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Group III secreted phospholipase A(2) transgenic mice spontaneously develop inflammation

PLA(2) (phospholipase A(2)) group III is an atypical sPLA(2) (secretory PLA(2)) that is homologous with bee venom PLA(2) rather than with other mammalian sPLA(2)s. In the present paper, we show that endogenous group III sPLA(2) (PLA2G3) is expressed in mouse skin and that Tg (transgenic) mice overex...

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Detalles Bibliográficos
Autores principales: Sato, Hiroyasu, Taketomi, Yoshitaka, Isogai, Yuki, Masuda, Seiko, Kobayashi, Tetsuyuki, Yamamoto, Kei, Murakami, Makoto
Formato: Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2708930/
https://www.ncbi.nlm.nih.gov/pubmed/19371233
http://dx.doi.org/10.1042/BJ20082429
Descripción
Sumario:PLA(2) (phospholipase A(2)) group III is an atypical sPLA(2) (secretory PLA(2)) that is homologous with bee venom PLA(2) rather than with other mammalian sPLA(2)s. In the present paper, we show that endogenous group III sPLA(2) (PLA2G3) is expressed in mouse skin and that Tg (transgenic) mice overexpressing human PLA2G3 spontaneously develop skin inflammation. Pla2g3-Tg mice over 9 months of age frequently developed dermatitis with hyperkeratosis, acanthosis, parakeratosis, erosion, ulcer and sebaceous gland hyperplasia. The dermatitis was accompanied by infiltration of neutrophils and macrophages and by elevated levels of pro-inflammatory cytokines, chemokines and prostaglandin E(2). In addition, Pla2g3-Tg mice had increased lymph aggregates and mucus in the airway, lymphocytic sialadenitis, hepatic extramedullary haemopoiesis, splenomegaly with increased populations of granulocytes and monocytes/macrophages, and increased serum IgG(1). Collectively, these observations provide the first demonstration of spontaneous development of inflammation in mice with Tg overexpression of mammalian sPLA(2).