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Ensor, C. M.

Publications and source records attributed to Ensor, C. M..

2 recordsLinked to original sources

Role of adipocyte angiotensinogen or angiotensin type 1a receptors in the development of diet-induced atherosclerosis or angiotensin II-induced abdominal aortic aneurysms

Adipocytes express renin-angiotensin system (RAS) components, including angiotensinogen (Agt), the precursor to angiotensin II (AngII), and the angiotensin type 1a receptor (AT1aR). The RAS contributes to atherosclerosis, and AngII infusion causes abdominal aortic aneurysm (AAA) formation. Obesity, an established vascular risk factor, exhibits a dysregulated RAS. We studied effects of adipocyte Agt or AT1aR deficiency on diet-induced atherosclerosis and AngII-induced AAAs in male low density lipoprotein receptor (Ldlr) deficient mice. For atherosclerosis, male control or adipocyte Agt/AT1aR deficient mice were fed Western diet for 3 months. There was no effect of adipocyte Agt or AT1aR deficiency on body weight, serum cholesterol concentrations, or atherosclerotic lesions. For AngII-induced AAAs, male control and adipocyte Agt/AT1aR deficient Ldlr-/- mice fed Western diet were infused with AngII. Adipocyte Agt deficiency had no effect on body weight, serum cholesterol concentrations, abdominal aortic lumen diameter, AAA incidence, or atherosclerosis. Control, but not adipocyte AT1aR deficient mice lost weight during AngII infusion. The size of adipocytes in white fat was increased in adipocyte AT1aR deficient mice with no significant influences on abdominal aortic lumen diameter, AAA incidence, or atherosclerosis. To define mechanisms, male Ldlr-/- mice were fed standard or Western diet (1 or 3 months) and Agt or AT1aR mRNA abundance quantified in periaortic fat (PAF). Agt mRNA abundance in abdominal PAF increased over time in both diet groups, with modest diet-induced reductions in thoracic PAF Agt mRNA abundance. There was an effect of diet duration on AT1aR mRNA abundance in thoracic PAF, and an interaction between diet and time on abdominal PAF AT1aR mRNA abundance. In conclusion, adipocyte Agt or AT1aR deficiency had minimal effects on atherosclerosis or AngII-induced AAAs. However, adipocyte AT1aR deficient mice exhibited increased adipocyte size. Diet-induced regulation of Agt or AT1aR mRNA abundance in PAF may have contributed to these findings.

pharmacology and toxicology↗

SARS-CoV-2 Spike Protein Regulation of Angiotensin Converting Enzyme 2 and Tissue Renin-Angiotensin Systems: Influence of Biologic Sex

Angiotensin converting enzyme 2 (ACE2) is an enzyme that limits activity of the renin-angiotensin system (RAS) and also serves as a receptor for the SARS-CoV-2 Spike (S) protein. Binding of S protein to ACE2 causes internalization which activates local RAS. ACE2 is on the X chromosome and its expression is regulated by sex hormones. In this study, we defined ACE2 mRNA abundance and examined effects of S protein on ACE2 activity and/or angiotensin II (AngII) levels in pivotal tissues (lung, adipose) from male and female mice. In lung, ACE2 mRNA abundance was reduced following gonadectomy (GDX) of male and female mice and was higher in XX than XY mice of the Four Core Genotypes (FCG). Reductions in lung ACE2 mRNA abundance by GDX occurred in XX, but not XY FCG female mice. Lung mRNA abundance of ADAM17 and TMPRSS2, enzymes that shed cell surface ACE2 and facilitate viral cell entry, was reduced by GDX in male but not female mice. For comparison, adipose ACE2 mRNA abundance was higher in female than male mice and higher in XX than XY FCG mice. Adipose ADAM17 mRNA abundance was increased by GDX of male and female mice. S protein reduced ACE2 activity in alveolar type II epithelial cells and 3T3-L1 adipocytes. Administration of S protein to male and female mice increased lung AngII levels and decreased adipose ACE2 activity in male but not female mice. These results demonstrate that sex differences in ACE2 expression levels may impact local RAS following S protein exposures.

physiology↗