Bone Morphogenetic Protein (BMP) signaling in development and human diseases

Richard N. Wang(University of Chicago), Jordan J. Green(University of Chicago), Zhongliang Wang(University of Chicago Medical Center), Youlin Deng(Molecular Oncology (United States)), Min Qiao(Molecular Oncology (United States)), Michael Peabody(Molecular Oncology (United States)), Qian Zhang(University of Chicago Medical Center), Jixing Ye(University of Chicago Medical Center), Zhengjian Yan(Chongqing Medical University), Sahitya K. Denduluri(Molecular Oncology (United States)), Olumuyiwa Idowu(University of Chicago), Melissa Li(University of Chicago Medical Center), Christine Shen(Molecular Oncology (United States)), Alan Hu(Molecular Oncology (United States)), Rex C. Haydon(University of Chicago Medical Center), Richard W. Kang(University of Chicago Medical Center), James M. Mok(University of Chicago Medical Center), Michael J. Lee(University of Chicago Medical Center), Hue L. Luu(University of Chicago Medical Center), Lewis L. Shi(University of Chicago Medical Center)
Genes & Diseases
July 27, 2014
Cited by 1,040Open Access
Full Text

Abstract

Bone Morphogenetic Proteins (BMPs) are a group of signaling molecules that belongs to the Transforming Growth Factor-β (TGF-β) superfamily of proteins. Initially discovered for their ability to induce bone formation, BMPs are now known to play crucial roles in all organ systems. BMPs are important in embryogenesis and development, and also in maintenance of adult tissue homeostasis. Mouse knockout models of various components of the BMP signaling pathway result in embryonic lethality or marked defects, highlighting the essential functions of BMPs. In this review, we first outline the basic aspects of BMP signaling and then focus on genetically manipulated mouse knockout models that have helped elucidate the role of BMPs in development. A significant portion of this review is devoted to the prominent human pathologies associated with dysregulated BMP signaling.


Related Papers

No related papers found

Powered by citation graph analysis