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利什曼原虫吞噬溶酶体:药物运输及跨区室的蛋白质分选

Leishmania phagolysosome: drug trafficking and protein sorting across the compartment.

作者信息

Chakraborty P, Basu M K

机构信息

Biomembrane Division, Indian Institute of Chemical Biology, Jadavpur, Calcutta, India.

出版信息

Crit Rev Microbiol. 1997;23(3):253-68. doi: 10.3109/10408419709115139.

Abstract

Survival or destruction of intramacrophage pathogen Leishmania depends in part on modulation of their host cell phagosome, capabilities of the infected macrophages to present parasite antigen to the host's immune system. Macrophages house these parasites as amastigotes in the acidic phagolysosomal compartment. Leishmania phagolysosome is the potential site for processing and presentation of its antigen as well as being the target site for chemotherapy in leishmaniasis. It is thought that the parasites are killed from macrophage activation by lymphokines secreted from either helper T1 cells or CD8+ T cells. Characterization of both the host and parasite molecules in the compartment in the context of biogenesis of Leishmania-phagolysosome and processing of the parasite antigen by this compartment are discussed. Trafficking of different drugs and new agents through this compartment and their role in chemotherapy and necessity of developing new drug carrier are also stressed.

摘要

巨噬细胞内病原体利什曼原虫的存活或消亡部分取决于其对宿主细胞吞噬体的调控,以及被感染巨噬细胞将寄生虫抗原呈递给宿主免疫系统的能力。巨噬细胞将这些寄生虫以无鞭毛体的形式容纳在酸性吞噬溶酶体区室中。利什曼原虫吞噬溶酶体是其抗原加工和呈递的潜在场所,也是利什曼病化疗的靶位点。据认为,寄生虫会被辅助性T1细胞或CD8 + T细胞分泌的淋巴因子激活的巨噬细胞杀死。本文讨论了在利什曼原虫 - 吞噬溶酶体生物发生以及该区室对寄生虫抗原加工的背景下,该区室中宿主和寄生虫分子的特征。还强调了不同药物和新制剂通过该区域的运输及其在化疗中的作用,以及开发新药物载体的必要性。

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