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Lactoferrin and lactoferricin endocytosis halt Giardia cell growth and prevent infective cyst production

机译:乳铁蛋白和乳铁蛋白的内吞作用阻止贾第鞭毛虫细胞生长并防止感染性囊肿的产生

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摘要

Lactoferrin (LF) is an 80 KDa iron-binding glycoprotein that plays a significant role in the innate immune system and is considered to be an important microbicide molecule. It has been suggested to be effective in the treatment of giardiasis, an intestinal disease caused by the protozoan parasite G. lamblia. However, the molecular mechanisms by which LF exerts its effect on this parasite are unknown. Most of the microbicidal activity of human or bovine LF (hLF or bLF) has been associated with the N-terminal region of the mature LF - lactoferricin (LFcin). LFcin is produced by pepsin cleavage of the native protein in vitro and likely in vivo. In this work, we analyse the participation of the endocytic machinery of G. lamblia in the internalization of bLF and bLFcin and their effects on cell homeostasis. Our results show that, when bLF or bLFcin are internalized by receptor-mediated endocytosis, cell growth stops, and morphological changes are produced in the trophozoites, which ultimately will produce immature cysts. Our findings contribute to disclose the fine mechanism by which bLF and bLFcin may function as an antigiardial molecule and why they have therapeutic potential to eradicate giardiasis.
机译:乳铁蛋白(LF)是一种80 KDa的铁结合糖蛋白,在先天免疫系统中起重要作用,被认为是重要的杀菌剂分子。有人认为对治疗贾第虫病是有效的,贾第虫病是由原生动物寄生虫G. lamblia引起的肠道疾病。但是,LF对这种寄生虫发挥作用的分子机制尚不清楚。人类或牛LF(hLF或bLF)的大部分杀微生物活性与成熟LF-乳铁蛋白(LFcin)的N端区域有关。 LFcin是通过胃蛋白酶在体外(可能在体内)切割天然蛋白而产生的。在这项工作中,我们分析了G.lamblia的内吞机制参与bLF和bLFcin的内在化及其对细胞稳态的影响。我们的结果表明,当bLF或bLFcin通过受体介导的内吞作用而被内在化时,细胞生长停止,并且滋养体中发生形态变化,最终将产生未成熟的囊肿。我们的发现有助于揭示bLF和bLFcin可能充当抗贾第鞭毛分子的精细机制,以及为什么它们具有消除贾第鞭毛虫病的治疗潜力。

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