The latent transforming growth factor β binding protein (LTBP) family

被引:150
作者
Öklü, R
Hesketh, R
机构
[1] Univ Cambridge, Dept Biochem, Sect Cardiovasc Biol, Cambridge CB2 1QW, England
[2] Northwestern Univ, Sch Med, Lake Shore Ctr, Chicago, IL 60611 USA
关键词
atherosclerosis; cancer; fibrillin; Marfan's syndrome; TGF beta;
D O I
10.1042/0264-6021:3520601
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
The transforming growth factor beta (TGF beta) cytokines are a multifunctional family that exert a wide variety of effects on both normal and transformed mammalian cells. The secretion and activation of TGF betas is regulated by their association with latency-associated proteins and latent TGF beta binding proteins (LTBPs). Over the past few years, three members of the LTBP family have been identified, in addition to the protoype LTBP1 first sequenced in 1990. Three of the LTBP family are expressed in a variety of isoforms as a consequence of alternative splicing. This review summarizes the differences between the isoforms in terms of the effects on domain structure and hence possible function. The close identity between LTBPs and members of the fibrillin family, mutations in which have been linked directly to Marfan's syndrome, suggests that anomalous expression of LTBPs may be associated with disease. Recent data indicating that differential expression of LTBP1 isoforms occurs during the development of coronary heart disease is considered, together with evidence that modulation of LTBP function, and hence of TGF beta activity, is associated with a variety of cancers.
引用
收藏
页码:601 / 610
页数:10
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