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[巨噬细胞与利什曼原虫相互作用的生物学]

[Biology of macrophages-Leishmania interactions].

作者信息

Antoine J C

机构信息

Unité d'Immunophysiologie Cellulaire, Institut Pasteur, Paris, France.

出版信息

Pathol Biol (Paris). 1995 Mar;43(3):215-23.

PMID:7675549
Abstract

Leishmania are trypanosomatidae which under their amastigote form behave as obligate intracellular parasites. At this stage, they multiply in macrophages of infected mammals (including man), within parasitophorous vacuoles (PV). These organelles of macrophage origin are part of the endocytic pathway. Study of their contents and membrane composition shows that they finally resemble lysosomes/prelysosomes. PV maintain a very acidic pH (< or = 5), and contain numerous functional lysosomal enzymes. They are limited by a membrane characterized by the presence of intrinsic and peripheral proteins described as being mainly associated with prelysosomal and/or lysosomal compartments (lamp-1, lamp-2, macrosialin, rab7p). Leishmania amastigotes appear to be acidophilic micro-organisms resistant to the action of lysosomal hydrolases and as such are fully adapted to the conditions encountered within prelysosomes/lysosomes. After stimulation of infected macrophages with interferon-gamma, we also note the presence of major histocompatibility complex (MHC) class II molecules in PV membrane but not that of MHC class I molecules. It is not yet known whether the PV-associated class II molecules play a role in the presentation of parasite antigens to protective specific T lymphocytes or whether parasites have developed strategies to inhibit or divert to their own advantage the antigen presentation process potentially detrimental to their survival. In any case, Leishmania-infected macrophages exhibit a deficiency in their capacity to present exogenous antigens in the context of MHC class II molecules. We are currently investigating whether this deficiency also extends to the presentation of parasite antigens.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

利什曼原虫属于锥虫科,其无鞭毛体形式为专性细胞内寄生虫。在此阶段,它们在被感染哺乳动物(包括人类)的巨噬细胞内的寄生泡(PV)中繁殖。这些源自巨噬细胞的细胞器是内吞途径的一部分。对其内容物和膜成分的研究表明,它们最终类似于溶酶体/前溶酶体。PV维持非常酸性的pH值(≤5),并含有多种功能性溶酶体酶。它们由一层膜界定,该膜的特征是存在被描述为主要与前溶酶体和/或溶酶体区室相关的内在蛋白和外周蛋白(lamp-1、lamp-2、巨唾液酸蛋白、rab7p)。利什曼原虫无鞭毛体似乎是对溶酶体水解酶作用具有抗性的嗜酸微生物,因此完全适应在前溶酶体/溶酶体内遇到的条件。在用γ干扰素刺激被感染的巨噬细胞后,我们还注意到PV膜中有主要组织相容性复合体(MHC)II类分子,但没有MHC I类分子。尚不清楚与PV相关的II类分子是否在将寄生虫抗原呈递给保护性特异性T淋巴细胞中起作用,或者寄生虫是否已制定策略来抑制或转向对其生存可能有害的抗原呈递过程以使其自身受益。无论如何,感染利什曼原虫的巨噬细胞在MHC II类分子背景下呈递外源性抗原的能力存在缺陷。我们目前正在研究这种缺陷是否也扩展到寄生虫抗原的呈递。(摘要截短于250字)

相似文献

1
[Biology of macrophages-Leishmania interactions].[巨噬细胞与利什曼原虫相互作用的生物学]
Pathol Biol (Paris). 1995 Mar;43(3):215-23.
2
Leishmania donovani-infected macrophages: characterization of the parasitophorous vacuole and potential role of this organelle in antigen presentation.杜氏利什曼原虫感染的巨噬细胞:寄生泡的特征及其在抗原呈递中的潜在作用。
J Cell Sci. 1994 Aug;107 ( Pt 8):2137-50. doi: 10.1242/jcs.107.8.2137.
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Antigen presentation by Leishmania mexicana-infected macrophages: activation of helper T cells by a model parasite antigen secreted into the parasitophorous vacuole or expressed on the amastigote surface.墨西哥利什曼原虫感染的巨噬细胞的抗原呈递:被分泌到寄生泡或在无鞭毛体表面表达的模型寄生虫抗原激活辅助性T细胞。
Eur J Immunol. 1996 Dec;26(12):3153-62. doi: 10.1002/eji.1830261248.
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Distribution of MHC class I and of MHC class II molecules in macrophages infected with Leishmania amazonensis.亚马逊利什曼原虫感染巨噬细胞中MHC I类分子和MHC II类分子的分布。
J Cell Sci. 1994 Jan;107 ( Pt 1):69-82. doi: 10.1242/jcs.107.1.69.
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Presentation of the protective parasite antigen LACK by Leishmania-infected macrophages.利什曼原虫感染的巨噬细胞呈递保护性寄生虫抗原LACK
J Immunol. 1996 Jun 1;156(11):4318-27.
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Dendritic cells as host cells for the promastigote and amastigote stages of Leishmania amazonensis: the role of opsonins in parasite uptake and dendritic cell maturation.作为亚马逊利什曼原虫前鞭毛体和无鞭毛体阶段宿主细胞的树突状细胞:调理素在寄生虫摄取和树突状细胞成熟中的作用
J Cell Sci. 2004 Jan 15;117(Pt 2):315-25. doi: 10.1242/jcs.00860. Epub 2003 Dec 2.
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Leishmania-infected macrophages sequester endogenously synthesized parasite antigens from presentation to CD4+ T cells.感染利什曼原虫的巨噬细胞会截留内源性合成的寄生虫抗原,使其无法呈递给CD4+T细胞。
Eur J Immunol. 1996 Dec;26(12):3163-9. doi: 10.1002/eji.1830261249.
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Biogenesis of Leishmania-harbouring parasitophorous vacuoles following phagocytosis of the metacyclic promastigote or amastigote stages of the parasites.寄生虫的循环前鞭毛体或无鞭毛体阶段被吞噬后,利什曼原虫寄生泡的生物发生。
J Cell Sci. 2002 Jun 1;115(Pt 11):2303-16. doi: 10.1242/jcs.115.11.2303.
9
Antigen presentation by Leishmania mexicana-infected macrophages: activation of helper T cells specific for amastigote cysteine proteinases requires intracellular killing of the parasites.墨西哥利什曼原虫感染的巨噬细胞的抗原呈递:对无鞭毛体半胱氨酸蛋白酶特异的辅助性T细胞的激活需要对寄生虫进行胞内杀伤。
Eur J Immunol. 1995 Apr;25(4):1094-100. doi: 10.1002/eji.1830250435.
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H-2M molecules, like MHC class II molecules, are targeted to parasitophorous vacuoles of Leishmania-infected macrophages and internalized by amastigotes of L. amazonensis and L. mexicana.H-2M分子与MHC II类分子一样,定位于感染利什曼原虫的巨噬细胞的寄生泡,并被亚马逊利什曼原虫和墨西哥利什曼原虫的无鞭毛体内化。
J Cell Sci. 1999 Aug;112 ( Pt 15):2559-70. doi: 10.1242/jcs.112.15.2559.

引用本文的文献

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Insulin-like growth factor I is a growth-promoting factor for Leishmania promastigotes and amastigotes.胰岛素样生长因子I是利什曼原虫前鞭毛体和无鞭毛体的生长促进因子。
Proc Natl Acad Sci U S A. 1998 Oct 27;95(22):13211-6. doi: 10.1073/pnas.95.22.13211.
2
Evidence for a major gene controlling susceptibility to tegumentary leishmaniasis in a recently exposed Bolivian population.在一个近期暴露于感染风险的玻利维亚人群中,存在一个控制皮肤利什曼病易感性的主要基因的证据。
Am J Hum Genet. 1997 Oct;61(4):968-79. doi: 10.1086/514882.