• 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

激活诱导的 B 细胞命运是由细胞内随机竞争决定的。

Activation-induced B cell fates are selected by intracellular stochastic competition.

机构信息

Hamilton Institute, National University of Ireland, Maynooth, Ireland.

出版信息

Science. 2012 Jan 20;335(6066):338-41. doi: 10.1126/science.1213230. Epub 2012 Jan 5.

DOI:10.1126/science.1213230
PMID:22223740
Abstract

In response to stimulation, B lymphocytes pursue a large number of distinct fates important for immune regulation. Whether each cell's fate is determined by external direction, internal stochastic processes, or directed asymmetric division is unknown. Measurement of times to isotype switch, to develop into a plasmablast, and to divide or to die for thousands of cells indicated that each fate is pursued autonomously and stochastically. As a consequence of competition between these processes, censorship of alternative outcomes predicts intricate correlations that are observed in the data. Stochastic competition can explain how the allocation of a proportion of B cells to each cell fate is achieved. The B cell may exemplify how other complex cell differentiation systems are controlled.

摘要

受到刺激后,B 淋巴细胞会选择多种不同的命运,这些命运对免疫调节很重要。目前尚不清楚每个细胞的命运是由外部导向、内部随机过程还是定向不对称分裂决定的。对数千个细胞的同种型转换、发育为浆母细胞、分裂或死亡的时间进行测量表明,每种命运都是自主和随机追求的。由于这些过程之间的竞争,对替代结果的审查预测了在数据中观察到的复杂相关性。随机竞争可以解释如何将一部分 B 细胞分配到每个细胞命运。B 细胞可以例证其他复杂的细胞分化系统是如何被控制的。

相似文献

1
Activation-induced B cell fates are selected by intracellular stochastic competition.激活诱导的 B 细胞命运是由细胞内随机竞争决定的。
Science. 2012 Jan 20;335(6066):338-41. doi: 10.1126/science.1213230. Epub 2012 Jan 5.
2
Evidence from the generation of immunoglobulin G-secreting cells that stochastic mechanisms regulate lymphocyte differentiation.来自分泌免疫球蛋白G细胞生成的证据表明,随机机制调节淋巴细胞分化。
Nat Immunol. 2004 Jan;5(1):55-63. doi: 10.1038/ni1016. Epub 2003 Nov 30.
3
B-cell differentiation: instructive one day, stochastic the next.B 细胞分化:有指导的一天,随机的下一天。
Curr Biol. 2012 Apr 10;22(7):R235-7. doi: 10.1016/j.cub.2012.02.045.
4
Models for the dynamics and order of immunoglobulin isotype switching.免疫球蛋白同种型转换的动力学和顺序模型。
Bull Math Biol. 2005 Jan;67(1):15-32. doi: 10.1016/j.bulm.2004.05.007.
5
Switching to IgG3, IgG2b, and IgA is division linked and independent, revealing a stochastic framework for describing differentiation.转换为IgG3、IgG2b和IgA是与细胞分裂相关且相互独立的,揭示了一个用于描述分化的随机框架。
J Immunol. 1999 Nov 1;163(9):4707-14.
6
Stochastically Timed Competition Between Division and Differentiation Fates Regulates the Transition From B Lymphoblast to Plasma Cell.随机定时的分裂与分化命运竞争调控 B 淋巴母细胞向浆细胞的转变。
Front Immunol. 2018 Sep 10;9:2053. doi: 10.3389/fimmu.2018.02053. eCollection 2018.
7
On the impact of correlation between collaterally consanguineous cells on lymphocyte population dynamics.关于旁系血亲细胞间相关性对淋巴细胞群体动态的影响。
J Math Biol. 2009 Aug;59(2):255-85. doi: 10.1007/s00285-008-0231-x. Epub 2008 Oct 28.
8
Modeling T- and B-cell growth and differentiation.模拟T细胞和B细胞的生长与分化。
Immunol Rev. 2007 Apr;216:119-29. doi: 10.1111/j.1600-065X.2006.00498.x.
9
Integrating signals from IFN-gamma and IL-4 by B cells: positive and negative effects on CD40 ligand-induced proliferation, survival, and division-linked isotype switching to IgG1, IgE, and IgG2a.B细胞整合来自IFN-γ和IL-4的信号:对CD40配体诱导的增殖、存活以及与分裂相关的向IgG1、IgE和IgG2a的同种型转换的正负效应。
J Immunol. 1999 Oct 15;163(8):4175-81.
10
T-BAM/CD40-L on helper T lymphocytes augments lymphokine-induced B cell Ig isotype switch recombination and rescues B cells from programmed cell death.辅助性T淋巴细胞上的T-BAM/CD40-L增强淋巴因子诱导的B细胞免疫球蛋白同种型转换重组,并使B细胞免于程序性细胞死亡。
J Immunol. 1994 Mar 1;152(5):2163-71.

引用本文的文献

1
Cell cycle-coupled transcriptional network orchestrates human B cell fate bifurcation.细胞周期耦合转录网络调控人类B细胞命运分化。
bioRxiv. 2025 Jun 25:2025.04.23.649973. doi: 10.1101/2025.04.23.649973.
2
Computational modelling of aggressive B-cell lymphoma.侵袭性B细胞淋巴瘤的计算建模
Biochem Soc Trans. 2025 Jul 4. doi: 10.1042/BST20253039.
3
Type I interferon promotes the fate of Toll-like receptor 9-stimulated follicular B cells to plasma cell differentiation.I型干扰素促进Toll样受体9刺激的滤泡B细胞向浆细胞分化的命运。
PNAS Nexus. 2024 Apr 17;3(4):pgae152. doi: 10.1093/pnasnexus/pgae152. eCollection 2024 Apr.
4
A neural network-based model framework for cell-fate decisions and development.基于神经网络的细胞命运决策与发育模型框架。
Commun Biol. 2024 Mar 14;7(1):323. doi: 10.1038/s42003-024-05985-1.
5
B cell memory: from generation to reactivation: a multipronged defense wall against pathogens.B细胞记忆:从产生到重新激活——抵御病原体的多层面防御壁垒
Cell Death Discov. 2024 Mar 7;10(1):117. doi: 10.1038/s41420-024-01889-5.
6
Reversible, tunable epigenetic silencing of TCF1 generates flexibility in the T cell memory decision.TCF1 的可逆、可调控表观遗传沉默赋予 T 细胞记忆决策的灵活性。
Immunity. 2024 Feb 13;57(2):271-286.e13. doi: 10.1016/j.immuni.2023.12.006. Epub 2024 Jan 31.
7
p53 and p21 dynamics encode single-cell DNA damage levels, fine-tuning proliferation and shaping population heterogeneity.p53 和 p21 的动态变化可编码单个细胞的 DNA 损伤水平,精细调节细胞增殖并塑造群体异质性。
Commun Biol. 2023 Nov 24;6(1):1196. doi: 10.1038/s42003-023-05585-5.
8
Modeling T Cell Fate.建模 T 细胞命运。
Annu Rev Immunol. 2023 Apr 26;41:513-532. doi: 10.1146/annurev-immunol-101721-040924.
9
Cyton2: A Model of Immune Cell Population Dynamics That Includes Familial Instructional Inheritance.Cyton2:一种包含家族性指令遗传的免疫细胞群体动力学模型。
Front Bioinform. 2021 Oct 26;1:723337. doi: 10.3389/fbinf.2021.723337. eCollection 2021.
10
Temporally dynamic antagonism between transcription and chromatin compaction controls stochastic photoreceptor specification in flies.转录和染色质紧缩之间的时间动态拮抗作用控制了果蝇中随机光感受器的特化。
Dev Cell. 2022 Aug 8;57(15):1817-1832.e5. doi: 10.1016/j.devcel.2022.06.016. Epub 2022 Jul 13.