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主要组织相容性复合体和免疫球蛋白重链可变区(Igh-V)连锁基因所控制的细胞相互作用分子之间的同源性,T细胞利用这些分子进行通讯。产生细胞和接受细胞的串联“适应性”分化。

Homologies between cell interaction molecular controlled by major histocompatibility complex- and Igh-V-linked genes that T cells use for communication. Tandem "adaptive" differentiation of producer and acceptor cells.

作者信息

Flood P, Yamauchi K, Singer A, Gershon R K

出版信息

J Exp Med. 1982 Nov 1;156(5):1390-7. doi: 10.1084/jem.156.5.1390.

DOI:10.1084/jem.156.5.1390
PMID:6982305
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2186833/
Abstract

We have asked the question: how do partner cells in immunoregulatory interactions between T cell subsets acquire the ability to recognize and react appropriately with one another? In particular, we have asked whether these communication events are completely determined by the cell's genetic constitution, or whether the recognition events can be learned during ontogeny. We have found that the T cells of parent into F1 chimeras and homozygous nude mice with F1 thymus grafts not only learn to react with genetically disparate acceptor cells, but that the receptors on the acceptor cells themselves learn to react with genetically disparate producer cells. This learning process can overcome both major histocompatibility complex- and immunoglobulin heavy chain variable region-linked restricted communication between T cell subsets. We interpret these findings to indicate that thymic elements can start a cascade of differential events. The thymic elements, whether endogenous or passively acquired, select from a pool of producer cells those that will react appropriately with the thymic selecting cells, and these cells become expanded. Then, the private markers (idiotype) on the expanded pool of producer cells act as selecting and expanding elements that choose from a pool of acceptor cells those that recognize the producer cells idiotype as self. This second differentiational event, although apparently thymus evidence that this type of acceptor cell differentiation could also take place during the course of an immune response.

摘要

我们提出了这样一个问题

在T细胞亚群之间的免疫调节相互作用中,伙伴细胞是如何获得相互识别并做出适当反应的能力的?具体而言,我们探讨了这些通讯事件是完全由细胞的遗传构成决定,还是识别事件可以在个体发育过程中习得。我们发现,亲代与F1嵌合体以及接受F1胸腺移植的纯合裸鼠的T细胞不仅学会了与基因上不同的受体细胞发生反应,而且受体细胞自身的受体也学会了与基因上不同的产生细胞发生反应。这个学习过程能够克服T细胞亚群之间主要组织相容性复合体和免疫球蛋白重链可变区相关的限制性通讯。我们对这些发现的解读是,胸腺成分能够引发一系列差异事件。胸腺成分,无论是内源性的还是被动获得的,会从产生细胞池中挑选出那些能与胸腺选择细胞做出适当反应的细胞,这些细胞会得到扩增。然后,扩增后的产生细胞池上的独特标记(独特型)作为选择和扩增元件,从受体细胞池中挑选出那些将产生细胞独特型识别为自身的细胞。这第二个分化事件,尽管显然胸腺证据表明这种类型的受体细胞分化也可能在免疫反应过程中发生。

相似文献

1
Homologies between cell interaction molecular controlled by major histocompatibility complex- and Igh-V-linked genes that T cells use for communication. Tandem "adaptive" differentiation of producer and acceptor cells.主要组织相容性复合体和免疫球蛋白重链可变区(Igh-V)连锁基因所控制的细胞相互作用分子之间的同源性,T细胞利用这些分子进行通讯。产生细胞和接受细胞的串联“适应性”分化。
J Exp Med. 1982 Nov 1;156(5):1390-7. doi: 10.1084/jem.156.5.1390.
2
Homologies between cell interaction molecules controlled by major histocompatibility complex- and Igh-V-linked genes that T cells use for communication; both molecules undergo "adaptive" differentiation in the thymus.主要组织相容性复合体和免疫球蛋白重链可变区(Igh-V)连锁基因所控制的、T细胞用于通讯的细胞相互作用分子之间的同源性;这两种分子在胸腺中都经历“适应性”分化。
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3
Influence of the major histocompatibility complex on positive thymic selection of V beta 17a+ T cells.
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4
Investigations into the nature of Igh-V region-restricted T cell interactions by using antibodies to antigens on methylcholanthrene-induced sarcomas. I. Analysis of an Igh-V-restricted suppressor-inducer factor.利用针对甲基胆蒽诱导肉瘤上抗原的抗体对Igh-V区限制性T细胞相互作用的性质进行研究。I. Igh-V限制性抑制诱导因子的分析。
J Immunol. 1985 Mar;134(3):1665-72.
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Adaptive differentiation of murine lymphocytes. II. The thymic microenvironment does not restrict the cooperative partner cell preference of helper T cells differentiating in F1 leads to F1 thymic chimeras.小鼠淋巴细胞的适应性分化。II. 胸腺微环境并不限制在F1→F1胸腺嵌合体中分化的辅助性T细胞的合作伴侣细胞偏好。
J Exp Med. 1979 Jun 1;149(6):1360-70. doi: 10.1084/jem.149.6.1360.
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Self recognition in allogeneic thymic chimeras. Self recognition by T helper cells from thymus-engrafted nude mice is restricted to the thymic H-2 haplotype.同种异体胸腺嵌合体中的自身识别。来自胸腺移植裸鼠的辅助性T细胞的自身识别局限于胸腺的H-2单倍型。
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Bone marrow-derived thymic antigen-presenting cells determine self-recognition of Ia-restricted T lymphocytes.骨髓来源的胸腺抗原呈递细胞决定了Ia限制型T淋巴细胞的自身识别。
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Ontogeny of MHC-linked, T cell-mediated suppression is regulated by the T cell genotype.与主要组织相容性复合体(MHC)相关的、T细胞介导的抑制作用的个体发生受T细胞基因型调控。
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The lymphoreticular system in triggering virus plus self-specific cytotoxic T cells: evidence for T help.触发病毒加自身特异性细胞毒性T细胞中的淋巴网状系统:T辅助的证据。
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引用本文的文献

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Antiidiotypes against anti-H-2 monoclonal antibodies. V. In vivo antiidiotype treatment induces idiotype-specific helper T cells.抗抗H-2单克隆抗体的抗独特型抗体。V. 体内抗独特型治疗诱导独特型特异性辅助性T细胞。
J Exp Med. 1983 Apr 1;157(4):1273-86. doi: 10.1084/jem.157.4.1273.
2
T cell regulation of B cell activation. I-A-restricted T suppressor cells inhibit the major histocompatibility complex-restricted interactions of T helper cells with B cells and accessory cells.T细胞对B细胞激活的调节作用。I-A限制性T抑制细胞抑制T辅助细胞与B细胞及辅助细胞之间主要组织相容性复合体限制性相互作用。
J Exp Med. 1983 Jun 1;157(6):1867-84. doi: 10.1084/jem.157.6.1867.
3
MHC-restricted minimal regulatory circuit initiated by a class II-autoreactive T cell clone.由II类自身反应性T细胞克隆启动的MHC限制的最小调节回路。
J Exp Med. 1987 May 1;165(5):1284-95. doi: 10.1084/jem.165.5.1284.

本文引用的文献

1
The H-2 phenotype of the thymus dictates the self-specificity expressed by thymic but not splenic cytotoxic T lymphocyte precursors in thymus-engrafted nude mice.胸腺的H-2表型决定了胸腺移植裸鼠中胸腺而非脾脏细胞毒性T淋巴细胞前体所表达的自身特异性。
J Immunol. 1981 Nov;127(5):2168-76.
2
Priming of T helper cells by antigen-activated B cells. B cell-primed Lyt-1+ helper cells are restricted to cooperate with B cells expressing the IgvH phenotype of the priming B cells.抗原激活的B细胞对辅助性T细胞的致敏作用。经B细胞致敏的Lyt-1⁺辅助性细胞只能与表达致敏B细胞IgvH表型的B细胞协同作用。
J Exp Med. 1981 May 1;153(5):1236-45. doi: 10.1084/jem.153.5.1236.
3
Influence of Igh-linked gene products on the generation of T helper cells in the response to sheep erythrocytes.Igh 连锁基因产物对绵羊红细胞应答中辅助性 T 细胞生成的影响。
J Exp Med. 1981 May 1;153(5):1225-35. doi: 10.1084/jem.153.5.1225.
4
Contrasuppression. A novel immunoregulatory activity.反向抑制。一种新型免疫调节活性。
J Exp Med. 1981 Jun 1;153(6):1533-46. doi: 10.1084/jem.153.6.1533.
5
Analysis of an antigen-specific H-2-restricted cell-free products(s) made by "I-J-" Ly-2 cells (Ly-2 TsF) that suppresses Ly-2 cell-depleted spleen cell activity.对由“I-J-”Ly-2细胞(Ly-2 TsF)产生的抑制Ly-2细胞耗竭的脾细胞活性的抗原特异性H-2限制性无细胞产物的分析。
Eur J Immunol. 1981 Nov;11(11):913-8. doi: 10.1002/eji.1830111111.
6
Analysis of antigen-specific, Ig-restricted cell-free material made by I-J+ Ly-1 cells (Ly-1 TsiF) that induces Ly-2+ cells to express suppressive activity.对由I-J⁺ Ly-1细胞(Ly-1 TsiF)产生的抗原特异性、Ig限制的无细胞物质的分析,该物质可诱导Ly-2⁺细胞表达抑制活性。
Eur J Immunol. 1981 Nov;11(11):905-12. doi: 10.1002/eji.1830111110.
7
Hapten-specific T cell responses to 4-hydroxy-3-nitrophenyl acetyl. XI. Pseudogenetic restrictions of hybridoma suppressor factors.对半抗原4-羟基-3-硝基苯乙酰的半抗原特异性T细胞应答。XI. 杂交瘤抑制因子的假基因限制
J Exp Med. 1981 Aug 1;154(2):468-79. doi: 10.1084/jem.154.2.468.
8
Self recognition in allogeneic radiation bone marrow chimeras. A radiation-resistant host element dictates the self specificity and immune response gene phenotype of T-helper cells.同种异体辐射骨髓嵌合体中的自我识别。一种抗辐射的宿主成分决定了辅助性T细胞的自我特异性和免疫反应基因表型。
J Exp Med. 1981 May 1;153(5):1286-301. doi: 10.1084/jem.153.5.1286.
9
Further improvements in the plaque technique for detecting single antibody-forming cells.用于检测单个抗体形成细胞的蚀斑技术的进一步改进。
Immunology. 1968 Apr;14(4):599-600.
10
Adaptive differentiation of murine lymphocytes. I. Both T and B lymphocytes differentiating in F1 transplanted to parental chimeras manifest preferential cooperative activity for partner lymphocytes derived from the same parental type corresponding to the chimeric host.小鼠淋巴细胞的适应性分化。I. 移植到亲代嵌合体中的F1代中分化的T淋巴细胞和B淋巴细胞,对源自与嵌合宿主相对应的同一亲代类型的伙伴淋巴细胞均表现出优先的协同活性。
J Exp Med. 1978 Sep 1;148(3):727-45. doi: 10.1084/jem.148.3.727.