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Renin cells orchestrate a neuro-endocrine microenvironment of the kidney arterial tree in health and disease
Manako Yamaguchi, Georgina Gyarmati, Liam McLaughlin, Hiroki Yamaguchi, Jason P. Smith, Lucas Ferreira de Almeida, Daisuke Matsuoka, Alexandre G. Martini, Sara M. Wilmsen, Sijie Hao, Kazuki Tainaka, Silvia Medrano, Sanjay Jain, Janos Peti-Peterdi, Maria Luisa S. Sequeira-Lopez, R. Ariel Gomez
Manako Yamaguchi, Georgina Gyarmati, Liam McLaughlin, Hiroki Yamaguchi, Jason P. Smith, Lucas Ferreira de Almeida, Daisuke Matsuoka, Alexandre G. Martini, Sara M. Wilmsen, Sijie Hao, Kazuki Tainaka, Silvia Medrano, Sanjay Jain, Janos Peti-Peterdi, Maria Luisa S. Sequeira-Lopez, R. Ariel Gomez
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Research Article Development Nephrology Vascular biology

Renin cells orchestrate a neuro-endocrine microenvironment of the kidney arterial tree in health and disease

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Abstract

Renin cells are essential for survival and serve as key regulators of blood pressure and fluid-electrolyte homeostasis. Their function and identity are dependent on signals from their local microenvironment afforded by neighboring cells and nerves. Whether and how renin cells contribute to the development and maintenance of this microenvironment remains unclear. Because renin cells are rare — 0.01 % of kidney cells — conventional histological approaches cannot capture their interaction with nerve fibers and surrounding cells within the nephron and its vasculature. Using high-resolution 3D imaging, cell-specific multicolor reporter mice, single-cell RNA-seq, and conditional gene deletions, we mapped how renin cells assemble within arterioles and communicate with axon fibers to organize the growth and orientation of the kidney arterioles during development and disease. This coinductive process is mediated by Ngf produced by renin cell precursors and is necessary for renin cell survival and innervation. Interestingly, renin enzymatic insufficiency elevates Ngf and drives arteriolar hypertrophy with aberrant axon sprouting and hyperinnervation. These findings indicate that renin cells regulate kidney neurovascular development, revealing them as active organizers of their local neuroregulatory microenvironment in health and disease.

Authors

Manako Yamaguchi, Georgina Gyarmati, Liam McLaughlin, Hiroki Yamaguchi, Jason P. Smith, Lucas Ferreira de Almeida, Daisuke Matsuoka, Alexandre G. Martini, Sara M. Wilmsen, Sijie Hao, Kazuki Tainaka, Silvia Medrano, Sanjay Jain, Janos Peti-Peterdi, Maria Luisa S. Sequeira-Lopez, R. Ariel Gomez

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Figure 2

Acute physiological stress markedly alters the number, volume, and distribution of renin cells in AAs.

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Acute physiological stress markedly alters the number, volume, and distr...
(A) Representative 3D images of kidney cortex from 3-month-old Ren1c-tdTomato/+ mice (control versus low-salt diet + captopril). Under physiological stress, renin cells exhibited enhanced brightness, swelled in JG regions, and extended upstream along the AAs, indicative of recruitment. Scale bars: 100 μm. (B) Schematic of cortical (C) and juxtamedullary (JM) AA structure. Renin cluster length was defined as the longitudinal extension of renin cells along the AA from the glomerular inlet. (C) Histogram showing elongated renin cluster lengths under physiological stress. (D) Renin clusters were shorter in JMAAs than cortical AAs in controls (P = 0.0009), but not under physiological stress (P = 0.3287). Data from 121 control and 129 treated AAs (2 mice/group; Mann-Whitney U test). (E) Three-dimensional reconstruction of renin cell nuclei (Imaris spot). Scale bar: 100 μm. (F–H) Cell number (F), cluster volume per cell (G), and volume per length (H) significantly increased by treatment. Data from 30 AAs/group (2 mice/group; Mann-Whitney U test). (I) Left panel: Classification and frequency of renin localization types. Data represent measurements from 2 mice per group. Right panels: Representative 3D images illustrating each type. White arrowheads indicate renin cell localization patterns. Scale bars: 100 μm. ***P < 0.001; ****P < 0.0001. Ctrl, control. See also Supplemental Figure 1.

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