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Bone morphogenetic protein receptors and signal transduction
Author(s) -
Kohei Miyazono,
Yuji Kamiya,
Masato Morikawa
Publication year - 2009
Publication title -
the journal of biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.28
H-Index - 115
eISSN - 1756-2651
pISSN - 0021-924X
DOI - 10.1093/jb/mvp148
Subject(s) - bone morphogenetic protein , smad , bmpr2 , bone morphogenetic protein receptor , signal transduction , receptor , biology , microbiology and biotechnology , bone morphogenetic protein 10 , cancer research , transforming growth factor beta , bone morphogenetic protein 2 , endocrinology , medicine , bone morphogenetic protein 7 , genetics , gene , in vitro
Bone morphogenetic proteins (BMPs) exhibit broad spectra of biological activities in various tissues, including bone, cartilage, blood vessels, heart, kidney, neurons, liver and lung. BMPs are members of the transforming growth factor-beta (TGF-beta) family that bind to type II and type I serine-threonine kinase receptors, and transduce signals through Smad and non-Smad signalling pathways. Recent findings have revealed that BMP signalling is finely tuned by various mechanisms in both positive and negative fashions. Perturbations of BMP signalling pathways are linked to a wide variety of clinical disorders, including vascular diseases, skeletal diseases and cancer. Administration of recombinant BMP ligands and increasing endogenous expression of BMPs provide therapeutic effects on some diseases. The recent development of BMP receptor inhibitors may also prove useful for some clinical diseases induced by hyperactivation of the BMP signalling pathways.

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