Angiotensin II enhances bacterial clearance via myeloid signaling in a murine sepsis model

Proc Natl Acad Sci U S A. 2022 Aug 23;119(34):e2211370119. doi: 10.1073/pnas.2211370119. Epub 2022 Aug 15.

Abstract

Sepsis, defined as organ dysfunction caused by a dysregulated host-response to infection, is characterized by immunosuppression. The vasopressor norepinephrine is widely used to treat low blood pressure in sepsis but exacerbates immunosuppression. An alternative vasopressor is angiotensin-II, a peptide hormone of the renin-angiotensin system (RAS), which displays complex immunomodulatory properties that remain unexplored in severe infection. In a murine cecal ligation and puncture (CLP) model of sepsis, we found alterations in the surface levels of RAS proteins on innate leukocytes in peritoneum and spleen. Angiotensin-II treatment induced biphasic, angiotensin-II type 1 receptor (AT1R)-dependent modulation of the systemic inflammatory response and decreased bacterial counts in both the blood and peritoneal compartments, which did not occur with norepinephrine treatment. The effect of angiotensin-II was preserved when treatment was delivered remote from the primary site of infection. At an independent laboratory, angiotensin-II treatment was compared in LysM-Cre AT1aR-/- (Myeloid-AT1a-) mice, which selectively do not express AT1R on myeloid-derived leukocytes, and littermate controls (Myeloid-AT1a+). Angiotensin-II treatment significantly reduced post-CLP bacteremia in Myeloid-AT1a+ mice but not in Myeloid-AT1a- mice, indicating that the AT1R-dependent effect of angiotensin-II on bacterial clearance was mediated through myeloid-lineage cells. Ex vivo, angiotensin-II increased post-CLP monocyte phagocytosis and ROS production after lipopolysaccharide stimulation. These data identify a mechanism by which angiotensin-II enhances the myeloid innate immune response during severe systemic infection and highlight a potential role for angiotensin-II to augment immune responses in sepsis.

Keywords: angiotensin II; immunity; innate; renin-angiotensin system; sepsis; vasoconstrictor agents.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Angiotensin II* / metabolism
  • Animals
  • Bacteremia / immunology*
  • Disease Models, Animal
  • Mice
  • Mice, Inbred C57BL
  • Myeloid Cells / metabolism*
  • Norepinephrine / metabolism
  • Receptor, Angiotensin, Type 1
  • Sepsis / immunology*
  • Sepsis / metabolism
  • Signal Transduction

Substances

  • Receptor, Angiotensin, Type 1
  • Angiotensin II
  • Norepinephrine