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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 4

Spatiotemporal organization of renin cells and axonal growth trajectories across the renal arterial tree during kidney development.

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Spatiotemporal organization of renin cells and axonal growth trajectorie...
(A) Three-dimensional views of renin expressing cells, arterial tree, and nerves at E17.5, P0, P5, P10, and 1 month in Ren1c-tdTomato/+ mice. Dashed lines indicate kidney surface. Scale bars: 100 μm. (B) Relative tdTomato intensity in juxtamedullary afferent arterioles (JMAA) and arterial branches from arcuate arteries to the outer cortex (AB-AAC) at E17.5 (n = 3) and P0 (n = 5) (linear mixed-effects model). Small colored circles indicate individual measurements, and large circles indicate the mean for each sample. (C–E) Distance-dependent distribution of TUBB3 and tdTomato signals from the kidney surface at P0 (n = 5) and P10 (n = 3). (C and D) Mean intensity profiles of TUBB3 and tdTomato. Solid lines indicate the mean across mice, and shaded areas represent mean ± SD. At P0, TUBB3 intensity rises closer to the surface than tdTomato, whereas at P10 the onset of TUBB3 and tdTomato signals is nearly coincident. (E) Δd, defined as the difference in onset distance between tdTomato and TUBB3 (Δd = d_onset[tdTomato] − d_onset[TUBB3]), is larger at P0 than at P10 (Mann-Whitney U test). *P < 0.05, ****P < 0.0001. See also Supplemental Figure 3 and Supplemental Video 5.

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