Fig. 8From: Microtubule destabilization caused by silicate via HDAC6 activation contributes to autophagic dysfunction in bone mesenchymal stem cellsInhibition of HDAC6 activity restored autophagic activity and improved cell viability after silicate exposure. a, b Autophagic flux-related proteins including p62 and LC3-II were identified by Western blot after transfection with siHDAC6 (n = 4). Data analysis showed that the expression of p62 and LC3-II after high-dose silicate treatment was partially downregulated via HDAC6 interference compared with that of the control group. c, d Autophagosome (LC3 dots) accumulation caused by high-dose silicate was partially improved with siHDAC6 treatment (n = 3, 10 random fields per sample). e CCK-8 assay was applied to evaluate cell viability after siHADC6 treatment. As the data show, the downregulation of cell viability caused by 1.5 mM and 3 mM silicate was significantly improved after siHDAC6 treatment (n = 4). (*p < 0.05, **p < 0.01, ***p < 0.001)Back to article page