromaffin cells and their preganglionic innervation. During migration of neural crest cells from the dorsal surface of the neural tube to their destinations in the sympathetic primordia and adrenal glands, precursors of the so-called sympathoadrenal (SA) cell lineage are exposed to signals from the notochord and ventral neural tube probably including the protein, Sonic hedgehog. These, and signals in the region of the dorsal aorta (members of the family of bone morphogentic proteins), where SA progenitor cells subsequently assemble, are essential for the induction of the adrenergic phenotype. SA progenitor cells subsequently differentiate into paravertebral and prevertebral sympathetic neurones, intra- and extra-adrenal chromaffin cells and intermediate SIF (small intensely fluorescent) cells. Based on in vitro studies with isolated SA and chromaffin progenitor cells, glucocortiocids have been claimed as essential for suppressing neuronal commitment and for channelling SA cells towards the chromaffin phenotype. However, mice deficient for a functional glucocorticoid receptor possess the full complement of adrenal chromaffin cells at birth, suggesting that signals other than glucocorticoid hormones may be important in triggering chromaffin cell differentiation. The cholinergic neurones that are preganglionic to adrenal chromaffin cells have their cell bodies located in the intermediolateral column (IML) of the spinal cord. For their normal development, these neurones require signals from the adrenal medulla, which include neurotrophin-4, a major neurotrophic factor of adrenal chromaffin cells. Taken together, these data provide a more complete picture of molecular signalling in the development of one of the most important neuroendocrine tissues in vertebrates.
基于近期体外实验以及基因敲除/插入研究的证据,本简短综述总结了肾上腺嗜铬细胞及其节前神经支配发育背后的分子情况。在神经嵴细胞从神经管背面向交感原基和肾上腺的迁移过程中,所谓交感肾上腺(SA)细胞谱系的前体细胞会接触到来自脊索和腹侧神经管的信号,可能包括蛋白质音猬因子。这些信号,以及SA祖细胞随后聚集的背主动脉区域的信号(骨形态发生蛋白家族成员),对于肾上腺素能表型的诱导至关重要。SA祖细胞随后分化为椎旁和椎前交感神经元、肾上腺内和肾上腺外嗜铬细胞以及中间型小而强荧光(SIF)细胞。基于对分离的SA和嗜铬祖细胞的体外研究,有人认为糖皮质激素对于抑制神经元定向分化以及引导SA细胞向嗜铬细胞表型分化至关重要。然而,缺乏功能性糖皮质激素受体的小鼠在出生时拥有完整的肾上腺嗜铬细胞,这表明除糖皮质激素外的其他信号可能在触发嗜铬细胞分化中起重要作用。肾上腺嗜铬细胞节前的胆碱能神经元的细胞体位于脊髓的中间外侧柱(IML)。对于这些神经元的正常发育,它们需要来自肾上腺髓质的信号,其中包括神经营养因子-4,这是肾上腺嗜铬细胞的一种主要神经营养因子。综上所述,这些数据为脊椎动物最重要的神经内分泌组织之一的发育中的分子信号传导提供了更完整的图景。