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Fig. 7. RNAi-induced loss of BMPR1A, by reducing MMP9 and MMP2
expression, impairs directed migration of human vascular smooth muscle
cells. (A) Gelatin zymography in response to PDGF-BB. Gelatin
zymography performed on conditioned media (left) and densitometric analysis
(right) show MMP9 and pro and active MMP2 activities in SiBMPR1A-treated
(SiBR1A) versus SiControl-treated (SiC) cells in response to PDGF-BB (20
ng/ml) stimulation for 6 hours. Bars indicate mean±s.e.m. of
densitometric values of SiBR1A MMP forms normalized to the corresponding SiC
values. (n=4). **P<0.01,
***P<0.001. (B) Migration in response to PDGF-BB
as assessed by modified Boyden Chamber assay. SiC- or SiBR1A-transfected
HPASMCs were stimulated with 20 ng/ml of PDGF-BB for 6 hours. Bars represent
mean±s.e.m. of migrating cells in 5-6 different microscopic fields.
(n=4).
P<0.05 for stimulated versus
unstimulated comparisons for each Si; ***P<0.001 for
comparisons between SiBR1A and SiC. Representative micrographs show the number
of migrating cells under each condition. Scale bar: 100 µm.