T-Cell Mineralocorticoid Receptor Controls Blood Pressure by Regulating Interferon-Gamma

Circ Res. 2017 May 12;120(10):1584-1597. doi: 10.1161/CIRCRESAHA.116.310480. Epub 2017 Mar 15.

Abstract

Rationale: Hypertension remains to be a global public health burden and demands novel intervention strategies such as targeting T cells and T-cell-derived cytokines. Mineralocorticoid receptor (MR) antagonists have been clinically used to treat hypertension. However, the function of T-cell MR in blood pressure (BP) regulation has not been elucidated.

Objective: We aim to determine the role of T-cell MR in BP regulation and to explore the mechanism.

Methods and results: Using T-cell MR knockout mouse in combination with angiotensin II-induced hypertensive mouse model, we demonstrated that MR deficiency in T cells strikingly decreased both systolic and diastolic BP and attenuated renal and vascular damage. Flow cytometric analysis showed that T-cell MR knockout mitigated angiotensin II-induced accumulation of interferon-gamma (IFN-γ)-producing T cells, particularly CD8+ population, in both kidneys and aortas. Similarly, eplerenone attenuated angiotensin II-induced elevation of BP and accumulation of IFN-γ-producing T cells in wild-type mice. In cultured CD8+ T cells, T-cell MR knockout suppressed IFN-γ expression whereas T-cell MR overexpression and aldosterone both enhanced IFN-γ expression. At the molecular level, MR interacted with NFAT1 (nuclear factor of activated T-cells 1) and activator protein-1 in T cells. Finally, T-cell MR overexpressing mice manifested more elevated BP compared with control mice after angiotensin II infusion and such difference was abolished by IFN-γ-neutralizing antibodies.

Conclusions: MR may interact with NFAT1 and activator protein-1 to control IFN-γ in T cells and to regulate target organ damage and ultimately BP. Targeting MR in T cells specifically may be an effective novel approach for hypertension treatment.

Keywords: T-cell; hypertension; inflammation; interferon-gamma; mineralocorticoid receptor.

MeSH terms

  • Acetylcholine / pharmacology
  • Animals
  • Blood Pressure / drug effects
  • Blood Pressure / physiology*
  • Cells, Cultured
  • Dose-Response Relationship, Drug
  • Hypertension / genetics
  • Hypertension / metabolism
  • Interferon-gamma / physiology*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Receptors, Mineralocorticoid / physiology*
  • T-Lymphocytes / physiology*

Substances

  • Receptors, Mineralocorticoid
  • Interferon-gamma
  • Acetylcholine