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Limited contribution of Toll-like receptor 2 and 4 to the host response to a fungal infectious pathogen, Cryptococcus neoformans
Authors:Nakamura Kiwamu  Miyagi Kazuya  Koguchi Yoshinobu  Kinjo Yuki  Uezu Kaori  Kinjo Takeshi  Akamine Morikazu  Fujita Jiro  Kawamura Ikuo  Mitsuyama Masao  Adachi Yoshiyuki  Ohno Naohito  Takeda Kiyoshi  Akira Shizuo  Miyazato Akiko  Kaku Mitsuo  Kawakami Kazuyoshi
Institution:Department of Medicine and Therapeutics, Control and Prevention of Infectious Diseases, Faculty of Medicine, University of the Ryukyus, Okinawa, Japan. kawakami@mail.tains.tohoku.ac.jp
Abstract:The present study was designed to elucidate the role of Toll-like receptor (TLR) 2 and TLR4 in the host response to Cryptococcus neoformans. Both TLR2 knockout (KO) and TLR4KO mice produced interleukin-1beta (IL-1beta), IL-6, IL-12p40 and tumor necrosis factor-alpha (TNF-alpha) in sera and cleared this fungal pathogen from infected lungs at a comparable level to control littermate (LM) mice. Synthesis of these cytokines was not significantly different in the lungs of these KO mice and LM mice, although IL-1beta, IL-6 and IL-12p40 tended to be lower in TLR2KO, but not TLR4KO, mice than in controls. In addition, there was no significant reduction detected in the synthesis of IL-12 and TNF-alpha by bone marrow-derived dendritic cells from TLR2KO and TLR4KO mice upon stimulation with live yeast cells. Finally, HEK293 cells expressing either TLR2/dectin-1 or TLR4/MD2/CD14 did not respond to C. neoformans in the activation of nuclear factor kappa B (NFkappaB) detected by a luciferase assay. Our results suggest that TLR2 and TLR4 do not or only marginally contribute to the host and cellular response to this pathogen.
Keywords:Cryptococcus neoformans            host response  TLR2  TLR4  dectin-1
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