scholarly journals Large-Scale Quantitatively Detecting and Analyzing of ceRNAs reveal NOTCH3 mRNA, miR-369-3p and rno-Rmdn2_0006 Together Regulate the Hepatocytes in G0 Phase and in G1 Phase During the Initiation Stage of Rat Liver Regeneration

Author(s):  
Xiayan Zang ◽  
Zihui Wang ◽  
Yafei Li ◽  
Han Gao ◽  
Jianlin Guo ◽  
...  

Abstract Aims:Generally, key events of the liver regeneration initiation (LRI) are how the hepatocytes in G0 phase change to G1 phase. We use the data from large-scale quantitatively detecting and analyzing (LQDA) to reveal ceRNAs together regulate the hepatocytes in G0 phase or in G1 phase during LRI.Main methods:The hepatocytes of the rat liver right lobe were isolated at 0 hour, 6 hour and 24 hour after partial hepatectomy (PH), their ceRNA expression abundance was measured by LQDA, and the correlation of their expression, interaction and role were revealed by ceRNA comprehensive analysis. Key findings:It was found that expression of NOTCH3 mRNA is up-regulated at 0 h, but miR-369-3p and rno-Rmdn2_0006 of hepatocytes not change significantly at that, meanwhile, the G0 phase-related gene CDKN1c promoted by NOTCH3 up-regulation, and the G1 phase-related gene PSEN2 inhibited by NOTCH3 down-regulation at that. On the contrary, NOTCH3 mRNA and rno-Rmdn2_0006 were up-regulated at 6 h, but miR-136-3p was down-regulated at that, the G1 phase-related genes CHUK, DDX24, HES1, NET1 and STAT3 promoted by NOTCH3 up-regulated, and the G0 phase-related gene CDKN1a inhibited by NOTCH3 down-regulated at that. These results suggested that the ceRNAs and the NOTCH3-regulated G0 phase- and G1 phase-related genes show a correlation in expression, interaction and role, they together regulate the hepatocytes in G0 phase at 0 h and in G1 phase at 6 h. Significance:These discovers are helpful to understand the mechanism which ceRNA together regulate the hepatocytes in G0 phase or G1 phase.

Author(s):  
Menghua Li ◽  
Xiaochun Zhou ◽  
Jinxin Mei ◽  
Xiaofang Geng ◽  
Yun Zhou ◽  
...  

AbstractUnder normal physiological conditions, the majority of hepatocytes are in the functional state (G0 phase). After injury or liver partial hepatectomy (PH), hepatocytes are rapidly activated to divide. To understand the mechanism underlying hepatocyte G0/G1 transition during rat liver regeneration, we used the Rat Genome 230 2.0 Array to determine the expression changes of genes, then searched the GO and NCBI databases for genes associated with the G0/G1 transition, and QIAGEN and KEGG databases for the G0/G1 transition signaling pathways. We used expression profile function (E t) to calculate the activity level of the known G0/G1 transition signal pathways, and Ingenuity Pathway Analysis 9.0 (IPA) to determine the interactions among these signaling pathways. The results of our study show that the activity of the signaling pathways of HGF, IL-10 mediated by p38MAPK, IL-6 mediated by STAT3, and JAK/STAT mediated by Ras/ERK and STAT3 are significantly increased during the priming phase (2–6 h after PH) of rat liver regeneration. This leads us to conclude that during rat liver regeneration, the HGF, IL-10, IL-6 and JAK/STAT signaling pathways play a major role in promoting hepatocyte G0/G1 transition in the regenerating liver.


Hepatology ◽  
1995 ◽  
Vol 21 (5) ◽  
pp. 1450-1454 ◽  
Author(s):  
Gianluigi Vendemiale ◽  
Ferruccio Guerrieri ◽  
Ignazio Grattagliano ◽  
Domenico Didonna ◽  
Leonilde Muolo ◽  
...  

IUBMB Life ◽  
1999 ◽  
Vol 47 (6) ◽  
pp. 1049-1059 ◽  
Author(s):  
Maria-Letizia Tomassoni ◽  
Elisabetta Albi ◽  
Mariapia Viola Magani

The Lancet ◽  
1989 ◽  
Vol 334 (8674) ◽  
pp. 1248-1249 ◽  
Author(s):  
A Francavilla ◽  
S Todo ◽  
K.A Porter ◽  
M Barone ◽  
Q Zeng ◽  
...  

1961 ◽  
Vol 39 (6) ◽  
pp. 1043-1054 ◽  
Author(s):  
D. K. Myers ◽  
C. Anne Hemphill ◽  
Constance M. Townsend

Deoxycytidylate deaminase activity and net synthesis of deoxyribonucleic acid (DNA) in vivo were found to increase at approximately the same time during the early stages of liver regeneration. However, deaminase activity in the regenerating liver remained at a high level for 1 day after DNA synthesis had slowed down again during the later stages of regeneration. The increase in deaminase activity was restricted as a result of exposure to 600 r X radiation during early regeneration, but this effect only became evident 11–16 hours after the irradiation. Irradiation on the second day after partial hepatectomy, when deaminase levels in control regenerating livers were relatively constant, failed to affect the deaminase activity immediately but did produce a 40–50% decrease in activity 11–16 hours later. Other antimitotic agents, e.g., colchicine, had little effect on deaminase activity.


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