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轴突相关施万细胞中髓鞘蛋白零基因的表达与基膜形成有关。

Expression of the protein zero myelin gene in axon-related Schwann cells is linked to basal lamina formation.

作者信息

Fernandez-Valle C, Fregien N, Wood P M, Bunge M B

机构信息

Miami Project to Cure Paralysis, Florida.

出版信息

Development. 1993 Nov;119(3):867-80. doi: 10.1242/dev.119.3.867.

DOI:10.1242/dev.119.3.867
PMID:7514526
Abstract

A Schwann cell has the potential to differentiate into either a myelinating or ensheathing cell depending upon signals received from the axon that it contacts. Studies focusing on the pathway leading to myelination demonstrated that Schwann cells must form a basal lamina in order to myelinate an axon. In this report, we describe studies that indicate that initiation of basal lamina synthesis is required for Schwann cells to distinguish between myelination-inducing axons and axons that do not induce myelination, and to respond by undergoing the appropriate genetic and cellular changes. We have used high resolution in situ hybridization, immunocytochemistry and electron microscopy to examine changes in gene expression and morphology of Schwann cells differentiating into myelin-forming cells in vitro. These experiments were carried out in dorsal root ganglion neuron/Schwann cell co-cultures maintained in either serum-free, serum-only or serum-plus-ascorbate-containing medium. We have made four novel observations that contribute significantly to our understanding of how basal lamina and myelination are linked. (1) The addition of ascorbate (in the presence of serum), which promotes basal lamina production, appears to induce expression of the protein zero gene encoding the major structural protein of myelin. Moreover, expression of protein zero mRNA and protein, and its insertion into myelin membranes, occurs only in the subset of Schwann cells contacting myelination-inducing axons. Schwann cells in contact with axons that do not induce myelination, or Schwann cells that have not established a unitary relationship with an axon, do not express protein zero mRNA although they produce basal lamina components. (2) In serum-free conditions, a majority of Schwann cells express protein zero mRNA and protein, but this change in gene expression is not associated with basal lamina formation or with elongation of the Schwann cell along the axon and elaboration of myelin. (3) In the presence of serum (and the absence of ascorbate), Schwann cells again fail to form basal lamina or elongate but no longer express protein zero mRNA or protein. (4) Myelin-associated glycoprotein and galactocerebroside, two additional myelin-specific components, can be expressed by Schwann cells under any of the three culture conditions. Therefore, we have demonstrated that axonal induction of protein zero gene expression in Schwann cells is subject to regulation by both serum- and ascorbate-dependent pathways and that not all myelin-specific proteins are regulated in the same manner.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

施万细胞有潜力根据从其接触的轴突接收到的信号分化为髓鞘形成细胞或包被细胞。专注于髓鞘形成途径的研究表明,施万细胞必须形成基膜才能使轴突髓鞘化。在本报告中,我们描述了一些研究,这些研究表明,施万细胞区分诱导髓鞘形成的轴突和不诱导髓鞘形成的轴突,并通过经历适当的基因和细胞变化做出反应,需要启动基膜合成。我们使用高分辨率原位杂交、免疫细胞化学和电子显微镜来检查体外分化为髓鞘形成细胞的施万细胞的基因表达和形态变化。这些实验在无血清、仅含血清或含血清加抗坏血酸的培养基中维持的背根神经节神经元/施万细胞共培养物中进行。我们有四个新的观察结果,对我们理解基膜与髓鞘形成之间的联系有很大帮助。(1)添加抗坏血酸(在有血清的情况下)可促进基膜产生,似乎能诱导编码髓鞘主要结构蛋白的蛋白零基因的表达。此外,蛋白零mRNA和蛋白的表达及其插入髓鞘膜仅发生在接触诱导髓鞘形成轴突的施万细胞亚群中。与不诱导髓鞘形成的轴突接触的施万细胞,或尚未与轴突建立单一关系的施万细胞,虽然产生基膜成分,但不表达蛋白零mRNA。(2)在无血清条件下,大多数施万细胞表达蛋白零mRNA和蛋白,但这种基因表达变化与基膜形成无关,也与施万细胞沿轴突的伸长和髓鞘的形成无关。(3)在有血清(且无抗坏血酸)的情况下,施万细胞再次无法形成基膜或伸长,但不再表达蛋白零mRNA或蛋白。(4)髓鞘相关糖蛋白和半乳糖脑苷脂,另外两种髓鞘特异性成分,可在三种培养条件中的任何一种下由施万细胞表达。因此,我们证明了施万细胞中蛋白零基因表达的轴突诱导受血清和抗坏血酸依赖性途径的调节,而且并非所有髓鞘特异性蛋白都以相同方式调节。(摘要截短至400字)

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Expression of the protein zero myelin gene in axon-related Schwann cells is linked to basal lamina formation.轴突相关施万细胞中髓鞘蛋白零基因的表达与基膜形成有关。
Development. 1993 Nov;119(3):867-80. doi: 10.1242/dev.119.3.867.
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P0 mRNA expression in cultures of Schwann cells and neurons that lack basal lamina and myelin.雪旺细胞和神经元培养物中P0 mRNA的表达,这些培养物缺乏基膜和髓磷脂。
J Neurosci Res. 1990 Oct;27(2):159-68. doi: 10.1002/jnr.490270206.
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P0 gene expression in cultured Schwann cells.培养的雪旺细胞中P0基因的表达。
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Negative regulation of the P0 gene in Schwann cells: suppression of P0 mRNA and protein induction in cultured Schwann cells by FGF2 and TGF beta 1, TGF beta 2 and TGF beta 3.施万细胞中P0基因的负调控:成纤维细胞生长因子2、转化生长因子β1、转化生长因子β2和转化生长因子β3对培养的施万细胞中P0 mRNA和蛋白诱导的抑制作用
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J Neurosci. 1997 Jan 1;17(1):241-50. doi: 10.1523/JNEUROSCI.17-01-00241.1997.

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