• 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

一种由活化的人T淋巴细胞分泌的新型多肽。

A novel polypeptide secreted by activated human T lymphocytes.

作者信息

Miller M D, Hata S, De Waal Malefyt R, Krangel M S

机构信息

Division of Tumor Virology, Dana-Farber Cancer Institute, Boston, MA 02115.

出版信息

J Immunol. 1989 Nov 1;143(9):2907-16.

PMID:2809212
Abstract

We have identified two cDNA clones, I-309 and G-26, which define genes expressed abundantly in activated human PBMC, but at low or undetectable levels in resting PBMC. Based upon nucleotide sequence analysis, both clones are predicted to encode small, structurally related polypeptides, each containing a hydrophobic leader sequence characteristic of secreted proteins and a motif of four conserved cysteine residues. Further, I-309 and G-26 are structurally related to a growing family of genes that apparently encode small polypeptides whose secretion is induced upon cell activation. I-309 represents a previously undescribed human gene. We have generated an anti-peptide antiserum to the I-309 gene product which recognizes proteins in culture supernatants of an activated T cell clone and of COS cells transfected with the I-309 cDNA, supporting the idea that I-309 encodes a secreted protein. Because I-309 encodes a small protein secreted by activated T cells that displays structural features similar to other cytokines, we believe that it defines a novel cytokine with as yet unknown function.

摘要

我们已鉴定出两个cDNA克隆,即I - 309和G - 26,它们所定义的基因在活化的人外周血单核细胞(PBMC)中大量表达,但在静息PBMC中表达水平很低或无法检测到。基于核苷酸序列分析,预计这两个克隆都编码小的、结构相关的多肽,每个多肽都含有分泌蛋白特有的疏水前导序列和四个保守半胱氨酸残基的基序。此外,I - 309和G - 26在结构上与一个不断扩大的基因家族相关,这些基因显然编码小多肽,其分泌在细胞活化时被诱导。I - 309代表一个以前未描述的人类基因。我们已针对I - 309基因产物产生了一种抗肽抗血清,该抗血清可识别活化T细胞克隆和用I - 309 cDNA转染的COS细胞培养上清液中的蛋白质,这支持了I - 309编码一种分泌蛋白的观点。由于I - 309编码一种由活化T细胞分泌的小蛋白,该蛋白具有与其他细胞因子相似的结构特征,我们认为它定义了一种功能未知的新型细胞因子。

相似文献

1
A novel polypeptide secreted by activated human T lymphocytes.一种由活化的人T淋巴细胞分泌的新型多肽。
J Immunol. 1989 Nov 1;143(9):2907-16.
2
Mitogenic activation of human T cells induces two closely related genes which share structural similarities with a new family of secreted factors.
J Immunol. 1989 Mar 1;142(5):1582-90.
3
Isolation and characterization of a cDNA encoding a putative cytokine which is induced by stimulation via the CD2 structure on human T lymphocytes.一种假定细胞因子的cDNA的分离与鉴定,该细胞因子由人T淋巴细胞上的CD2结构刺激诱导产生。
Eur J Immunol. 1989 Jun;19(6):1045-51. doi: 10.1002/eji.1830190614.
4
Isolation and characterization of an expressible cDNA encoding human IL-3. Induction of IL-3 mRNA in human T cell clones.编码人白细胞介素-3的可表达互补DNA的分离与特性鉴定。人T细胞克隆中白细胞介素-3信使核糖核酸的诱导。
J Immunol. 1988 Apr 1;140(7):2288-95.
5
Identification of a mouse protein homologous to the human CD6 T cell surface protein and sequence of the corresponding cDNA.与人类CD6 T细胞表面蛋白同源的小鼠蛋白的鉴定及相应cDNA的序列分析
J Immunol. 1995 Nov 15;155(10):4739-48.
6
Isolation and characterization of a novel B cell activation gene.一种新型B细胞激活基因的分离与鉴定
J Immunol. 1993 May 1;150(9):3895-904.
7
A cDNA clone encoding a product of activated human T lymphocytes.
Mol Biol Med. 1984 Apr;2(2):151-65.
8
Cloning and characterization of a novel T cell activation gene.
J Immunol. 1987 Nov 1;139(9):3126-31.
9
RP1, a new member of the adenomatous polyposis coli-binding EB1-like gene family, is differentially expressed in activated T cells.
J Immunol. 1997 Aug 1;159(3):1276-83.
10
Molecular cloning, expression and chromosomal localization of a novel human REG family gene, REG III.一种新型人类REG家族基因REG III的分子克隆、表达及染色体定位
Gene. 2004 Sep 29;340(1):161-70. doi: 10.1016/j.gene.2004.06.010.

引用本文的文献

1
Emerging Immunotherapy Targets in Early Drug Development.早期药物研发中新兴的免疫治疗靶点
Int J Mol Sci. 2025 Jun 4;26(11):5394. doi: 10.3390/ijms26115394.
2
CC Chemokine Family Members' Modulation as a Novel Approach for Treating Central Nervous System and Peripheral Nervous System Injury-A Review of Clinical and Experimental Findings.CC 趋化因子家族成员的调节作为治疗中枢神经系统和周围神经系统损伤的新方法——临床和实验研究结果综述。
Int J Mol Sci. 2024 Mar 28;25(7):3788. doi: 10.3390/ijms25073788.
3
Development of a cellular model to study CCR8 signaling in tumor-infiltrating regulatory T cells.
建立一个细胞模型来研究肿瘤浸润调节性 T 细胞中的 CCR8 信号转导。
Cancer Immunol Immunother. 2024 Jan 17;73(1):11. doi: 10.1007/s00262-023-03607-z.
4
Protective action of ultrasound-guided electrolysis technique on the muscle damage induced by notexin in rats.超声引导电解技术对肌肉损伤的保护作用,notexin 诱导的大鼠。
PLoS One. 2022 Nov 28;17(11):e0276634. doi: 10.1371/journal.pone.0276634. eCollection 2022.
5
Research progress on Th17 and T regulatory cells and their cytokines in regulating atherosclerosis.Th17细胞与调节性T细胞及其细胞因子在调控动脉粥样硬化中的研究进展
Front Cardiovasc Med. 2022 Sep 21;9:929078. doi: 10.3389/fcvm.2022.929078. eCollection 2022.
6
Chemokine Receptor-Targeted Therapies: Special Case for CCR8.趋化因子受体靶向疗法:CCR8的特殊情况
Cancers (Basel). 2022 Jan 20;14(3):511. doi: 10.3390/cancers14030511.
7
How Phagocytes Acquired the Capability of Hunting and Removing Pathogens From a Human Body: Lessons Learned From Chemotaxis and Phagocytosis of (Review).吞噬细胞如何获得从人体中搜寻和清除病原体的能力:从趋化性和吞噬作用中汲取的经验教训(综述)
Front Cell Dev Biol. 2021 Aug 20;9:724940. doi: 10.3389/fcell.2021.724940. eCollection 2021.
8
Combined tumor-directed recruitment and protection from immune suppression enable CAR T cell efficacy in solid tumors.联合肿瘤靶向招募和免疫抑制保护可增强 CAR T 细胞在实体瘤中的疗效。
Sci Adv. 2021 Jun 9;7(24). doi: 10.1126/sciadv.abi5781. Print 2021 Jun.
9
A Critical Update of the Assessment and Acute Management of Patients with Severe Burns.严重烧伤患者评估与急性处理的重要更新
Adv Wound Care (New Rochelle). 2019 Dec 1;8(12):607-633. doi: 10.1089/wound.2019.0963. Epub 2019 Nov 6.
10
M2b macrophage polarization and its roles in diseases.M2b 型巨噬细胞极化及其在疾病中的作用。
J Leukoc Biol. 2019 Aug;106(2):345-358. doi: 10.1002/JLB.3RU1018-378RR. Epub 2018 Dec 21.