Proximal tubule cells contribute to the thin descending limb of the loop of Henle during mouse kidney development.

Eunah Chung, Fariba Nosrati, Mike Adam, Andrew Potter, Mohammed Sayed, Christopher Ahn, Benjamin D Humphreys, Hee-Woong Lim, Yueh-Chiang Hu, S Steven Potter, Joo-Seop Park
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Abstract

Background: The thin descending limb of the loop of Henle is crucial for urine concentration, as it facilitates passive water reabsorption. Despite its importance, little is known about how this nephron segment forms during kidney development.

Methods: We assembled a large single-cell RNA sequencing (scRNA-seq) dataset by integrating multiple datasets of non-mutant developing mouse kidneys to identify developing thin descending limb cells. To test whether those cells originate from proximal tubule cells, we generated a proximal tubule-specific Cre line, Slc34a1eGFPCre , and conducted lineage tracing. Additionally, given that the transcription factor Hnf4a directly binds to the Aqp1 gene, we examined whether the loss of Hnf4a affects Aqp1 expression in thin descending limb cells.

Results: From our scRNA-seq dataset, we identified a small cluster of cells distinct from both the proximal tubule and the thick ascending limb of the loop of Henle. Those cells exhibited high expression of thin descending limb marker genes, including Aqp1 and Bst1 . Notably, a subset of proximal tubule cells also expressed thin descending limb marker genes, suggesting that proximal tubule cells may give rise to thin descending limb cells. Using lineage tracing with the Slc34a1eGFPCre line, we found that, at least, a subset of thin descending limb cells are descendants of proximal tubule cells. Furthermore, the loss of Hnf4a, a transcription factor essential for mature proximal tubule cell formation, disrupted proper Aqp1 expression in thin descending limb cells, providing additional evidence of a developmental link between proximal tubule cells and thin descending limb cells.

Conclusion: Our findings shed new light on the developmental origin of thin descending limb cells and highlight the importance of Hnf4a in regulating their formation.

Key points: Reference single cell RNA-seq dataset of the developing mouse kidney was assembled and used to identify the thin descending limb of the loop of Henle.Lineage analysis of proximal tubules in the mouse kidney shows that proximal tubule cells give rise to the thin descending limb of the loop of Henle. Deletion of Hnf4a disrupts the expression of Aqp1 in the thin descending limb of the loop of Henle, highlighting a developmental link between proximal tubules and the loop of Henle.

背景:亨氏襻的细降支(DTL)对尿液浓缩至关重要,因为它有利于被动水重吸收。尽管DTL非常重要,但人们对其在肾脏发育过程中如何形成知之甚少。单细胞 RNA 测序(scRNA-seq)研究尚未明确确定发育中小鼠肾脏中的 DTL 细胞:我们整合了多个非突变发育期小鼠肾脏的数据集,建立了一个大型scRNA-seq数据集,以鉴定发育中的DTL细胞。为了检测DTL细胞是否起源于近端肾小管(PT)细胞,我们生成了PT特异性Cre系Slc34a1eGFPCre,并对PT细胞进行了系谱追踪。此外,鉴于转录因子Hnf4a直接与Aqp1基因结合,我们研究了Hnf4a的缺失是否会影响Aqp1在DTL细胞中的表达:从我们的scRNA-seq数据集中,我们发现了一小簇细胞,它们与亨氏襻近端小管和粗升支细胞截然不同。这些细胞表现出 DTL 标记基因的高表达,包括 Aqp1 和 Bst1。值得注意的是,一部分 PT 细胞也表达 DTL 标记基因,这表明 PT 细胞可能产生 DTL 细胞。通过使用 Slc34a1eGFPCre 株系进行系谱追踪,我们发现 DTL 细胞的 Rosa26 报告呈阳性,这证实了 DTL 细胞是 PT 细胞的后代。此外,成熟PT细胞形成所必需的转录因子Hnf4a的缺失破坏了DTL细胞中Aqp1的正常表达,为PT细胞和DTL细胞之间的发育联系提供了更多证据:我们的发现揭示了DTL细胞的发育起源,并强调了Hnf4a在调节其形成过程中的重要性:小鼠肾脏近端小管的系谱分析表明,近端小管细胞产生了亨勒襻的细降肢。Hnf4a的缺失破坏了Aqp1在亨勒襻细降肢中的表达,突显了近端小管和亨勒襻之间的发育联系。
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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