{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Qian W"],"funding":["American Heart Association","U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences","NHLBI NIH HHS","NIGMS NIH HHS","U.S. Department of Health & Human Services | National Institutes of Health"],"pagination":["512"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC8791986"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["13(1)"],"pubmed_abstract":["Mechanical overload of the vascular wall is a pathological hallmark of life-threatening abdominal aortic aneurysms (AAA). However, how this mechanical stress resonates at the unicellular level of vascular smooth muscle cells (VSMC) is undefined. Here we show defective mechano-phenotype signatures of VSMC in AAA measured with ultrasound tweezers-based micromechanical system and single-cell RNA sequencing technique. Theoretical modelling predicts that cytoskeleton alterations fuel cell membrane tension of VSMC, thereby modulating their mechanoallostatic responses which are validated by live micromechanical measurements. Mechanistically, VSMC gradually adopt a mechanically solid-like state by upregulating cytoskeleton crosslinker, α-actinin2, in the presence of AAA-promoting signal, Netrin-1,"],"journal":["Nature communications"],"pubmed_title":["Microskeletal stiffness promotes aortic aneurysm by sustaining pathological vascular smooth muscle cell mechanosensation via Piezo1."],"pmcid":["PMC8791986"],"funding_grant_id":["R35GM133646","R35 GM133646","16SDG31020038","R01HL146627","R01 HL146627"],"pubmed_authors":["Zias AL","Tellaoui RS","Ma X","Silvestro M","Qu H","Li R","Bajpai A","Garg K","Hadi T","Qian W","Zhang Z","Maldonado T","Chen W","Rivera CF","Corsica A","Ramkhelawon B"],"additional_accession":[]},"is_claimable":false,"name":"Microskeletal stiffness promotes aortic aneurysm by sustaining pathological vascular smooth muscle cell mechanosensation via Piezo1.","description":"Mechanical overload of the vascular wall is a pathological hallmark of life-threatening abdominal aortic aneurysms (AAA). However, how this mechanical stress resonates at the unicellular level of vascular smooth muscle cells (VSMC) is undefined. Here we show defective mechano-phenotype signatures of VSMC in AAA measured with ultrasound tweezers-based micromechanical system and single-cell RNA sequencing technique. Theoretical modelling predicts that cytoskeleton alterations fuel cell membrane tension of VSMC, thereby modulating their mechanoallostatic responses which are validated by live micromechanical measurements. Mechanistically, VSMC gradually adopt a mechanically solid-like state by upregulating cytoskeleton crosslinker, α-actinin2, in the presence of AAA-promoting signal, Netrin-1,","dates":{"release":"2022-01-01T00:00:00Z","publication":"2022 Jan","modification":"2025-04-25T22:24:26.755Z","creation":"2025-04-06T09:05:46.914Z"},"accession":"S-EPMC8791986","cross_references":{"pubmed":["35082286"],"doi":["10.1038/s41467-021-27874-5"]}}