Ma Debin,Shen Yanbing,Wang Baolin,Chen Ping.Influence of Tmub1 silencing on proliferation of rat hepatocytes after partial hepatectomy[J].J Amry Med Univ (J Third Mil Med Univ),2013,35(09):850-853.
Ma Debin,Shen Yanbing,Wang Baolin,Chen Ping.Influence of Tmub1 silencing on proliferation of rat hepatocytes after partial hepatectomy[J].J Amry Med Univ (J Third Mil Med Univ),2013,35(09):850-853.DOI:
Influence of Tmub1 silencing on proliferation of rat hepatocytes after partial hepatectomy
Objective To investigate the role of transmembrane and ubiquitin-like domain-containing protein 1 (Tmub1) protein in the liver regeneration and its impact on the expression of securin in the process. Methods A total of 54 adult male SD rats were randomly divided into Tmub1 RNAi lentivirus group
blank lenitiviral vector group
and control
and they received an injection of lentivirus (3×10
7
TU) or PBS through ileocaecal vein. In 2 d later
partial hepatectomy (PH) were carried out in all rats. Then the liver tissue was collected in 0
2
6
12
24 and 48 h after model establishment to extract primary hepatocytes and preserve liver tissue. Effect of Tmub1 RNAi lentivirus interference on rat primary hepatocytes was detected by real-time PCR and Western blotting
respectively. Effect of Tmub1 RNAi lentivirus on the growth and cell cycle in rat primary hepatocytes was detected by MTT assay and flow cytometry
respectively. Results Real-time PCR and Western blotting showed that the expression of Tmub1 at mRNA and protein levels was significantly inhibited
and the expression of securin at mRNA level had no change
but the expression of securin at protein level was significantly down-regulated. MTT assay showed that Tmub1 gene silencing significantly improved the proliferation in liver cells in 6 to 24 h after PH. Flow cytometry displayed that the liver cells were arrested in G
2
/M phase. Conclusion Tmub1 protein plays a negative role in the process of liver cells’ proliferation
which may be closely related to its effect on the expression of securin at protein level.