• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Structure and function of the CD16:zeta:gamma complex expressed on human natural-killer cells.

作者信息

Vivier E, Ackerly M, Rochet N, Anderson P

机构信息

Division of Tumor Immunology, Dana Farber Cancer Institute, Boston, MA.

出版信息

Int J Cancer Suppl. 1992;7:11-4.

PMID:1428397
Abstract

Natural-killer (NK) cells are large granular lymphocytes involved in host defense against tumor cells and virally-infected cells. In addition to natural cytotoxicity, NK cells can effect antibody-dependent cytotoxicity mediated by CD16 (Fc gamma RIIIA alpha). It has recently been shown that CD16 is associated with disulfide-linked dimers composed of 2 homologous sub-units, zeta and gamma. These transducing molecules are also associated with other multimeric cell-surface receptors such as the T-cell antigen receptor (CD3:TCR) complex (zeta and gamma) and the high-affinity Fc receptor for IgE (Fc epsilon RI) expressed on basophils and mast cells (gamma). These results show that distinct cell-surface receptors utilize common transducing sub-units, and emphasize the homology between the CD16, Fc epsilon RI and CD3:TCR complexes. However within the lymphoid cells, the gamma-gamma homodimer is preferentially expressed in NK cells and cytotoxic T cells, suggesting that specific combinations of these transducing dimers might sub-serve distinct signal-transducing functions, and contribute to lymphocyte heterogeneity.

摘要

相似文献

1
Structure and function of the CD16:zeta:gamma complex expressed on human natural-killer cells.
Int J Cancer Suppl. 1992;7:11-4.
2
Structural similarity between Fc receptors and T cell receptors. Expression of the gamma-subunit of Fc epsilon RI in human T cells, natural killer cells and thymocytes.Fc受体与T细胞受体之间的结构相似性。人T细胞、自然杀伤细胞和胸腺细胞中FcεRIγ亚基的表达。
J Immunol. 1991 Dec 15;147(12):4263-70.
3
Association of the p56lck protein tyrosine kinase with the Fc gamma RIIIA/CD16 complex in human natural killer cells.人自然杀伤细胞中p56lck蛋白酪氨酸激酶与FcγRIIIA/CD16复合物的关联。
Eur J Immunol. 1993 Oct;23(10):2488-97. doi: 10.1002/eji.1830231017.
4
The human natural killer cell receptor for major histocompatibility complex class I molecules. Surface modulation of p58 molecules and their linkage to CD3 zeta chain, Fc epsilon RI gamma chain and the p56lck kinase.人类主要组织相容性复合体I类分子的自然杀伤细胞受体。p58分子的表面调节及其与CD3ζ链、FcεRIγ链和p56lck激酶的联系。
Eur J Immunol. 1994 Oct;24(10):2527-34. doi: 10.1002/eji.1830241040.
5
Tyrosine phosphorylation of the Fc gamma RIII(CD16): zeta complex in human natural killer cells. Induction by antibody-dependent cytotoxicity but not by natural killing.
J Immunol. 1991 Jan 1;146(1):206-10.
6
Co-association of CD3 zeta with a receptor (CD16) for IgG Fc on human natural killer cells.CD3ζ与人类自然杀伤细胞上IgG Fc受体(CD16)的共关联。
Nature. 1989 Dec 14;342(6251):803-5. doi: 10.1038/342803a0.
7
Expression of the zeta protein subunit in CD3- NK effectors derived from human thymus.ζ蛋白亚基在源自人胸腺的CD3 - 自然杀伤效应细胞中的表达。
Cell Immunol. 1994 May;155(2):508-16. doi: 10.1006/cimm.1994.1143.
8
Platelet-induced expression of Fc gamma RIII (CD16) on human monocytes.血小板诱导人单核细胞上FcγRIII(CD16)的表达。
Eur J Immunol. 1991 Apr;21(4):895-9. doi: 10.1002/eji.1830210406.
9
Alterations in expression and function of signal-transducing proteins in tumor-associated T and natural killer cells in patients with ovarian carcinoma.卵巢癌患者肿瘤相关T细胞和自然杀伤细胞中信号转导蛋白的表达及功能改变。
Clin Cancer Res. 1996 Jan;2(1):161-73.
10
Characterization of the family of dimers associated with Fc receptors (Fc epsilon RI and Fc gamma RIII).
J Immunol. 1991 Oct 15;147(8):2652-6.

引用本文的文献

1
Natural killer cell-based cancer immunotherapy: from basics to clinical trials.基于自然杀伤细胞的癌症免疫疗法:从基础到临床试验。
Exp Hematol Oncol. 2024 Oct 16;13(1):101. doi: 10.1186/s40164-024-00561-z.
2
Multivariate analysis of FcR-mediated NK cell functions identifies unique clustering among humans and rhesus macaques.FcR 介导的 NK 细胞功能的多变量分析在人类和恒河猴中确定了独特的聚类。
Front Immunol. 2023 Dec 6;14:1260377. doi: 10.3389/fimmu.2023.1260377. eCollection 2023.
3
The Frequency and Function of NKG2CCD57 Adaptive NK Cells in Cytomagalovirus Co-Infected People Living with HIV Decline with Duration of Antiretroviral Therapy.
在接受抗逆转录病毒治疗的时间延长后,人巨细胞病毒合并感染 HIV 的患者体内 NKG2CCD57 适应性自然杀伤细胞的频率和功能下降。
Viruses. 2023 Jan 24;15(2):323. doi: 10.3390/v15020323.
4
CD4 and MHCII phenotypic variability of peripheral blood monocytes in dogs.犬外周血单核细胞中 CD4 和 MHCII 表型的可变性。
PLoS One. 2019 Jul 3;14(7):e0219214. doi: 10.1371/journal.pone.0219214. eCollection 2019.
5
The Natural Cytotoxicity Receptors in Health and Disease.天然细胞毒性受体在健康和疾病中的作用。
Front Immunol. 2019 May 7;10:909. doi: 10.3389/fimmu.2019.00909. eCollection 2019.
6
Exploiting NK Cell Surveillance Pathways for Cancer Therapy.利用自然杀伤细胞监测途径进行癌症治疗。
Cancers (Basel). 2019 Jan 8;11(1):55. doi: 10.3390/cancers11010055.
7
IgG-Independent Co-aggregation of FcεRI and FcγRIIB Results in LYN- and SHIP1-Dependent Tyrosine Phosphorylation of FcγRIIB in Murine Bone Marrow-Derived Mast Cells.IgG 非依赖性 FcεRI 和 FcγRIIB 的共聚集导致鼠骨髓来源肥大细胞中 FcγRIIB 的 LYN 和 SHIP1 依赖性酪氨酸磷酸化。
Front Immunol. 2018 Aug 27;9:1937. doi: 10.3389/fimmu.2018.01937. eCollection 2018.
8
Chimeric Antigen Receptor Expressing Natural Killer Cells for the Immunotherapy of Cancer.嵌合抗原受体表达的自然杀伤细胞用于癌症的免疫治疗。
Front Immunol. 2018 Feb 15;9:283. doi: 10.3389/fimmu.2018.00283. eCollection 2018.
9
p46, a novel natural killer cell-specific surface molecule that mediates cell activation.p46,一种介导细胞活化的新型自然杀伤细胞特异性表面分子。
J Exp Med. 1997 Oct 6;186(7):1129-36. doi: 10.1084/jem.186.7.1129.
10
Systemic T cell-independent tumor immunity after transplantation of universal receptor-modified bone marrow into SCID mice.将通用受体修饰的骨髓移植到SCID小鼠体内后的全身性非T细胞依赖性肿瘤免疫。
J Exp Med. 1996 Dec 1;184(6):2261-9. doi: 10.1084/jem.184.6.2261.