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加工后的抗原与抗原呈递细胞膜的稳定结合。

Stable association of processed antigen with antigen-presenting cell membranes.

作者信息

Jensen P E

机构信息

Department of Pathology, Emory University School of Medicine, Atlanta, GA 30322.

出版信息

J Immunol. 1989 Jul 15;143(2):420-5.

PMID:2786907
Abstract

Th cells recognize a processed form of Ag in association with class II histocompatibility molecules expressed on the surface of APC. The physical nature of the cell surface association of physiologically processed Ag was investigated by using membranes isolated from Ag-pulsed APC. Such membranes were sufficient to directly activate class II-restricted T cell hybridomas without further Ag processing. T cell-stimulating activity remained after treatment of membranes in harsh conditions, including pH 4.0, pH 9.0, high salt, and chaotropic solvents. Activity was lost after exposure to pH 2.0 or protease. The capacity of pH 2.0 (but not protease) treated membranes to present artificially processed, peptide Ag to T cells suggests that exposure to pH 2.0 results in the selective dissociation of processed Ag from membranes. Similar results were obtained in parallel experiments with peptide-pulsed membranes. No qualitative differences were found between physiologically processed Ag and peptide Ag with respect to their remarkably stable association with the APC plasma membrane.

摘要

辅助性T细胞识别与抗原呈递细胞(APC)表面表达的II类组织相容性分子相关的经加工的抗原形式。通过使用从经抗原脉冲处理的APC分离的膜,研究了生理加工抗原在细胞表面结合的物理性质。这种膜足以直接激活II类限制性T细胞杂交瘤,而无需进一步的抗原加工。在包括pH 4.0、pH 9.0、高盐和离液剂等苛刻条件下处理膜后,T细胞刺激活性仍然存在。暴露于pH 2.0或蛋白酶后活性丧失。经pH 2.0(而非蛋白酶)处理的膜将人工加工的肽抗原呈递给T细胞的能力表明,暴露于pH 2.0会导致加工后的抗原从膜上选择性解离。在肽脉冲膜的平行实验中也获得了类似结果。在生理加工抗原和肽抗原与APC质膜的显著稳定结合方面,未发现定性差异。

相似文献

1
Stable association of processed antigen with antigen-presenting cell membranes.加工后的抗原与抗原呈递细胞膜的稳定结合。
J Immunol. 1989 Jul 15;143(2):420-5.
2
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引用本文的文献

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HLA-DM and the MHC class II antigen presentation pathway.HLA-DM与MHC II类抗原呈递途径。
Immunol Res. 1999;20(3):195-205. doi: 10.1007/BF02790403.
2
Membrane interactions influence the peptide binding behavior of DR1.膜相互作用影响DR1的肽结合行为。
J Exp Med. 1994 Jan 1;179(1):229-34. doi: 10.1084/jem.179.1.229.
3
Regulation of antigen presentation by acidic pH.酸性pH值对抗抗原呈递的调节作用。
J Exp Med. 1990 May 1;171(5):1779-84. doi: 10.1084/jem.171.5.1779.
4
Effects of pH and polysaccharides on peptide binding to class II major histocompatibility complex molecules.pH值和多糖对肽与II类主要组织相容性复合体分子结合的影响。
Proc Natl Acad Sci U S A. 1991 Apr 1;88(7):2740-4. doi: 10.1073/pnas.88.7.2740.
5
Reduction of disulfide bonds during antigen processing: evidence from a thiol-dependent insulin determinant.抗原加工过程中二硫键的还原:来自硫醇依赖性胰岛素决定簇的证据。
J Exp Med. 1991 Nov 1;174(5):1121-30. doi: 10.1084/jem.174.5.1121.
6
Enhanced binding of peptide antigen to purified class II major histocompatibility glycoproteins at acidic pH.在酸性pH条件下,肽抗原与纯化的II类主要组织相容性糖蛋白的结合增强。
J Exp Med. 1991 Nov 1;174(5):1111-20. doi: 10.1084/jem.174.5.1111.
7
Antigen-presenting cells constitutively bind tumor antigens in the tumor-bearing state in vivo to construct an effective immunogenic unit.抗原呈递细胞在体内荷瘤状态下持续结合肿瘤抗原,以构建有效的免疫原性单位。
Jpn J Cancer Res. 1991 Mar;82(3):262-5. doi: 10.1111/j.1349-7006.1991.tb01840.x.
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A first-order reaction controls the binding of antigenic peptides to major histocompatibility complex class II molecules.一级反应控制抗原肽与主要组织相容性复合体II类分子的结合。
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