CCL17 acts as a novel therapeutic target in pathological cardiac hypertrophy and heart failure

Circulating proteomic signatures of age are closely associated with aging and age-related diseases; however, the utility of changes in secreted proteins in identifying therapeutic targets for diseases remains unclear. Serum proteomic profiling of an age-stratified healthy population and further comm...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:The Journal of experimental medicine 2022-08, Vol.219 (8)
Hauptverfasser: Zhang, Yang, Ye, Yicong, Tang, Xiaoqiang, Wang, Hui, Tanaka, Toshiko, Tian, Ran, Yang, Xufei, Wang, Lun, Xiao, Ying, Hu, Xiaomin, Jin, Ye, Pang, Haiyu, Du, Tian, Liu, Honghong, Sun, Lihong, Xiao, Shuo, Dong, Ruijia, Ferrucci, Luigi, Tian, Zhuang, Zhang, Shuyang
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Circulating proteomic signatures of age are closely associated with aging and age-related diseases; however, the utility of changes in secreted proteins in identifying therapeutic targets for diseases remains unclear. Serum proteomic profiling of an age-stratified healthy population and further community-based cohort together with heart failure patients study demonstrated that circulating C-C motif chemokine ligand 17 (CCL17) level increased with age and correlated with cardiac dysfunction. Subsequent animal experiments further revealed that Ccll7-KO significantly repressed aging and angiotensin II (Ang II)-induced cardiac hypertrophy and fibrosis, accompanied by the plasticity and differentiation of T cell subsets. Furthermore, the therapeutic administration of an anti-CCL17 neutralizing antibody inhibited Ang II-induced pathological cardiac remodeling. Our findings reveal that chemokine CCL17 is identifiable as a novel therapeutic target in age-related and Ang II-induced pathological cardiac hypertrophy and heart failure.
ISSN:0022-1007
1540-9538
DOI:10.1084/jem.20200418