Fibrosis in Pathology of Heart and Kidney: From Deep RNA-Sequencing to Novel Molecular Targets

被引:21
|
作者
Schreibing, Felix [1 ,2 ]
Anslinger, Teresa M. [1 ,2 ]
Kramann, Rafael [1 ,2 ,3 ]
机构
[1] Rhein Westfal TH Aachen, Med Fac, Inst Expt Med & Syst Biol, Aachen, Germany
[2] Rhein Westfal TH Aachen, Med Fac, Div Nephrol & Clin Immunol, Aachen, Germany
[3] Erasmus MC, Dept Internal Med Nephrol & Transplantat, Rotterdam, Netherlands
基金
欧洲研究理事会;
关键词
chronic renal insufficiency; fibrosis; heart failure; myofibroblasts; RNA-seq; CARDIAC FIBROBLASTS; TUBULOINTERSTITIAL CHANGES; MYOFIBROBLAST TRANSITION; CARDIORENAL SYNDROME; SEQ; TISSUE; REVEALS; IDENTIFICATION; HETEROGENEITY; MACROPHAGES;
D O I
10.1161/CIRCRESAHA.122.321761
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Diseases of the heart and the kidney, including heart failure and chronic kidney disease, can dramatically impair life expectancy and the quality of life of patients. The heart and kidney form a functional axis; therefore, functional impairment of 1 organ will inevitably affect the function of the other. Fibrosis represents the common final pathway of diseases of both organs, regardless of the disease entity. Thus, inhibition of fibrosis represents a promising therapeutic approach to treat diseases of both organs and to resolve functional impairment. However, despite the growing knowledge in this field, the exact pathomechanisms that drive fibrosis remain elusive. RNA-sequencing approaches, particularly single-cell RNA-sequencing, have revolutionized the investigation of pathomechanisms at a molecular level and facilitated the discovery of disease-associated cell types and mechanisms. In this review, we give a brief overview over the evolution of RNA-sequencing techniques, summarize most recent insights into the pathogenesis of heart and kidney fibrosis, and discuss how transcriptomic data can be used, to identify new drug targets and to develop novel therapeutic strategies.
引用
收藏
页码:1013 / 1033
页数:21
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