Activation of TLR3 induces osteogenic responses in human aortic valve interstitial cells through the NF-kappaB and ERK1/2 pathways.

作者：Zhan Qiong; Song Rui; Zeng Qingchun; Yao Qingzhou; Ao Lihua; Xu Dingli; Fullerton David A; Meng Xianzhong

来源：International Journal of Biological Sciences, 2015, 11(4): 482-493.

DOI：10.7150/ijbs.10905

• Aortic valve interstitial cells.
• BMP-2
• Calcification
• TGF-beta1
• TLR3

UNLABELLED: Calcific aortic valve disease (CAVD) is characterized by chronic inflammation and progressive calcification in valve leaflets. Aortic valve interstitial cells (AVICs) play a critical role in the pathogenesis of CAVD. Previous studies show that stimulation of Toll-like receptor (TLR) 2 or TLR4 in AVICs in vitro up-regulates the expression of osteogenic mediators. Double-stranded RNA (dsRNA) can activate pro-inflammatory signaling through TLR3, the NLRP3 inflammasome and RIG-I-like receptors. The objective of this study is to determine the effect of dsRNA on AVIC osteogenic activities and the mechanism of its action. METHODS AND RESULTS: AVICs isolated from normal human valves were exposed to polyinosinic-polycytidylic acid [poly(I:C)], a mimic of dsRNA. Treatment with poly(I:C) increased the production of bone morphogenetic protein-2 (BMP-2), transforming growth factor beta-1 (TGF-beta1) and alkaline phosphatase (ALP), and resulted in calcium deposit formation. Poly(I:C) induced the phosphorylation of NF-kappaB and ERK1/2. Knockdown of TLR3 essentially abrogated NF-kappaB and ERK1/2 phosphorylation, and markedly reduced the effect of poly(I:C) on the production of BMP-2, TGF-beta1 and ALP. Further, inhibition of either NF-kappaB or ERK1/2 markedly reduced the levels of BMP-2, TGF-beta1 and ALP in cells exposed to poly(I:C). CONCLUSION: Poly(I:C) up-regulates the production of BMP-2, TGF-beta1 and ALP, and promotes calcium deposit formation in human AVICs. The pro-osteogenic effect of poly(I:C) is mediated primarily by TLR3 and the NF-kappaB and ERK1/2 pathways. These findings suggest that dsRNA, when present in aortic valve tissue, may promote CAVD progression through up-regulation of AVIC osteogenic activities.

• 出版日期2015
• 单位南方医科大学