Literature DB >> 1328400

Gap-junctional protein connexin 43 is expressed in dermis and epidermis of human skin: differential modulation by retinoids.

H Guo1, P Acevedo, F D Parsa, J S Bertram.   

Abstract

Retinoids are effective modulators of proliferation and differentiation of keratinocytes in vivo and in vitro. In mouse 10T1/2 cells, retinoid action on proliferation and neoplastic transformation is correlated with the upregulation of gap-junctional communication and expression of connexin 43 (Cx43). In the present study we have determined if retinoids induce similar effects on gene expression in human skin. Studies were conducted in intact skin and on cultured keratinocytes and dermal fibroblasts. In a clinical study, 2 weeks of treatment with 0.05% all-trans retinoic acid resulted in increased expression of Cx43 mRNA and protein in epidermis. Expression occurred predominantly in the suprabasal layer. Cultured cells exhibited a differential response to retinoic acid. In keratinocytes, increased expression of Cx43 occurred at low (10(-11) M) concentrations, whereas inhibition occurred at high (10(-7) M) concentrations; however, junctional communication, measured by dye transfer, was not altered over this concentration range. Dermal fibroblasts, in contrast, exhibited a dose-dependent increased expression of Cx43 at concentrations up to 10(-7) M retinoic acid and proportionately increased their junctional communication over this dose range. These data indicate that control of Cx43 gene expression by retinoids in human skin cells is complex. The production of gradients of junctional channels could play a role in the control of growth and differentiation in epidermis.

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Year:  1992        PMID: 1328400     DOI: 10.1111/1523-1747.ep12616154

Source DB:  PubMed          Journal:  J Invest Dermatol        ISSN: 0022-202X            Impact factor:   8.551


  10 in total

1.  Differentiation of organotypic epidermis in the presence of skin disease-linked dominant-negative Cx26 mutants and knockdown Cx26.

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Authors:  G D Carystinos; A Bier; G Batist
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Journal:  Mol Biol Cell       Date:  2011-03-16       Impact factor: 4.138

4.  Characterisation of Peptide5 systemic administration for treating traumatic spinal cord injured rats.

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Journal:  Exp Brain Res       Date:  2017-07-19       Impact factor: 1.972

5.  The potency of the fs260 connexin43 mutant to impair keratinocyte differentiation is distinct from other disease-linked connexin43 mutants.

Authors:  Jared M Churko; Stephanie Langlois; Xinyue Pan; Qing Shao; Dale W Laird
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Review 6.  Embryonic wound healing: a primer for engineering novel therapies for tissue repair.

Authors:  Katherine E Degen; Robert G Gourdie
Journal:  Birth Defects Res C Embryo Today       Date:  2012-09

Review 7.  Connexin43 phosphorylation: structural changes and biological effects.

Authors:  Joell L Solan; Paul D Lampe
Journal:  Biochem J       Date:  2009-04-15       Impact factor: 3.857

8.  Targeting Cx43 and N-cadherin, which are abnormally upregulated in venous leg ulcers, influences migration, adhesion and activation of Rho GTPases.

Authors:  Ariadna Mendoza-Naranjo; Peter Cormie; Antonio E Serrano; Rebecca Hu; Shay O'Neill; Chiuhui Mary Wang; Christopher Thrasivoulou; Kieran T Power; Alexis White; Thomas Serena; Anthony R J Phillips; David L Becker
Journal:  PLoS One       Date:  2012-05-15       Impact factor: 3.240

9.  Differential dose-dependent effects of alpha-, beta-carotenes and lycopene on gap-junctional intercellular communication in rat liver in vivo.

Authors:  V Krutovskikh; M Asamoto; N Takasuka; M Murakoshi; H Nishino; H Tsuda
Journal:  Jpn J Cancer Res       Date:  1997-12

10.  Connexin26 Mutations Causing Palmoplantar Keratoderma and Deafness Interact with Connexin43, Modifying Gap Junction and Hemichannel Properties.

Authors:  Zunaira Shuja; Leping Li; Shashank Gupta; Gülistan Meşe; Thomas W White
Journal:  J Invest Dermatol       Date:  2016-01       Impact factor: 8.551

  10 in total

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