Acid beta-Glucosidase 1 Counteracts p38 delta-dependent Induction of Interleukin-6 POSSIBLE ROLE FOR CERAMIDE AS AN ANTI-INFLAMMATORY LIPID

作者：Kitatani Kazuyuki; Sheldon Kely; Anelli Viviana; Jenkins Russell W; Sun Ying; Grabowski Gregory A; Obeid Lina M; Hannun Yusuf A^*

来源：Journal of Biological Chemistry, 2009, 284(19): 12979-12988.

DOI：10.1074/jbc.M809500200

Activation of protein kinase C (PKC) by the phorbol ester (phorbol 12-myristate 13-acetate) induces ceramide formation through the salvage pathway involving, in part, acid beta-glucosidase 1 (GBA1), which cleaves glucosylceramide to ceramide. Here, we examine the role of the GBA1-ceramide pathway, in regulating a pro-inflammatory pathway initiated by PKC and leading to activation of p38 and induction of interleukin 6 (IL-6). Inhibition of ceramide formation by fumonisin B1 or down-regulation of PKC delta potentiated PMA-induced activation of p38 in human breast cancer MCF-7 cells. Similarly, knockdown of GBA1 by small interfering RNAs or pharmacological inhibition of GBA1 promoted further activation of p38 after PMA treatment, implicating the GBA1-ceramide pathway in the termination of p38 activation. Knockdown of GBA1 also evoked the hyperproduction of IL-6 in response to 4 beta phorbol 12-myristate 13-acetate. On the other hand, increasing cellular ceramide with cell-permeable ceramide treatment resulted in attenuation of the IL-6 response. Importantly, silencing the delta isoform of the p38 family significantly attenuated the hyperproduction of IL-6. Reciprocally, p38 delta overexpression induced IL-6 biosynthesis. Thus, the GBA1-ceramide pathway is suggested to play an important role in terminating p38 delta activation responsible for IL-6 biosynthesis. Furthermore, the p38 delta isoform was identified as a novel and predominant target of ceramide signaling as well as a regulator of IL-6 biosynthesis.

• 出版日期2009-5-8