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单细胞转录揭示胚胎肾脏发育中的关键转录因子。

Single cell transcription revealing key transcription factors in embryonic kidney development.

作者信息

Huang Jingxian, Yan Bing, Wu Hongwei, Yang Hougang, Luan Shaodong, Yu Haiyan, Shi Wei, Ye Pingping, Yuan Fang, Yan Qiang, Liu Fanna, Yin Lianghong, Tang Donge, Dai Yong

机构信息

Guangdong Provincial Autoimmune Disease Precision Medicine Engineering Research Center, Shenzhen Autoimmune Disease Engineering Research Center, Shenzhen Geriatrics Clinical Research Center, Shenzhen People's Hospital, Second Clinical Medical College of Jinan University, Shenzhen, 518020, China.

Institute of Kidney Disease and Blood Purification, The First Affiliated Hospital of Jinan University, Guangzhou, 510630, China.

出版信息

Mol Cell Biochem. 2025 May 20. doi: 10.1007/s11010-025-05307-x.


DOI:10.1007/s11010-025-05307-x
PMID:40392427
Abstract

The development of the kidney is a complex process involving the differentiation of renal progenitor cells into various specialized cell types, including renal tubular epithelial cells and podocytes. Understanding the molecular mechanisms that govern this differentiation process is crucial for unraveling the intricacies of kidney development. Recent advances in single-cell RNA sequencing technology have enabled researchers to explore the heterogeneity of renal progenitor cells at an unprecedented resolution, offering new insights into the distinct subpopulations and transcriptional landscapes within these cells. Our analysis revealed the presence of distinct subpopulations within renal progenitor cells. Furthermore, we identified key transcription factors that are crucial for the differentiation of these progenitors into renal tubular epithelial cells and podocytes. These findings provide new insights into the molecular mechanisms of kidney development, highlighting the role of specific transcription factors in the differentiation of renal progenitor cells. Although further research is needed to fully validate these findings and their therapeutic potential, this study provides a valuable foundation for future exploration of kidney regeneration strategies.

摘要

肾脏的发育是一个复杂的过程,涉及肾祖细胞分化为各种特化细胞类型,包括肾小管上皮细胞和足细胞。了解调控这一分化过程的分子机制对于阐明肾脏发育的复杂性至关重要。单细胞RNA测序技术的最新进展使研究人员能够以前所未有的分辨率探索肾祖细胞的异质性,为这些细胞内不同的亚群和转录图谱提供了新的见解。我们的分析揭示了肾祖细胞内存在不同的亚群。此外,我们确定了对于这些祖细胞分化为肾小管上皮细胞和足细胞至关重要的关键转录因子。这些发现为肾脏发育的分子机制提供了新的见解,突出了特定转录因子在肾祖细胞分化中的作用。尽管需要进一步研究来充分验证这些发现及其治疗潜力,但这项研究为未来探索肾脏再生策略提供了有价值的基础。

相似文献

[1]
Single cell transcription revealing key transcription factors in embryonic kidney development.

Mol Cell Biochem. 2025-5-20

[2]
Cell therapy for kidney injury: different options and mechanisms--kidney progenitor cells.

Nephron Exp Nephrol. 2014

[3]
The transcription factor TCF21 is necessary for adoption of cell fates by Foxd1+ stromal progenitors during kidney development.

bioRxiv. 2024-12-14

[4]
Modeled microgravity unravels the roles of mechanical forces in renal progenitor cell physiology.

Stem Cell Res Ther. 2024-1-17

[5]
Tcf21 as a founder transcription factor in specifying Foxd1 cells to the juxtaglomerular cell lineage.

Am J Physiol Renal Physiol. 2025-1-1

[6]
Single-Cell Chromatin and Gene-Regulatory Dynamics of Mouse Nephron Progenitors.

J Am Soc Nephrol. 2022-7

[7]
Sex-specific proximal tubular cell differentiation pathways identified by single-nucleus RNA sequencing.

Sci Rep. 2024-10-14

[8]
Epithelial cell fate in the nephron tubule is mediated by the ETS transcription factors etv5a and etv4 during zebrafish kidney development.

Dev Biol. 2016-3-15

[9]
Possible mechanisms of kidney repair.

Fibrogenesis Tissue Repair. 2009-6-26

[10]
Kidney Cells Regeneration: Dedifferentiation of Tubular Epithelium, Resident Stem Cells and Possible Niches for Renal Progenitors.

Int J Mol Sci. 2019-12-15

本文引用的文献

[1]
Correction: Qin et al. Production and Stabilization of Specific Upregulated Long Noncoding RNA HOXD-AS2 in Glioblastomas Are Mediated by TFE3 and miR-661, Respectively. 2022, , 2828.

Int J Mol Sci. 2024-12-31

[2]
Systemic immune-inflammation Index is associated with chronic kidney disease in the U.S. population: insights from NHANES 2007-2018.

Front Immunol. 2024

[3]
Domain generalization enables general cancer cell annotation in single-cell and spatial transcriptomics.

Nat Commun. 2024-3-2

[4]
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology.

Nature. 2024-3

[5]
Liquid Biopsy: A New Avenue for the Diagnosis of Kidney Disease: Diabetic Kidney Disease, Renal Cancer, and IgA Nephropathy.

Genes (Basel). 2024-1-7

[6]
Plays Independent Roles in Congenital Heart Disease and Neurodevelopmental Disability.

Int J Mol Sci. 2023-12-28

[7]
The chromatin landscape of healthy and injured cell types in the human kidney.

Nat Commun. 2024-1-10

[8]
Single-cell transcriptome sequencing reveals aberrantly activated inter-tumor cell signaling pathways in the development of clear cell renal cell carcinoma.

J Transl Med. 2024-1-8

[9]
The SOX4/EZH2/SLC7A11 signaling axis mediates ferroptosis in calcium oxalate crystal deposition-induced kidney injury.

J Transl Med. 2024-1-2

[10]
Cortical somatostatin long-range projection neurons and interneurons exhibit divergent developmental trajectories.

Neuron. 2024-2-21

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