Transcription factor Tcf21 modulates urinary bladder size and differentiation

IF 1.7 4区 生物学 Q4 CELL BIOLOGY Development Growth & Differentiation Pub Date : 2024-01-10 DOI:10.1111/dgd.12906
Elizabeth A. Mann, Melissa S. Mogle, Joo-Seop Park, Pramod Reddy
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Abstract

Urinary bladder organogenesis requires coordinated cell growth, specification, and patterning of both mesenchymal and epithelial compartments. Tcf21, a gene that encodes a helix–loop–helix transcription factor, is specifically expressed in the mesenchyme of the bladder during development. Here we show that Tcf21 is required for normal development of the bladder. We found that the bladders of mice lacking Tcf21 were notably hypoplastic and that the Tcf21 mutant mesenchyme showed increased apoptosis. There was also a marked delay in the formation of visceral smooth muscle, accompanied by a defect in myocardin (Myocd) expression. Interestingly, there was also a marked delay in the formation of the basal cell layer of the urothelium, distinguished by diminished expression of Krt5 and Krt14. Our findings suggest that Tcf21 regulates the survival and differentiation of mesenchyme cell-autonomously and the maturation of the adjacent urothelium non-cell-autonomously during bladder development.

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转录因子 Tcf21 可调节膀胱大小和分化。
膀胱器官的形成需要间质和上皮细胞的协调生长、规格化和模式化。Tcf21是一种编码螺旋-环-螺旋转录因子的基因,在膀胱间质的发育过程中特异性表达。在这里,我们发现 Tcf21 是膀胱正常发育所必需的。我们发现,缺乏 Tcf21 的小鼠膀胱明显发育不良,Tcf21 突变体间质的凋亡增加。内脏平滑肌的形成也明显延迟,同时伴有心肌蛋白(Myocd)表达缺陷。有趣的是,尿路上皮基底细胞层的形成也明显延迟,表现为 Krt5 和 Krt14 的表达减少。我们的研究结果表明,在膀胱发育过程中,Tcf21自主调节间充质细胞的存活和分化,非自主调节邻近尿路上皮细胞的成熟。
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来源期刊
Development Growth & Differentiation
Development Growth & Differentiation 生物-发育生物学
CiteScore
4.60
自引率
4.00%
发文量
62
审稿时长
6 months
期刊介绍: Development Growth & Differentiation (DGD) publishes three types of articles: original, resource, and review papers. Original papers are on any subjects having a context in development, growth, and differentiation processes in animals, plants, and microorganisms, dealing with molecular, genetic, cellular and organismal phenomena including metamorphosis and regeneration, while using experimental, theoretical, and bioinformatic approaches. Papers on other related fields are also welcome, such as stem cell biology, genomics, neuroscience, Evodevo, Ecodevo, and medical science as well as related methodology (new or revised techniques) and bioresources. Resource papers describe a dataset, such as whole genome sequences and expressed sequence tags (ESTs), with some biological insights, which should be valuable for studying the subjects as mentioned above. Submission of review papers is also encouraged, especially those providing a new scope based on the authors’ own study, or a summarization of their study series.
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