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SDF-1/CXCR4/CXCR7在脑缺血后神经元再生中的作用

The Role of SDF-1/CXCR4/CXCR7 in Neuronal Regeneration after Cerebral Ischemia.

作者信息

Cheng Xi, Wang Huibin, Zhang Xiuchun, Zhao Shanshan, Zhou Zhike, Mu Xiaopeng, Zhao Chuansheng, Teng Weiyu

机构信息

Neurology, The First Hospital of China Medical University, Shenyang, China.

Geriatrics, The First Hospital of China Medical University, Shenyang, China.

出版信息

Front Neurosci. 2017 Oct 24;11:590. doi: 10.3389/fnins.2017.00590. eCollection 2017.


DOI:10.3389/fnins.2017.00590
PMID:29123467
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5662889/
Abstract

Stromal cell-derived factor-1 is a chemoattractant produced by bone marrow stromal cell lines. It is recognized as a critical factor in the immune and central nervous systems (CNSs) as well as exerting a role in cancer. SDF-1 activates two G protein-coupled receptors, CXCR4 and CXCR7; these are expressed in both developing and mature CNSs and participate in multiple physiological and pathological events, e.g., inflammatory response, neurogenesis, angiogenesis, hematopoiesis, cancer metastasis, and HIV infection. After an ischemic stroke, SDF-1 levels robustly increase in the penumbra regions and participate in adult neural functional repair. Here we will review recent findings about SDF-1 and its receptor, analyse their functions in neurogeneration after brain ischemic injury: i.e., how the system promotes the proliferation, differentiation and migration of neural precursor cells and mediates axonal elongation and branching.

摘要

基质细胞衍生因子-1是一种由骨髓基质细胞系产生的趋化因子。它被认为是免疫和中枢神经系统中的关键因子,同时在癌症中也发挥作用。SDF-1激活两种G蛋白偶联受体,即CXCR4和CXCR7;它们在发育中的和成熟的中枢神经系统中均有表达,并参与多种生理和病理过程,例如炎症反应、神经发生、血管生成、造血、癌症转移和HIV感染。缺血性中风后,SDF-1水平在半暗带区域显著升高,并参与成年神经功能修复。在此,我们将综述关于SDF-1及其受体的最新研究发现,分析它们在脑缺血损伤后神经发生中的作用:即该系统如何促进神经前体细胞的增殖、分化和迁移,并介导轴突的伸长和分支。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d7b/5662889/67c69d104faa/fnins-11-00590-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d7b/5662889/01278d656a8a/fnins-11-00590-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d7b/5662889/47cd2d44b489/fnins-11-00590-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d7b/5662889/67c69d104faa/fnins-11-00590-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d7b/5662889/01278d656a8a/fnins-11-00590-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d7b/5662889/47cd2d44b489/fnins-11-00590-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d7b/5662889/67c69d104faa/fnins-11-00590-g0003.jpg

相似文献

[1]
The Role of SDF-1/CXCR4/CXCR7 in Neuronal Regeneration after Cerebral Ischemia.

Front Neurosci. 2017-10-24

[2]
SDF-1/CXCR7 Chemokine Signaling is Induced in the Peri-Infarct Regions in Patients with Ischemic Stroke.

Aging Dis. 2018-4-1

[3]
Regional and cellular localization of the CXCl12/SDF-1 chemokine receptor CXCR7 in the developing and adult rat brain.

J Comp Neurol. 2008-9-10

[4]
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Curr Drug Targets. 2012-2

[5]
Stromal cell-derived factor-1 and its receptor CXCR4 in adult neurogenesis after cerebral ischemia.

Restor Neurol Neurosci. 2013

[6]
Pattern of CXCR7 Gene Expression in Mouse Brain Under Normal and Inflammatory Conditions.

J Neuroimmune Pharmacol. 2015-5-22

[7]
A dual role for the SDF-1/CXCR4 chemokine receptor system in adult brain: isoform-selective regulation of SDF-1 expression modulates CXCR4-dependent neuronal plasticity and cerebral leukocyte recruitment after focal ischemia.

J Neurosci. 2002-7-15

[8]
The role of SDF-1-CXCR4/CXCR7 axis in biological behaviors of adipose tissue-derived mesenchymal stem cells in vitro.

Biochem Biophys Res Commun. 2013-10-30

[9]
CXCR7 Mediates Neural Progenitor Cells Migration to CXCL12 Independent of CXCR4.

Stem Cells. 2015-8

[10]
CXCR4 and CXCR7 form a functional receptor unit for SDF-1/CXCL12 in primary rodent microglia.

Neuropathol Appl Neurobiol. 2013-10

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本文引用的文献

[1]
A Novel CXCR4 Antagonist CX549 Induces Neuroprotection in Stroke Brain.

Cell Transplant. 2017-4-13

[2]
Intrinsic Axonal Growth and the Drive for Regeneration.

Front Neurosci. 2016-10-27

[3]
CXCR7 Participates in CXCL12-mediated Cell Cycle and Proliferation Regulation in Mouse Neural Progenitor Cells.

Curr Mol Med. 2016

[4]
SDF-1 and CXCR4 play an important role in adult SVZ lineage cell proliferation and differentiation.

Brain Res. 2017-2-15

[5]
Oligodendrocyte precursors migrate along vasculature in the developing nervous system.

Science. 2016-1-22

[6]
Oligodendrocyte Development and Plasticity.

Cold Spring Harb Perspect Biol. 2015-8-20

[7]
CXCL12 Gene Therapy Ameliorates Ischemia-Induced White Matter Injury in Mouse Brain.

Stem Cells Transl Med. 2015-10

[8]
Mechanisms of cell-cell interaction in oligodendrogenesis and remyelination after stroke.

Brain Res. 2015-10-14

[9]
bFGF Protects Pre-oligodendrocytes from Oxygen/Glucose Deprivation Injury to Ameliorate Demyelination.

Cell Mol Neurobiol. 2015-10

[10]
CXCR7 Mediates Neural Progenitor Cells Migration to CXCL12 Independent of CXCR4.

Stem Cells. 2015-8

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