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The Journal of Immunology, 2000, 165: 4024-4031.
Copyright © 2000 by The American Association of Immunologists

Studies on a Mechanism by Which Cytosolic Phospholipase A2 Regulates the Expression and Function of Type IIA Secretory Phospholipase A21

Hiroshi Kuwata*, Shinji Yamamoto*, Yoshitaka Miyazaki*, Satoko Shimbara*, Yoshihito Nakatani*, Hiroshi Suzuki{dagger}, Natsuo Ueda{dagger}, Shozo Yamamoto{dagger}, Makoto Murakami* and Ichiro Kudo2,*

* Department of Health Chemistry, Showa University School of Pharmaceutical Sciences, Tokyo, Japan; and {dagger} Department of Biochemistry, Tokushima University School of Medicine, Tokushima, Japan

Although it has been proposed that arachidonate release by several secretory phospholipase A2 (sPLA2) isozymes is modulated by cytosolic PLA2 (cPLA2), the cellular component(s) that intermediates between these two signaling PLA2s remains unknown. Here we provide evidence that 12- or 15-lipoxygenase (12/15-LOX), which lies downstream of cPLA2, plays a pivotal role in cytokine-induced gene expression and function of sPLA2-IIA. The sPLA2-IIA expression and associated PGE2 generation induced by cytokines in rat fibroblastic 3Y1 cells were markedly attenuated by antioxidants that possess 12/15-LOX inhibitory activity. 3Y1 cells expressed 12/15-LOX endogenously, and forcible overexpression of 12/15-LOX in these cells greatly enhanced cytokine-induced expression of sPLA2-IIA, with a concomitant increase in delayed PG generation. Moreover, studies using 293 cells stably transfected with sPLA2-IIA revealed that stimulus-dependent hydrolysis of membrane phospholipids by sPLA2-IIA was enhanced by overexpression of 12/15-LOX. These results indicate that the product(s) generated by the cPLA2-12/15-LOX pathway following cell activation may play two roles: enhancement of sPLA2-IIA gene expression and membrane sensitization that leads to accelerated sPLA2-IIA-mediated hydrolysis.




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