Rictor in Perivascular Adipose Tissue Controls Vascular Function by Regulating Inflammatory Molecule Expression
Author(s) -
Indranil Bhattacharya,
Katja Drägert,
Verena Albert,
Emmanuel Contassot,
Marlen Damjanović,
Asami Hagiwara,
Lukas Zimmerli,
Rok Humar,
Michael N. Hall,
Edouard Battegay,
Elvira Haas
Publication year - 2013
Publication title -
arteriosclerosis thrombosis and vascular biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.007
H-Index - 270
eISSN - 1524-4636
pISSN - 1079-5642
DOI - 10.1161/atvbaha.112.301001
Subject(s) - mtorc2 , adipose tissue , endocrinology , downregulation and upregulation , inflammation , medicine , proinflammatory cytokine , brown adipose tissue , nitric oxide synthase , tumor necrosis factor alpha , biology , adipose tissue macrophages , protein kinase b , chemistry , nitric oxide , white adipose tissue , microbiology and biotechnology , phosphorylation , mtorc1 , immunology , biochemistry , gene
Perivascular adipose tissue (PVAT) wraps blood vessels and modulates vasoreactivity by secretion of vasoactive molecules. Mammalian target of rapamycin complex 2 (mTORC2) has been shown to control inflammation and is expressed in adipose tissue. In this study, we investigated whether adipose-specific deletion of rictor and thereby inactivation of mTORC2 in PVAT may modulate vascular function by increasing inflammation in PVAT.
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