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1
Imogen 38: a novel 38-kD islet mitochondrial autoantigen recognized by T cells from a newly diagnosed type 1 diabetic patient.伊莫金38:一种新发现的38-kD胰岛线粒体自身抗原,可被一名新诊断的1型糖尿病患者的T细胞识别。
J Clin Invest. 1996 Jan 15;97(2):551-61. doi: 10.1172/JCI118448.
2
Altered peptide ligands of islet autoantigen Imogen 38 inhibit antigen specific T cell reactivity in human type-1 diabetes.胰岛自身抗原Imogen 38的改变肽配体抑制人类1型糖尿病中抗原特异性T细胞反应性。
J Autoimmun. 1998 Aug;11(4):353-61. doi: 10.1006/jaut.1998.0207.
3
Islet cell autoantigen 69 kD (ICA69). Molecular cloning and characterization of a novel diabetes-associated autoantigen.胰岛细胞自身抗原69kD(ICA69)。一种新型糖尿病相关自身抗原的分子克隆与特性分析。
J Clin Invest. 1993 Jul;92(1):359-71. doi: 10.1172/JCI116574.
4
T-cell epitope analysis using subtracted expression libraries (TEASEL): application to a 38-kDA autoantigen recognized by T cells from an insulin-dependent diabetic patient.使用消减表达文库的T细胞表位分析(TEASEL):应用于一名胰岛素依赖型糖尿病患者T细胞识别的38-kDA自身抗原
Proc Natl Acad Sci U S A. 1996 Mar 5;93(5):2014-8. doi: 10.1073/pnas.93.5.2014.
5
An islet-cell protein tyrosine phosphatase is a likely precursor to the 37-kDa autoantigen in type 1 diabetes: human and macaque sequences, tissue distribution, unique and shared epitopes, and predictive autoantibodies.一种胰岛细胞蛋白酪氨酸磷酸酶可能是1型糖尿病中37 kDa自身抗原的前体:人类和猕猴序列、组织分布、独特和共同表位以及预测性自身抗体。
Mol Med. 1997 Mar;3(3):163-73.
6
Identification of an MHC class I-restricted autoantigen in type 1 diabetes by screening an organ-specific cDNA library.通过筛选器官特异性cDNA文库鉴定1型糖尿病中一种MHC I类限制性自身抗原。
Nat Med. 1999 Sep;5(9):1026-31. doi: 10.1038/12465.
7
Autoantigens in insulin-dependent diabetes mellitus: molecular cloning and characterization of human IA-2 beta.胰岛素依赖型糖尿病中的自身抗原:人IA-2β的分子克隆与特性分析
Proc Assoc Am Physicians. 1997 Jul;109(4):429-39.
8
HLA-DR-restricted T cell lines from newly diagnosed type 1 diabetic patients specific for insulinoma and normal islet beta cell proteins: lack of reactivity to glutamic acid decarboxylase.来自新诊断的1型糖尿病患者的HLA - DR限制性T细胞系,对胰岛素瘤和正常胰岛β细胞蛋白具有特异性:对谷氨酸脱羧酶无反应性。
Clin Exp Immunol. 1995 Oct;102(1):152-8. doi: 10.1111/j.1365-2249.1995.tb06649.x.
9
Evidence for recognition of novel islet T cell antigens by granule-specific T cell lines from new onset type 1 diabetic patients.新发病1型糖尿病患者的颗粒特异性T细胞系识别新型胰岛T细胞抗原的证据。
Clin Exp Immunol. 2000 Jul;121(1):100-5. doi: 10.1046/j.1365-2249.2000.01279.x.
10
Islet cell antigen 512 is a diabetes-specific islet autoantigen related to protein tyrosine phosphatases.胰岛细胞抗原512是一种与蛋白酪氨酸磷酸酶相关的糖尿病特异性胰岛自身抗原。
J Immunol. 1994 Mar 15;152(6):3183-8.

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4
Novel autoantigens in type 1 diabetes.1 型糖尿病中的新型自身抗原。
Am J Transl Res. 2013 May 24;5(4):379-92. Print 2013.
5
Antigen targets of type 1 diabetes autoimmunity.1 型糖尿病自身免疫的抗原靶点。
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6
NCI60 cancer cell line panel data and RNAi analysis help identify EAF2 as a modulator of simvastatin and lovastatin response in HCT-116 cells.NCI60 癌细胞系panel 数据和 RNAi 分析有助于确定 EAF2 是辛伐他汀和洛伐他汀在 HCT-116 细胞中反应的调节剂。
PLoS One. 2011 Apr 4;6(4):e18306. doi: 10.1371/journal.pone.0018306.
7
An update on the use of NOD mice to study autoimmune (Type 1) diabetes.NOD 小鼠在自身免疫性(1 型)糖尿病研究中的应用进展。
Expert Rev Clin Immunol. 2010 Nov;6(6):939-55. doi: 10.1586/eci.10.68.
8
Selective screening of secretory vesicle-associated proteins for autoantigens in type 1 diabetes: VAMP2 and NPY are new minor autoantigens.1型糖尿病中分泌囊泡相关蛋白作为自身抗原的选择性筛查:囊泡相关膜蛋白2和神经肽Y是新的次要自身抗原。
Clin Immunol. 2008 Jun;127(3):366-74. doi: 10.1016/j.clim.2008.01.018. Epub 2008 Mar 24.
9
The cation efflux transporter ZnT8 (Slc30A8) is a major autoantigen in human type 1 diabetes.阳离子外流转运蛋白ZnT8(溶质载体家族30成员8)是人类1型糖尿病中的主要自身抗原。
Proc Natl Acad Sci U S A. 2007 Oct 23;104(43):17040-5. doi: 10.1073/pnas.0705894104. Epub 2007 Oct 17.
10
T-cell epitopes in type 1 diabetes.1型糖尿病中的T细胞表位
Curr Diab Rep. 2004 Apr;4(2):87-94. doi: 10.1007/s11892-004-0062-0.

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A microspectrophotometric method for the determination of cytochrome oxidase.一种测定细胞色素氧化酶的显微分光光度法。
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The sulphatase of ox liver. I. The complex nature of the enzyme.牛肝硫酸酯酶。I. 该酶的复合性质。
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Transcription factor jun-B is target of autoreactive T-cells in IDDM.转录因子Jun-B是胰岛素依赖型糖尿病中自身反应性T细胞的靶点。
Diabetes. 1993 Apr;42(4):626-30. doi: 10.2337/diab.42.4.626.
4
Islet cell autoantigen 69 kD (ICA69). Molecular cloning and characterization of a novel diabetes-associated autoantigen.胰岛细胞自身抗原69kD(ICA69)。一种新型糖尿病相关自身抗原的分子克隆与特性分析。
J Clin Invest. 1993 Jul;92(1):359-71. doi: 10.1172/JCI116574.
5
Detection of pancreatic islet 64,000 M(r) autoantigens in insulin-dependent diabetes distinct from glutamate decarboxylase.在胰岛素依赖型糖尿病中检测到与谷氨酸脱羧酶不同的胰岛64,000 M(r)自身抗原。
J Clin Invest. 1993 Jul;92(1):240-8. doi: 10.1172/JCI116556.
6
A multiplicity of protein antigens in subcellular fractions of rat insulinoma tissue are able to stimulate T cells obtained from non-obese diabetic mice.大鼠胰岛素瘤组织亚细胞组分中的多种蛋白质抗原能够刺激从非肥胖糖尿病小鼠获得的T细胞。
Diabetologia. 1993 May;36(5):385-90. doi: 10.1007/BF00402272.
7
Islet-specific T-cell clones from the NOD mouse respond to beta-granule antigen.来自非肥胖糖尿病(NOD)小鼠的胰岛特异性T细胞克隆对β颗粒抗原产生反应。
Diabetes. 1994 Feb;43(2):197-203. doi: 10.2337/diab.43.2.197.
8
Isolation of nonobese diabetic mouse T-cells that recognize novel autoantigens involved in the early events of diabetes.分离识别参与糖尿病早期事件的新型自身抗原的非肥胖糖尿病小鼠T细胞。
Diabetes. 1994 Jan;43(1):33-9. doi: 10.2337/diab.43.1.33.
9
Molecular cloning of mouse pancreatic islet R-cadherin: differential expression in endocrine and exocrine tissue.小鼠胰岛R-钙黏蛋白的分子克隆:在内分泌和外分泌组织中的差异表达。
Mol Endocrinol. 1993 Sep;7(9):1151-60. doi: 10.1210/mend.7.9.8247017.
10
Immune response to glutamic acid decarboxylase correlates with insulitis in non-obese diabetic mice.对谷氨酸脱羧酶的免疫反应与非肥胖糖尿病小鼠的胰岛炎相关。
Nature. 1993 Nov 4;366(6450):72-5. doi: 10.1038/366072a0.

伊莫金38:一种新发现的38-kD胰岛线粒体自身抗原,可被一名新诊断的1型糖尿病患者的T细胞识别。

Imogen 38: a novel 38-kD islet mitochondrial autoantigen recognized by T cells from a newly diagnosed type 1 diabetic patient.

作者信息

Arden S D, Roep B O, Neophytou P I, Usac E F, Duinkerken G, de Vries R R, Hutton J C

机构信息

Department of Clinical Biochemistry, University of Cambridge, Addenbrooke's Hospital, United Kingdom.

出版信息

J Clin Invest. 1996 Jan 15;97(2):551-61. doi: 10.1172/JCI118448.

DOI:10.1172/JCI118448
PMID:8567980
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC507050/
Abstract

Cell-mediated autoimmune attack directed against islet proteins of approximately 38 kD in size has been associated with type 1 diabetes. A novel murine cDNA encoding an antigen of this size was cloned using a screening procedure based on the proliferative response of a human diabetic T cell clone (1C6) to a recombinant antigen epitope library. Membrane preparations from COS 7 cells transfected with the full-length 1,267-bp cDNA elicited a proliferative response from the reporter T cells comparable to that of the defined peptide epitope and native insulinoma antigen. In vitro translation and transfection experiments suggested that the protein is initially synthesized as a 44-kD protein and then processed to the native 38-kD form through the proteolytic removal of a 54-aa NH2-terminal mitochondrial targeting sequence. Differential centrifugation, Percoll density gradient centrifugation, and immunofluorescence studies confirmed localization of the antigen to mitochondria. Northern blot, Western blot, and 1C6 T cell proliferation assays showed that, although imogen 38 was more highly expressed in beta cell than alpha cell lines, it was also present in other tissues. It is concluded that imogen 38 may be a target for bystander autoimmune attack in diabetes rather than a primary autoantigen.

摘要

针对大小约为38 kD的胰岛蛋白的细胞介导的自身免疫攻击与1型糖尿病有关。利用基于人糖尿病T细胞克隆(1C6)对重组抗原表位文库的增殖反应的筛选程序,克隆了编码这种大小抗原的新型鼠cDNA。用全长1267 bp cDNA转染的COS 7细胞的膜制剂引发了报告T细胞的增殖反应,其与确定的肽表位和天然胰岛素瘤抗原的增殖反应相当。体外翻译和转染实验表明,该蛋白最初以44 kD蛋白的形式合成,然后通过蛋白水解去除54个氨基酸的NH2末端线粒体靶向序列加工成天然的38 kD形式。差速离心、Percoll密度梯度离心和免疫荧光研究证实了该抗原定位于线粒体。Northern印迹、Western印迹和1C6 T细胞增殖试验表明,尽管免疫原38在β细胞系中比α细胞系中表达更高,但它也存在于其他组织中。得出的结论是,免疫原38可能是糖尿病中旁观者自身免疫攻击的靶点,而不是主要自身抗原。