Ras-related C3 Botulinum Toxin Substrate (Rac) and Src Family Kinases (SFK) Are Proximal and Essential for Phosphatidylinositol 3-Kinase (PI3K) Activation in Natural Killer (NK) Cell-mediated Direct Cytotoxicity against Cryptococcus neoformans

Ras 相关的 C3 肉毒杆菌毒素底物 (Rac) 和 Src 家族激酶 (SFK) 是自然杀伤 (NK) 细胞介导的针对新型隐球菌的直接细胞毒性中磷脂酰肌醇 3-激酶 (PI3K) 激活的近端和必需物

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作者:Richard F Xiang, Danuta Stack, Shaunna M Huston, Shu Shun Li, Henry Ogbomo, Stephen K Kyei, Christopher H Mody

Abstract

The activity of Rac in leukocytes is essential for immunity. However, its role in NK cell-mediated anti-microbial signaling remains unclear. In this study, we investigated the role of Rac in NK cell mediated anti-cryptococcal killing. We found thatCryptococcus neoformansindependently activates both Rac and SFK pathways in NK cells, and unlike in tumor killing,Cryptococcusinitiated a novel Rac → PI3K → Erk cytotoxicity cascade. Remarkably, Rac was not required for conjugate formation, despite its essential role in NK cytotoxicity againstC. neoformans Taken together, our data show that, unlike observations with tumor cells, NK cells use a novel Rac cytotoxicity pathway in conjunction with SFK, to killC. neoformans.

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