Expression of TGF-β1, -β2 and -β3 in localized and systemic scleroderma

被引:83
作者
Querfeld, C [1 ]
Eckes, B [1 ]
Huerkamp, C [1 ]
Krieg, T [1 ]
Sollberg, S [1 ]
机构
[1] Univ Cologne, Dept Dermatol, D-50924 Cologne, Germany
关键词
localized scleroderma; systemic scleroderma; TGF-beta; transforming growth factor-beta;
D O I
10.1016/S0923-1811(99)00008-0
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Scleroderma is a generalized or localized disorder which leads to fibrosis of the affected organs. TGF-beta has been implicated as a causal agent in its pathogenesis. In mammals, TGF-beta comprises a family of three members, beta 1, beta 2 and beta 3. Since cutaneous wound healing is thought to result either in formation of a scar or in scar-free tissue regeneration, depending on the relative amounts of the beta 3 isoform, the expression of all three isoforms was studied in skin biopsies of patients with either localized or systemic scleroderma. mRNA for all three isoforms was detected in inflammatory skin areas of both disease forms, but never in sclerotic or healthy skin. Immunohistochemical analysis confirmed expression of beta 1 and beta 2 proteins in inflammatory skin of patients, whereas beta 3 protein appeared to be present in the subepidermal area and also found throughout the dermis of patients and healthy dermis as well. (C) 1999 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:13 / 22
页数:10
相关论文
共 28 条
[1]   PRELIMINARY CRITERIA FOR THE CLASSIFICATION OF SYSTEMIC-SCLEROSIS (SCLERODERMA) [J].
不详 .
ARTHRITIS AND RHEUMATISM, 1980, 23 (05) :581-590
[2]   TRANSFORMING GROWTH FACTOR-BETA-1 INDUCES EXTRACELLULAR-MATRIX FORMATION IN GLOMERULONEPHRITIS [J].
BORDER, WA ;
RUOSLAHTI, E .
CELL DIFFERENTIATION AND DEVELOPMENT, 1990, 32 (03) :425-432
[3]  
BORDER WA, 1994, NEW ENGL J MED, V331, P1286
[4]   TRANSFORMING GROWTH FACTOR-BETA-1 IS PRESENT AT SITES OF EXTRACELLULAR-MATRIX GENE-EXPRESSION IN HUMAN PULMONARY FIBROSIS [J].
BROEKELMANN, TJ ;
LIMPER, AH ;
COLBY, TV ;
MCDONALD, JA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (15) :6642-6646
[5]  
Coker RK, 1997, AM J PATHOL, V150, P981
[6]  
CONNOR TB, 1989, J EXP MED, V163, P1661
[7]   INVITRO AND INVIVO ASSOCIATION OF TRANSFORMING GROWTH FACTOR-BETA-1 WITH HEPATIC-FIBROSIS [J].
CZAJA, MJ ;
WEINER, FR ;
FLANDERS, KC ;
GIAMBRONE, MA ;
WIND, R ;
BIEMPICA, L ;
ZERN, MA .
JOURNAL OF CELL BIOLOGY, 1989, 108 (06) :2477-2482
[8]   PATHOPHYSIOLOGY OF SCLERODERMA [J].
FLEISCHMAJER, R .
INTERNATIONAL JOURNAL OF DERMATOLOGY, 1977, 16 (05) :310-318
[9]   TRANSCRIPTION AND EXPRESSION OF TRANSFORMING GROWTH-FACTOR TYPE-BETA IN THE SKIN OF PROGRESSIVE SYSTEMIC-SCLEROSIS - A MEDIATOR OF FIBROSIS [J].
GRUSCHWITZ, M ;
MULLER, PU ;
SEPP, N ;
HOFER, E ;
FONTANA, A ;
WICK, G .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1990, 94 (02) :197-203
[10]   TGF-beta signalling from cell membrane to nucleus through SMAD proteins [J].
Heldin, CH ;
Miyazono, K ;
tenDijke, P .
NATURE, 1997, 390 (6659) :465-471