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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 5

Stage-specific expression of axon guidance and neurotrophic factors by FoxD1-lineage cells during kidney development.

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Stage-specific expression of axon guidance and neurotrophic factors by F...
(A) Representative XY-plane (100 μm thickness) 3D imaging of renal cortex from P5 FoxD1GC; R26RtdTomato; Ren1c-YFP mice, showing spatial distribution and relationship of renin-expressing cells (YFP) with FoxD1-lineage cells (tdTomato). Scale bar: 100 μm. (B) Immunofluorescence staining of P5 kidneys from FoxD1GC; R26RtdTomato; Ren1c-YFP mice illustrating the spatial relationships among renin cells, nerves, SMCs, and endothelial cells. Scale bars: 100 μm. (C–F) Violin plots showing cell-specific single pathway analysis scores for neurogenesis (C), regulation of synapse structure or activity (D), positive regulation of axon extension involved in axon guidance (E), and nerve growth factor signaling pathway (F) across MM progenitors, renin precursors, early renin cells (RCs), and late RCs. Statistical comparisons were performed using pairwise t tests with Benjamini-Hochberg multiple comparisons corrections; *Padj < 0.05, ****Padj < 0.0001. (G) Dot plot showing stage-specific expression patterns of selected nerve-related genes and cell markers (Foxd1 and Ren1) across different populations of FoxD1-lineage renal cells at multiple developmental stages (E12, E18, P5, P30). Genes are color-coded by their associated GO pathways. Dot size: percentage of cells expressing the gene; color: expression levels (z score). MC, mesangial cell; PC, pericyte; FB, fibroblast. See also Supplemental Figure 4 and Supplemental Video 6.

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ISSN 2379-3708

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