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激活素作为体内胆碱能分化因子的候选物。

Activins as candidate cholinergic differentiation factors in vivo.

作者信息

Fann M J, Patterson P H

机构信息

Biology Division, California Institute of Technology, Pasadena 91125, USA.

出版信息

Int J Dev Neurosci. 1995 Jun-Jul;13(3-4):317-30. doi: 10.1016/0736-5748(94)00075-e.

Abstract

A number of cytokine families have been implicated in shaping neuronal survival, growth and gene expression. The neuropoietic and transforming growth factor-beta (TGF-beta) cytokines, in particular, have emerged as candidates for regulating the phenotype of sympathetic neurons. Culture studies have shown that neuropoietic cytokines (such as leukemia inhibitory factor, ciliary neurotrophic factor, oncostatin M, growth promoting activity) can induce the cholinergic enzyme, choline acetyltransferase (ChAT) and several neuropeptides, whereas certain members of the TGF-beta family (activin A, bone morphogenetic proteins-2 and -6) induce partially overlapping but distinct sets of transmitter and neuropeptide genes in sympathetic neurons. Since activins can induce ChAT in cultured neurons, we have investigated whether these cytokines are expressed by the appropriate cells and tissues to make them candidates for the cholinergic differentiation factor that is known to alter the phenotype of sympathetic neurons that innervate the sweat gland in the footpad in vivo. In-situ hybridization with the anti-sense probe for activin beta B specifically labels the sweat glands but not other tissues in the footpads of developing rats. Ribonuclease protection assays indicate that beta B as well as the other activin and inhibin subunit mRNAs are expressed by a number of tissues, including footpad, hairy skin and submaxillary gland. Homogenates of developing rat footpads, however, failed to induce the set of neuropeptide genes in cultured sympathetic neurons that is characteristic for activins, although neuropoietic cytokine activity was readily detectable in this assay. Thus, while activin beta B mRNA is expressed in the sweat gland, this tissue does not contain detectable activin protein as assayed by its ability to regulate neuronal gene expression. Moreover, activin subunit mRNAs are expressed by targets of noradrenergic sympathetic neurons in vivo, indicating that activin expression is not limited to targets of cholinergic neurons.

摘要

许多细胞因子家族都与神经元的存活、生长和基因表达的形成有关。特别是神经营养性细胞因子和转化生长因子-β(TGF-β)细胞因子,已成为调节交感神经元表型的候选因子。培养研究表明,神经营养性细胞因子(如白血病抑制因子、睫状神经营养因子、制瘤素M、生长促进活性因子)可诱导胆碱能酶、胆碱乙酰转移酶(ChAT)和几种神经肽的产生,而TGF-β家族的某些成员(激活素A、骨形态发生蛋白-2和-6)在交感神经元中诱导部分重叠但不同的递质和神经肽基因组合。由于激活素可在培养的神经元中诱导ChAT的产生,我们研究了这些细胞因子是否由合适的细胞和组织表达,使其成为胆碱能分化因子的候选者,已知该因子可改变体内支配足垫汗腺的交感神经元的表型。用激活素βB的反义探针进行原位杂交,可特异性标记发育中大鼠足垫的汗腺,但不标记其他组织。核糖核酸酶保护试验表明,βB以及其他激活素和抑制素亚基的mRNA在包括足垫、多毛皮肤和颌下腺在内的多种组织中表达。然而,发育中大鼠足垫的匀浆未能在培养的交感神经元中诱导出激活素特有的神经肽基因组合,尽管在该试验中很容易检测到神经营养性细胞因子活性。因此,虽然激活素βB mRNA在汗腺中表达,但通过其调节神经元基因表达的能力检测,该组织中不含可检测到的激活素蛋白。此外,激活素亚基的mRNA在体内去甲肾上腺素能交感神经元的靶组织中表达,表明激活素的表达不限于胆碱能神经元的靶组织。

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