Adiponectin association with T-cadherin protects against neointima proliferation and atherosclerosis

被引:107
作者
Fujishima, Yuya [1 ]
Maeda, Norikazu [1 ,2 ]
Matsuda, Keisuke [1 ]
Masuda, Shigeki [1 ]
Mori, Takuya [1 ]
Fukuda, Shiro [1 ]
Sekimoto, Ryohei [1 ]
Yamaoka, Masaya [1 ]
Obata, Yoshinari [1 ]
Kita, Shunbun [1 ,2 ]
Nishizawa, Hitoshi [1 ]
Funahashi, Tohru [1 ,2 ]
Ranscht, Barbara [3 ]
Shimomura, Iichiro [1 ]
机构
[1] Osaka Univ, Grad Sch Med, Dept Metab Med, 2-2-B5 Yamada Oka, Suita, Osaka 5650871, Japan
[2] Osaka Univ, Grad Sch Med, Dept Metab & Atherosclerosis, Osaka, Japan
[3] Sanford Burnham Prebys Med Discovery Inst, La Jolla, CA USA
基金
日本学术振兴会;
关键词
ADIPOSE-SPECIFIC PROTEIN; GENOME-WIDE ASSOCIATION; CELL-ADHESION MOLECULE; SMOOTH-MUSCLE-CELLS; INSULIN-RESISTANCE; EXPRESSION; PLASMA; ACTIVATION; GROWTH; CDH13;
D O I
10.1096/fj.201601064R
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Adiponectin, an adipocyte-derived protein abundant in the circulation, is thought to be protective against atherosclerosis. However, it is not fully understood how the association of adiponectin with vascular cells and its antiatherogenic effect are connected. In this study, T-cadherin was essential for accumulation of adiponectin in the neointima and atherosclerotic plaque lesions, and the adiponectin-T-cadherin association protected against vascular injury. In the apolipoprotein E-knockout (ApoE-KO) mice, adiponectin and T-cadherin colocalized on endothelial cells and synthetic smooth muscle cells in the aortic intima. Notably, aortic adiponectin protein disappeared in T-cadherin/ApoE double-knockout (Tcad/ApoE-DKO) mice with significant elevation of blood adiponectin concentration. Furthermore, in Tcad/ApoE-DKO mice, carotid artery ligation resulted in a significant increase of neointimal thickness compared with ApoE-KO mice. Finally, on a high-cholesterol diet, Tcad/ApoE-DKO mice increased atherosclerotic plaque formation, despite a 5-fold increase in plasma adiponectin level compared with that in ApoE-KO mice. In vitro, knockdown of T-cadherin from human aortic smooth muscle cells (HASMCs) with synthetic phenotype significantly reduced adiponectin accumulation on HASMCs and negated the inhibitory effect of adiponectin on proinflammatory change. Collective evidence showed that adiponectin accumulates in the vasculature via T-cadherin, and the adiponectin-T-cadherin association plays a protective role against neointimal and atherosclerotic plaque formations.-Fujishima, Y., Maeda, N., Matsuda, K., Masuda, S., Mori, T., Fukuda, S., Sekimoto, R., Yamaoka, M., Obata, Y., Kita, S., Nishizawa, H., Funahashi, T., Ranscht, B., Shimomura, I. Adiponectin association with T-cadherin protects against neointima proliferation and atherosclerosis.
引用
收藏
页码:1571 / 1583
页数:13
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