Proximal Tubule Cells Contribute to the Thin Descending Limb of the Loop of Henle during Mouse Kidney Development

Key Points Reference single-cell RNA-seq dataset of the developing mouse kidney was used to identify the thin descending limb of the loop of Henle. Lineage analysis of proximal tubules in the mouse kidney shows that proximal tubules give rise to the thin descending limb of the loop of Henle. Hnf4a deletion disrupts Aqp1 expression in the thin descending limb, suggesting a developmental link between proximal tubules and the loop of Henle. 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 dataset by integrating multiple datasets of nonmutant 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. In addition, 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 single-cell RNA sequencing 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. Conclusions Our findings shed new light on the developmental origin of thin descending limb cells and highlight the importance of Hnf4a in regulating their formation.