中国康复理论与实践2016，Vol.22Issue(7)：769-773,5.DOI:10.3969/j.issn.1006-9771.2016.07.006
高压氧对脑外伤外源性骨髓间充质干细胞归巢的影响
Effects of Hyperbaric Oxygen on Homing of Exogenous Bone Marrow Mesenchymal Stem Cells after Traumatic Brain Injury
摘要
Abstract
Objective To investigate the effects of hyperbaric oxygen (HBO) on homing of exogenous bone marrow mesenchymal stem cells (BMSCs) after traumatic brain injury (TBI) in rats. Methods BMSCs were isolated and cultured with Ficoll density gradient centrifuga-tion, and the surface markers (CD29, CD90, CD45, CD11b) of the third generation were identified with flow cytometry. The authenticated BM-SCs were processed by the cell membrane fluorescent probe CM-DiI before transplantation. Thirty-six Sprague-Dawley rats were divided in-to Sham group (n=6), TBI group (n=6), BMSCs group (n=12), HBO+BMSCs group (n=12). The number and locations of homing of tracing BMSCs were observed under fluorescent microscope after frozen sections, and the expression of stromal cell-derived factor 1 (SDF-1) and CXC chemokine receptor type 4 (CXCR4) proteins were detected with Western blotting one and three days after BMSCs transplantation. Re-sults The fluorescence-labeled BMSCs focused on the injured hemisphere, especially around the damaged brain tissue. The number of hom-ing was more in HBO+BMSCs group than in BMSCs group at the same time (P<0.01), and increased in both groups three days after trans-plantation compared with those of one day after transplantation (P<0.01). The expression of SDF-1 and CXCR4 protein were more in HBO+BMSCs group than in BMSCs group (P<0.05). Conclusion HBO can promote the exogenous BMSCs homing to damaged brain tissue in rats after traumatic brain injury, which is related to the enhancement of SDF-1/CXCR4 axis.关键词
脑外伤/高压氧/骨髓间充质干细胞/归巢/大鼠Key words
traumatic brain injury/hyperbaric oxygen/bone marrow mesenchymal stem cells/homing/rats分类
医药卫生引用本文复制引用
刘杨,丁政,唐朝正,周苏键,卢晓欣,彭慧平..高压氧对脑外伤外源性骨髓间充质干细胞归巢的影响[J].中国康复理论与实践,2016,22(7):769-773,5.基金项目
1.南京军区福州总医院专项基金项目(No.2011-009)；2.南京军区福州总医院创新团队基金项目(No.2014CXTD08)。 （No.2011-009）
