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
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Abstract

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 Foxd1Cre/+;Tcf21f/f and Ren1dCre/+;Tcf21f/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 Foxd1Cre/+;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/+;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+ cells (stromal lineage) from E12, E18, P5, and P30 Foxd1Cre/+;Rosa26mTmG 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 是将 Foxd1 细胞分化为绒毛膜细胞系的创始转录因子
肾素对血压调节和电解质平衡至关重要,其表达细胞来自 Foxd1+ 基质祖细胞。然而,引导这些祖细胞走向分泌肾素细胞命运的因素仍不清楚。Tcf21是一种基本螺旋环螺旋(bHLH)转录因子,在肾脏发育过程中至关重要。我们利用Foxd1Cre/+;Tcf21f/f和Ren1dCre/+;Tcf21f/f小鼠模型,研究了Tcf21在Foxd1+祖细胞分化成并肾小球(JG)细胞过程中的作用。免疫染色和原位杂交显示,与对照组相比,Foxd1Cre/+;Tcf21f/f 肾脏中肾素阳性区域较少,肾动脉形态(包括传入动脉)也发生了改变,这表明 Tcf21 在肾素表达细胞的出现过程中起着关键作用。然而,肾素表达细胞(Ren1dCre/+;Tcf21f/f)中的Tcf21失活并不能再现这种表型,这表明一旦肾素细胞身份确立,Tcf21就不再需要了。通过对来自E12、E18、P5和P30 Foxd1Cre/+;Rosa26mTmG对照肾脏的GFP+细胞(基质系)进行单细胞RNA测序(scRNA-seq)和单细胞转座酶可检测染色质测序(scATAC-seq)的综合分析,我们分析了Tcf21在JG系细胞(n=2,054)中的表达时间动态。伪时间轨迹分析显示,Tcf21在肾间质和基质细胞的早期发育阶段(E12)表达量最高,随着细胞成熟为表达肾素的JG细胞,其表达量下降。动因富集分析证实了 Tcf21 在肾脏早期发育中的重要作用。这些发现强调了Tcf21在肾脏早期发育阶段Foxd1+细胞分化为JG细胞的过程中发挥的关键作用,有助于深入了解JG细胞分化的分子机制,并突出了Tcf21在肾脏发育过程中的关键作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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