Key result
Human kidney pericytes express and secrete enzymatically functional renin, which is inducible by cyclic AMP and capable of generating angiotensin I.
Human kidney pericytes are capable of producing and secreting functional renin, highlighting their developmental plasticity and potential role in regulating the renin-angiotensin system.
Suggests pericytes contribute to renal renin production; leaves open their role in hypertension pathogenesis and targeted therapies.
Pericytes, perivascular cells embedded in the microvascular wall, are crucial for vascular homeostasis. These cells also play diverse roles in tissue development and regeneration as multi-lineage progenitors, immunomodulatory cells and as sources of trophic factors. Here, we establish that pericytes are renin producing cells in the human kidney. Renin was localized by immunohistochemistry in CD146 and NG2 expressing pericytes, surrounding juxtaglomerular and afferent arterioles. Similar to pericytes from other organs, CD146 + CD34 – CD45 – CD56 – renal fetal pericytes, sorted by flow cytometry, exhibited tri-lineage mesodermal differentiation potential in vitro . Additionally, renin expression was triggered in cultured kidney pericytes by cyclic AMP as confirmed by immuno-electron microscopy, and secretion of enzymatically functional renin, capable of generating angiotensin I. Pericytes derived from second trimester human placenta also expressed renin in an inducible fashion although the renin activity was much lower than in renal pericytes. Thus, our results confirm and extend the recently discovered developmental plasticity of microvascular pericytes, and may open new perspectives to the therapeutic regulation of the renin-angiotensin system.
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Stefańska et al. (2016) studied this question. cyclic AMP was evaluated on Renin expression and secretion. Human kidney pericytes express and secrete enzymatically functional renin, which is inducible by cyclic AMP and capable of generating angiotensin I.
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