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. 2018 Jun 1;37(39):5305–5324. doi: 10.1038/s41388-018-0294-0

Fig. 5.

Fig. 5

Effects of DKK3 silencing on TGFBI and ECM-1 protein and mRNA levels in WPMY-1 and RWPE-1 cells. a Western blots of CM from equal numbers of shCTRL (PSM2) and shDKK3 (Wsh8) WPMY-1 cells cultured in serum-free medium for 48 h were probed for TGFBI; a Coomassie Blue (CB)-stained gel of samples run in parallel was used as a loading control. b Densitometry analysis of TGFBI in CM; graph shows average intensity normalized to PSM2, error bars show SD, **p < 0.01, n = 5. c q-RT-PCR analysis of TGFBI mRNA levels, relative to 36B4, in shCTRL (PSM2/PSM3) and shDKK3 (Wsh7/Wsh8) WPMY-1 cells; error bars show SD. d Western blots of CM from equal numbers of shCTRL (NS11) and shDKK3 (sh6) RWPE-1 cells cultured in serum-free medium for 48 h were probed for TGFBI; a CB-stained gel of samples run in parallel was used as a loading control. e Densitometry analysis of TGFBI in CM; graph shows average intensity normalized to NS11, error bars show SD, **p < 0.01, n = 3. f q-RT-PCR analysis of TGFBI mRNA levels, relative to 36B4, in shCTRL (NS11) and shDKK3 (sh6) RWPE-1 cells; error bars show SD, n = 3, *p < 0.05. gl ECM-1 protein and ECM1 mRNA levels were analyzed as in af; h **p < 0.01, n = 6, k *p < 0.05, n = 3