MODULATION OF KERATINOCYTE GROWTH-FACTOR AND ITS RECEPTOR IN REEPITHELIALIZING HUMAN SKIN

被引:145
作者
MARCHESE, C
CHEDID, M
DIRSCH, OR
CSAKY, KG
SANTANELLI, F
LATINI, C
LAROCHELLE, WJ
TORRISI, MR
AARONSON, SA
机构
[1] MT SINAI SCH MED,DERALD H RUTTENBERG CANC CTR,NEW YORK,NY 10029
[2] UNIV ROMA LA SAPIENZA,NATL INST CANC RES,BIOTECHNOL SECT,I-00161 ROME,ITALY
[3] NEI,IMMUNOL LAB,BETHESDA,MD 20892
[4] NCI,CELLULAR & MOLEC BIOL LAB,BETHESDA,MD 20892
[5] UNIV ROMA LA SAPIENZA,DEPT PLAST SURG & RECONSTRUCT,I-00161 ROME,ITALY
[6] UNIV ROMA LA SAPIENZA,DEPT EXPTL MED & PATHOL,I-00161 ROME,ITALY
关键词
D O I
10.1084/jem.182.5.1369
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We investigated the expression and distribution of keratinocyte growth factor (FGF) (FGF-7) and its receptor (KGFR) during reepithelialization of human skin. KGF mRNA levels increased rapidly by 8-10-fold and remained elevated for several days. In contrast, KGFR transcript levels decreased early but were significantly elevated by 8-9 d. A KGF-immunoglobulin G fusion protein (KGF-HFc), which specifically and sensitively detects the KGFR, localized the receptor to differentiating keratinocytes of control epidermis, but revealed a striking decrease in receptor protein expression during the intermediate period of reepithelization. Suramin, which blocked KGF binding and stripped already bound KGF from its receptor, failed to unmask KGFRs in tissue sections from the intermediate phase of wound repair. The absence of KGFR protein despite increased KGFR transcript levels implies functional receptor downregulation in the presence of increased KGF. This temporal modulation of KGF and KGFRs provides strong evidence for the functional involvement of KGF in human skin reepithelialization.
引用
收藏
页码:1369 / 1376
页数:8
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