Effect of AMD3100 on SDF-1 induced proliferation and migration of endothelial progenitor cells
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Effect of AMD3100 on SDF-1 induced proliferation and migration of endothelial progenitor cells
Journal of Army Medical UniversityVol. 29, Issue 6, Pages: 475-478(2007)
作者机构:
第三军医大学:新桥医院心血管内科,全军心血管内科研究所,大坪医院野战外科研究所心血管内科
作者简介:
基金信息:
DOI:
CLC:R322.12;R329.28;R392.12
Published:2007,
Published Online:30 March 2007,
稿件说明:
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YIN YANG-GUANG, HUANG LAN, ZHAO XIAO-HUI, et al. Effect of AMD3100 on SDF-1 induced proliferation and migration of endothelial progenitor cells. [J]. Journal of army medical university, 2007, 29(6): 475-478.
DOI:
YIN YANG-GUANG, HUANG LAN, ZHAO XIAO-HUI, et al. Effect of AMD3100 on SDF-1 induced proliferation and migration of endothelial progenitor cells. [J]. Journal of army medical university, 2007, 29(6): 475-478.DOI:
Effect of AMD3100 on SDF-1 induced proliferation and migration of endothelial progenitor cells
Objective To investigate the effect of stromal cell derived factor-1 (SDF-1) on the proliferation and migration of endothelial progenitor cells (EPCs) and whether such an effect could be blocked with AMD3100. Methods EPCs in 96-well plates were co-cultured with SDF-1α (1
5
10 ng/ml)
or AMD3100 or 5 ng/ml SDF-1α +AMD3100 (10
50
100 ng/ml) for 24 h. EPCs proliferation was assayed with MTT. EPCs was incubated with or without 10 ng/ml AMD3100 for 1 h
then induced by SDF-1α or without to start migration at 37 ℃ for 6 h. EPCs migration was evaluated by using a modified Boyden chamber assay. Results SDF-1α increased EPCs proliferation activity in a dose-dependent manner
but its effect induced by 5 ng/ml SDF-1α was inhibited completely with 10 ng/ml AMD3100. The proliferation of EPCs treated with AMD3100 alone was inhibited. SDF-1α increased EPCs migration
but this effect was completely blocked by AMD3100. The migration of EPCs was reduced by AMD3100 alone. Conclusion SDF-1α can improve EPCs proliferation and migration
and its effect could be blocked with AMD3100. The treatment of AMD3100 alone decreases the proliferation and migration of EPCs.