| Literature DB >> 22450320 |
Masashi Okada1, Yasukazu Hozumi, Kiyoshi Iwazaki, Kentaro Misaki, Mitsuaki Yanagida, Yoshihiko Araki, Takashi Watanabe, Hitoshi Yagisawa, Matthew K Topham, Kozo Kaibuchi, Kaoru Goto.
Abstract
Diacylglycerol kinase (DGK) plays an important role in phosphoinositide signaling cascade by regulating the intracellular level of diacylglycerol and phosphatidic acid. The DGK family is involved in various pathophysiological responses that are mediated through unique binding partners in different tissues and cells. In this study, we identified a small GTPase effector protein, IQGAP1, as a novel DGKζ-associated complex protein. A bacterial endotoxin, lipopolysaccharide (LPS), facilitated the complex formation in macrophages. Both proteins co-localized at the edge and phagocytic cup of the cell. Furthermore, RNA interference-mediated knockdown of DGKζ or IQGAP1 impaired LPS-induced Rac1 activation. Primary macrophages derived from DGKζ(-/-) mice attenuated LPS-induced phagocytosis of bacteria. These results suggest that DGKζ is involved in IQGAP1/Rac1-mediated phagocytosis upon LPS stimulation in macrophages.Entities:
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Year: 2012 PMID: 22450320 DOI: 10.1016/j.bbrc.2012.03.057
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575