Literature DB >> 12406338

Identification of platelet-activating factor acetylhydrolase II in human skin.

Mariangela Marques1, Yong Pei, Michael D Southall, John M Johnston, Hiroyuki Arai, Junken Aoki, Takao Inoue, Holger Seltmann, Christos C Zouboulis, Jeffrey B Travers.   

Abstract

Platelet-activating factor acetylhydrolases are a family of specialized phospholipase A2 enzymes. They serve an anti-inflammatory function by converting the proinflammatory autocoid, PAF, into biologically inactive lyso-PAF, by the removal of the sn-2 acetyl group of this glycerophospholipid. Similarly, platelet-activating factor acetylhydrolases can also degrade oxidatively modified sn-2 polyunsaturated-fatty-acid-containing phospholipids, which are toxic to cells. Platelet-activating factor acetylhydrolase II is a recently cloned member of this family of specialized phospholipases. Consistent with a potential role of this intracellular enzyme in protecting membrane phospholipids against oxidative stress, platelet-activating factor acetylhydrolase II has been shown to translocate from cytosol to membranes in response to pro-oxidative stressors, and overexpression of this enzyme decreases the cytotoxic effects of these agents. The objective of this study was to assess whether platelet-activating factor acetylhydrolase II is involved in protecting skin against oxidative stress. Platelet-activating factor acetylhydrolase II protein was demonstrated in human skin by immunohistochemistry, with the highest levels of the enzyme found in sebaceous glands and lesser amounts in epidermal keratinocytes. Treatment of epidermal cells with t-butylhydroperoxide or ultraviolet B radiation resulted in platelet-activating factor acetylhydrolase II translocation from cytosol to membranes. To assess the role of this enzyme in epidermal function, a recombinant retroviral strategy was used to overexpress platelet-activating factor acetylhydrolase II in the human keratinocyte-derived cell line HaCaT. Overexpression of platelet-activating factor acetylhydrolase II protected HaCaT cells against apop tosis induced by oxidative stressors t-butylhydroperoxide and ultraviolet B radiation. Similar levels of apoptosis, however, were seen in both control and platelet-activating-factor-acetylhydrolase-II-over expressing HaCaT cells in response to C2 ceramide. These studies demonstrate the presence of platelet-activating factor acetylhydrolase II in a restricted pattern in human skin, and provide evidence that this specialized phospholipase is involved in protecting this organ against oxidative stress through the degradation of oxidatively modified bioactive phospholipids.

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Year:  2002        PMID: 12406338     DOI: 10.1046/j.1523-1747.2002.01859.x

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


  18 in total

1.  An essential role for platelet-activating factor in activating mast cell migration following ultraviolet irradiation.

Authors:  Rommel Chacón-Salinas; Limo Chen; Alma D Chávez-Blanco; Alberto Y Limón-Flores; Ying Ma; Stephen E Ullrich
Journal:  J Leukoc Biol       Date:  2013-09-05       Impact factor: 4.962

Review 2.  To hydrolyze or not to hydrolyze: the dilemma of platelet-activating factor acetylhydrolase.

Authors:  Gopal Kedihitlu Marathe; Chaitanya Pandit; Chikkamenahalli Lakshminarayana Lakshmikanth; Vyala Hanumanthareddy Chaithra; Shancy Petsel Jacob; Cletus Joseph Michael D'Souza
Journal:  J Lipid Res       Date:  2014-05-23       Impact factor: 5.922

3.  Trafficking of platelet-activating factor acetylhydrolase type II in response to oxidative stress.

Authors:  Anastasia F Thévenin; Elizabeth S Monillas; Jason M Winget; Kirk Czymmek; Brian J Bahnson
Journal:  Biochemistry       Date:  2011-09-12       Impact factor: 3.162

Review 4.  Bioactive oxidatively truncated phospholipids in inflammation and apoptosis: formation, targets, and inactivation.

Authors:  Thomas M McIntyre
Journal:  Biochim Biophys Acta       Date:  2012-03-16

5.  Platelet-activating factor is crucial in psoralen and ultraviolet A-induced immune suppression, inflammation, and apoptosis.

Authors:  Peter Wolf; Dat X Nghiem; Jeffrey P Walterscheid; Scott Byrne; Yumi Matsumura; Yasuhiro Matsumura; Cora Bucana; Honnavara N Ananthaswamy; Stephen E Ullrich
Journal:  Am J Pathol       Date:  2006-09       Impact factor: 4.307

6.  Lipid profiling of the Arabidopsis hypersensitive response reveals specific lipid peroxidation and fragmentation processes: biogenesis of pimelic and azelaic acid.

Authors:  Maria Zoeller; Nadja Stingl; Markus Krischke; Agnes Fekete; Frank Waller; Susanne Berger; Martin J Mueller
Journal:  Plant Physiol       Date:  2012-07-22       Impact factor: 8.340

7.  Normal fur development and sebum production depends on fatty acid 2-hydroxylase expression in sebaceous glands.

Authors:  Helena Maier; Marion Meixner; Dieter Hartmann; Roger Sandhoff; Lihua Wang-Eckhardt; Inge Zöller; Volkmar Gieselmann; Matthias Eckhardt
Journal:  J Biol Chem       Date:  2011-05-31       Impact factor: 5.157

Review 8.  Lipid mediators in acne.

Authors:  Monica Ottaviani; Emanuela Camera; Mauro Picardo
Journal:  Mediators Inflamm       Date:  2010-08-25       Impact factor: 4.711

9.  Cytotoxic phospholipid oxidation products. Cell death from mitochondrial damage and the intrinsic caspase cascade.

Authors:  Rui Chen; Lili Yang; Thomas M McIntyre
Journal:  J Biol Chem       Date:  2007-06-27       Impact factor: 5.157

10.  Platelet activating factor stimulates arachidonic acid release in differentiated keratinocytes via arachidonyl non-selective phospholipase A2.

Authors:  Katarina Mariann Jørgensen; Hanne Solvang Felberg; Rolf K Berge; Astrid Laegreid; Berit Johansen
Journal:  Arch Dermatol Res       Date:  2009-12-30       Impact factor: 3.017

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