前往化源商城

Wound Repair And Regeneration 2015-01-01

The role of SDF-1 in homing of human adipose-derived stem cells.

Ewa K Stuermer, Alexandra Lipenksy, Oliver Thamm, Edmund Neugebauer, Nadine Schaefer, Paul Fuchs, Bertil Bouillon, Paola Koenen

文献索引:Wound Repair Regen. 23 , 82-9, (2015)

全文:HTML全文

摘要

One of the putative pathophysiological mechanisms of chronic wounds is a disturbed homing of stem cells. In this project, the stromal cell-derived factor 1 (SDF-1)/C-X-C chemokine receptor (CXCR) 4 and SDF-1/CXCR7 pathway were focused in human adipose-derived stem cells (ASCs). ASCs were incubated with acute (AWF) or chronic wound fluid (CWF) to analyze their effects by quantitative real-time polymerase chain reaction (SDF-1, CXCR4, CXCR7, TIMP3), enzyme-linked immunosorbent assay (SDF-1 in WFs and supernatant), and transwell migration assay with/without antagonization. Whereas SDF-1 amounted 73.5 pg/mL in AWF, it could not be detected in CWF. Incubation with AWF led to a significant enhancement (129.7 pg/mL vs. 95.5 pg/mL), whereas CWF resulted in a significant reduction (30 pg/mL vs. 95.5 pg/mL) of SDF-1 in ASC supernatant. The SDF-1 receptor CXCR7 was detected on ASCs. AWF but not CWF significantly induced ASC migration, which was inhibited by CXCR4 and CXCR7 antagonists. Expressions of SDF-1, CXCR4, and CXCR7 were significantly stimulated by AWF while TIMP3 expression was reduced. In conclusion, an uncontrolled inflammation in the chronic wound environment, indicated by a reduced SDF-1 expression, resulted in a decreased ASC migration. A disturbed SDF-1/CXCR4 as well as SDF-1/CXCR7 pathway seems to play an important role in the impaired healing of chronic wounds. © 2015 by the Wound Healing Society.

相关化合物

结构式 名称/CAS号 全部文献
硫氰酸胍 结构式 硫氰酸胍
CAS:593-84-0
氢氧化钙 结构式 氢氧化钙
CAS:1305-62-0
4',6-二脒基-2-苯基吲哚二盐酸盐 结构式 4',6-二脒基-2-苯基吲哚二盐酸盐
CAS:28718-90-3