Suppr超能文献

基质转录因子 21 调节肾脏基质的发育 与 Wnt/-连环蛋白信号的相互作用。

Stromal Transcription Factor 21 Regulates Development of the Renal Stroma Interaction with Wnt/-Catenin Signaling.

机构信息

Division of Nephrology, Ann and Robert H. Lurie Children's Hospital of Chicago, Chicago, Illinois.

Feinberg Cardiovascular and Renal Research Institute, Northwestern University Feinberg School of Medicine, Chicago, Illinois.

出版信息

Kidney360. 2022 May 6;3(7):1228-1241. doi: 10.34067/KID.0005572021. eCollection 2022 Jul 28.

Abstract

BACKGROUND

Kidney formation requires coordinated interactions between multiple cell types. Input from the interstitial progenitor cells is implicated in multiple aspects of kidney development. We previously reported that transcription factor 21 (Tcf21) is required for ureteric bud branching. Here, we show that Tcf21 in Foxd1+ interstitial progenitors regulates stromal formation and differentiation interaction with -catenin.

METHODS

We utilized the Foxd1Cre;Tcf21 murine kidney for morphologic analysis. We used the murine clonal mesenchymal cell lines MK3/M15 to study Tcf21 interaction with Wnt/-catenin.

RESULTS

Absence of Tcf21 from Foxd1+ stromal progenitors caused a decrease in stromal cell proliferation, leading to marked reduction of the medullary stromal space. Lack of Tcf21 in the Foxd1+ stromal cells also led to defective differentiation of interstitial cells to smooth-muscle cells, perivascular pericytes, and mesangial cells. Foxd1Cre;Tcf21 kidney showed an abnormal pattern of the renal vascular tree. The stroma of Foxd1Cre;Tcf21 kidney demonstrated marked reduction in -catenin protein expression compared with wild type. Tcf21 was bound to -catenin both upon -catenin stabilization and at basal state as demonstrated by immunoprecipitation . In MK3/M15 metanephric mesenchymal cells, Tcf21 enhanced TCF/LEF promoter activity upon -catenin stabilization, whereas DNA-binding deficient mutated Tcf21 did not enhance TCF/LEF promoter activity. Kidney explants of Foxd1Cre;Tcf21 showed low mRNA expression of stromal Wnt target genes. Treatment of the explants with CHIR, a Wnt ligand mimetic, restored Wnt target gene expression. Here, we also corroborated previous evidence that normal development of the kidney stroma is required for normal development of the Six2+ nephron progenitor cells, loop of Henle, and the collecting ducts.

CONCLUSIONS

These findings suggest that stromal Tcf21 facilitates medullary stroma development by enhancing Wnt/-catenin signaling and promotes stromal cell proliferation and differentiation. Stromal Tcf21 is also required for the development of the adjacent nephron epithelia.

摘要

背景

肾脏的形成需要多种细胞类型之间的协调相互作用。间质祖细胞的输入涉及肾脏发育的多个方面。我们之前报道过转录因子 21(Tcf21)是输尿管芽分支所必需的。在这里,我们表明 Foxd1+间质祖细胞中的 Tcf21 调节基质形成和分化,与β-连环蛋白相互作用。

方法

我们利用 Foxd1Cre;Tcf21 小鼠肾脏进行形态分析。我们使用小鼠克隆间充质细胞系 MK3/M15 研究 Tcf21 与 Wnt/β-连环蛋白的相互作用。

结果

Foxd1+基质祖细胞中 Tcf21 的缺失导致基质细胞增殖减少,导致髓质基质空间明显减少。Foxd1+基质细胞中 Tcf21 的缺失也导致间质细胞向平滑肌细胞、血管周周细胞和系膜细胞的分化缺陷。Foxd1Cre;Tcf21 肾脏的肾血管树呈现异常模式。与野生型相比,Foxd1Cre;Tcf21 肾脏的基质中β-连环蛋白蛋白表达明显减少。免疫沉淀证实 Tcf21 在β-连环蛋白稳定和基础状态下与β-连环蛋白结合。在 MK3/M15 肾间充质细胞中,Tcf21 在β-连环蛋白稳定时增强 TCF/LEF 启动子活性,而 DNA 结合缺陷突变的 Tcf21 则不能增强 TCF/LEF 启动子活性。Foxd1Cre;Tcf21 肾脏外植体的基质 Wnt 靶基因的 mRNA 表达降低。用 Wnt 配体模拟物 CHIR 处理外植体可恢复 Wnt 靶基因的表达。在这里,我们还证实了之前的证据,即正常的肾脏基质发育对于 Six2+肾祖细胞、Henle 袢和收集管的正常发育是必需的。

结论

这些发现表明,基质 Tcf21 通过增强 Wnt/β-连环蛋白信号促进间质细胞增殖和分化,促进髓质基质的发育。基质 Tcf21 对于相邻肾上皮的发育也是必需的。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验