Tropism mechanism of stem cells targeting injured brain tissues by stromal cell-derived factor-1.
- Author:
Sai ZHANG
1
;
Xiao-zhi LIU
;
Zhen-lin LIU
;
Chong-zhi SHANG
;
Qun-liang HU
Author Information
- Publication Type:Journal Article
- MeSH: Animals; Brain Injuries; pathology; Cell Movement; Cells, Cultured; Chemokine CXCL12; analysis; physiology; Neurons; cytology; Rats; Receptors, CXCR4; analysis; physiology; Stem Cells; physiology; Tropism
- From: Chinese Journal of Traumatology 2009;12(5):263-268
- CountryChina
- Language:English
-
Abstract:
OBJECTIVETo explore the role and function of stromal cell-derived factor-1 (SDF-1) in stem cells migrating into injured brain area.
METHODSRat-derived nerve stem cells (NSCs) were isolated and cultured routinely. Transwell system was used to observe the migration ability of NSCs into injured nerve cells. Immunocytochemistry was used to explore the expression of chemotactic factor receptor-4 (CXCR-4) in NSCs. In vivo, we applied immunofluorescence technique to observe the migration of NSCs into injured brain area. Immunofluorescence technique and Western blotting were used to test expression level of SDF-1. After AMD3100 (a special chemical blocker) blocking CXCR-4, the migration ability of NSCs was tested in vivo and in vitro, respectively.
RESULTSNSCs displayed specific tropism for injured nerve cells or traumatic brain area in vivo and in vitro. The expression level of SDF-1 in traumatic brain area increased remarkably and the expression level of CXCR-4 in the NSCs increased simultaneously. After AMD3100 blocking the expression of CXCR-4, the migration ability of NSCs decreased significantly both in vivo and in vitro.
CONCLUSIONSSDF-1 may play a key role in stem cells migrating into injured brain area through specially combining with CXCR-4.
