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维生素 B12 通过对 PTP-3/LAR PRTP 表达的异构体特异性调控,调节神经胶质细胞迁移和突触形成。

Vitamin B12 Regulates Glial Migration and Synapse Formation through Isoform-Specific Control of PTP-3/LAR PRTP Expression.

机构信息

Department of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, NC 27710, USA.

Department of Molecular Biosciences, The University of Kansas, Lawrence, KS 66045, USA.

出版信息

Cell Rep. 2020 Mar 24;30(12):3981-3988.e3. doi: 10.1016/j.celrep.2020.02.113.

Abstract

Vitamin B12 is known to play critical roles during the development and aging of the brain, and vitamin B12 deficiency has been linked to neurodevelopmental and degenerative disorders. However, the underlying molecular mechanisms of how vitamin B12 affects the development and maintenance of the nervous system are still unclear. Here, we report that vitamin B12 can regulate glial migration and synapse formation through control of isoform-specific expression of PTP-3/LAR PRTP (leukocyte-common antigen-related receptor-type tyrosine-protein phosphatase). We found the uptake of diet-supplied vitamin B12 in the intestine to be critical for the expression of a long isoform of PTP-3 (PTP-3A) in neuronal and glial cells. The expression of PTP-3A cell autonomously regulates glial migration and synapse formation through interaction with an extracellular matrix protein NID-1/nidogen 1. Together, our findings demonstrate that isoform-specific regulation of PTP-3/ LAR PRTP expression is a key molecular mechanism that mediates vitamin-B12-dependent neuronal and glial development.

摘要

维生素 B12 在大脑的发育和衰老过程中起着至关重要的作用,维生素 B12 缺乏与神经发育和退行性疾病有关。然而,维生素 B12 如何影响神经系统的发育和维持的潜在分子机制仍不清楚。在这里,我们报告维生素 B12 可以通过控制 PTP-3/LAR PRTP(白细胞共同抗原相关受体型酪氨酸蛋白磷酸酶)的异构体特异性表达来调节神经胶质细胞迁移和突触形成。我们发现,肠道中饮食供应的维生素 B12 的摄取对于神经元和神经胶质细胞中长异构体 PTP-3(PTP-3A)的表达至关重要。PTP-3A 的表达通过与细胞外基质蛋白 NID-1/nidogen 1 的相互作用,自主调节神经胶质细胞的迁移和突触形成。总之,我们的研究结果表明,PTP-3/LAR PRTP 表达的异构体特异性调节是介导维生素 B12 依赖性神经元和神经胶质发育的关键分子机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1320/7281833/664a32f248c1/nihms-1593798-f0002.jpg

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