| Literature DB >> 24830537 |
Asako Kurauchi-Mito1, Atsuhiro Ichihara2, Kanako Bokuda1, Mariyo Sakoda1, Kenichiro Kinouchi1, Tomonori Yaguchi3, Taketo Yamada4, Ge-Hong Sun-Wada5, Yoh Wada6, Hiroshi Itoh1.
Abstract
The (pro)renin receptor ((P)RR) is known to play an important role in the pathogenesis of vascular complications in diabetes mellitus and hypertension through its function in activating the local renin-angiotensin system. Recent studies have shown that the (P)RR is an accessory protein of the vacuolar H(+)-ATPase, suggesting a more fundamental and developmental function. In this study, smooth muscle cell-specific (P)RR/Atp6ap2 conditional knockout mice were generated. Smooth muscle cell-specific ablation of the (P)RR resulted in nonatherogenic sclerosis in the abdominal aorta. The deletion of the (P)RR did not affect ambulatory blood pressure levels. In cultured murine vascular smooth muscle cells (VSMCs), ablation of the (P)RR suppressed the expression of the Vo subunit c of the vacuolar H(+)-ATPase and impaired the cell recycling system, leading to autophagic cell death. In addition, loss of the (P)RR in VSMCs induced the expression of monocyte chemotactic protein-1 and interleukin-6 mRNAs. These results suggest that the (P)RR is essential for cell survival and downregulation of vascular inflammation in murine VSMCs through maintaining normal function of the vacuolar H(+)-ATPase.Entities:
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Year: 2014 PMID: 24830537 DOI: 10.1038/hr.2014.92
Source DB: PubMed Journal: Hypertens Res ISSN: 0916-9636 Impact factor: 3.872