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肾脏疾病:新技术将机制转化为治疗方法。

Kidney disease: new technologies translate mechanisms to cure.

出版信息

J Clin Invest. 2014 Jun;124(6):2294-8. doi: 10.1172/JCI76825. Epub 2014 Jun 2.

DOI:10.1172/JCI76825
PMID:24892702
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4089455/
Abstract

Kidney disease is one of the most prevalent chronic conditions and is a frequent complication of diabetes, cardiovascular disease, and obesity. Recent advances in biomedical research and novel technologies have created opportunities to study kidney disease in a variety of platforms, applied to human populations. The Reviews in this series discuss the kidney in hypertension, diabetes, and monogenic forms of kidney disease, as well as the cellular and molecular mediators of acute kidney injury and fibrosis, IgA nephropathy and idiopathic membranous nephropathy, and kidney transplantation. In this introduction, we briefly review new insights into focal segmental glomerulosclerosis and the role of podocytes in health and disease. Additionally, we discuss how new technologies, therapeutics, and the availability of patient data can help shape the study of kidney disease and ultimately inform policies concerning biomedical research and health care.

摘要

肾脏病是最常见的慢性疾病之一,也是糖尿病、心血管疾病和肥胖症的常见并发症。生物医学研究和新技术的最新进展为在各种平台上研究肾脏病提供了机会,这些平台适用于人类群体。本系列评论讨论了高血压、糖尿病和单基因形式的肾脏病中的肾脏,以及急性肾损伤和纤维化、IgA 肾病和特发性膜性肾病的细胞和分子介质,以及肾移植。在这篇介绍中,我们简要回顾了局灶节段性肾小球硬化的新见解以及足细胞在健康和疾病中的作用。此外,我们还讨论了新技术、疗法以及患者数据的可用性如何帮助塑造肾脏病的研究,并最终为生物医学研究和医疗保健政策提供信息。

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Kidney disease: new technologies translate mechanisms to cure.肾脏疾病:新技术将机制转化为治疗方法。
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Replication of European hypertension associations in a case-control study of 9,534 African Americans.在一项针对 9534 名非裔美国人的病例对照研究中,欧洲高血压协会的研究结果得到了复制。
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Quercetin Inhibits Fibroblast Activation and Kidney Fibrosis Involving the Suppression of Mammalian Target of Rapamycin and β-catenin Signaling.槲皮素通过抑制雷帕霉素哺乳动物靶蛋白和β-连环蛋白信号传导来抑制成纤维细胞活化和肾脏纤维化。
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本文引用的文献

1
Therapeutic translation in acute kidney injury: the epithelial/endothelial axis.急性肾损伤的治疗性转化:上皮/内皮轴。
J Clin Invest. 2014 Jun;124(6):2355-63. doi: 10.1172/JCI72269. Epub 2014 Jun 2.
2
Complement as a multifaceted modulator of kidney transplant injury.补体作为肾脏移植损伤的多功能调节剂。
J Clin Invest. 2014 Jun;124(6):2348-54. doi: 10.1172/JCI72273. Epub 2014 Jun 2.
3
The inextricable role of the kidney in hypertension.肾脏在高血压中的不可分割的作用。
J Clin Invest. 2014 Jun;124(6):2341-7. doi: 10.1172/JCI72274. Epub 2014 Jun 2.
4
Molecular mechanisms of diabetic kidney disease.糖尿病肾病的分子机制。
J Clin Invest. 2014 Jun;124(6):2333-40. doi: 10.1172/JCI72271. Epub 2014 Jun 2.
5
The genetics and immunobiology of IgA nephropathy.IgA 肾病的遗传学和免疫生物学。
J Clin Invest. 2014 Jun;124(6):2325-32. doi: 10.1172/JCI74475. Epub 2014 Jun 2.
6
Genetic mechanisms and signaling pathways in autosomal dominant polycystic kidney disease.常染色体显性遗传性多囊肾病的遗传机制和信号通路。
J Clin Invest. 2014 Jun;124(6):2315-24. doi: 10.1172/JCI72272. Epub 2014 Jun 2.
7
Membranous nephropathy: from models to man.膜性肾病:从模型到人类。
J Clin Invest. 2014 Jun;124(6):2307-14. doi: 10.1172/JCI72270. Epub 2014 Jun 2.
8
Cellular and molecular mechanisms in kidney fibrosis.肾脏纤维化的细胞和分子机制。
J Clin Invest. 2014 Jun;124(6):2299-306. doi: 10.1172/JCI72267. Epub 2014 Jun 2.
9
Epigenomics starts to make its mark.表观基因组学开始崭露头角。
Nature. 2014 Apr 3;508(7494):22. doi: 10.1038/508022a.
10
Role of podocyte B7-1 in diabetic nephropathy.足细胞 B7-1 在糖尿病肾病中的作用。
J Am Soc Nephrol. 2014 Jul;25(7):1415-29. doi: 10.1681/ASN.2013050518. Epub 2014 Mar 27.