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

被引:0
|
作者
Faissner, Andreas [1 ]
机构
[1] Ruhr Univ Bochum, Dept Cell Morphol & Mol Neurobiol, Bochum, Germany
来源
关键词
astrocyte; Emx1; epilepsy; low-density lipoprotein receptor-related protein-1 (LRP1); NG2 (CSPG4) chondroitin sulfate proteoglycan; radial glia; tissue plasminogen activator (tPA); (GLAST) glutamate aspartate transporter; TISSUE-PLASMINOGEN ACTIVATOR; METHYL-D-ASPARTATE; NMDA RECEPTOR; NEURAL STEM; NEURITE OUTGROWTH; RADIAL GLIA; A-BETA; TYROSINE PHOSPHORYLATION; CONDITIONAL DELETION; MEDIATED ACTIVATION;
D O I
10.3389/fnetp.2023.1190240
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
The low-density lipoprotein related protein receptor 1 (LRP1), also known as CD91 or alpha-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 A beta-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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页数:15
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