• 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

蛋白 4.1R 通过抑制 C-Kit 介导的信号转导负调控 P815 细胞的增殖。

Protein 4.1R negatively regulates P815 cells proliferation by inhibiting C-Kit-mediated signal transduction.

机构信息

School of Life Sciences, Zhengzhou University, 100 Science Road, Zhengzhou, 450001, PR China.

The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, 450001, PR China.

出版信息

Exp Cell Res. 2021 Jan 15;398(2):112403. doi: 10.1016/j.yexcr.2020.112403. Epub 2020 Nov 30.

DOI:10.1016/j.yexcr.2020.112403
PMID:33271128
Abstract

The proliferation of mast cells (MCs) plays a crucial role in either physiological or pathological progression of human physical. C-Kit-mediated signaling pathway has been confirmed to play a key role in MCs proliferation, and the regulatory mechanisms of C-Kit-mediated MCs proliferation need to be further explored. Our previous study found that protein 4.1R could negatively regulate T cell receptor (TCR) mediated signal pathways in CD4 T cells. Little is known about the function of 4.1R in C-Kit-mediated proliferation of MCs. In this study, P815-4.1R cells were constructed by using CRISPR/Cas9 technique. Lack of 4.1R significantly enhanced P815 cells proliferation by accelerating the progression of cell cycle. 4.1R could also significantly alleviate the clinical symptoms of systemic mastocytosis (SM) and improve the overall survival of SM mice. Further study showed that 4.1R could interact directly with C-Kit to inhibit the activation of C-Kit-mediated Ras-Raf-MAPKs and PI3K-AKT signal pathways. Taken together, our findings demonstrate that protein 4.1R, a novel negative regulator, negatively regulates MCs proliferation by inhibiting C-Kit-mediated signal transduction, which maybe provide a potential target to the prevention and treatment of abnormal MCs proliferation-related diseases.

摘要

肥大细胞(MCs)的增殖在人体生理或病理进程中起着至关重要的作用。C-Kit 介导的信号通路已被证实在 MCs 增殖中发挥关键作用,需要进一步探索 C-Kit 介导的 MCs 增殖的调控机制。我们之前的研究发现,蛋白 4.1R 可以负调控 CD4 T 细胞中 T 细胞受体(TCR)介导的信号通路。关于 4.1R 在 C-Kit 介导的 MCs 增殖中的作用知之甚少。在这项研究中,我们使用 CRISPR/Cas9 技术构建了 P815-4.1R 细胞。缺乏 4.1R 可通过加速细胞周期进程显著增强 P815 细胞的增殖。4.1R 还可显著减轻系统性肥大细胞增多症(SM)的临床症状并提高 SM 小鼠的总生存率。进一步的研究表明,4.1R 可以直接与 C-Kit 相互作用,抑制 C-Kit 介导的 Ras-Raf-MAPKs 和 PI3K-AKT 信号通路的激活。综上所述,我们的研究结果表明,蛋白 4.1R 作为一种新型负调控因子,通过抑制 C-Kit 介导的信号转导来负调控 MCs 的增殖,这可能为预防和治疗异常 MCs 增殖相关疾病提供潜在靶点。

相似文献

1
Protein 4.1R negatively regulates P815 cells proliferation by inhibiting C-Kit-mediated signal transduction.蛋白 4.1R 通过抑制 C-Kit 介导的信号转导负调控 P815 细胞的增殖。
Exp Cell Res. 2021 Jan 15;398(2):112403. doi: 10.1016/j.yexcr.2020.112403. Epub 2020 Nov 30.
2
Oncogenic KIT-induced aggressive systemic mastocytosis requires SHP2/PTPN11 phosphatase for disease progression in mice.致癌性KIT诱导的侵袭性系统性肥大细胞增多症在小鼠疾病进展中需要SHP2/PTPN11磷酸酶。
Oncotarget. 2014 Aug 15;5(15):6130-41. doi: 10.18632/oncotarget.2177.
3
Activation of KIT modulates the function of tumor necrosis factor-related apoptosis-inducing ligand receptor (TRAIL-R) in mast cells.KIT 的激活调节肥大细胞中肿瘤坏死因子相关凋亡诱导配体受体(TRAIL-R)的功能。
Allergy. 2015 Jul;70(7):764-74. doi: 10.1111/all.12612. Epub 2015 Apr 16.
4
KIT signaling regulates MITF expression through miRNAs in normal and malignant mast cell proliferation.KIT 信号通路通过 microRNA 调控正常和恶性肥大细胞增殖中的 MITF 表达。
Blood. 2011 Mar 31;117(13):3629-40. doi: 10.1182/blood-2010-07-293548. Epub 2011 Jan 27.
5
RabGEF1 regulates stem cell factor/c-Kit-mediated signaling events and biological responses in mast cells.RabGEF1调节肥大细胞中干细胞因子/c-Kit介导的信号转导事件和生物学反应。
Proc Natl Acad Sci U S A. 2006 Feb 21;103(8):2659-64. doi: 10.1073/pnas.0511191103.
6
Lnk adaptor protein down-regulates specific Kit-induced signaling pathways in primary mast cells.衔接蛋白Lnk下调原代肥大细胞中特定的Kit诱导信号通路。
Blood. 2008 Nov 15;112(10):4039-47. doi: 10.1182/blood-2008-05-154849. Epub 2008 Aug 27.
7
The antitumor activity of homoharringtonine against human mast cells harboring the KIT D816V mutation.高三尖杉酯碱对携带 KIT D816V 突变的人肥大细胞的抗肿瘤活性。
Mol Cancer Ther. 2010 Jan;9(1):211-23. doi: 10.1158/1535-7163.MCT-09-0468. Epub 2010 Jan 6.
8
SWAP-70 regulates c-kit-induced mast cell activation, cell-cell adhesion, and migration.交换蛋白70(SWAP-70)调节c-kit诱导的肥大细胞活化、细胞间黏附及迁移。
Mol Cell Biol. 2004 Dec;24(23):10277-88. doi: 10.1128/MCB.24.23.10277-10288.2004.
9
Mechanisms of STAT protein activation by oncogenic KIT mutants in neoplastic mast cells.致癌性 KIT 突变体激活 STAT 蛋白的机制。
J Biol Chem. 2011 Feb 25;286(8):5956-66. doi: 10.1074/jbc.M110.182642. Epub 2010 Dec 6.
10
Signal transduction-associated and cell activation-linked antigens expressed in human mast cells.在人类肥大细胞中表达的信号转导相关和细胞活化相关抗原。
Int J Hematol. 2002 May;75(4):357-62. doi: 10.1007/BF02982124.

引用本文的文献

1
Cytoskeletal Protein 4.1R in Health and Diseases.细胞骨架蛋白 4.1R 在健康与疾病中的作用
Biomolecules. 2024 Feb 11;14(2):214. doi: 10.3390/biom14020214.