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髓鞘蛋白脂蛋白:在髓鞘结构中的功能与其在少突胶质细胞发育中的作用不同。

Myelin proteolipid protein: function in myelin structure is distinct from its role in oligodendrocyte development.

作者信息

Nadon N L, West M

机构信息

Oklahoma Medical Research Foundation, Oklahoma City, Okla., USA.

出版信息

Dev Neurosci. 1998;20(6):533-9. doi: 10.1159/000017354.

Abstract

The myelin proteolipid proteins PLP and DM20 are essential for the compaction of central nervous system myelin and they play an important role in the maturation of the oligodendrocyte. The specific function of the less abundant DM20 isoform is still unknown, but rescue experiments previously indicated that both isoforms are necessary for oligodendrocyte maturation. In vitro experiments have suggested DM20 may assist in the translocation of PLP into the membrane. We tested this hypothesis in vivo, by investigating whether wild-type PLP derived from a transgene could be incorporated into the myelin membrane of Plp mutant rumpshaker mice. We previously demonstrated that expression of the PLP transgene alone in a more severe Plp mutant, jimpy mouse, did not result in PLP incorporation into the myelin. Here we report that there was significantly more PLP in white matter from rumpshaker expressing the PLP transgene than their nontransgenic rumpshaker littermates and that myelin structure was improved. The delay in oligodendrocyte development was not alleviated by expression of the PLP transgene however, supporting an essential role for DM20 in oligodendrocyte maturation.

摘要

髓磷脂蛋白脂蛋白(PLP)和DM20对于中枢神经系统髓磷脂的紧密化至关重要,并且它们在少突胶质细胞的成熟过程中发挥重要作用。含量较少的DM20异构体的具体功能仍然未知,但先前的拯救实验表明这两种异构体对于少突胶质细胞的成熟都是必需的。体外实验表明,DM20可能有助于PLP转运到膜中。我们通过研究源自转基因的野生型PLP是否可以整合到Plp突变体摇尾小鼠的髓磷脂膜中,在体内验证了这一假设。我们先前证明,在更严重的Plp突变体jimpy小鼠中单独表达PLP转基因不会导致PLP整合到髓磷脂中。在此我们报告,与未转基因的摇尾同窝小鼠相比,表达PLP转基因的摇尾小鼠白质中的PLP明显更多,并且髓磷脂结构得到改善。然而,PLP转基因的表达并未缓解少突胶质细胞发育的延迟,这支持了DM20在少突胶质细胞成熟中的重要作用。

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