Rothman T P, Nilaver G, Gershon M D
J Comp Neurol. 1984 May 1;225(1):13-23. doi: 10.1002/cne.902250103.
The development of peptidergic neurons was analyzed in the murine bowel. Neurons, detected immunocytochemically with antisera to substance P (SP) and vasoactive intestinal polypeptide (VIP), respectively, were selected for study. Explantation of the primordial bowel with subsequent growth in organotypic tissue culture served as an assay for the presence of neuronal precursor cells within the developing gut. One objective of the study was to determine whether the neural crest population that initially colonizes the mammalian bowel contains the precursors of peptidergic neurons as well as those of neurons that contain small molecule neurotransmitters, or whether peptidergic neurons are derived from a later migration of emigr és to the gut. A second objective was to compare the timing of peptidergic phenotypic expression with that of the small molecule neurotransmitters, acetylcholine (ACh) and serotonin (5-HT). The precursors of peptidergic neurons were found to have colonized the bowel prior to the appearance of recognizable neurons of any type. The immunocytochemical detection of SP and VIP in vivo lagged behind the appearance of cholinergic and serotonergic markers by at least 2 days in the foregut and by greater than 3 days in the hindgut. Peptidergic neurons showed a proximodistal pattern of phenotypic expression. These observations support the hypothesis that the murine bowel is colonized by a single wave of precursor cells that contains the primordia of peptidergic neurons as well as neurons that use small molecule neurotransmitters. Data are consistent with the earlier expression of the small molecule phenotype. The proximodistal sequence of phenotypic expression in the absence of a similar sequence in precursor colonization supports an interaction between the precursors of enteric neurons and the microenvironment of the gut that modulates neuronal phenotypic expression.
对小鼠肠道中肽能神经元的发育进行了分析。分别用抗P物质(SP)和血管活性肠肽(VIP)的抗血清通过免疫细胞化学方法检测到的神经元被选作研究对象。将原始肠道进行外植,并在器官型组织培养中使其生长,以此作为检测发育中的肠道内神经前体细胞是否存在的一种方法。该研究的一个目的是确定最初定殖于哺乳动物肠道的神经嵴群体是否既包含肽能神经元的前体,也包含含有小分子神经递质的神经元的前体,或者肽能神经元是否源自后来迁移到肠道的移民。第二个目的是比较肽能表型表达与小分子神经递质乙酰胆碱(ACh)和5-羟色胺(5-HT)的表型表达时间。发现肽能神经元的前体在任何类型的可识别神经元出现之前就已定殖于肠道。在体内,SP和VIP的免疫细胞化学检测在前肠比胆碱能和5-羟色胺能标志物的出现至少滞后2天,在后肠则滞后超过3天。肽能神经元呈现出从近端到远端的表型表达模式。这些观察结果支持这样一种假说,即小鼠肠道由一波单一的前体细胞定殖,这些前体细胞包含肽能神经元以及使用小分子神经递质的神经元的原基。数据与小分子表型的早期表达一致。在没有类似的前体定殖序列的情况下,表型表达的从近端到远端的序列支持肠神经元前体与调节神经元表型表达的肠道微环境之间存在相互作用。