Literature DB >> 10366436

Expression of a Cx43 deletion mutant in 3T3 A31 fibroblasts prevents PDGF-induced inhibition of cell communication and suppresses cell growth.

C D Moorby1, E Gherardi.   

Abstract

Communication through gap junctions was first suggested to have a role in the social control of cell growth over 30 years ago. However, despite extensive experimentation, the importance of gap junctions as a general mechanism of growth control remains to be established. A number of different studies have shown that a common early response of cells in culture to polypeptide growth factors such as PDGF is a rapid and transient inhibition of cell communication suggesting that a cell may have to lose communication with its neighbors before it can undergo cell division. Here we show that 3T3 A31 fibroblasts exposed to PDGF exhibit a 50% decrease in cell communication as measured by dye transfer in the absence of significant changes in the cellular content and distribution of Cx43. Likewise, PDGF inhibited cell communication in cells transfected either with a vector which did not contain a cDNA or with an expression vector encoding full-length Cx43 fused to a c-myc tag (Cx43-M). In contrast, 3T3 A31 fibroblasts transfected with an expression construct encoding a deletion mutant of Cx43 (Cx43-256M) consisting of amino acids 1-256 of Cx43 fused to a c-myc tag maintain high levels of gap junction activity following exposure to PDGF. These results suggest that sites which trigger loss of cell communication in response to PDGF are located within amino acids 257 to 382 of the Cx43 molecule. Cells transfected with an expression vector encoding full-length Cx43 fused to a c-myc tail exhibited a reduced basal growth rate compared to both parent cells and cells transfected with a control vector but maintained a strong mitogenic response to PDGF. In contrast, both the basal growth rate and the mitogenic response to PDGF was markedly reduced in cells which expressed Cx43-256M consistent with the hypothesis that loss of cell communication is required before a cell can respond to mitogenic stimuli. Copyright 1999 Academic Press.

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Year:  1999        PMID: 10366436     DOI: 10.1006/excr.1999.4485

Source DB:  PubMed          Journal:  Exp Cell Res        ISSN: 0014-4827            Impact factor:   3.905


  10 in total

Review 1.  Pathophysiological roles of gap junction in glomerular mesangial cells.

Authors:  Jian Yao; Ying Zhu; Tetsuo Morioka; Takashi Oite; Masanori Kitamura
Journal:  J Membr Biol       Date:  2007-07-11       Impact factor: 1.843

2.  Regulation of connexin-43-mediated growth inhibition by a phosphorylatable amino-acid is independent of gap junction-forming ability.

Authors:  Xitong Dang; Madhumathy Jeyaraman; Elissavet Kardami
Journal:  Mol Cell Biochem       Date:  2006-05-23       Impact factor: 3.396

3.  MAPK phosphorylation of connexin 43 promotes binding of cyclin E and smooth muscle cell proliferation.

Authors:  Scott R Johnstone; Brett M Kroncke; Adam C Straub; Angela K Best; Clarence A Dunn; Leslie A Mitchell; Yelena Peskova; Robert K Nakamoto; Michael Koval; Cecilia W Lo; Paul D Lampe; Linda Columbus; Brant E Isakson
Journal:  Circ Res       Date:  2012-05-31       Impact factor: 17.367

4.  Oxidized phospholipid species promote in vivo differential cx43 phosphorylation and vascular smooth muscle cell proliferation.

Authors:  Scott R Johnstone; Jeremy Ross; Michael J Rizzo; Adam C Straub; Paul D Lampe; Norbert Leitinger; Brant E Isakson
Journal:  Am J Pathol       Date:  2009-07-16       Impact factor: 4.307

5.  Defective epidermal barrier in neonatal mice lacking the C-terminal region of connexin43.

Authors:  Karen Maass; Alexander Ghanem; Jung-Sun Kim; Manuela Saathoff; Stephanie Urschel; Gregor Kirfel; Ruth Grümmer; Markus Kretz; Thorsten Lewalter; Klaus Tiemann; Elke Winterhager; Volker Herzog; Klaus Willecke
Journal:  Mol Biol Cell       Date:  2004-07-28       Impact factor: 4.138

6.  Glomerular expression of connexin 40 and connexin 43 in rat experimental glomerulonephritis.

Authors:  Tetsuo Morioka; Shinichi Okada; Masaaki Nameta; Fadia Kamal; Nadia T Yanakieva-Georgieva; Jian Yao; Ayako Sato; Honglan Piao; Takashi Oite
Journal:  Clin Exp Nephrol       Date:  2012-09-04       Impact factor: 2.801

7.  Ser364 of connexin43 and the upregulation of gap junction assembly by cAMP.

Authors:  E M TenBroek; P D Lampe; J L Solan; J K Reynhout; R G Johnson
Journal:  J Cell Biol       Date:  2001-12-24       Impact factor: 10.539

8.  Spatio-temporal patterning of different connexins in developing and postnatal human kidneys and in nephrotic syndrome of the Finnish type (CNF).

Authors:  Ivona Kosovic; Natalija Filipovic; Benjamin Benzon; Katarina Vukojevic; Marijan Saraga; Merica Glavina Durdov; Ivana Bocina; Mirna Saraga-Babic
Journal:  Sci Rep       Date:  2020-05-29       Impact factor: 4.379

9.  The C-terminal domain of connexin43 modulates cartilage structure via chondrocyte phenotypic changes.

Authors:  Raquel Gago-Fuentes; John F Bechberger; Marta Varela-Eirin; Adrian Varela-Vazquez; Benigno Acea; Eduardo Fonseca; Christian C Naus; Maria D Mayan
Journal:  Oncotarget       Date:  2016-11-08

Review 10.  Gap junction-mediated cell-to-cell communication in oral development and oral diseases: a concise review of research progress.

Authors:  Wenjing Liu; Yujia Cui; Jieya Wei; Jianxun Sun; Liwei Zheng; Jing Xie
Journal:  Int J Oral Sci       Date:  2020-06-12       Impact factor: 6.344

  10 in total

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