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单克隆抗体14F7可识别阶段特异性未成熟少突胶质细胞表面分子,它能抑制与星形胶质细胞共培养介导的少突胶质细胞分化。

Monoclonal antibody 14F7, which recognizes a stage-specific immature oligodendrocyte surface molecule, inhibits oligodendrocyte differentiation mediated in co-culture with astrocytes.

作者信息

Yoshimura K, Sakurai Y, Nishimura D, Tsuruo Y, Nomura M, Kawato S, Seiwa C, Iguchi T, Itoh K, Asou H

机构信息

Department of Neuro-cell Biology, Tokyo Metropolitan Institute of Gerontology, Japan.

出版信息

J Neurosci Res. 1998 Oct 1;54(1):79-96. doi: 10.1002/(SICI)1097-4547(19981001)54:1<79::AID-JNR9>3.0.CO;2-E.

Abstract

Cells at an intermediate stage of oligodendrocyte lineage are not only well characterized by biochemical studies but also are likely to relate to the outcome of physiological events. To elucidate the molecular events leading to the development of oligodendrocyte lineage cells, we have raised monoclonal antibodies against stage-specific immature oligodendrocytes, which have previously been isolated by a novel oligodendrocyte-lineage cell culture technique (Sakurai et al.: J Neurosci Res 52:17-26, 1998). We have isolated a mouse monoclonal antibody termed 14F7 which predominantly labels stage-specific immature oligodendrocytes and have found that the expression of 14F7 immunoreactivity in the developing neonatal rat forebrain is closely associated with cells expressing the oligodendrocyte progenitor marker A2B5 and to immature oligodendrocyte expressing O4 antigen. 14F7+ cells were distributed in the ventricular and subventricular zone and the nearby forming corpus callosum as non-myelinating cells. In contrast to cell culture observations, 14F7+ cells were seen only in oligodendrocyte lineage cells. For instance, dissociated cell culture studies indicated that 14F7 labels a cell surface molecule, and its cellular distribution is coincident with all of O4+ cells and A2B5+ cells, and even A2B5- cells. By contrast, 14F7-positive cells did not label astrocytes and, furthermore, did not label myelin basic protein (MBP)-positive oligodendrocytes. 14F7 recognized a 48-kDa protein on sodium dodecyl sulfate polyacrylamide gel electrophoresis. 14F7 immunoreactivity was detectable in rat brain as early as embryonic day 18. Furthermore, in these cells, the total time for differentiation was extended, and on maturation, these cells subsequently expressed an array of myelin-specific proteins, which normally occurs by direct contact with type-1 astrocytes. However, in the presence of 14F7, stage-specific oligodendrocytes co-cultured with astrocytes completely failed to express MBP. These data suggest that the 14F7 antigen is a novel cell surface molecule that is expressed in the intermediate stage of oligodendrocyte-lineage cells, and it is expected that it regulates the differentiation of oligodendrocyte throughout development.

摘要

少突胶质细胞谱系中间阶段的细胞不仅通过生化研究得到了充分表征,而且可能与生理事件的结果相关。为了阐明导致少突胶质细胞谱系细胞发育的分子事件,我们制备了针对阶段特异性未成熟少突胶质细胞的单克隆抗体,这些细胞先前已通过一种新型的少突胶质细胞谱系细胞培养技术分离出来(樱井等人:《神经科学研究杂志》52:17 - 26, 1998)。我们分离出一种名为14F7的小鼠单克隆抗体,它主要标记阶段特异性未成熟少突胶质细胞,并发现14F7免疫反应性在新生大鼠发育中的前脑的表达与表达少突胶质细胞祖细胞标志物A2B5的细胞以及表达O4抗原的未成熟少突胶质细胞密切相关。14F7 +细胞作为非髓鞘形成细胞分布在脑室和室下区以及附近正在形成的胼胝体中。与细胞培养观察结果不同,14F7 +细胞仅在少突胶质细胞谱系细胞中可见。例如,解离细胞培养研究表明14F7标记一种细胞表面分子,其细胞分布与所有O4 +细胞、A2B5 +细胞甚至A2B5 -细胞一致。相比之下,14F7阳性细胞不标记星形胶质细胞,而且也不标记髓鞘碱性蛋白(MBP)阳性的少突胶质细胞。14F7在十二烷基硫酸钠聚丙烯酰胺凝胶电泳上识别一种48 kDa的蛋白质。早在胚胎第18天,大鼠脑中就可检测到14F7免疫反应性。此外,在这些细胞中,分化的总时间延长,并且在成熟时,这些细胞随后表达一系列髓鞘特异性蛋白质,而这些蛋白质通常通过与1型星形胶质细胞直接接触而出现。然而,在存在14F7的情况下,与星形胶质细胞共培养的阶段特异性少突胶质细胞完全无法表达MBP。这些数据表明14F7抗原是一种在少突胶质细胞谱系细胞中间阶段表达的新型细胞表面分子,预计它在整个发育过程中调节少突胶质细胞的分化。

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