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Review
. 2017 Oct 24:11:590.
doi: 10.3389/fnins.2017.00590. eCollection 2017.

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

Affiliations
Review

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

Xi Cheng et al. Front Neurosci. .

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.

Keywords: CXCR4; CXCR7; ischemic stroke; neurogenesis; stromal cell-derived factor-1.

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Figures

Figure 1
Figure 1
Overview of signaling pathways of the SDF-1/CXCR4/CXCR7 network. formula image,formula image, formula image,+P indicate processes involving in direct promoting effect, indirect promoting effect, inhibitory effect, and phosphorylation effect, respectively.
Figure 2
Figure 2
Schematic overview of SDF-1/CXCR4/CXCR7 interactions and their effects in neurogenesis.
Figure 3
Figure 3
Schematic overview of signaling pathways involved in the SDF-1/CXCR4/CXCR7 mediated axonal outgrowth, cells migration, and chemotaxis.

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