Tcf21 as a founder transcription factor in specifying Foxd1 cells to the juxtaglomerular cell lineage

Hina Anjum, Jason P. Smith, Alexandre G. Martini, George S. Yacu, Silvia Medrano, R. Ariel Gomez, Maria Luisa S. Sequeira-Lopez, Susan E. Quaggin, Gal Finer*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

Renin is crucial for blood pressure regulation and electrolyte balance, and its expressing cells arise from Forkhead box D1-positive (Foxd1 þ ) stromal progenitors. However, factors guiding these progenitors toward renin-secreting cell fate remain unclear. Tcf21, a basic helix-loop-helix (bHLH) transcription factor, is essential in kidney development. Using Foxd1Cre/ þ ;Tcf21f/f and Ren1dCre/ þ ;Tcf21f/f mouse models, we investigated the role of Tcf21 in the differentiation of Foxd1 þ progenitor cells into juxtaglomerular (JG) cells. Immunostaining and in situ hybridization demonstrated fewer renin-positive areas and altered renal arterial morphology, including the afferent arteriole, in Foxd1Cre/ þ ;Tcf21f/f kidneys compared with controls, indicating Tcf21’s critical role in the emergence of renin-expressing cells. However, Tcf21 inactivation in renin-expressing cells (Ren1dCre/ þ ;Tcf21f/f) did not recapitulate this phenotype, suggesting Tcf21 is dispensable once renin cell identity is established. Using an integrated analysis of single-cell RNA sequencing (scRNA-seq) and single-cell assay for transposase-accessible chromatin sequencing (scATAC-seq) on GFP þ cells (stromal lineage) from E12, E18, P5, and P30 Foxd1Cre/ þ ;Rosa26mTmG control kidneys, we analyzed the temporal dynamics of Tcf21 expression in cells comprising the JG lineage (n ¼ 2,054). A pseudotime trajectory analysis revealed that Tcf21 expression is highest in metanephric mesenchyme and stromal cells at early developmental stages (E12), with a decline in expression as cells mature into renin-expressing JG cells. Motif enrichment analyses supported Tcf21’s significant involvement in early kidney development. These findings underscore the critical role of Tcf21 in Foxd1 þ cell differentiation into JG cells during early stages of kidney development, offering insights into the molecular mechanisms governing JG cell differentiation and highlighting Tcf21’s pivotal role in kidney development.

Original languageEnglish (US)
Pages (from-to)F121-F130
JournalAmerican Journal of Physiology - Renal Physiology
Volume328
Issue number1
DOIs
StatePublished - Jan 2025

Funding

Confocal microscopy was provided by the Center for Advanced Microscopy of Northwestern University and by the Microscopy and Histology Group at Stanley Manne Children\u2019s Research Institute affiliated with Ann and Robert H. Lurie Children\u2019s Hospital of Chicago. With gratitude to the Zell Family Foundation. This work was supported by National Institutes of Health, National Institutes of Diabetes and Digestive and Kidney Diseases, K08 DK-118180 (to G. Finer), and National Institutes of Health, UVA Pediatric Center of Excellence in Nephrology, P50 DK-096373 (to G. Finer).

Keywords

  • Foxd1 stromal progenitors
  • Tcf21
  • kidney development
  • renin

ASJC Scopus subject areas

  • Physiology

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