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. 2022 Jan 27;12:1459. doi: 10.1038/s41598-022-05408-3

Figure 2.

Figure 2

Treatment with bile acids inhibits LPS-induced PKM1 and PKM2 transcription in cell cultures. The mRNA expression for (a, c) PKM2 and (b, d) PKM1, and (e) PKM2/PKM1 transcript ratio was determined by qRT-PCR in microglia and in Raw264.7 cultures. Cells were preincubated with TLCA (40 μM), TUDCA (200 μM) for 2 h followed by LPS (10 ng/ml for microglia and 50 ng/ml for Raw264.7 respectively) was added for further 24 h. The expression of 36B4  for microglia or RPS29 for Raw264.7 cells respectively was used as a housekeeping gene to normalize the data. ANOVA revealed significant treatment effects on the transcription of PKM1 in (a) microglial cells [F(5, 28) = 9,3, p < 0.001] and (d) in Raw264.7 cells, [F(7, 21) = 4.7 p < 0.01] and PKM2 (b) in microglial cells [F(5, 29) = 13.7, p < 0.001] and (e) in Raw264.7 cells [F(5, 23) = 3.7, p < 0.05] respectively. Changes of PKM2/PKM1 ratio in (c) microglial cells and (f) Raw264.7 cells were not statistically significant. Results of Dunnett’s post hoc tests are indicated as in Fig. 1 (* vs. control, # vs. LPS, n ≥ 3 independent experiments).