Low-density lipoprotein receptor-related protein-1 (LRP1) in the glial lineage modulates neuronal excitability.

Andreas Faissner
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Abstract

The low-density lipoprotein related protein receptor 1 (LRP1), also known as CD91 or α-Macroglobulin-receptor, is a transmembrane receptor that interacts with more than 40 known ligands. It plays an important biological role as receptor of morphogens, extracellular matrix molecules, cytokines, proteases, protease inhibitors and pathogens. In the CNS, it has primarily been studied as a receptor and clearance agent of pathogenic factors such as Aβ-peptide and, lately, Tau protein that is relevant for tissue homeostasis and protection against neurodegenerative processes. Recently, it was found that LRP1 expresses the Lewis-X (Lex) carbohydrate motif and is expressed in the neural stem cell compartment. The removal of Lrp1 from the cortical radial glia compartment generates a strong phenotype with severe motor deficits, seizures and a reduced life span. The present review discusses approaches that have been taken to address the neurodevelopmental significance of LRP1 by creating novel, lineage-specific constitutive or conditional knockout mouse lines. Deficits in the stem cell compartment may be at the root of severe CNS pathologies.

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神经胶质谱系中的低密度脂蛋白受体相关蛋白-1 (LRP1)调节神经元兴奋性。
低密度脂蛋白相关蛋白受体1 (LRP1),也称为CD91或α-巨球蛋白受体,是一种跨膜受体,可与40多种已知配体相互作用。它作为形态因子、细胞外基质分子、细胞因子、蛋白酶、蛋白酶抑制剂和病原体的受体发挥着重要的生物学作用。在中枢神经系统中,它主要被研究为致病因子的受体和清除剂,如a β-肽和最近的Tau蛋白,它们与组织稳态和保护神经退行性过程有关。最近,研究发现LRP1表达Lewis-X (Lex)碳水化合物基序,并在神经干细胞隔室中表达。从皮质放射状胶质细胞室中去除Lrp1会产生强烈的表型,导致严重的运动缺陷、癫痫发作和寿命缩短。本综述讨论了通过创建新颖的、谱系特异性的构成或条件敲除小鼠系来解决LRP1神经发育意义的方法。干细胞区室的缺陷可能是严重中枢神经系统病变的根源。
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