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利用大鼠-小鼠异种培养物分析轴突-神经胶质细胞相互作用过程中少突胶质细胞上整合素的表达。

Analysis of integrin expression on oligodendrocytes during axo-glial interaction by using rat-mouse xenocultures.

作者信息

Shaw C E, Milner R, Compston A S, ffrench-Constant C

机构信息

University of Cambridge Neurology Unit, Addenbrookes Hospital, United Kingdom.

出版信息

J Neurosci. 1996 Feb 1;16(3):1163-72. doi: 10.1523/JNEUROSCI.16-03-01163.1996.

Abstract

To analyze the expression of cell-surface molecules on neurons or glia during myelination, we have developed a xenotypic coculture system in which mouse oligodendrocytes interact with rat dorsal root ganglion neurons. The axo-glial interactions in these cultures promote oligodendrocyte precursor cell proliferation, survival, and differentiation as in vivo, thus supporting the validity of the xenocultures as a model system to study myelination in which the molecules on the neurons or the glia can be distinguished using species-specific antibodies. We examined the expression of integrins, the major family of cell-surface extracellular matrix receptors, on oligodendrocytes during the early stages of myelination and found that, unlike Schwann cells, oligodendrocytes do not express alpha 6 beta 4 in association with myelin sheath formation. The pattern of integrin expression observed on oligodendrocytes in these cultures is similar to that seen in oligodendrocytes that differentiate in purified cultures, and it comprises alpha 6 beta 1, alpha v beta 5, and an as yet uncharacterized alpha v-associated beta subunit of 80 kDa. Changes in integrin expression associated with differentiation, therefore, do not depend on axonal contact, and beta 4 is not required for myelin sheath formation, although its expression may contribute to the individual properties of oligodendrocytes and Schwann cells.

摘要

为了分析髓鞘形成过程中神经元或神经胶质细胞表面分子的表达情况,我们开发了一种异种共培养系统,其中小鼠少突胶质细胞与大鼠背根神经节神经元相互作用。这些培养物中的轴突-神经胶质相互作用促进少突胶质前体细胞的增殖、存活和分化,与体内情况相同,从而支持了异种培养作为研究髓鞘形成的模型系统的有效性,在该系统中,可以使用物种特异性抗体区分神经元或神经胶质细胞上的分子。我们研究了髓鞘形成早期少突胶质细胞上主要的细胞表面细胞外基质受体家族整合素的表达情况,发现与施万细胞不同,少突胶质细胞在髓鞘形成过程中不表达α6β4。在这些培养物中观察到的少突胶质细胞上整合素的表达模式与在纯化培养物中分化的少突胶质细胞中看到的模式相似,它包括α6β1、αvβ5和一个尚未鉴定的与αv相关的80 kDaβ亚基。因此,与分化相关的整合素表达变化不依赖于轴突接触,并且虽然β4的表达可能有助于少突胶质细胞和施万细胞的个体特性,但髓鞘形成不需要β4。

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