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C-Kit Ligand Promotes Mast Cell Infection by Toxoplasma gondii

机译:C-Kit配体通过弓形虫促进肥大细胞感染

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Biological functions of mast cells include a functional role in innate immunity against parasitic infections.Here, we demonstrated that mast cells could also play a role in the anti-microbial defenses regulation and might participateas a parasite reservoir. We observed that Toxoplasma gondii infected massively in vitro mouse bone marrow derivedmast cells (BMMC), a mucosal mast cell (MMC) phenotype, followed by substantial cell lysis. This induced release of ??-hexosaminidase, but not of preformed or neosynthesized TNF-. Culturing MMC in the presence of recombinant mousestem cell factor (c-kit ligand) led to their maturation into connective tissue-like mast cells (CTMC), which T. gondii wasable to adhere on and to infect more. T. gondii infection did not induce release of ??-hexosaminidase and serotonin fromBMMC. These results demonstrated that mast cells interact with T. gondii and are massively infected, especially aftertheir maturation by c-kit ligand.
机译:肥大细胞的生物学功能包括在抵抗寄生虫感染的先天免疫中的功能。这里,我们证明了肥大细胞还可以在抗微生物防御调节中发挥作用,并且可能作为寄生虫的贮藏库参与。我们观察到弓形虫在体外大量感染小鼠骨髓源性肥大细胞(BMMC),粘膜肥大细胞(MMC)表型,随后大量细胞裂解。这诱导释放β-己糖胺酶,但不释放预先形成的或新合成的TNF-。在重组小鼠干细胞因子(c-kit配体)存在下培养MMC导致它们成熟,成为结缔组织样肥大细胞(CTMC),弓形虫可以粘附并感染更多。刚地弓形虫感染不会诱导BMMC释放γ-己糖胺酶和5-羟色胺。这些结果表明,肥大细胞与弓形虫相互作用并被大量感染,特别是在它们被c-kit配体成熟后。

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