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神经胶质原代培养中的少突胶质细胞分化:对甲羟戊酸的需求。

Oligodendroglial differentiation in glial primary cultures: requirement for mevalonate.

作者信息

Langan T J, Volpe J J

出版信息

J Neurochem. 1987 Jun;48(6):1804-8. doi: 10.1111/j.1471-4159.1987.tb05739.x.

DOI:10.1111/j.1471-4159.1987.tb05739.x
PMID:3033149
Abstract

The oligodendroglial enzyme, 2',3'-cyclic nucleotide 3'-phosphohydrolase (CNP), is a valuable marker for expression of oligodendroglial differentiation in glial primary cultures, and the inducibility of this enzyme by dibutyryl-3',5'-cyclic AMP (dBcAMP) appears to be limited to immature or developing oligodendroglia. To investigate the relationship between the induction of CNP and the sterol biosynthetic pathway, primary cultures of glia dissociated from the brains of newborn rats were maintained in 10% fetal calf serum (FCS) and exposed to 1 mM dBcAMP on day 7 in culture. Cultures so treated for either 48 h or 72 h demonstrated a three- to fourfold induction of CNP specific activity. The magnitude of this induction was not affected when the cholesterol content of the culture medium was reduced by greater than 95% by placing the cultures in 10% lipoprotein-poor serum rather than 10% FCS during the exposure to dBcAMP. Mevinolin (10 microM), a specific inhibitor of 3-hydroxy-3-methylglutaryl coenzyme A reductase, the rate-limiting enzyme of the sterol biosynthetic pathway, completely inhibited the induction of CNP by dBcAMP, while not affecting either the accumulation of cellular protein per flask or rate of protein synthesis. Simultaneous addition of mevalonate (20 mM) prevented the inhibition of the induction of CNP by mevinolin. However, simultaneous addition of low-density lipoprotein sufficient to increase the cholesterol content of the medium 80-fold failed to correct mevinolin's inhibition of the induction of CNP.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

少突胶质细胞酶2',3'-环核苷酸3'-磷酸水解酶(CNP)是胶质细胞原代培养中少突胶质细胞分化表达的一种重要标志物,该酶被二丁酰-3',5'-环磷酸腺苷(dBcAMP)诱导的现象似乎仅限于未成熟或正在发育的少突胶质细胞。为了研究CNP的诱导与固醇生物合成途径之间的关系,将新生大鼠脑部分离的胶质细胞原代培养物置于10%胎牛血清(FCS)中,并在培养第7天暴露于1 mM dBcAMP。如此处理48小时或72小时的培养物显示CNP比活性有三到四倍的诱导。当在暴露于dBcAMP期间将培养物置于10%低脂蛋白血清而非10% FCS中,使培养基中胆固醇含量降低超过95%时,这种诱导的幅度不受影响。美伐他汀(10 microM)是固醇生物合成途径的限速酶3-羟基-3-甲基戊二酰辅酶A还原酶的特异性抑制剂,它完全抑制了dBcAMP对CNP的诱导,同时不影响每个培养瓶中细胞蛋白的积累或蛋白质合成速率。同时添加甲羟戊酸(20 mM)可防止美伐他汀对CNP诱导的抑制。然而,同时添加足以使培养基中胆固醇含量增加80倍的低密度脂蛋白未能纠正美伐他汀对CNP诱导的抑制。(摘要截断于250字)

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Oligodendroglial differentiation in glial primary cultures: requirement for mevalonate.神经胶质原代培养中的少突胶质细胞分化:对甲羟戊酸的需求。
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