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Article

Cathepsin S Activity Controls Injury-Related Vascular Repair in Mice via the TLR2-Mediated p38MAPK and PI3K-Akt/p-HDAC6 Signaling Pathway.

Arteriosclerosis, thrombosis, and vascular biology - 1 Aug 2016

Wu Hongxian, Cheng Xian Wu, Hu Lina, Takeshita Kyosuke, Hu Chen, Du Qiuna, Li Xiang, Zhu Enbo, Huang Zhe, Yisireyili Maimaiti, Zhao Guangxian, Piao Limei, Inoue Aiko, Jiang Haiying, Lei Yanna, Zhang Xiaohong, Liu Shaowen, Dai Qiuyan, Kuzuya Masafumi, Shi Guo-Ping, Murohara Toyoaki

Abstract excerpt

OBJECTIVE: Cathepsin S (CatS) participates in atherogenesis through several putative mechanisms. The ability of cathepsins to modify histone tail is likely to contribute to stem cell development. Histone deacetylase 6 (HDAC6) is required in modulating the proliferation and migration of various types of cancer cells. Here, we investigated the cross talk between CatS and HADC6 in injury-related vascular repair in...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 27365406
DOI: 10.1161/ATVBAHA.115.307110
PMCID: PMC4961274

Genes

HDAC6
TLR2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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