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Human epidermis is a novel site of phospholipase B expression
Authors:Maury Eric  Prévost Marie Claude  Nauze Michel  Redoulès Daniel  Tarroux Roger  Charvéron Marie  Salles Jean Pierre  Perret Bertrand  Chap Hugues  Gassama-Diagne Ama
Affiliation:Institut de recherche Pierre Fabre, CERPER/H?tel Dieu Saint Jacques, F31052 Toulouse, France.
Abstract:Phospholipase B (PLB) is an enzyme that displays both phospholipase A(2) and lysophospholipase activities. Analysis of human epidermis homogenates indicated the presence of a 97 kDa PLB protein, as well as a phospholipase A(2) activity, both being enriched in the soluble fraction. Immunolabelling and in situ hybridization experiments showed that this enzyme is expressed in the different layers of epidermis with an accumulation at the dermo-epidermis junction. RT-PCR data indicated that PLB is specifically expressed in natural and reconstructed epidermis. By 3'-RACE-PCR and screening of human genome databases, we obtained a 3600 bp cDNA coding for human PLB highly homologous to already described intestinal brush border PLBs. These data led us to conclude that the soluble PLB corresponds to a proteolytic cleavage of the membrane anchored protein. Altogether, our results provide the first characterization of human PLB which should play an important role in epidermal barrier function.
Keywords:Phospholipase B   Human   Epidermis   Keratinocyte   Molecular cloning
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