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. 2012 Oct 15;17(8):1053–1065. doi: 10.1089/ars.2012.4518

FIG. 2.

FIG. 2.

HIF-1α-dependent induction of miR-107 improved PCMSC survival. (A) Western blot showing the successful abrogation of HIF-1α in the nuclear fraction of PCMSC with PCx2 and transfected with HIF-1α siRNA as compared with Sc siRNA-transfected PCMSC. Native non-PCMSC were used as controls. (B) RT-PCR showing the abrogation of miR-107 in PCMC (PCx2) in response to HIF-1α siRNA transfection as compared with Sc siRNA-transfected PCMSC. (C) The abrogation of HIF-1α led to the loss of cytoprotection in PCMSC as determined by LDH-release assay. PCMSC (both PCx1 and PCx2) with HIF-1α siRNA transfection had a significantly higher release of LDH under 6 h of lethal anoxia as compared with ScMSC. (D) Representative fluorescence images and quantitative analysis of TUNEL positivity (green) showed that the abrogation of HIF-1α significantly increased TUNEL-positive PCMSC as compared with Sc siRNA-transfected PCMSC. DAPI was used to visualize nuclei. HIF-1α, hypoxia inducible factor-1α; N.S., non-significant; RT-PCR, reverse transcription polymerase chain reaction; Sc, scramble; TUNEL, transferase-mediated dUTP nick-end labeling. (To see this illustration in color the reader is referred to the web version of this article at www.liebertpub.com/ars).