Chalazonitis A, Rothman T P, Chen J, Vinson E N, MacLennan A J, Gershon M D
Department of Anatomy and Cell Biology, Columbia University, College of Physicians and Surgeons, New York, New York 10032, USA.
Dev Biol. 1998 Jun 15;198(2):343-65.
Neurotrophin-3 (NT-3) is known to promote enteric neuronal and glial development. Ciliary neurotrophic factor (CNTF) and leukemia inhibitory factor (LIF) were investigated to test the hypothesis that the development of subsets of enteric neurons and/or glia is also affected by a neuropoietic cytokine, by itself, or together with NT-3. Crest-derived cells, immunoselected from the fetal rat gut (E14) with antibodies to p75NTR, were found by RT-PCR and immunocytochemistry (after culture) to express both alpha (CNTER alpha) and beta components (gp130 and LIFR beta) of the tripartite CNTF receptor. In situ, myenteric ganglia below the esophagus were CNTFR alpha-immunoreactive by E16-E18. In vitro, CNTF and LIF induced in crest-derived cells nuclear translocation of STAT3 (signal transducer and activator of transcription 3), a concentration-dependent increase in expression of neuronal or glial markers, and a decrease in expression of the precursor marker, nestin. LIFR beta was expressed by more cells than CNTFR alpha; therefore, although the factors were equipotent, the maximal effect of LIF > CNTF. The cytokines and NT-3 were additive in promoting neuronal but not glial development. Specifically, the development of neurons expressing NADPH-diaphorase activity (an early marker found in inhibitory motor neurons) was promoted by CNTF and NT-3. These observations support the idea that a ligand for the tripartite CNTF receptor complex plays a role in ENS development.
已知神经营养因子-3(NT-3)可促进肠神经元和神经胶质细胞的发育。研究了睫状神经营养因子(CNTF)和白血病抑制因子(LIF),以检验肠神经元和/或神经胶质细胞亚群的发育也受一种神经生成细胞因子单独或与NT-3共同影响的假说。用抗p75NTR抗体从胎鼠肠道(E14)免疫筛选出的嵴衍生细胞,通过逆转录聚合酶链反应(RT-PCR)和免疫细胞化学(培养后)发现其表达CNTF三方受体的α(CNTERα)和β成分(gp130和LIFRβ)。在原位,食管下方的肌间神经节在E16-E18时呈CNTFRα免疫反应性。在体外,CNTF和LIF可诱导嵴衍生细胞中信号转导子和转录激活子3(STAT3)的核转位,神经元或神经胶质细胞标志物表达呈浓度依赖性增加,前体标志物巢蛋白的表达减少。表达LIFRβ的细胞比表达CNTFRα的细胞多;因此,尽管这些因子的效力相同,但LIF的最大效应>CNTF。这些细胞因子和NT-3在促进神经元而非神经胶质细胞发育方面具有相加作用。具体而言,CNTF和NT-3可促进表达烟酰胺腺嘌呤二核苷酸磷酸黄递酶活性(一种在抑制性运动神经元中发现的早期标志物)的神经元的发育。这些观察结果支持了CNTF三方受体复合物的配体在肠神经系统发育中起作用这一观点。