Literature DB >> 12535213

Fas ligand in pemphigus sera induces keratinocyte apoptosis through the activation of caspase-8.

Mario Puviani1, Alessandra Marconi, Emanuele Cozzani, Carlo Pincelli.   

Abstract

The Fas/Fas ligand system triggers the extrinsic apoptotic pathway and is involved in several inflammatory conditions, also at the skin level. The Fas/Fas ligand cell death pathway plays a major role in anoikis, a type of apoptosis characterized by cell detachment. As pemphigus is characterized by loss of cell to cell adhesion, we evaluated the role of anoikis and Fas ligand in this bullous disease. We report that, in suprabasal epidermis from perilesional pemphigus skin, most keratinocytes are apoptotic. Moreover, Fas ligand levels are markedly increased in sera from pemphigus patients, whereas they are undetectable in sera from patients undergoing steroid treatment. Sera from untreated patients but not from patients under steroids induce keratinocyte apoptosis. Pemphigus-sera-induced cell death is partially inhibited by pretreatment with anti-Fas ligand antibodies and by incubation with caspase-8 inhibitor Z-IETD-FMK. Finally, caspase-8 is activated in keratinocytes provided with sera from pemphigus patients, whereas cleavage is partially blocked by pretreatment of sera with anti-Fas ligand antibody. These results suggest that increased Fas ligand in pemphigus sera is responsible for keratinocyte apoptosis, which occurs through the activation of a caspase-8-driven extrinsic apoptotic pathway.

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Year:  2003        PMID: 12535213     DOI: 10.1046/j.1523-1747.2003.12014.x

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


  35 in total

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Authors:  Robert Pollmann; Thomas Schmidt; Rüdiger Eming; Michael Hertl
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2.  Novel mechanisms of target cell death and survival and of therapeutic action of IVIg in Pemphigus.

Authors:  Juan Arredondo; Alexander I Chernyavsky; Ali Karaouni; Sergei A Grando
Journal:  Am J Pathol       Date:  2005-12       Impact factor: 4.307

3.  Genome-wide gene expression profiling reveals unsuspected molecular alterations in pemphigus foliaceus.

Authors:  Danielle Malheiros; Rodrigo A Panepucci; Ana M Roselino; Amélia G Araújo; Marco A Zago; Maria Luiza Petzl-Erler
Journal:  Immunology       Date:  2014-11       Impact factor: 7.397

4.  Antimitochondrial autoantibodies in pemphigus vulgaris: a missing link in disease pathophysiology.

Authors:  Steve Marchenko; Alexander I Chernyavsky; Juan Arredondo; Vivian Gindi; Sergei A Grando
Journal:  J Biol Chem       Date:  2009-12-10       Impact factor: 5.157

5.  Pemphigus vulgaris IgG cause loss of desmoglein-mediated adhesion and keratinocyte dissociation independent of epidermal growth factor receptor.

Authors:  Wolfgang-Moritz Heupel; Peter Engerer; Enno Schmidt; Jens Waschke
Journal:  Am J Pathol       Date:  2009-01-15       Impact factor: 4.307

6.  Experimental human cell and tissue models of pemphigus.

Authors:  Gerda van der Wier; Hendri H Pas; Marcel F Jonkman
Journal:  Dermatol Res Pract       Date:  2010-05-26

7.  A hypothesis concerning a potential involvement of ceramide in apoptosis and acantholysis induced by pemphigus autoantibodies.

Authors:  Wendy B Bollag
Journal:  Dermatol Res Pract       Date:  2010-05-18

8.  Apoptotic pathways in pemphigus.

Authors:  Meryem Bektas; Puneet Jolly; David S Rubenstein
Journal:  Dermatol Res Pract       Date:  2010-06-15

9.  p38MAPK signaling and desmoglein-3 internalization are linked events in pemphigus acantholysis.

Authors:  Puneet S Jolly; Paula Berkowitz; Meryem Bektas; Hua-En Lee; Michael Chua; Luis A Diaz; David S Rubenstein
Journal:  J Biol Chem       Date:  2010-01-21       Impact factor: 5.157

10.  Protein kinase Cdelta regulates keratinocyte death and survival by regulating activity and subcellular localization of a p38delta-extracellular signal-regulated kinase 1/2 complex.

Authors:  Tatiana Efimova; Ann-Marie Broome; Richard L Eckert
Journal:  Mol Cell Biol       Date:  2004-09       Impact factor: 4.272

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