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抗L1黏附分子抗体在体外对雪旺细胞髓鞘形成的抑制作用。

Inhibition of Schwann cell myelination in vitro by antibody to the L1 adhesion molecule.

作者信息

Wood P M, Schachner M, Bunge R P

机构信息

Department of Anatomy and Neurobiology, Washington University School of Medicine, St. Louis, Missouri 63110.

出版信息

J Neurosci. 1990 Nov;10(11):3635-45. doi: 10.1523/JNEUROSCI.10-11-03635.1990.

Abstract

The specific axonal and Schwann cell surface molecules that mediate the initiation of myelination have not been identified. We have used cocultures of purified rat dorsal root ganglion neurons and Schwann cells and purified polyclonal antibodies to the L1 adhesion molecule to study the role of L1 in myelin formation. Schwann cells were first arrested in a basal-lamina-free premyelination stage (by serum/ascorbate deprivation), then manipulated to allow basal lamina deposition and myelination (by serum/ascorbate addition) in the absence or presence of anti-L1. Using electron microscopy, immunocytochemistry, and myelin sheath quantitation after Sudan-black staining, we determined the effect of anti-L1 on (1) basal lamina formation, (2) the segregation by Schwann cells of axons into a 1:1 relationship, (3) galactocerebroside (Gal-C) expression, (4) laminin deposition, and (5) myelin formation. Anti-L1 strongly blocked myelin formation, Gal-C expression, and axon segregation but did not block basal lamina formation. In controls, elongated Schwann cell processes completely covered the axons and exhibited uniform surface staining for laminin; in anti-L1-treated cultures, shortened Schwann cells, intensely stained for laminin, were observed in clusters separated by unstained lengths of axons. When 50 micrograms/ml exogenous purified laminin was added to the medium, Schwann cell length and laminin staining were similar in control and treated cultures. However, the inhibition of myelination of anti-L1 was not altered by the addition of laminin. Myelination was also inhibited with antigen-binding fragments (Fab) of polyclonal anti-L1, but an antibody to liver membranes did not block myelination. These results indicate that L1 is involved in the linear extension of Schwann cell processes along axons, the engulfment of axons, and the induction of myelin-specific components within the Schwann cell. We conclude that anti-L1 prevents myelination by blocking these events rather than by blocking basal lamina deposition.

摘要

介导髓鞘形成起始的特定轴突和施万细胞表面分子尚未被鉴定出来。我们利用纯化的大鼠背根神经节神经元与施万细胞的共培养物以及针对L1黏附分子的纯化多克隆抗体,来研究L1在髓鞘形成中的作用。首先使施万细胞停滞于无基膜的髓鞘形成前期阶段(通过血清/抗坏血酸剥夺),然后在不存在或存在抗L1的情况下,通过添加血清/抗坏血酸来促使基膜沉积和髓鞘形成。通过电子显微镜、免疫细胞化学以及苏丹黑染色后的髓鞘定量分析,我们确定了抗L1对以下方面的影响:(1)基膜形成;(2)施万细胞将轴突分隔成1:1关系;(3)半乳糖脑苷脂(Gal-C)表达;(4)层粘连蛋白沉积;(5)髓鞘形成。抗L1强烈阻断髓鞘形成、Gal-C表达和轴突分隔,但不阻断基膜形成。在对照中,伸长的施万细胞突起完全覆盖轴突,并对层粘连蛋白呈现均匀的表面染色;在抗L1处理的培养物中,观察到缩短的施万细胞,其层粘连蛋白染色强烈,聚集成簇,被未染色的轴突段分隔开。当向培养基中添加50微克/毫升外源性纯化层粘连蛋白时,对照和处理培养物中的施万细胞长度和层粘连蛋白染色相似。然而,添加层粘连蛋白并未改变抗L1对髓鞘形成的抑制作用。多克隆抗L1的抗原结合片段(Fab)也抑制髓鞘形成,但针对肝细胞膜的抗体不阻断髓鞘形成。这些结果表明,L1参与施万细胞突起沿轴突的线性延伸、轴突的吞噬以及施万细胞内髓鞘特异性成分的诱导。我们得出结论,抗L1通过阻断这些事件而非阻断基膜沉积来阻止髓鞘形成。

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