Protein expression of fibroblast growth factor receptor-1 in keratinocytes during wound healing in rat skin

被引:20
作者
Takenaka, H [1 ]
Kishimoto, S [1 ]
Tooyama, I [1 ]
Kimura, H [1 ]
Yasuno, H [1 ]
机构
[1] SHIGA UNIV MED SCI,INST MOL NEUROL,OTSU,SHIGA 52021,JAPAN
关键词
immunohistochemistry; epidermis; blood vessel;
D O I
10.1111/1523-1747.ep12276740
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Fibroblast growth factors have been shown to play important roles in wound healing, To define their sites of action, we examined the expression of fibroblast growth factor receptor-1 (FGFR-1) during burn wound healing in rat skin by immunohistochemistry and western blot analysis. In cryostat sections of intact skin, little or no staining was observed, After a burn, however, staining for FGFR-1 was found in newly forming epidermis. The suprabasal layer of such epidermis, composed mostly of regenerating keratinocytes, was stained intensely, whereas keratinocytes in newly forming hair follicles were devoid of staining. Staining gradually decreased week by week after wound closure and was hardly visible 10 weeks after the burn, when the thickness of the epidermis had returned to the normal level, Staining was also found in small blood vessels and capillaries of granulation tissues of the dermis. Western blot analysis using the same antiserum was performed in the newly forming epidermis 10 d after the burn. A single band was detected with an apparent molecular weight of 120 kDa, corresponding to the short membrane-bound form of rat FGFR-1. Our study indicates that FGFR-1 is expressed during wound healing, mainly in regenerating epidermis and to some extent in blood vessels of the dermis, Fibroblast growth factors may affect the proliferation and differentiation of epidermal keratinocytes as well as angiogenesis in the dermis via the FGFR-1 expressed during wound healing.
引用
收藏
页码:108 / 112
页数:5
相关论文
共 44 条
[1]   KERATINOCYTE GROWTH-FACTOR - A FIBROBLAST GROWTH-FACTOR FAMILY MEMBER WITH UNUSUAL TARGET-CELL SPECIFICITY [J].
AARONSON, SA ;
BOTTARO, DP ;
MIKI, T ;
RON, D ;
FINCH, PW ;
FLEMING, TP ;
AHN, J ;
TAYLOR, WG ;
RUBIN, JS .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1991, 638 :62-77
[2]  
ANTONIADES HN, 1993, AM J PATHOL, V142, P1099
[3]   INJURY INDUCES INVIVO EXPRESSION OF PLATELET-DERIVED GROWTH-FACTOR (PDGF) AND PDGF RECEPTOR MESSENGER-RNAS IN SKIN EPITHELIAL-CELLS AND PDGF MESSENGER-RNA IN CONNECTIVE-TISSUE FIBROBLASTS [J].
ANTONIADES, HN ;
GALANOPOULOS, T ;
NEVILLEGOLDEN, J ;
KIRITSY, CP ;
LYNCH, SE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (02) :565-569
[4]   STIMULATION OF WOUND-HEALING, USING BRAIN EXTRACT WITH FIBROBLAST GROWTH-FACTOR (FGF) ACTIVITY .1. QUANTITATIVE AND BIOCHEMICAL-STUDIES INTO FORMATION OF GRANULATION-TISSUE [J].
BUNTROCK, P ;
JENTZSCH, KD ;
HEDER, G .
EXPERIMENTAL PATHOLOGY, 1982, 21 (01) :46-53
[5]   GROWTH-FACTORS IN DEVELOPMENT, TRANSFORMATION, AND TUMORIGENESIS [J].
CROSS, M ;
DEXTER, TM .
CELL, 1991, 64 (02) :271-280
[6]  
DANILENKO DM, 1995, AM J PATHOL, V147, P145
[7]  
Davidson J, 1988, Prog Clin Biol Res, V266, P63
[8]   ACCELERATED WOUND REPAIR, CELL-PROLIFERATION, AND COLLAGEN ACCUMULATION ARE PRODUCED BY A CARTILAGE-DERIVED GROWTH-FACTOR [J].
DAVIDSON, JM ;
KLAGSBRUN, M ;
HILL, KE ;
BUCKLEY, A ;
SULLIVAN, R ;
BREWER, PS ;
WOODWARD, SC .
JOURNAL OF CELL BIOLOGY, 1985, 100 (04) :1219-1227
[9]   CLONING AND EXPRESSION OF 2 DISTINCT HIGH-AFFINITY RECEPTORS CROSS-REACTING WITH ACIDIC AND BASIC FIBROBLAST GROWTH-FACTORS [J].
DIONNE, CA ;
CRUMLEY, G ;
BELLOT, F ;
KAPLOW, JM ;
SEARFOSS, G ;
RUTA, M ;
BURGESS, WH ;
JAYE, M ;
SCHLESSINGER, J .
EMBO JOURNAL, 1990, 9 (09) :2685-2692
[10]   BASIC FIBROBLAST GROWTH-FACTOR IN THE EARLY HUMAN BURN WOUND [J].
GIBRAN, NS ;
ISIK, FF ;
HEIMBACH, DM ;
GORDON, D .
JOURNAL OF SURGICAL RESEARCH, 1994, 56 (03) :226-234