期刊文献+

Role of connexin-related signalling in hepatic homeostasis and its relevance for liver-based in vitro modelling

Role of connexin-related signalling in hepatic homeostasis and its relevance for liver-based in vitro modelling
下载PDF
导出
摘要 Direct intercellular communication mediated by gap junctions constitutes a major regulatory platform in the control of hepatic homeostasis.Hepatocellular gap junctions are composed of two hemichannels of adjacent cells which are built up by connexin proteins,in casu Cx32.Mathieu Vinken,Pofessor at the Department of Toxicology of the Free University BrusselsBelgium,was one of the first investigators to demonstrate that hepatic connexin expression is controlled by epigenetic mechanisms.In particular,he found that inhibitors of histone deacetylase enzymes enhance Cx32 production and gap junction activity in cultures of primary hepatocytes,a finding that is of importance for liver-based in vitro modelling.Professor Dr.Mathieu Vinken's recent work is focussed on the elucidation of the role of connexin proteins and their channels in the hepatocyte life cycle.Specific attention is paid to apoptosis in this context,whereby it has been found that Cx32 hemichannels control the termination of induced cell death in cultures of primary hepatocytes. Overall,Professor Dr.Mathieu Vinken's research can be considered as an important contribution to the field of hepatic connexin physiology. Direct intercellular communication mediated by gap junctions constitutes a major regulatory platform in the control of hepatic homeostasis. Hepatocellular gap junctions are composed of two hemichannels of adjacent cells which are built up by connexin proteins, in casu Cx32. Mathieu Vinken, Pofessor at the Department of Toxicology of the Free University Brussels-Belgium, was one of the first investigators to demonstrate that hepatic connexin expression is controlled by epigenetic mechanisms. In particular, he found that inhibitors of histone deacetylase enzymes enhance Cx32 production and gap junction activity in cultures of primary hepatocytes, a finding that is of importance for liver-based in vitro modelling. Professor Dr. Mathieu Vinken’s recent work is focussed on the elucidation of the role of connexin proteins and their channels in the hepatocyte life cycle. Specific attention is paid to apoptosis in this context, whereby it has been found that Cx32 hemichannels control the termination of induced cell death in cultures of primary hepatocytes. Overall, Professor Dr. Mathieu Vinken’s research can be considered as an important contribution to the field of hepatic connexin physiology.
出处 《World Journal of Gastrointestinal Pathophysiology》 CAS 2011年第5期82-87,共6页 世界胃肠病理生理学杂志(英文版)(电子版)
基金 supported by grants of the FWO,the research council of the VUB and the European Union
关键词 CONNEXIN HEMICHANNEL Gap junction Primary HEPATOCYTE In VITRO modelling Epigenetics HISTONE modifications Cell death Apoptosis HEPATOTOXICITY Connexin Hemichannel Gap junction Primary hepatocyte In vitro modelling Epigenetics Histone modifications Cell death Apoptosis Hepatotoxicity
  • 相关文献

参考文献25

  • 1Mathieu Vinken,Elke Decrock,Elke Vuyst,Marijke Bock,Roosmarijn E. Vandenbroucke,Bruno G. Geest,Joseph Demeester,Niek N. Sanders,Tamara Vanhaecke,Luc Leybaert,Vera Rogiers.Connexin32 hemichannels contribute to the apoptotic-to-necrotic transition during Fas-mediated hepatocyte cell death[J]. Cellular and Molecular Life Sciences . 2010 (6)
  • 2Henkens T,Vinken M,Lukaszuk A,TourwéD,Vanhaecke T,Rogiers V.Differential effects of hydroxamate histone deacetylase inhibitors on cellular functionality and gap junc- tions in primary cultures of mitogen-stimulated hepatocytes. Toxicology Letters . 2008
  • 3Vinken M,Decrock E,De Vuyst E,Leybaert L,Vanhaecke T,Rogiers V.Biochemical characterisation of an in vitro model of hepatocellular apoptotic cell death. Alternatives to Laboratory Animals . 2009
  • 4Vinken M,Snykers S,Fraczek J,Decrock E,Leybaert L,Ro- giers V,Vanhaecke T.DNA methyltransferase 3a expression decreases during apoptosis in primary cultures of hepato-cytes. Toxicology in Vitro . 2010
  • 5Vinken M,Decrock E,Leybaert L,Vanhaecke T,Rogiers V.Proteolytic cleavage of adherens junction components dur- ing Fas-dependent cell death in primary cultures of rat hepa- tocytes. ALTEX Alternativen zu Tierexperimenten . 2010
  • 6Decrock E,De Vuyst E,Vinken M,Van Moorhem M,Vranckx K,Wang N,Van Laeken L,De Bock M,D’’Herde K,Lai CP,Rogiers V,Evans WH,Naus CC,Leybaert L.Connex- in 43 hemichannels contribute to the propagation of apoptotic cell death in a rat C6 glioma cell model. Cell Death and Differentiation . 2009
  • 7Papeleu P,Vanhaecke T,Rogiers V.Histone deacetylase inhibition:a differentiation therapy for cultured primary hepatocytes. Curr Enzym Inhib . 2006
  • 8Vanhaecke T,Papeleu P,Elaut G,Rogiers V.Trichostatin A-like hydroxamate histone deacetylase inhibitors as thera- peutic agents:toxicological point of view. Current Medicinal Chemistry . 2004
  • 9Vinken M,Peggy P,Vera R,Tamara V.Histone deacetylase inhibitors as potent modulators of cellular contacts. Current Drug Targets . 2006
  • 10Papeleu P,Loyer P,Vanhaecke T,Elaut G,Geerts A,Guguen- Guillouzo C,Rogiers V.Trichostatin A induces differential cell cycle arrests but does not induce apoptosis in primary cultures of mitogen-stimulated rat hepatocytes. Journal of Hepatology . 2003

共引文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部