Frozen cultured sheets of human epidermal keratinocytes enhance healing of full-thickness wounds in mice

被引:0
|
作者
Elisa Tamariz
Meytha Marsch-Moreno
Federico Castro-Muñozledo
Victor Tsutsumi
W. Kuri-Harcuch
机构
[1] Department of Cell Biology,
[2] Centro de Investigación y Estudios Avanzados del IPN,undefined
[3] Apdo,undefined
[4] PO Box 14–740,undefined
[5] Mexico City,undefined
[6] 07000,undefined
[7] Mexico e-mail: walid@cell.cinvestav.mx; Tel.: +1–525 747 7000,undefined
[8] ext. 5521; Fax: +1–525 747 7081,undefined
[9] Department of Experimental Pathology,undefined
[10] Centro de Investigación y Estudios Avanzados del IPN,undefined
[11] Apdo,undefined
[12] PO Box 14–740,undefined
[13] Mexico City 07000,undefined
[14] Mexico,undefined
来源
Cell and Tissue Research | 1999年 / 296卷
关键词
Key words Cultured epidermis; Keratinocyte; Epithelialization; Wound healing; Human; Mouse (NMRI);
D O I
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中图分类号
学科分类号
摘要
 Sheets of cultured allogeneic human keratinocytes have been used for the treatment of burns and chronic leg ulcers but there has been no animal assay for the therapeutic action of these cultures. In order to analyze the effects of frozen cultures of human keratinocytes on wound healing, we have developed such an assay based on the rate of repair of full-thickness skin wounds in immunocompetent NMR1 mice. Reepithelialization of the control wounds, originating from the murine epithelium at the edge of the wound, occurred at a constant rate of advance of 150 µm/day. When frozen cultured human epidermal sheets were thawed at room temperature for 5–10 min and applied to the surface of the wound, the murine epithelium advanced at 267 µm/day. Most wounds treated with frozen cultures completely healed after 10 days, whereas most control wounds required 16 days. The accelerated reepithelialization did not depend on the presence of proliferative human keratinocytes in the frozen cultures. The cultures also promoted early formation of granulation tissue and laminin deposition over the surface of the wound bed. This simple assay should permit quantitative analysis of the effects on healing exerted not only by cultured cells, but also by proteins and small molecules.
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页码:575 / 585
页数:10
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