Ernsberger Uwe, Esposito Lorena, Partimo Sandra, Huber Katrin, Franke Aylin, Bixby John L, Kalcheim Chaya, Unsicker Klaus
Department of Neuroanatomy, Interdisciplinary Center for Neurosciences (IZN), University of Heidelberg, INF 307, 69120 Heidelberg, Germany.
Cell Tissue Res. 2005 Jan;319(1):1-13. doi: 10.1007/s00441-004-0996-1. Epub 2004 Nov 25.
We have analyzed the distribution of neural crest-derived precursors and the expression of catecholaminergic and neuronal markers in developing adrenal tissue of chick embryos. Undifferentiated neural crest cells are found in presumptive adrenal regions from embryonic day 3 (E3) onward. An increasing proportion of cells expressing tyrosine hydroxylase (TH) mRNA indicates catecholaminergic differentiation of precursors not only in primary sympathetic ganglia, but also in presumptive adrenal regions. Whereas precursors and differentiating cells show mesenchymal distribution until E5, discrete adrenal anlagen form during E6. Even during E5, catecholaminergic cells with low or undetectable neurofilament M (NF-M) mRNA expression prevail in positions at which adrenal anlagen become distinct during E6. The predominance of TH-positive and NF-M-negative cells is maintained throughout embryogenesis in adrenal tissue. RNA encoding SCG10, a pan-neuronal marker like NF-M, is strongly expressed throughout adrenal anlagen during E6 but is found at reduced levels in chromaffin cells compared with neuronal cells at E15. Two additional neuronal markers, synaptotagmin 1 and neurexin 1, are expressed at low to undetectable levels in developing chromaffin cells throughout embryogenesis. The developmental regulation of neuronal markers shows at least three different patterns among the four mRNAs analyzed. Importantly, there is no generalized downregulation of neuronal markers in developing adrenal anlagen. Thus, our observations question the classical concept of chromaffin differentiation from a common sympathoadrenal progenitor expressing neuronal properties and suggest alternative models with changing instructive signals or separate progenitor populations for sympathetic neuronal and chromaffin endocrine cells.
我们分析了鸡胚发育中肾上腺组织里神经嵴衍生前体细胞的分布以及儿茶酚胺能和神经元标志物的表达情况。从胚胎第3天(E3)起,在假定的肾上腺区域发现了未分化的神经嵴细胞。表达酪氨酸羟化酶(TH)mRNA的细胞比例不断增加,这表明前体细胞不仅在初级交感神经节,而且在假定的肾上腺区域都发生了儿茶酚胺能分化。在前体细胞和分化细胞在E5之前呈现间充质分布,而在E6期间形成离散的肾上腺原基。即使在E5时,神经丝M(NF-M)mRNA表达低或无法检测到的儿茶酚胺能细胞在肾上腺原基在E6时变得明显的位置占主导。在肾上腺组织的整个胚胎发育过程中,TH阳性和NF-M阴性细胞一直占优势。编码SCG10(一种像NF-M一样的泛神经元标志物)的RNA在E6期间在整个肾上腺原基中强烈表达,但与E15时的神经元细胞相比,在嗜铬细胞中的水平较低。另外两种神经元标志物,突触结合蛋白1和接触蛋白1,在整个胚胎发育过程中,在发育中的嗜铬细胞中表达水平低至无法检测到。在所分析的四种mRNA中,神经元标志物的发育调控至少呈现出三种不同模式。重要的是,在发育中的肾上腺原基中,神经元标志物并没有普遍下调。因此,我们的观察结果对嗜铬细胞从表达神经元特性的共同交感肾上腺祖细胞分化而来的经典概念提出了质疑,并提出了具有变化的诱导信号或交感神经元和嗜铬内分泌细胞的单独祖细胞群体的替代模型。