| Literature DB >> 32730927 |
Gregory R Gipson1, Erich J Goebel1, Kaitlin N Hart2, Emily C Kappes1, Chandramohan Kattamuri1, Jason C McCoy1, Thomas B Thompson3.
Abstract
The Bone Morphogenetic Proteins (BMPs) are the largest class signaling molecules within the greater Transforming Growth Factor Beta (TGFβ) family, and are responsible for a wide array of biological functions, including dorsal-ventral patterning, skeletal development and maintenance, as well as cell homeostasis. As such, dysregulation of BMPs results in a number of diseases, including fibrodysplasia ossificans progressiva (FOP) and pulmonary arterial hypertension (PAH). Therefore, understanding BMP signaling and regulation at the molecular level is essential for targeted therapeutic intervention. This review discusses the recent advances in the structural and biochemical characterization of BMPs, from canonical ligand-receptor interactions to co-receptors and antagonists. This work aims to highlight how BMPs differ from other members of the TGFβ family, and how that information can be used to further advance the field. Lastly, this review discusses several gaps in the current understanding of BMP structures, with the aim that discussion of these gaps will lead to advancements in the field.Entities:
Keywords: BMP; Review; Structure
Mesh:
Substances:
Year: 2020 PMID: 32730927 PMCID: PMC7502536 DOI: 10.1016/j.bone.2020.115549
Source DB: PubMed Journal: Bone ISSN: 1873-2763 Impact factor: 4.398