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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 7

Renin enzymatic insufficiency leads to overstimulation of renin cells, NGF synthesis, and aberrant vascular hyperinnervation.

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Renin enzymatic insufficiency leads to overstimulation of renin cells, N...
(A) Representative 3D reconstructions of renin cells (tdTomato), vascular mural cells, and nerve fibers in kidneys of Ren1c-tdTomato/tdTomato (homo) mice at 7 months. Renin cells exhibit concentric expansion and progressive hyperinnervation. Lower panels separately show renin cells and nerve fibers. Scale bars: 100 μm. (B) Sagittal and coronal sections from 3D imaging illustrate progressive concentric thickening of AAs and increased perivascular innervation in homo kidneys at 1 and 7 months. Coronal views highlight lumen narrowing and the increasing complexity of nerve fiber organization. Scale bars: 20 μm. (C) qPCR for Ngf in kidneys from Ren1c-tdTomato/+ (het) and homo mice at 2–5 months (Mann-Whitney U test, het n = 13, homo n = 13) (left). Pearson’s correlation between age and Ngf expression in homo mice (n = 13) (right). (D) Representative 3D reconstructions of renin-plexus networks generated with NetTracer3D from 7-month-old het and homo kidneys. Nodes represent renin cell clusters and nerve/plexus structures; edges indicate connections defined by an unbroken segmented nerve path between nodes. Scale bars: 200 μm. (E and F) Communicability betweenness centrality (E) and node connectivity (F). Overlaid histograms (left) show node-level distributions for representative networks. Group comparisons (right) show per-animal means analyzed by a linear mixed-effects model (het n = 3, homo n = 4); data are shown as mean ± SD; circles denote females and triangles denote males. Each histogram also reports a distribution-shape similarity score (0–1; higher indicates more similar), derived from the Jensen-Shannon distance. Triangles, males; circles, females, *P < 0.05, **P < 0.01. See also Supplemental Figures 5 and 6, and Supplemental Videos 7 and 8.

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ISSN 2379-3708

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