Skip to main content
Cellular & Molecular Biology Letters logoLink to Cellular & Molecular Biology Letters
. 2014 Mar 19;19(2):181–200. doi: 10.2478/s11658-014-0188-2

Study on the activity of the signaling pathways regulating hepatocytes from G0 phase into G1 phase during rat liver regeneration

Menghua Li 1,2, Xiaochun Zhou 1,2, Jinxin Mei 1,2, Xiaofang Geng 1,2, Yun Zhou 1,2, Weimin Zhang 2, Cunshuan Xu 1,2,
PMCID: PMC6275877  PMID: 24643584

Abstract

Under 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.

Keywords: Rat liver regeneration, Signal transduction, Hepatocyte G0/G1 transition, HGF, IL-10, IL-6, JAK/STAT, p38MAPK, Ras/ERK, STAT3, Ingenuity pathway analysis 9.0 (IPA)

Full Text

The Full Text of this article is available as a PDF (2.5 MB).

Abbreviations used

ERK

extracellular regulated protein kinases

HGF

hepatocyte growth factor

IL-6

interleukin-6

IL-10

interleukin-10

JAK

Janus kinase

JNK

c-Jun NH2-terminal kinase

MAPK

mitogen-activated protein kinase

NF-κB

nuclear factor κB

STAT3

signal transducer and activator of transcription

References

  • 1.Yokoyama Y, Nagino M, Nimura Y. Mechanisms of hepatic regeneration following portal vein embolization and partial hepatectomy: a review. World J. Surg. 2007;31:367–374. doi: 10.1007/s00268-006-0526-2. [DOI] [PubMed] [Google Scholar]
  • 2.Vondran FW, Katenz E, Schwartlander R, Morgul RS, Haluk M, Raschzok N, Gong XB, Cheng XD, Kehr D, Sauer IM. Isolation of primary human hepatocytes after partial hepatectomy: criteria for identification of the most promising liver specimen. Artif. Organs. 2008;32:205–213. doi: 10.1111/j.1525-1594.2007.00524.x. [DOI] [PubMed] [Google Scholar]
  • 3.Estes MD, Do J, Ahn CH. On chip cell separator using magnetic bead-based enrichment and depletion of various surface markers. Biomed. Microdevices. 2009;11:509–515. doi: 10.1007/s10544-008-9257-5. [DOI] [PubMed] [Google Scholar]
  • 4.Michalopoulos GK. Liver regeneration. J. Cell Physiol. 2007;213:286–300. doi: 10.1002/jcp.21172. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Kountouras J, Boura P, Lygidakis NJ. Liver regeneration after hepatectomy. Hepatogastroenterology. 2001;48:556–562. [PubMed] [Google Scholar]
  • 6.Sell S. The hepatocyte: heperogeneity and plasticity of liver cells. Int. J. Biochem. Cell Biol. 2003;35:267–271. doi: 10.1016/s1357-2725(02)00182-6. [DOI] [PubMed] [Google Scholar]
  • 7.Zimmermann A. Regulation of liver regeneration. Nephrol. Dial. Transplant. 2004;19:iv6–iv10. doi: 10.1093/ndt/gfh1034. [DOI] [PubMed] [Google Scholar]
  • 8.Fausto N, Laird AD, Webber EM. Liver regeneration. 2. Role of growth factors and cytokines in hepatic regeneration. FASEB J. 1995;9:1527–1536. doi: 10.1096/fasebj.9.15.8529831. [DOI] [PubMed] [Google Scholar]
  • 9.Cantz T, Manns MP, Ott M. Stem cells in liver regeneration and therapy. Cell Tissue Res. 2008;331:271–282. doi: 10.1007/s00441-007-0483-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Xu CS, Chen XG, Chang CF, Wang GP, Wang WB, Zhang LX, Zhu QS, Wang L, Zhang FC. Transcriptional profiles of biliary epithelial cells from rat regenerating liver after partial hepatectomy. Genes Genomics. 2012;34:245–256. [Google Scholar]
  • 11.Xu CS, Yang YJ, Yang JY, Chen XG, Wang GP. Analysis of the role of the integrin signaling pathway in hepatocytes during rat liver regeneration. Cell. Mol. Biol. Lett. 2012;17:274–288. doi: 10.2478/s11658-012-0011-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Michalopeulos GK. Liver regeneration. J. Cell Physiol. 2007;213:286–300. doi: 10.1002/jcp.21172. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Gómez-Lechón MJ, Guillén I, Ponsoda X, Fabra R, Trullenque R, Nakamura T, Castell JV. Cell cycle progression proteins (cyclins), oncogene expression, and signal transduction during the proliferative response of human hepatocytes to hepatocyte growth factor. Hepatology. 1996;23:1012–1019. doi: 10.1002/hep.510230511. [DOI] [PubMed] [Google Scholar]
  • 14.Morello D, Fitzgerald MJ, Babinet C, Fausto N. C-myc, c-fos and c-jun regulation in the regeneration livers of normal and H-2K/c-myc transgenic mice. Mol. Cell Biol. 1990;10:3185–3193. doi: 10.1128/mcb.10.6.3185. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Akira S, Isshiki H, Sugita T, Tanabe O, Kinoshita S, Nishio Y, Nakajima T, Hirano T, Kishimoto T. A nuclear factor for IL-6 expression (NF-IL6) is a member of a C/EBP family. EMBO J. 1990;9:1897–1906. doi: 10.1002/j.1460-2075.1990.tb08316.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Zhong Z, Wen Z, Darnell JE. Stat3: a STAT family member activated by tyrosine phosphorylation in response to epidermal growth factor and interleukin-6. Science. 1994;264:95–98. doi: 10.1126/science.8140422. [DOI] [PubMed] [Google Scholar]
  • 17.Trautwein C, Caelles C, Vander GP, Hunter T, Karin M, Chojkier M. Transactivation by NF-IL6/LAP is enhanced by phosphorylation of its activation domain. Nature. 1993;364:544–547. doi: 10.1038/364544a0. [DOI] [PubMed] [Google Scholar]
  • 18.Cressmann DE, Diamond RH, Taub R. Rapid activation of the Stat3 tran-scription complex in liver regeneration. Hepatology. 1995;21:1443–1449. [PubMed] [Google Scholar]
  • 19.Trautwein C, Rakemann T, Niehof M, Rose-John S, Manns MP. Acute-phase response factor, increased binding, and target gene transcription during liver regeneration. Gastroenterology. 1996;110:1854–1862. doi: 10.1053/gast.1996.v110.pm8964411. [DOI] [PubMed] [Google Scholar]
  • 20.Niehof M, Manns MP, Trautwein C. CREB controls LAP/C/EBP beta transcription. Mol. Cell Biol. 1997;17:3600–3613. doi: 10.1128/mcb.17.7.3600. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Fujiyoshi M, Ozaki M. Molecular mechanisms of liver regeneration and protection for treatment of liver dysfunction and diseases. J. Hepatobiliary Pancreat. Sci. 2011;18:13–22. doi: 10.1007/s00534-010-0304-2. [DOI] [PubMed] [Google Scholar]
  • 22.Higgins GM, Anderson RM. Experimental pathology of the liver: Restoration of the liver of the white rat following partial surgical removal. Arch. Pathol. 1931;12:186–202. [Google Scholar]
  • 23.Grisham JW. Cell types in rat liver cultures: their identification and isolation. Mol. Cell Biochem. 1983;54:23–33. doi: 10.1007/BF00225244. [DOI] [PubMed] [Google Scholar]
  • 24.Wang WB, Xie LF, Wang W, Wang L, Xu CS. Isolation, purity and identification of hepatocytes in rat normal liver and regenerating liver. Henan Sci. 2008;26:1492–1498. [Google Scholar]
  • 25.Strober W. Curr. Protoc. Immunol. 2001. Trypan blue exclusion test of cell viability. [DOI] [PubMed] [Google Scholar]
  • 26.Twigger SN, Smith J, Zuniga-Meyer A, Bromberg SK. Curr. Protoc. Bioinformatics. 2006. Exploring phenotypic data at the rat genome database. [DOI] [PubMed] [Google Scholar]
  • 27.Wang JZ, Du Z, Payattakool R, Yu PS, Chen CF. A new method to measure the semantic similarity of GO terms. Bioinformatics. 2007;23:1274–1281. doi: 10.1093/bioinformatics/btm087. [DOI] [PubMed] [Google Scholar]
  • 28.Guo W, Cai C, Wang C, Zhao L, Wang L, Zhang T. A preliminary analysis of genome structure and composition in Gossypium hirsutum. BMC Genomics. 2008;9:314. doi: 10.1186/1471-2164-9-314. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Xu CS, Wang GP, Zhang LX, Chang CF, Zhi J, Hao YP. Correlation between liver cancer occurrence and gene expression profiles in rat liver tissue. Genet. Mol. Res. 2011;10:3480–3513. doi: 10.4238/2011.December.14.3. [DOI] [PubMed] [Google Scholar]
  • 30.Jiang C, Xuan Z, Zhao F, Zhang MQ. TRED: a transcriptional regulatory element database, new entries and other development. Nucleic Acids Res. 2007;35:137–140. doi: 10.1093/nar/gkl1041. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31.Childress PJ, Flepcher RL, Perumal NB. LymphTF-DB: a database of transcription factors involved in lymphocyte development. Genes Immun. 2007;8:360–365. doi: 10.1038/sj.gene.6364386. [DOI] [PubMed] [Google Scholar]
  • 32.Wang GP, Xu CS. Reference gene selection for real-time RT-PCR in eight kinds of rat regenerating hepatic cells. Mol. Biotechnol. 2010;46:49–57. doi: 10.1007/s12033-010-9274-5. [DOI] [PubMed] [Google Scholar]
  • 33.Kost DP, Michalpopulos GK. Effect of epidermal growth factor on the expression of protooncogenes c-myc and c-Ha-ras in short-term primary hepatocyte culture. J. Cell. Physiol. 1990;144:122–127. doi: 10.1002/jcp.1041440116. [DOI] [PubMed] [Google Scholar]
  • 34.Borowiak M, Garratt AN, Wustefeld T, Strehle M, Trautwein C, Birchmeier C. Met provides essential signals for liver regeneration. Proc. Natl. Acad. Sci.USA. 2004;101:10608–10613. doi: 10.1073/pnas.0403412101. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35.Okano J, Shiota G, Matsumoto K, Yasui S, Kurimasa A, Hisatome I, Steinbergd P, Murawakia Y. Hepatocyte growth factor exerts a proliferative effect on oval cells through the PI3K/AKT signaling pathway. Biochem. Biophys. Res. Commun. 2003;309:298–304. doi: 10.1016/j.bbrc.2003.04.002. [DOI] [PubMed] [Google Scholar]
  • 36.Stolz DB, Mars WM, Petersen BE, Kim TH, Michalopoulos GK. Growth factor signal transduction immediately after two-thirds partial hepatectomy in the rat. Cancers Res. 1999;59:3954–3960. [PubMed] [Google Scholar]
  • 37.Boccaccio C, Ando M, Tamagnone L, Bardelli A, Michieli P, Battistini C, Comoglio PM. Induction of epithelial tubules by growth factor HGF depends on the STAT pathway. Nature. 1998;391:285–288. doi: 10.1038/34657. [DOI] [PubMed] [Google Scholar]
  • 38.Zhang YW, Wang LM, Jove R, Van de Woude GF. Requirement of Stat3 signaling for HGF/SF-Met mediated tumorigenesis. Oncogene. 2002;21:217–226. doi: 10.1038/sj.onc.1205004. [DOI] [PubMed] [Google Scholar]
  • 39.Hirano T. Interleukin 6 and its receptor: Ten years later. Int. Rev. Immunol. 1998;16:249–284. doi: 10.3109/08830189809042997. [DOI] [PubMed] [Google Scholar]
  • 40.Lutticken C, Wegenka UM, Yuan J, Buschmann J, Schindler C, Ziemiecki A, Harpur AG, Wilks AF, Yasukawa K, Taga T, Kishimoto T, Barbieri G, Sendtner M, Pellegrini S, Heinrich C P, Horn F. Association of transcription factor APRF and protein kinase Jak1 with the interleukin-6 signaltransducer gp130. Science. 1994;263:89–92. doi: 10.1126/science.8272872. [DOI] [PubMed] [Google Scholar]
  • 41.Stahl N, Boulton TG, Farruggella T, Ip NY, Davis S, Witthuhn BA, Quelle FW, Silvennoinen O, Barbieri G, Pellegrini S, Ihle JN, Yancopoulos GD. Association and activation of Jak Tyk kinases by CNTF-LIF-OSM-IL-6 beta receptor components. Science. 1994;263:92–95. doi: 10.1126/science.8272873. [DOI] [PubMed] [Google Scholar]
  • 42.Gerhartz C, Heesel B, Sasse J, Hemmann U, Landgraf C, Schneider-Mergener J, Horn F, Heinrich PC, Graeve L. Differential activation of acute phase response factor/STAT3 and STAT1 via the cytoplasmic domain of the interleukin 6 signal transducer gp130. I. Definition of a novel phosphotyrosine motif mediating STAT1 activation. J. Biol. Chem. 1996;271:12991–12998. doi: 10.1074/jbc.271.22.12991. [DOI] [PubMed] [Google Scholar]
  • 43.Streetz KL, Luedde T, Manns MP, Trautwein C. Interleukin 6 and liver regeneration. Gut. 2000;47:309–312. doi: 10.1136/gut.47.2.309. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 44.Marshall C J. Specificity of receptor tyrosine kinase signaling: transient versus sustained extracellular signal-regulated kinase activation. Cell. 1995;80:179–185. doi: 10.1016/0092-8674(95)90401-8. [DOI] [PubMed] [Google Scholar]
  • 45.Cohen CB, Ren R, Baltimore D. Modular binding domains in signal transduction proteins. Cell. 1995;80:237–248. doi: 10.1016/0092-8674(95)90406-9. [DOI] [PubMed] [Google Scholar]
  • 46.Hunter T. Protein kinases and phosphatases: the yin and yang of protein phosphorylation and signaling. Cell. 1995;80:225–236. doi: 10.1016/0092-8674(95)90405-0. [DOI] [PubMed] [Google Scholar]
  • 47.Heldin CH. Dimerization of cell surface receptors in signal transduction. Cell. 1995;80:213–224. doi: 10.1016/0092-8674(95)90404-2. [DOI] [PubMed] [Google Scholar]
  • 48.Hill CS, Treisman R. Transcriptional regulation by extracellular signals: mechanisms and specificity. Cell. 1995;80:199–212. doi: 10.1016/0092-8674(95)90403-4. [DOI] [PubMed] [Google Scholar]

Articles from Cellular & Molecular Biology Letters are provided here courtesy of BMC

RESOURCES