Journal
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY
Volume 313, Issue 4, Pages F847-F853Publisher
AMER PHYSIOLOGICAL SOC
DOI: 10.1152/ajprenal.00175.2017
Keywords
sex; cytokines; hypertension; lymphocytes
Categories
Funding
- National Institutes of Health [R01 HL-127091-02]
- American Heart Association [17EIA33410565, 13PRE16110000]
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Female spontaneously hypertensive rats (STIR) have more renal regulatory T cells (Tregs) than males, and greater levels of Tregs in female SHR are dependent on blood pressure (BP). However, the molecular mechanism responsible for greater Tregs in female SHR is unknown. Transforming growth factor (TGF)-beta is a pleiotropic cytokine critical in the differentiation of naive T cells into Tregs, and female SHR have higher TGF-beta excretion than male SHR. The goals of the current study were to test the hypotheses that 1) female SHR have greater renal TGF-beta expression than male SHR, which is dependent on BP and 2) neutralizing TGF-beta will decrease renal Tregs in female SHR. Renal cortices were isolated from 5- and 13-wk-old male and female SHR, and TGF-beta levels were measured via Western blot and ELIS A. Adult female SHR have more free, active TGF-beta(1), than 5-wk-old female SHR (46% more) or male SUR (44% more than 5-wk-old males and 56% more than 13-wk-old male SHR). We confirmed greater TGF-beta(1) in adult female SHR was due to increases in BP and not sexual maturation by measuring TGF-beta(1) levels following treatment with BP-lowering drugs or ovariectomy. Separate female SHR were treated with an antibody to TGF-beta; BP was measured, and T cells were assessed in whole blood and the kidney. Neutralizing TGE-beta had no effect on BP, although circulating Tregs decreased by 32%, while Th17 cells increased by 64%. Renal Tregs were not altered by antibody treatment, although Th17 cells were decreased by 61%. In conclusion, although TGF-beta promotes circulating Tregs in female SHR, it does not account for the sex difference in renal Tregs in SHR.
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