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本文引用的文献

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Sodium-Glucose Co-Transporter 2 Inhibitors Correct Metabolic Maladaptation of Proximal Tubular Epithelial Cells in High-Glucose Conditions.钠-葡萄糖协同转运蛋白 2 抑制剂纠正高糖条件下近端肾小管上皮细胞的代谢适应不良。
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Identification of hub genes in diabetic kidney disease via multiple-microarray analysis.通过多重微阵列分析鉴定糖尿病肾病中的枢纽基因
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Fc-Elabela fusion protein attenuates lipopolysaccharide-induced kidney injury in mice.Fc-Elabela 融合蛋白可减轻脂多糖诱导的小鼠肾损伤。
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Butyrate alleviates diabetic kidney disease by mediating the miR-7a-5p/P311/TGF-β1 pathway.丁酸盐通过调控 miR-7a-5p/P311/TGF-β1 通路缓解糖尿病肾病。
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Runx-mediated regulation of CCL5 via antagonizing two enhancers influences immune cell function and anti-tumor immunity.Runx 通过拮抗两个增强子对 CCL5 的调节影响免疫细胞功能和抗肿瘤免疫。
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APELA/ELA32 Reduces Iodixanol-induced Apoptosis, Inflammatory Response and Mitochondrial and DNA Damage in Renal Tubular Epithelial Cells.APELA/ELA32 降低碘克沙醇诱导的肾小管上皮细胞凋亡、炎症反应以及线粒体和 DNA 损伤。
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通过对db/db小鼠肾脏进行单细胞转录组分析预测糖尿病肾病中的细胞靶点

Prediction of cellular targets in diabetic kidney diseases with single-cell transcriptomic analysis of db/db mouse kidneys.

作者信息

Wu Chenhua, Tao Yingjun, Li Nan, Fei Jingjin, Wang Yurong, Wu Jie, Gu Harvest F

机构信息

Laboratory of Molecular Medicine, School of Basic Medicine and Clinical Pharmacy, China Pharmaceutical University, Nanjing, 210009, China.

Laboratory of Minigene Pharmacy, School of Life Science and Technology, China Pharmaceutical University, Nanjing, 211198, China.

出版信息

J Cell Commun Signal. 2023 Mar;17(1):169-188. doi: 10.1007/s12079-022-00685-z. Epub 2022 Jul 9.

DOI:10.1007/s12079-022-00685-z
PMID:35809207
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10030752/
Abstract

Diabetic kidney disease is the leading cause of impaired kidney function, albuminuria, and renal replacement therapy (dialysis or transplantation), thus placing a large burden on health-care systems. This urgent event requires us to reveal the molecular mechanism of this disease to develop more efficacious treatment. Herein, we reported single-cell RNA sequencing analyses in kidneys of db/db mouse, an animal model for type 2 diabetes and diabetic kidney disease. We first analyzed the hub genes expressed differentially in the single cell resolution transcriptome map of the kidneys. Then we figured out the communication among the renal and immune cells in the kidneys. Data from this report may provide novel information for better understanding the cell-specific targets involved in the aetiologia of type 2 diabetic kidney disease and for cell communication and signaling between renal cells and immune cells of this complex disease.

摘要

糖尿病肾病是肾功能受损、蛋白尿和肾脏替代治疗(透析或移植)的主要原因,给医疗保健系统带来了沉重负担。这一紧急情况要求我们揭示该疾病的分子机制,以开发更有效的治疗方法。在此,我们报告了对db/db小鼠肾脏进行的单细胞RNA测序分析,db/db小鼠是2型糖尿病和糖尿病肾病的动物模型。我们首先分析了在肾脏单细胞分辨率转录组图谱中差异表达的枢纽基因。然后我们弄清楚了肾脏中肾细胞和免疫细胞之间的通讯。本报告的数据可能为更好地理解2型糖尿病肾病病因中涉及的细胞特异性靶点以及这种复杂疾病的肾细胞与免疫细胞之间的细胞通讯和信号传导提供新信息。