Involvement of the CXCL12/CXCR4 pathway in the recovery of skin following burns

被引:118
作者
Avniel, Shani
Arik, Zaretski
Maly, Alex
Sagie, Assa
Ben Basst, Hanna
Yahana, Merav Darash
Weiss, Ido D.
Pal, Boaz
Wald, Ori
Ad-El, Dean
Fujii, Nobutaka
Arenzana-Seisdedos, Fernando
Jung, Steffen
Galun, Eithan
Gur, Eyal
Peled, Amnon
机构
[1] Hadassah Univ Hosp, Goldyne Savad Inst Gene Therapy, IL-91120 Jerusalem, Israel
[2] Tel Aviv Sourasky Med Ctr, Dept Plast & Reconstruct Surg, Pethach Tikva, Israel
[3] Hadassah Univ Hosp, Dept Pathol, IL-91120 Jerusalem, Israel
[4] Hadassah Univ Hosp, Expt Surg Lab, IL-91120 Jerusalem, Israel
[5] Rabbin Med Ctr, Dept Plast & Reconstruct Surg, Pethach Tikva, Israel
[6] Kyoto Univ, Grad Sch Pharmaceut Sci, Sakyo Ku, Kyoto, Japan
[7] Inst Pasteur, Paris, France
[8] Weizmann Inst Sci, Dept Immunol, IL-76100 Rehovot, Israel
关键词
D O I
10.1038/sj.jid.5700069
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Burn wound healing is a complex process consisting of an inflammatory phase, the formation of granulation tissue, and remodeling. The role of the CXCL12/CXCR4 pathway in the recovery of skin following burns is unknown. We found that CXCL12 is similarly expressed in human, swine, and rat skin by pericyte and endothelial cells, fibrous sheet, fibroblasts, and axons. Following burns, the levels of CXCL12 were markedly increased in human burn blister fluids. One day after injury, there was a gradual increase in the expression of CXCL12 in the hair follicles and in blood vessel endothelium surrounding the burn. Three to 11 days following burns, an increased number of fibroblasts expressing CXCL12 were observed in the recovering dermis of rat, swine, and human skin. In contrast to CXCL12, CXCR4 expression was detected in proliferating epithelial cells as well as in eosinophils and mononuclear cells infiltrating the skin. In vitro, CXCL12 was expressed by primary human skin fibroblasts, but not by keratinocytes, and was stimulated by wounding a confluent cell layer of these fibroblasts. Blocking the CXCR4/CXCL12 axis resulted in the significant reduction in eosinophil accumulation in the dermis and improved epithelialization. Thus, blocking CXCR4/CXCL12 interaction may significantly improve skin recovery after burns.
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收藏
页码:468 / 476
页数:9
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