Cardiovascular Research Advance Access first published online on October 13, 2008
This version [Corrected Proof] published online on October 30, 2008
Cardiovascular Research, doi:10.1093/cvr/cvn278
MMP-9 and -12 cause N-cadherin shedding and thereby β-catenin signalling and vascular smooth muscle cell proliferation
Bristol Heart Institute, University of Bristol, Level 7, Bristol Royal Infirmary, Bristol BS2 8HW, UK
* Corresponding author. Tel: +44 117 9283154; fax: +44 117 9283581.E-mail address: s.j.george{at}bris.ac.uk
Aims: Vascular smooth muscle cell (VSMC) proliferation contributes to intimal thickening in restenosis and atherosclerosis. Previously, we demonstrated that matrix-degrading metalloproteinase (MMP)-dependent shedding of the extracellular portion of N-cadherin increased VSMC proliferation via elevation of β-catenin signalling and cyclin D1 expression. In this study, we aimed to determine whether MMP-2, -9, -12, or -14 regulates VSMC proliferation via N-cadherin shedding.
Methods and results: N-cadherin shedding was significantly impaired in proliferating mouse aortic VSMCs deficient in MMP-9 (MMP-9–/–) and MMP-12 (MMP-12–/–) compared with wild-type controls (1.1 ± 0.7- and 1.0 ± 0.1- vs. 2.0 ± 0.2-fold). Furthermore, proliferating VSMCs subjected to MMP-9 or -12 siRNA knockdown or deficient in MMP-9 or -12 showed significantly increased cellular levels of N-cadherin compared with controls (1.7 ± 0.2-, 2.7 ± 0.6-, and 3.5 ± 1.6-, 1.7 ± 0.2-fold, respectively). Incubation of VSMCs with active MMP-9 or -12 independently increased N-cadherin cleavage. Additionally, β-catenin signalling was significantly reduced by 52 ± 17 and 81 ± 12% in MMP-9–/– and -12–/– proliferating VSMCs, respectively, and this was corroborated by siRNA knockdown of MMP-9 and -12. Decreased β-catenin signalling coincided with significantly reduced proliferation and cyclin D1 protein levels in MMP-9–/– and -12–/– cells. Little or no additive effect was observed with combined modulation of MMP-9 and -12 in all experiments. In contrast, N-cadherin shedding and VSMC proliferation were not modulated by MMP-2 and -14.
Conclusion: In conclusion, we propose that MMP-9 and -12 promote intimal thickening by independent cleavage of N-cadherin, which elevates VSMC proliferation via β-catenin signalling.
KEYWORDS MMP; N-cadherin; Intimal thickening; Smooth muscle cell; Proliferation
Time for primary review: 22 days
Present address. Paul O'Gorman Lifeline Centre, Southmead Hospital, Bristol BS10 5NB, UK.