Go to The Journal of Clinical Investigation
  • About
  • Editors
  • Consulting Editors
  • For authors
  • Journal stats
  • Publication ethics
  • Publication alerts by email
  • Transfers
  • Advertising
  • Job board
  • Contact
  • Physician-Scientist Development
  • Current issue
  • Past issues
  • By specialty
    • COVID-19
    • Cardiology
    • Immunology
    • Metabolism
    • Nephrology
    • Oncology
    • Pulmonology
    • All ...
  • Videos
  • Collections
    • In-Press Preview
    • Resource and Technical Advances
    • Clinical Research and Public Health
    • Research Letters
    • Editorials
    • Perspectives
    • Physician-Scientist Development
    • Reviews
    • Top read articles

  • Current issue
  • Past issues
  • Specialties
  • In-Press Preview
  • Resource and Technical Advances
  • Clinical Research and Public Health
  • Research Letters
  • Editorials
  • Perspectives
  • Physician-Scientist Development
  • Reviews
  • Top read articles
  • About
  • Editors
  • Consulting Editors
  • For authors
  • Journal stats
  • Publication ethics
  • Publication alerts by email
  • Transfers
  • Advertising
  • Job board
  • Contact
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
View: Text | PDF
Research Article Development Nephrology Vascular biology

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

  • Text
  • PDF
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

×

Figure 3

Dense sympathetic innervation of renin cell clusters in AAs.

Options: View larger image (or click on image) Download as PowerPoint
Dense sympathetic innervation of renin cell clusters in AAs.
(A) Three-d...
(A) Three-dimensional images of Ren1c-tdTomato/+ mouse kidney cortex showing renin cells, arterial tree, and nerve fibers. The enlarged XY view (right panels) highlights nerve fibers enveloping the renin cells, with fine branching of nerve fibers indicated by arrowheads. Bottom panels depict separate channels. Scale bars: 100 μm (left and bottom panels); 50 μm (enlarged view). (B) Three-dimensional images from Ren1c+/–; Ren1c-Cre; R26RmTmG mice labeled for renin-lineage cells (GFP), other tissue structures (tdTomato), and nerve fibers. Enlarged XY view highlights nerve fiber arrangement along afferent and efferent arterioles, avoiding glomeruli. Bottom panels depict separate channels. Scale bars: 100 μm. (C) Immunofluorescence staining of Ren1c-tdTomato/+ mouse kidneys for TH and TUBB3, confirming sympathetic innervation of renin cells. Dashed circle: glomerulus. Scale bars: 50 μm. (D) Synaptic marker synaptophysin (SYN) colocalized with TUBB3+ nerve fibers, suggesting synaptic connections with renin cells. Right panels: Enlarged views showing colocalization. Dashed circle indicates glomerulus. Scale bars: 50 μm (enlarged view); 10 μm (right enlarged panels). (E) Electron microscopy image illustrating nerve terminal containing synaptic vesicles (arrowhead), closely associated with a renin-secreting cell containing renin granules (labeled G). Inset: low-magnification view of a renin cell. The main panel is an enlarged view of the region indicated by an asterisk (*). Scale bars: 500 nm. See also Supplemental Figure 2 and Supplemental Videos 3 and 4.

Copyright © 2026 American Society for Clinical Investigation
ISSN 2379-3708

Sign up for email alerts