Human amnion epithelial cell therapy reduces hypertension-induced vascular stiffening and cognitive impairment

Sci Rep. 2024 Jan 22;14(1):1837. doi: 10.1038/s41598-024-52214-0.

Abstract

Vascular inflammation and fibrosis are hallmarks of hypertension and contribute to the development of cardiovascular disease and cognitive impairment. However, current anti-hypertensive drugs do not treat the underlying tissue damage, such as inflammation-associated fibrosis. Human amnion epithelial cells have several properties amenable for treating vascular pathology. This study tested the effect of amnion epithelial cells on vascular pathology and cognitive impairment during hypertension. Male C57Bl6 mice (8-12 weeks) were administered vehicle (saline; n = 58) or angiotensin II (0.7 mg/kg/d, n = 56) subcutaneously for 14 d. After surgery, a subset of mice were injected with 106 amnion epithelial cells intravenously. Angiotensin II infusion increased systolic blood pressure, aortic pulse wave velocity, accumulation of aortic leukocytes, and aortic mRNA expression of collagen subtypes compared to vehicle-infused mice (n = 9-11, P < 0.05). Administration of amnion epithelial cells attenuated these effects of angiotensin II (P < 0.05). Angiotensin II-induced cognitive impairment was prevented by amnion epithelial cell therapy (n = 7-9, P < 0.05). In the brain, amnion epithelial cells modulated some of the inflammatory genes that angiotensin II promoted differential expression of (n = 6, p-adjusted < 0.05). These findings suggest that amnion epithelial cells could be explored as a potential therapy to inhibit vascular pathology and cognitive impairment during hypertension.

MeSH terms

  • Amnion
  • Angiotensin II
  • Animals
  • Cognitive Dysfunction* / etiology
  • Cognitive Dysfunction* / therapy
  • Epithelial Cells
  • Fibrosis
  • Humans
  • Hypertension* / therapy
  • Inflammation
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Pulse Wave Analysis

Substances

  • Angiotensin II