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神经生长相关蛋白GAP - 43的过表达诱导转基因小鼠成年神经系统中的神经发芽。

Overexpression of the neural growth-associated protein GAP-43 induces nerve sprouting in the adult nervous system of transgenic mice.

作者信息

Aigner L, Arber S, Kapfhammer J P, Laux T, Schneider C, Botteri F, Brenner H R, Caroni P

机构信息

Friedrich Miescher Institute, Basel, Switzerland.

出版信息

Cell. 1995 Oct 20;83(2):269-78. doi: 10.1016/0092-8674(95)90168-x.

Abstract

Regulation of neurite outgrowth and structural plasticity may involve the expression of intrinsic determinants controlling growth competence. We have tested this concept by targeting constitutive expression of the growth-associated protein GAP-43 to the neurons of adult transgenic mice. Such mice showed striking spontaneous nerve sprouting at the neuromuscular junction and in the terminal field of hippocampal mossy fibers. In control mice, these nerve fibers did not express GAP-43, and did not sprout spontaneously. Lesion-induced nerve sprouting and terminal arborization during reinnervation were greatly potentiated in GAP-43-overexpressing mice. A mutant GAP-43 that cannot be phosphorylated by PKC had reduced sprout-promoting activity. The results establish GAP-43 as an intrinsic presynaptic determinant for neurite outgrowth and plasticity.

摘要

神经突生长和结构可塑性的调节可能涉及控制生长能力的内在决定因素的表达。我们通过将生长相关蛋白GAP-43的组成型表达靶向成年转基因小鼠的神经元来验证这一概念。此类小鼠在神经肌肉接头处和海马苔藓纤维的终末区域出现了显著的自发性神经芽生。在对照小鼠中,这些神经纤维不表达GAP-43,也不会自发芽生。在GAP-43过表达的小鼠中,损伤诱导的神经芽生和再支配过程中的终末分支显著增强。一种不能被蛋白激酶C磷酸化的突变型GAP-43具有降低的促芽活性。这些结果确立了GAP-43作为神经突生长和可塑性的内在突触前决定因素。

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