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An HDAC9-MALAT1-BRG1 complex mediates smooth muscle dysfunction in thoracic aortic aneurysm.

Christian L Lino Cardenas | Chase W Kessinger | Yisha Cheng | Carolyn MacDonald | Thomas MacGillivray | Brian Ghoshhajra | Luai Huleihel | Saifar Nuri | Ashish S Yeri | Farouc A Jaffer | Naftali Kaminski | Patrick Ellinor | Neal L Weintraub | Rajeev Malhotra | Eric M Isselbacher | Mark E Lindsay
Nature communications | 2018

Thoracic aortic aneurysm (TAA) has been associated with mutations affecting members of the TGF-β signaling pathway, or components and regulators of the vascular smooth muscle cell (VSMC) actomyosin cytoskeleton. Although both clinical groups present similar phenotypes, the existence of potential common mechanisms of pathogenesis remain obscure. Here we show that mutations affecting TGF-β signaling and VSMC cytoskeleton both lead to the formation of a ternary complex comprising the histone deacetylase HDAC9, the chromatin-remodeling enzyme BRG1, and the long noncoding RNA MALAT1. The HDAC9-MALAT1-BRG1 complex binds chromatin and represses contractile protein gene expression in association with gain of histone H3-lysine 27 trimethylation modifications. Disruption of Malat1 or Hdac9 restores contractile protein expression, improves aortic mural architecture, and inhibits experimental aneurysm growth. Thus, we highlight a shared epigenetic pathway responsible for VSMC dysfunction in both forms of TAA, with potential therapeutic implication for other known HDAC9-associated vascular diseases.

Pubmed ID: 29520069

Associated grants

  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL126949
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL112640
  • Agency: NIAMS NIH HHS, United States
    Id: R01 AR070029
  • Agency: NHLBI NIH HHS, United States
    Id: K08 HL111210
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL130113
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL134354

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