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Published in: Journal of Cardiovascular Translational Research 2/2020

01-04-2020 | Arterial Occlusive Disease | Original Article

Foam Cell-Derived CXCL14 Muti-Functionally Promotes Atherogenesis and Is a Potent Therapeutic Target in Atherosclerosis

Authors: Weilin Tong, Yaqi Duan, Rumeng Yang, Ying Wang, Changqing Peng, Zitian Huo, Guoping Wang

Published in: Journal of Cardiovascular Translational Research | Issue 2/2020

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Abstract

CXC chemokine family has been related to atherogenesis for long. However, the relationship between CXCL14 and atherogenesis is still unclear. This study preliminarily detected CXCL14 expression at foam cells in atherosclerosis specimens by immunohistochemistry. In vitro foam cells were derived from THP-1 after phorbol-12-myristate-13-acetate (PMA) and oxidized low-density lipoprotein (ox-LDL) stimulation. Immunoblotting and qPCR convinced CXCL14 expression variation during foam cell formation. We further demonstrated that ox-LDL regulated CXCL14 expression by AP-1. AP-1 could bind to CXCL14 promoter and up-regulate CXCL14 mRNA expression. Besides, CXCL14 promoted THP-1 migration, macrophage lipid phagocytosis, and smooth muscle cell migration as well as proliferation mainly via the ERK1/2 pathway. Additionally, a CXCL14 peptide-induced immune therapy showed efficacy in ApoE−/− mouse model. In conclusion, our study demonstrated that CXCL14 is highly up-regulated during foam cell formation and promotes atherogenesis in various ways. CXCL14 may be a potent therapeutic target for atherosclerosis.
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Metadata
Title
Foam Cell-Derived CXCL14 Muti-Functionally Promotes Atherogenesis and Is a Potent Therapeutic Target in Atherosclerosis
Authors
Weilin Tong
Yaqi Duan
Rumeng Yang
Ying Wang
Changqing Peng
Zitian Huo
Guoping Wang
Publication date
01-04-2020
Publisher
Springer US
Published in
Journal of Cardiovascular Translational Research / Issue 2/2020
Print ISSN: 1937-5387
Electronic ISSN: 1937-5395
DOI
https://doi.org/10.1007/s12265-019-09915-z

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