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1
Leishmania promastigotes are recognized by the macrophage receptor for advanced glycosylation endproducts.利什曼原虫前鞭毛体可被巨噬细胞晚期糖基化终产物受体识别。
J Exp Med. 1987 Jan 1;165(1):140-5. doi: 10.1084/jem.165.1.140.
2
The mouse macrophage receptor for C3bi (CR3) is a major mechanism in the phagocytosis of Leishmania promastigotes.小鼠C3bi巨噬细胞受体(CR3)是吞噬利什曼原虫前鞭毛体的主要机制。
J Immunol. 1985 Oct;135(4):2785-9.
3
Complement receptor type 3 (CR3) binds to an Arg-Gly-Asp-containing region of the major surface glycoprotein, gp63, of Leishmania promastigotes.3型补体受体(CR3)与利什曼原鞭毛虫主要表面糖蛋白gp63的一个含精氨酸-甘氨酸-天冬氨酸的区域结合。
J Exp Med. 1988 Jul 1;168(1):279-92. doi: 10.1084/jem.168.1.279.
4
Identification of a macrophage-binding determinant on lipophosphoglycan from Leishmania major promastigotes.鉴定来自硕大利什曼原虫前鞭毛体的脂磷壁酸上的巨噬细胞结合决定簇。
Proc Natl Acad Sci U S A. 1992 Jan 1;89(1):6-10. doi: 10.1073/pnas.89.1.6.
5
Monoclonal antibodies that recognize distinct epitopes of the macrophage type three complement receptor differ in their ability to inhibit binding of Leishmania promastigotes harvested at different phases of their growth cycle.识别巨噬细胞三型补体受体不同表位的单克隆抗体,在抑制处于生长周期不同阶段收获的利什曼原虫前鞭毛体结合的能力上存在差异。
Immunology. 1988 Dec;65(4):511-4.
6
CR1, the C3b receptor, mediates binding of infective Leishmania major metacyclic promastigotes to human macrophages.CR1,即C3b受体,介导感染性硕大利什曼原虫成熟前鞭毛体与人类巨噬细胞的结合。
J Immunol. 1989 Jul 15;143(2):617-22.
7
The Abl and Arg kinases mediate distinct modes of phagocytosis and are required for maximal Leishmania infection.Abl 和 Arg 激酶介导不同模式的吞噬作用,并且是最大程度感染利什曼原虫所必需的。
Mol Cell Biol. 2012 Aug;32(15):3176-86. doi: 10.1128/MCB.00086-12. Epub 2012 Jun 4.
8
Cutaneous host defense in leishmaniasis: interaction of isolated dermal macrophages and epidermal Langerhans cells with the insect-stage promastigote.利什曼病中的皮肤宿主防御:分离的真皮巨噬细胞和表皮朗格汉斯细胞与昆虫阶段前鞭毛体的相互作用。
Infect Immun. 1988 Feb;56(2):336-42. doi: 10.1128/iai.56.2.336-342.1988.
9
Modulation of macrophage mannose receptor affects the uptake of virulent and avirulent Leishmania donovani promastigotes.巨噬细胞甘露糖受体的调节影响有毒力和无毒力杜氏利什曼原虫前鞭毛体的摄取。
J Parasitol. 2001 Oct;87(5):1023-7. doi: 10.1645/0022-3395(2001)087[1023:MOMMRA]2.0.CO;2.
10
The involvement of the major surface glycoprotein (gp63) of Leishmania promastigotes in attachment to macrophages.利什曼原虫前鞭毛体的主要表面糖蛋白(gp63)在与巨噬细胞附着中的作用。
J Immunol. 1986 Apr 1;136(7):2613-20.

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Immune Responses in Leishmaniasis: An Overview.利什曼病中的免疫反应:概述
Trop Med Infect Dis. 2022 Mar 31;7(4):54. doi: 10.3390/tropicalmed7040054.
2
Complement Receptor 3-Mediated Inhibition of Inflammasome Priming by Ras GTPase-Activating Protein During Phagocytosis by Human Mononuclear Phagocytes.补体受体 3 介导的 Ras GTP 酶激活蛋白在人单核吞噬细胞吞噬作用过程中对炎症小体的起始抑制作用。
Front Immunol. 2018 Mar 26;9:561. doi: 10.3389/fimmu.2018.00561. eCollection 2018.
3
Redundant and regulatory roles for Toll-like receptors in Leishmania infection.Toll样受体在利什曼原虫感染中的冗余和调节作用
Clin Exp Immunol. 2017 Nov;190(2):167-186. doi: 10.1111/cei.13014. Epub 2017 Aug 7.
4
Immunoregulation in human American leishmaniasis: balancing pathology and protection.人类美洲利什曼病中的免疫调节:平衡病理与保护
Parasite Immunol. 2014 Aug;36(8):367-76. doi: 10.1111/pim.12100.
5
Fine tuning inflammation at the front door: macrophage complement receptor 3-mediates phagocytosis and immune suppression for Francisella tularensis.精细调控炎症反应的“前门”:巨噬细胞补体受体 3 介导的弗朗西斯氏菌属土拉弗朗西斯菌的吞噬作用和免疫抑制。
PLoS Pathog. 2013 Jan;9(1):e1003114. doi: 10.1371/journal.ppat.1003114. Epub 2013 Jan 24.
6
Differences in human macrophage receptor usage, lysosomal fusion kinetics and survival between logarithmic and metacyclic Leishmania infantum chagasi promastigotes.人巨噬细胞受体利用、溶酶体融合动力学和对数期与循环期婴儿利什曼原虫之间差异。
Cell Microbiol. 2009 Dec;11(12):1827-41. doi: 10.1111/j.1462-5822.2009.01374.x. Epub 2009 Aug 20.
7
Role of beta-D-galactofuranose in Leishmania major macrophage invasion.β-D-呋喃半乳糖在硕大利什曼原虫巨噬细胞侵袭中的作用。
Infect Immun. 2002 Dec;70(12):6592-6. doi: 10.1128/IAI.70.12.6592-6596.2002.
8
Intracellular survival of Leishmania major in neutrophil granulocytes after uptake in the absence of heat-labile serum factors.在缺乏热不稳定血清因子的情况下,利什曼原虫主要亚种被中性粒细胞摄取后在细胞内的存活情况。
Infect Immun. 2002 Feb;70(2):826-35. doi: 10.1128/IAI.70.2.826-835.2002.
9
Regulation of the expression of nitric oxide synthase and leishmanicidal activity by glycoconjugates of Leishmania lipophosphoglycan in murine macrophages.利什曼原虫脂磷壁酸糖缀合物对小鼠巨噬细胞中一氧化氮合酶表达及杀利什曼原虫活性的调控
Proc Natl Acad Sci U S A. 1996 Oct 1;93(20):10984-9. doi: 10.1073/pnas.93.20.10984.
10
Leishmania major-human macrophage interactions: cooperation between Mac-1 (CD11b/CD18) and complement receptor type 1 (CD35) in promastigote adhesion.硕大利什曼原虫与人类巨噬细胞的相互作用:前鞭毛体黏附中Mac-1(CD11b/CD18)与1型补体受体(CD35)之间的协同作用
Infect Immun. 1996 Jun;64(6):2206-15. doi: 10.1128/iai.64.6.2206-2215.1996.

本文引用的文献

1
Phagocytosis and killing of the protozoan Leishmania donovani by human polymorphonuclear leukocytes.人类多形核白细胞对杜氏利什曼原虫的吞噬与杀伤作用。
J Immunol. 1981 Oct;127(4):1438-43.
2
Nonenzymatic glycosylation of peripheral nerve protein in diabetes mellitus.糖尿病中周围神经蛋白的非酶糖基化
Proc Natl Acad Sci U S A. 1981 Aug;78(8):5190-2. doi: 10.1073/pnas.78.8.5190.
3
Accumulation of diabetic rat peripheral nerve myelin by macrophages increases with the presence of advanced glycosylation endproducts.随着晚期糖基化终末产物的出现,巨噬细胞对糖尿病大鼠周围神经髓磷脂的积累会增加。
J Exp Med. 1984 Jul 1;160(1):197-207. doi: 10.1084/jem.160.1.197.
4
Aging of proteins: isolation and identification of a fluorescent chromophore from the reaction of polypeptides with glucose.蛋白质老化:从多肽与葡萄糖反应产物中分离并鉴定一种荧光发色团。
Proc Natl Acad Sci U S A. 1984 May;81(9):2684-8. doi: 10.1073/pnas.81.9.2684.
5
Nonenzymatic glycosylation and the pathogenesis of diabetic complications.非酶糖基化与糖尿病并发症的发病机制
Ann Intern Med. 1984 Oct;101(4):527-37. doi: 10.7326/0003-4819-101-4-527.
6
Activation of the alternative complement pathway by Leishmania promastigotes: parasite lysis and attachment to macrophages.利什曼原虫前鞭毛体激活替代补体途径:寄生虫裂解及与巨噬细胞的附着
J Immunol. 1984 Mar;132(3):1501-5.
7
Macrophage complement and lectin-like receptors bind Leishmania in the absence of serum.在无血清情况下,巨噬细胞补体和凝集素样受体可结合利什曼原虫。
J Exp Med. 1985 Jul 1;162(1):324-31. doi: 10.1084/jem.162.1.324.
8
The mouse macrophage receptor for C3bi (CR3) is a major mechanism in the phagocytosis of Leishmania promastigotes.小鼠C3bi巨噬细胞受体(CR3)是吞噬利什曼原虫前鞭毛体的主要机制。
J Immunol. 1985 Oct;135(4):2785-9.
9
A model in mice for experimental leishmaniasis with a West African strain of Leishmania tropica.一种用于实验性利什曼病的小鼠模型,使用热带利什曼原虫的西非菌株。
Am J Trop Med Hyg. 1979 May;28(3):472-9. doi: 10.4269/ajtmh.1979.28.472.
10
Mac-1: a macrophage differentiation antigen identified by monoclonal antibody.Mac-1:一种由单克隆抗体识别的巨噬细胞分化抗原。
Eur J Immunol. 1979 Apr;9(4):301-6. doi: 10.1002/eji.1830090410.

利什曼原虫前鞭毛体可被巨噬细胞晚期糖基化终产物受体识别。

Leishmania promastigotes are recognized by the macrophage receptor for advanced glycosylation endproducts.

作者信息

Mosser D M, Vlassara H, Edelson P J, Cerami A

出版信息

J Exp Med. 1987 Jan 1;165(1):140-5. doi: 10.1084/jem.165.1.140.

DOI:10.1084/jem.165.1.140
PMID:3025330
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2188265/
Abstract

In this paper we demonstrate the involvement of the macrophage receptor for advanced glycosylation endproducts (AGE) in the phagocytosis of Leishmania major promastigotes. Blocking of this receptor with the ligand, AGE-BSA, leads to a 50% decrease in phagocytosis relative to controls, and a comparable decrease in the respiratory burst. The inhibition of phagocytosis by AGE-BSA was specific to leishmania. The binding of zymosan or C3bi-RBC and the phagocytosis of IgG-RBC or latex beads was not affected by the presence of AGE-BSA. Blocking of both the AGE receptor and CR3 decreases leishmania binding by nearly 90%, and reduces the respiratory burst by 80%, indicating that the two receptors account for the bulk of L. tropica promastigote recognition and uptake by the macrophage.

摘要

在本文中,我们证明了晚期糖基化终产物(AGE)巨噬细胞受体参与了巨噬细胞对利什曼原虫前鞭毛体的吞噬作用。用配体AGE-BSA阻断该受体后,相对于对照组,吞噬作用降低了50%,呼吸爆发也有类似程度的降低。AGE-BSA对吞噬作用的抑制作用对利什曼原虫具有特异性。酵母聚糖或C3bi-RBC的结合以及IgG-RBC或乳胶珠的吞噬作用不受AGE-BSA的影响。同时阻断AGE受体和CR3可使利什曼原虫的结合减少近90%,并使呼吸爆发降低80%,这表明这两种受体在巨噬细胞对热带利什曼原虫前鞭毛体的识别和摄取中起主要作用。