Tcf21 是将 Foxd1 细胞分化为绒毛膜细胞系的创始转录因子

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
{"title":"Tcf21 是将 Foxd1 细胞分化为绒毛膜细胞系的创始转录因子","authors":"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","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>Renin is crucial for blood pressure regulation and electrolyte balance, and its expressing cells arise from 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. Utilizing <i>Foxd1<sup>Cre/+</sup>;Tcf21<sup>f/f</sup></i> and <i>Ren1<sup>dCre/+</sup>;Tcf21<sup>f/f</sup></i> 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 <i>Foxd1<sup>Cre/+</sup>;Tcf21<sup>f/f</sup></i> kidneys compared to controls, indicating Tcf21's critical role in the emergence of renin-expressing cells. However, Tcf21 inactivation in renin-expressing cells (<i>Ren1<sup>dCre/+</sup>;Tcf21<sup>f/f</sup></i>) 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 <i>Foxd1<sup>Cre/+</sup>;Rosa26<sup>mTmG</sup></i> control kidneys, we analyzed the temporal dynamics of Tcf21 expression in cells comprising the JG lineage (<i>n</i>=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 highlight Tcf21's pivotal role in kidney development.</p>","PeriodicalId":93867,"journal":{"name":"American journal of physiology. Renal physiology","volume":" ","pages":"None"},"PeriodicalIF":0.0000,"publicationDate":"2024-11-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Tcf21 as a Founder Transcription Factor in Specifying Foxd1 Cells to the Juxtaglomerular Cell Lineage.\",\"authors\":\"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\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Renin is crucial for blood pressure regulation and electrolyte balance, and its expressing cells arise from 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. Utilizing <i>Foxd1<sup>Cre/+</sup>;Tcf21<sup>f/f</sup></i> and <i>Ren1<sup>dCre/+</sup>;Tcf21<sup>f/f</sup></i> 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 <i>Foxd1<sup>Cre/+</sup>;Tcf21<sup>f/f</sup></i> kidneys compared to controls, indicating Tcf21's critical role in the emergence of renin-expressing cells. However, Tcf21 inactivation in renin-expressing cells (<i>Ren1<sup>dCre/+</sup>;Tcf21<sup>f/f</sup></i>) 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 <i>Foxd1<sup>Cre/+</sup>;Rosa26<sup>mTmG</sup></i> control kidneys, we analyzed the temporal dynamics of Tcf21 expression in cells comprising the JG lineage (<i>n</i>=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 highlight Tcf21's pivotal role in kidney development.</p>\",\"PeriodicalId\":93867,\"journal\":{\"name\":\"American journal of physiology. Renal physiology\",\"volume\":\" \",\"pages\":\"None\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-11-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"American journal of physiology. Renal physiology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"American journal of physiology. Renal physiology","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

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。
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Tcf21 as a Founder Transcription Factor in Specifying Foxd1 Cells to the Juxtaglomerular Cell Lineage.

Renin is crucial for blood pressure regulation and electrolyte balance, and its expressing cells arise from 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. Utilizing 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 to 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 highlight Tcf21's pivotal role in kidney development.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Sex differences in the adrenal circadian clock: a role for BMAL1 in the regulation of urinary aldosterone excretion and renal electrolyte balance in mice. Phosphoproteomic response to epidermal growth factor in native rat inner medullary collecting duct. Western diet exacerbates a murine model of Balkan nephropathy. Intestinal Barrier Function Declines During Polycystic Kidney Disease Progression. Remote organ cancer induces kidney injury, inflammation, and fibrosis and adversely alters renal function.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1