| Literature DB >> 32039915 |
Guangxin Li1,2, Mo Wang1, Alexander W Caulk3, Nicholas A Cilfone4, Sharvari Gujja4, Lingfeng Qin1, Pei-Yu Chen5, Zehua Chen4, Sameh Yousef1, Yang Jiao1, Changshun He1, Bo Jiang1, Arina Korneva3, Matthew R Bersi3, Guilin Wang6, Xinran Liu7,8, Sameet Mehta9, Arnar Geirsson1,10, Jeffrey R Gulcher4, Thomas W Chittenden4, Michael Simons5,10, Jay D Humphrey3,10, George Tellides1,10,11.
Abstract
Smooth muscle cell (SMC) proliferation has been thought to limit the progression of thoracic aortic aneurysm and dissection (TAAD) because loss of medial cells associates with advanced disease. We investigated effects of SMC proliferation in the aortic media by conditional disruption of Tsc1, which hyperactivates mTOR complex 1. Consequent SMC hyperplasia led to progressive medial degeneration and TAAD. In addition to diminished contractile and synthetic functions, fate-mapped SMCs displayed increased proteolysis, endocytosis, phagocytosis, and lysosomal clearance of extracellular matrix and apoptotic cells. SMCs acquired a limited repertoire of macrophage markers and functions via biogenesis of degradative organelles through an mTOR/β-catenin/MITF-dependent pathway, but were distinguishable from conventional macrophages by an absence of hematopoietic lineage markers and certain immune effectors even in the context of hyperlipidemia. Similar mTOR activation and induction of a degradative SMC phenotype in a model of mild TAAD due to Fbn1 mutation greatly worsened disease with near-uniform lethality. The finding of increased lysosomal markers in medial SMCs from clinical TAAD specimens with hyperplasia and matrix degradation further supports the concept that proliferation of degradative SMCs within the media causes aortic disease, thus identifying mTOR-dependent phenotypic modulation as a therapeutic target for combating TAAD.Entities:
Keywords: Cardiovascular disease; Vascular Biology
Year: 2020 PMID: 32039915 PMCID: PMC7269581 DOI: 10.1172/JCI131048
Source DB: PubMed Journal: J Clin Invest ISSN: 0021-9738 Impact factor: 14.808