| Literature DB >> 32151560 |
Diana Fulmer1, Katelynn A Toomer2, Janiece Glover1, Lilong Guo1, Kelsey Moore1, Reece Moore1, Rebecca Stairley1, Cortney Gensemer1, Sameer Abrol1, Mary Kate Rumph1, Faith Emetu1, Joshua H Lipschutz3, Colin McDowell1, Justin Bian1, Christina Wang1, Tyler Beck1, Andy Wessels1, Marie-Ange Renault4, Russell A Norris5.
Abstract
Non-syndromic mitral valve prolapse (MVP) is the most common heart valve disease affecting 2.4% of the population. Recent studies have identified genetic defects in primary cilia as causative to MVP, although the mechanism of their action is currently unknown. Using a series of gene inactivation approaches, we define a paracrine mechanism by which endocardially-expressed Desert Hedgehog (DHH) activates primary cilia signaling on neighboring valve interstitial cells. High-resolution imaging and functional assays show that DHH de-represses smoothened at the primary cilia, resulting in kinase activation of RAC1 through the RAC1-GEF, TIAM1. Activation of this non-canonical hedgehog pathway stimulates α-smooth actin organization and ECM remodeling. Genetic or pharmacological perturbation of this pathway results in enlarged valves that progress to a myxomatous phenotype, similar to valves seen in MVP patients. These data identify a potential molecular origin for MVP as well as establish a paracrine DHH-primary cilium cross-talk mechanism that is likely applicable across developmental tissue types.Entities:
Keywords: Desert hedgehog signaling; Myxomatous degeneration; Primary cilia; Valve development
Mesh:
Substances:
Year: 2020 PMID: 32151560 PMCID: PMC7281834 DOI: 10.1016/j.ydbio.2020.03.003
Source DB: PubMed Journal: Dev Biol ISSN: 0012-1606 Impact factor: 3.582