SELECTIVE INACTIVITY OF TGF-BETA DECORIN COMPLEXES

被引:100
作者
HAUSSER, H
GRONING, A
HASILIK, A
SCHONHERR, E
KRESSE, H
机构
[1] Institute of Physiological Chemistry and Pathobiochemistry, University of Münster, D-48149 Münster
关键词
TGF-BETA; DECORIN; BIGLYCAN; PROTEOGLYCAN-100; COLLAGEN-GEL RETRACTION;
D O I
10.1016/0014-5793(94)01044-7
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
Previous studies had shown that binding of TGF-beta to the small proteoglycan decorin results in its inactivation. Indeed, in osteosarcoma cells the addition of decorin prevented the TGF-beta 1-mediated up-regulation of biglycan synthesis. However, the down-regulation of proteoglycan-100 remained unaltered. Even in the presence of a 100,000-fold molar excess of decorin, TGF-beta 1 was fully active in U937 monocytes with respect to the inhibition of cell proliferation. There was no inhibition of the TGF-beta-mediated stimulation of the retraction of fibroblast-populated collagen lattices. Thus, the formation of TGF-beta/decorin complexes leads to the neutralization of distinct effects only.
引用
收藏
页码:243 / 245
页数:3
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