EXPRESSION OF IMMUNOREACTIVE AND BIOACTIVE ACTIVIN-A PROTEIN IN ADULT MURINE LUNG AFTER BLEOMYCIN TREATMENT

被引:49
作者
MATSUSE, T
FUKUCHI, Y
ETO, Y
MATSUI, H
HOSOI, T
OKA, T
OHGA, E
NAGASE, T
ORIMO, H
机构
[1] UNIV TOKYO,FAC MED,DEPT PATHOL,BUNKYO KU,TOKYO 113,JAPAN
[2] AJINOMOTO CO INC,CENT RES LABS,KAWASAKI,KANAGAWA 210,JAPAN
关键词
D O I
10.1165/ajrcmb.13.1.7541220
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Activin A is a homodimeric protein structurally and functionally related to transforming growth factor beta (TGF-beta), and the expression of activin A is modulated by TGF-beta. Here, we demonstrate the expression of activin A in normal and bleomycin (BLM)-treated murine lungs. ICR mice were treated with BLM intraperitoneally for 10 days, whereas saline vehicle was injected into control mice. Intra-alveolar fibrotic changes were observed in the lung tissue obtained from the mice at day 14 after the final BLM administration. Immunohistochemical studies using a polyclonal antibody to activin A revealed the presence of activin A in the bronchiolar epithelium and smooth muscle cells of veins in both control and BLM-treated mice. In the BLM-treated mice at days 7 and 14, the marked infiltration of immunoreactive alveolar macrophages was observed in the area of fibrotic changes. Bioactivity of activin A measured by erythroid differentiation factor assay in the conditioned medium of alveolar macrophages obtained from BLM-treated mice at day 14 was significantly increased. These findings indicate that alveolar macrophages are a potent source of activin A after BLM treatment. The present study demonstrates for the first time the abundant expression of activin A in murine lung tissues after BLM administration, suggesting that activin A may play a role in the pathogenesis of BLM-induced pulmonary fibrosis.
引用
收藏
页码:17 / 24
页数:8
相关论文
共 37 条
[1]  
Brain JD, 1977, LUNG BIOL HLTH DISEA, P849
[2]   BLEOMYCIN REGULATION OF TRANSFORMING GROWTH-FACTOR-BETA MESSENGER-RNA IN RAT LUNG FIBROBLASTS [J].
BREEN, E ;
SHULL, S ;
BURNE, S ;
ABSHER, M ;
KELLEY, J ;
PHAN, S ;
CUTRONEO, KR .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1992, 6 (02) :146-152
[3]   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
[4]   INTERSTITIAL LUNG-DISEASES OF UNKNOWN CAUSE .1. DISORDERS CHARACTERIZED BY CHRONIC INFLAMMATION OF THE LOWER RESPIRATORY-TRACT [J].
CRYSTAL, RG ;
BITTERMAN, PB ;
RENNARD, SI ;
HANCE, AJ ;
KEOGH, BA .
NEW ENGLAND JOURNAL OF MEDICINE, 1984, 310 (03) :154-166
[5]   ACTIVIN-A ERYTHROID-DIFFERENTIATION FACTOR IS INDUCED DURING HUMAN MONOCYTE ACTIVATION [J].
ERAMAA, M ;
HURME, M ;
STENMAN, UH ;
RITVOS, O .
JOURNAL OF EXPERIMENTAL MEDICINE, 1992, 176 (05) :1449-1452
[6]   PURIFICATION AND CHARACTERIZATION OF ERYTHROID-DIFFERENTIATION FACTOR (EDF) ISOLATED FROM HUMAN-LEUKEMIA CELL-LINE THP-1 [J].
ETO, Y ;
TSUJI, T ;
TAKEZAWA, M ;
TAKANO, S ;
YOKOGAWA, Y ;
SHIBAI, H .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1987, 142 (03) :1095-1103
[7]  
FUKUDA Y, 1987, AM J PATHOL, V126, P171
[8]  
HASHIMOTO M, 1992, J BIOL CHEM, V267, P4999
[9]   ACTIVIN EDF AS AN INHIBITOR OF NEURAL DIFFERENTIATION [J].
HASHIMOTO, M ;
KONDO, S ;
SAKURAI, T ;
ETOH, Y ;
SHIBAI, H ;
MURAMATSU, M .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1990, 173 (01) :193-200
[10]   INHIBIN AND ACTIVIN REGULATE [H-3]THYMIDINE UPTAKE BY RAT THYMOCYTES AND 3T3 CELLS-INVITRO [J].
HEDGER, MP ;
DRUMMOND, AE ;
ROBERTSON, DM ;
RISBRIDGER, GP ;
DEKRETSER, DM .
MOLECULAR AND CELLULAR ENDOCRINOLOGY, 1989, 61 (01) :133-138