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施万细胞在特定培养基中增殖但无法分化。

Schwann cells proliferate but fail to differentiate in defined medium.

作者信息

Moya F, Bunge M B, Bunge R P

出版信息

Proc Natl Acad Sci U S A. 1980 Nov;77(11):6902-6. doi: 10.1073/pnas.77.11.6902.

Abstract

Primary cultures of dorsal root ganglia cells from 18- to 21-day rodent embryos were studied for their ability to express Schwann cell function in a defined medium lacking serum and embryo extract. It was confirmed that Schwann cells, but not fibroblasts, are able to proliferate in response to contact with axons when cultured in this defined medium. We here report that in this medium, however, differentiation of Schwann cells was arrested before completion of ensheathment and before initiation of myelin formation. Electron microscopic analysis confirmed this ensheathment failure and showed that the extracellular matrix components (basal lamina and thin collagenous fibrils) normally produced by axon-related Schwann cells had not been formed. This absence of extracellular matrix, as well as the presence in the Schwann cell of an increased cytoplasmic granularity (observed in the light microscope) and numerous distended cisterns of rough endoplasmic reticulum, suggest a failure in Schwann cell secretion. However, within one week after addition of serum and embryo extract to the culture medium, the ensheathment failure was corrected and myelination occurred; electron microscopic observations showed the presence of basal lamina and collagen fibrils in association with Schwann cells. These results suggest the presence in serum or embryo extract (or both) of factors necessary for the full expression of Schwann cell function (although a similar requirement is not present for the expression of oligodendrocyte function in culture). We propose that these observations indicate a linkage between Schwann cell secretion and axonal ensheathment, including myelin formation.

摘要

研究了来自18至21天龄啮齿动物胚胎的背根神经节细胞的原代培养物,以观察它们在缺乏血清和胚胎提取物的限定培养基中表达施万细胞功能的能力。已证实,当在这种限定培养基中培养时,施万细胞而非成纤维细胞能够响应与轴突的接触而增殖。然而,我们在此报告,在这种培养基中,施万细胞的分化在髓鞘形成开始之前以及包绕完成之前就停止了。电子显微镜分析证实了这种包绕失败,并表明通常由与轴突相关的施万细胞产生的细胞外基质成分(基膜和细胶原纤维)尚未形成。这种细胞外基质的缺失,以及施万细胞中细胞质颗粒增多(在光学显微镜下观察到)和大量扩张的粗面内质网池的存在,提示施万细胞分泌功能障碍。然而,在向培养基中添加血清和胚胎提取物后一周内,包绕失败得到纠正且发生了髓鞘形成;电子显微镜观察显示与施万细胞相关的基膜和胶原纤维的存在。这些结果表明血清或胚胎提取物(或两者)中存在施万细胞功能充分表达所必需的因子(尽管培养中少突胶质细胞功能的表达不存在类似需求)。我们提出,这些观察结果表明施万细胞分泌与轴突包绕之间存在联系,包括髓鞘形成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e06/350399/c089b814f9de/pnas00498-0657-a.jpg

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