IMMUNOHISTOCHEMICAL LOCALIZATION OF CYTOKINES IN NEVI

被引:23
作者
FLEMING, MG
HOWE, SF
CANDEL, AG
机构
[1] LOYOLA UNIV, MED CTR, DEPT PATHOL, MAYWOOD, IL 60153 USA
[2] RUSH PRESBYTERIAN ST LUKES MED CTR, DEPT PATHOL, CHICAGO, IL 60612 USA
关键词
D O I
10.1097/00000372-199212000-00002
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Eight common nevi and 11 dysplastic nevi were evaluated for the presence of basic fibroblast growth factor, platelet-derived growth factor, transforming growth factor-alpha, interleukin-1-alpha, and interleukin-1-beta by immunohistochemical labelling with highly specific monoclonal antibodies. Basic fibroblast growth factor was abundant in the nevus cells and keratinocytes of nevi. Dysplastic nevus cells on average stained less intensely for basic fibroblast growth factor than did common nevus cells. In both types of nevi, basic fibroblast growth factor was identified in the basement membranes at the dermoepidermal junction and surrounding nevus celt nests and individual nevus celts. Labelling of nevus cells for transforming growth factor-alpha was variable, while there was moderate labelling for platelet-derived growth factor and light labelling for interleukin-1-alpha. Only two nevi, both dysplastic, stained (very faintly) for interleukin-1-beta. It is possible that these cytokines, especially basic fibroblast growth factor, act in autocrine fashion to maintain nevocellular growth and may also contribute to the epidermal hyperplasia and fibrosis frequently observed in nevi.
引用
收藏
页码:496 / 503
页数:8
相关论文
共 50 条
[1]   BASIC FIBROBLAST GROWTH-FACTOR BINDS TO SUBENDOTHELIAL EXTRACELLULAR-MATRIX AND IS RELEASED BY HEPARITINASE AND HEPARIN-LIKE MOLECULES [J].
BASHKIN, P ;
DOCTROW, S ;
KLAGSBRUN, M ;
SVAHN, CM ;
FOLKMAN, J ;
VLODAVSKY, I .
BIOCHEMISTRY, 1989, 28 (04) :1737-1743
[2]  
BENNICELLI JL, 1989, CANCER RES, V49, P930
[3]  
BERGMAN W, 1988, CANCER, V61, P1660, DOI 10.1002/1097-0142(19880415)61:8<1660::AID-CNCR2820610825>3.0.CO
[4]  
2-X
[5]  
BERNSTEIN MJ, 1984, JAMA-J AM MED ASSOC, V251, P1864
[6]   GROWTH-FACTOR MODULATION OF MELANOMA GROWTH STIMULATORY ACTIVITY MESSENGER-RNA EXPRESSION IN HUMAN-MALIGNANT MELANOMA-CELLS CORRELATES WITH CELL-GROWTH [J].
BORDONI, R ;
THOMAS, G ;
RICHMOND, A .
JOURNAL OF CELLULAR BIOCHEMISTRY, 1989, 39 (04) :421-428
[7]   ORIGIN OF FAMILIAL MALIGNANT MELANOMAS FROM HERITABLE MELANOCYTIC LESIONS - B-K MOLE SYNDROME [J].
CLARK, WH ;
REIMER, RR ;
GREENE, M ;
AINSWORTH, AM ;
MASTRANGELO, MJ .
ARCHIVES OF DERMATOLOGY, 1978, 114 (05) :732-738
[8]   A STUDY OF TUMOR PROGRESSION - THE PRECURSOR LESIONS OF SUPERFICIAL SPREADING AND NODULAR MELANOMA [J].
CLARK, WH ;
ELDER, DE ;
GUERRY, D ;
EPSTEIN, MN ;
GREENE, MH ;
VANHORN, M .
HUMAN PATHOLOGY, 1984, 15 (12) :1147-1165
[9]   PRODUCTION AND AUTOINDUCTION OF TRANSFORMING GROWTH FACTOR-ALPHA IN HUMAN KERATINOCYTES [J].
COFFEY, RJ ;
DERYNCK, R ;
WILCOX, JN ;
BRINGMAN, TS ;
GOUSTIN, AS ;
MOSES, HL ;
PITTELKOW, MR .
NATURE, 1987, 328 (6133) :817-820
[10]   UVR INDUCTION OF TGF-ALPHA - A POSSIBLE AUTOCRINE MECHANISM FOR THE EPIDERMAL MELANOCYTIC RESPONSE AND FOR PROMOTION OF EPIDERMAL CARCINOGENESIS [J].
ELLEM, KAO ;
CULLINAN, M ;
BAUMANN, KC ;
DUNSTAN, A .
CARCINOGENESIS, 1988, 9 (05) :797-801