Renin is crucial for blood pressure regulation and electrolyte balance, and its expressing cells arise from Forkhead box D1-positive (Foxd1(+)) 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 Foxd1(Cre/+);Tcf21(f/f) and Ren1(dCre/+);Tcf21(f/f) mouse models, we investigated the role of Tcf21 in the differentiation of Foxd1(+) 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 Foxd1(Cre/+);Tcf21(f/f) kidneys compared with controls, indicating Tcf21's critical role in the emergence of renin-expressing cells. However, Tcf21 inactivation in renin-expressing cells (Ren1(dCre/+);Tcf21(f/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(+) cells (stromal lineage) from E12, E18, P5, and P30 Foxd1(Cre/+);Rosa26(mTmG) control kidneys, we analyzed the temporal dynamics of Tcf21 expression in cells comprising the JG lineage (n = 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(+) 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.NEW & NOTEWORTHY This manuscript provides novel insights into the role of Tcf21 in the differentiation of Foxd1(+) cells into JG cells. Using integrated scRNA-seq and scATAC-seq, the study reveals that Tcf21 expression is crucial during early embryonic stages, with its peak at embryonic day 12. The findings demonstrate that inactivation of Tcf21 leads to fewer renin-positive areas and altered renal arterial morphology, underscoring the importance of Tcf21 in the specification of renin-expressing JG cells and kidney development.
Tcf21 as a founder transcription factor in specifying Foxd1 cells to the juxtaglomerular cell lineage.
Tcf21 作为创始转录因子,将 Foxd1 细胞指定为肾小球旁细胞谱系
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作者:Anjum Hina, Smith Jason P, Martini Alexandre G, Yacu George S, Medrano Silvia, Gomez R Ariel, Sequeira-Lopez Maria Luisa S, Quaggin Susan E, Finer Gal
| 期刊: | American Journal of Physiology-Renal Physiology | 影响因子: | 3.400 |
| 时间: | 2025 | 起止号: | 2025 Jan 1; 328(1):F121-F130 |
| doi: | 10.1152/ajprenal.00235.2024 | 研究方向: | 细胞生物学 |
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