ELEVATED BASIC FIBROBLAST GROWTH-FACTOR IN THE SERUM OF PATIENTS WITH DUCHENNE MUSCULAR-DYSTROPHY

被引:76
作者
DAMORE, PA
BROWN, RH
KU, PT
HOFFMAN, EP
WATANABE, H
ARAHATA, K
ISHIHARA, T
FOLKMAN, J
机构
[1] HARVARD UNIV,SCH MED,PROGRAM CELL & DEV BIOL,BOSTON,MA 02115
[2] HARVARD UNIV,SCH MED,DEPT PATHOL,BOSTON,MA 02115
[3] HARVARD UNIV,SCH MED,DEPT ANAT,BOSTON,MA 02115
[4] MASSACHUSETTS GEN HOSP,CECIL B DAY LAB NEUROMUSCULAR RES,BOSTON,MA 02114
[5] UNIV PITTSBURGH,SCH MED,DEPT MOLEC GENET & BIOCHEM,PITTSBURGH,PA 15261
[6] TAKEDA CHEM CORP,OSAKA,JAPAN
[7] NATL INST NEUROSCI,TOKYO,JAPAN
[8] NATL HIGASHI SAITAMA HOSP,SAITAMA,JAPAN
关键词
D O I
10.1002/ana.410350320
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The mechanism whereby dystrophin deficiency leads to excessive fibrosis and muscle degeneration is not known. The absence of dystrophin in skeletal muscle is associated with reduced plasma membrane stability as evidenced by elevated serum levels of the cytoplasmic enzyme creatine kinase. Basic fibroblast growth factor, a cytoplasmic polypeptide growth regulator that stimulates connective tissue synthesis, induces satellite cell proliferation, and suppresses myogenic differentiation, is made by skeletal muscle. We hypothesize that dystrophin deficiency leads to the constant release of basic fibroblast growth factor, which in turn contributes to fibrosis and muscle weakness by stimulating connective tissue and suppressing skeletal muscle differentiation. As an initial step in testing this hypothesis, we measured basic fibroblast growth factor in the serum of Duchenne muscular dystrophy patients. We found that whereas basic fibroblast growth factor was undetectable in the serum of normal individuals (n = 200), levels were elevated in 11 of 18 patients with Duchenne muscular dystrophy. Copyright © 1994 American Neurological Association
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页码:362 / 365
页数:4
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