The role of Gata3 in renin cell identity.

IF 3.7 2区 医学 Q1 PHYSIOLOGY
Jesus S Neyra, Silvia Medrano, Alexandre De Goes Martini, Maria Luisa S Sequeira-Lopez, R Ariel Gomez
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引用次数: 0

Abstract

Renin cells are precursors for other cell types in the kidney and show high plasticity in postnatal life in response to challenges to homeostasis. Our previous single-cell RNA-sequencing studies revealed that the dual zinc-finger transcription factor Gata3, which is important for cell lineage commitment and differentiation, is expressed in mouse renin cells under normal conditions and homeostatic threats. We identified a potential Gata3-binding site upstream of the renin gene leading us to hypothesize that Gata3 is essential for renin cell identity. We studied adult mice with conditional deletion of Gata3 in renin cells: Gata3fl/fl;Ren1dCre/+ (Gata3-cKO) and control Gata3fl/fl;Ren1d+/+ counterparts. Gata3 immunostaining revealed that Gata3-cKO mice had significantly reduced Gata3 expression in juxtaglomerular, mesangial, and smooth muscle cells, indicating a high degree of deletion of Gata3 in renin lineage cells. Gata3-cKO mice exhibited a significant increase in blood urea nitrogen, suggesting hypovolemia and/or compromised renal function. By immunostaining, renin-expressing cells appeared very thin compared with their normal plump shape in control mice. Renin cells were ectopically localized to Bowman's capsule in some glomeruli, and there was aberrant expression of actin-α2 signals in the mesangium, interstitium, and Bowman's capsule in Gata3-cKO mice. Distal tubules showed dilated morphology with visible intraluminal casts. Under physiological threat, Gata3-cKO mice exhibited a lower increase in mRNA levels than controls. Hematoxylin-eosin, periodic acid-Schiff, and Masson's trichrome staining showed increased glomerular fusion, absent cubical epithelial cells in Bowman's capsule, intraglomerular aneurysms, and tubular dilation. In conclusion, our results indicate that Gata3 is crucial to the identity of cells of the renin lineage.NEW & NOTEWORTHY Gata3, a dual zinc-finger transcription factor, is responsible for the identity and localization of renin cells in the kidney. Mice with a conditional deletion of Gata3 in renin lineage cells have abnormal kidneys with juxtaglomerular cells that lose their characteristic location and are misplaced outside and around arterioles and glomeruli. The fundamental role of Gata3 in renin cell development offers a new model to understand how transcription factors control cell location, function, and pathology.

Gata3在肾素细胞特性中的作用。
肾素细胞是肾脏中其他细胞类型的前体,在出生后的生活中表现出高可塑性,以应对体内平衡的挑战。我们之前的单细胞RNA测序研究表明,在正常条件和稳态威胁下,对细胞谱系承诺和分化很重要的双锌指转录因子Gata3在小鼠肾素细胞中表达。我们在肾素基因上游发现了一个潜在的Gata3结合位点,从而推测Gata3对肾素细胞身份至关重要。我们研究了肾素细胞中Gata3条件性缺失的成年小鼠:Gata3fl/fl;Ren1dCre/+(Gata3 cKO)和控制Gata3fl/fl;Ren1d+/+对应项。Gata3免疫染色显示,Gata3-cKO小鼠在肾小球旁、系膜和平滑肌细胞中的Gata3表达显著降低,表明肾素谱系细胞中Gata3高度缺失。Gata3-cKO小鼠表现出血尿素氮的显著增加,表明低血容量和/或肾功能受损。通过免疫染色,与对照小鼠的正常肥大形状相比,肾素表达细胞显得非常薄。在某些肾小球中,肾素细胞异位定位于鲍曼囊,并且在Gata3-cKO小鼠的系膜、间质和鲍曼囊中存在肌动蛋白-α2信号的异常表达。远端小管扩张,管腔内可见铸型。在生理威胁下,Gata3-cKO小鼠表现出比对照组更低的mRNA水平增加。苏木精-伊红、碘酸Schiff和Masson三色染色显示肾小球融合增加,Bowman囊中没有立方上皮细胞,肾小球内动脉瘤和肾小管扩张。总之,我们的研究结果表明,Gata3对肾素谱系细胞的身份至关重要。NEW&NOTEWORTHY Gata3是一种双锌指转录因子,负责肾脏中肾素细胞的识别和定位。肾素谱系细胞中Gata3条件性缺失的小鼠具有异常肾脏,肾小球旁细胞失去其特征位置,并错位在小动脉和肾小球外和周围。Gata3在肾素细胞发育中的基本作用为了解转录因子如何控制细胞位置、功能和病理提供了一个新的模型。
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来源期刊
CiteScore
8.40
自引率
7.10%
发文量
154
审稿时长
2-4 weeks
期刊介绍: The American Journal of Physiology - Renal Physiology publishes original manuscripts on timely topics in both basic science and clinical research. Published articles address a broad range of subjects relating to the kidney and urinary tract, and may involve human or animal models, individual cell types, and isolated membrane systems. Also covered are the pathophysiological basis of renal disease processes, regulation of body fluids, and clinical research that provides mechanistic insights. Studies of renal function may be conducted using a wide range of approaches, such as biochemistry, immunology, genetics, mathematical modeling, molecular biology, as well as physiological and clinical methodologies.
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