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. 2018 Jul 23;40(4):477–485. doi: 10.1038/s41401-018-0076-9

Fig. 2.

Fig. 2

The effect of early or late miR-135a-5p mimic or inhibitor treatment on hypoxia-induced proliferation of PASMCs. ac After PASMCs were exposed to 21% O2 (normoxia) or 3% O2 (hypoxia) for 48 h together with a miR-135a-5p mimic or inhibitor treatment that started at the beginning of the hypoxic treatment, the cell viability of the PASMCs was determined by CCK-8 assays (a), cell proliferation was determined by [3H]-leucine incorporation (b) and the expression of the PCNA gene and protein (c, d) were determined in PASMCs. eg PASMCs were exposed to 21% O2 (normoxia) or 3% O2 (hypoxia) for 48 h together with a miR-135a-5p mimic or inhibitor treatment that started after 12 h of hypoxic treatment, and the cell viability and proliferation of the PASMCs were determined by CCK-8 assays (e) and by the mRNA expression of the PCNA gene and protein (f, g) in PASMCs. Data are presented as the mean ± s.d., and n = 3 independent experiments for each panel. *P < 0.05, **P < 0.01 vs. normoxia; ##P < 0.01 vs. hypoxia