In IL-1β-stimulated human hepatic stellate cells, Tβ4 treatment increased the number of cells in G0/G1 phase arrest compared with the model group and the siRNA-Tβ4 knockdown group.
In plain wordsIn liver cells, thymosin beta‑4 increased cells arrested in the G0/G1 phase compared with IL-1β-treated cells and Tβ4-knockdown cells.
- Peptide
- Thymosin beta-4 (human)
- Outcome
- IncreaseCells in G0/G1 phase arrest
- Study
humann: not reported in source
HSC-LX2 human hepatic stellate cell line with IL-1β- Comparator
- IL-1β model group and siRNA-Tβ4 knockdown group
- Outcome group
- Liver fat and liver function · Liver
- Studied dose
- 1000 ng/mlAs given in this study (human).
Source sentences
Due to the G0/G1 phase arrest, the number of cells in the Tβ4 treatment group increased, compared with the model group and the siRNA-Tβ4 knockdown group (p<0.01).
2 context sentences(design, population, supporting numbers)
To investigate the inhibitory effect of thymosin-β4 (Tβ4) on the activation of the human hepatic stellate cell line (HSC-LX2) induced by interleukin (IL)-1β.
There were 5 groups in this study, i.e., blank control group, negative control group (SI-NC, empty plasmid), model group (20 ng/ml of IL-1β), siRNA-Tβ4 knockdown group (IL-1β and si-Tβ4) and Tβ4 treatment group (IL-1β and 1000 ng/ml of Tβ4).