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tRNA Activation02:26

tRNA Activation

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Ribosome Profiling02:24

Ribosome Profiling

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Ribosome profiling or ribo-sequencing is a deep sequencing technique that produces a snapshot of active translation in a cell. It selectively sequences the mRNAs protected by ribosomes to get an insight into a cell’s translation landscape at any given point in time.
Applications of ribosome profiling
Ribosome profiling has many applications, including in vivo monitoring of translation inside a particular organ or tissue type and quantifying new protein synthesis levels.
The technique...
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T Cell Activation and Clonal Selection

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T cells are integral to our adaptive immune system, recognizing and effectively responding to foreign antigens. T cell activation and clonal selection are pivotal in orchestrating this immune response. This article elucidates these mechanisms, detailing the roles of cluster of differentiation (CD) markers, major histocompatibility complex (MHC) molecules, costimulatory signals, and the process of clonal selection.
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When T cells with CD4 markers are activated, they give rise to two types of effector cells: helper T cells and regulatory T cells. Meanwhile, T cells with CD8 markers differentiate into effector cytotoxic T cells. The differentiation of CD4 T cells into helper T cell subsets, such as Th1, Th2, and Th17 cells, is dependent on the antigen type, antigen-presenting cell, and regulatory cytokines.
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General Transcription Factors

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Tissue-specific transcription factors contribute to diverse cellular functions in mammals. For example, the gene for beta globin, a major component of hemoglobin, is present in all cells of the body. However, it is only expressed in red blood cells because the transcription factors that can bind to the promoter sequences of the beta globin gene are only expressed in these cells. Tissue-specific transcription factors also ensure that mutations in these factors may impair only the function of...
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相关实验视频

Updated: Sep 16, 2025

In Vitro Differentiation of Human CD4+FOXP3+ Induced Regulatory T Cells (iTregs) from Naïve CD4+ T Cells Using a TGF-β-containing Protocol
08:20

In Vitro Differentiation of Human CD4+FOXP3+ Induced Regulatory T Cells (iTregs) from Naïve CD4+ T Cells Using a TGF-β-containing Protocol

Published on: December 30, 2016

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全长转录组测序揭示了Treg特定的异形表达在激活时.

Yohei Sato1,2, Erika Osada2, Yoshinobu Manome2

  • 1Project Research Unit, Laboratory of Immune Cell Therapy, The Jikei University School of Medicine, Tokyo 105-8461, Japan.

International journal of molecular sciences
|July 12, 2025
PubMed
概括

调节性T细胞 (Tregs) 呈现出独特的异型组合,包括一个独特的FOXP3异型,这对免疫系统调节至关重要. 这种Treg特异性特征是在T细胞受体刺激后显现的.

关键词:
这是FOXP3P3的.在ISO-seqq中使用.在PD-L1中.在RNA-seqqq.监管性T细胞 (Tregs) 是一种

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Adenoviral Transduction of Naive CD4 T Cells to Study Treg Differentiation
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Adenoviral Transduction of Naive CD4 T Cells to Study Treg Differentiation

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Generation of Induced Regulatory T Cells from Primary Human Naïve and Memory T Cells
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Generation of Induced Regulatory T Cells from Primary Human Naïve and Memory T Cells

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相关实验视频

Last Updated: Sep 16, 2025

In Vitro Differentiation of Human CD4+FOXP3+ Induced Regulatory T Cells (iTregs) from Naïve CD4+ T Cells Using a TGF-β-containing Protocol
08:20

In Vitro Differentiation of Human CD4+FOXP3+ Induced Regulatory T Cells (iTregs) from Naïve CD4+ T Cells Using a TGF-β-containing Protocol

Published on: December 30, 2016

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Adenoviral Transduction of Naive CD4 T Cells to Study Treg Differentiation
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Adenoviral Transduction of Naive CD4 T Cells to Study Treg Differentiation

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Generation of Induced Regulatory T Cells from Primary Human Naïve and Memory T Cells
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Generation of Induced Regulatory T Cells from Primary Human Naïve and Memory T Cells

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科学领域:

  • 免疫学 免疫学 免疫学
  • 分子生物学分子生物学
  • 基因组学就是基因组学.

背景情况:

  • 调节FOXP3+的T细胞 (Tregs) 对免疫平衡至关重要.
  • 人类Tregs独特地表达了一种缺少2 (三角形) 异构体的FOXP3异构体.
  • 假设Tregs具有独特的基因和异型表达特征.

研究的目的:

  • 识别和确认Treg特定的异型组.
  • 调查异形表达在Treg功能中的作用.
  • 分析Tregs与常规T细胞 (Tconvs) 之间的异型使用差异.

主要方法:

  • 长读高通量异形序列化 (Iso-seq) 用于全基因组异形使用分析.
  • 在Tregs和Tconvs之间比较异型表达特征.
  • T细胞受体 (TCR) 刺激试验和PD-L1抗体阻断实验.

主要成果:

  • 通过使用Iso-seq.确定了一个独特的Treg-特定的异型谱.
  • 与Tconvs.不同的是,Tregs优先表达全长FOXP3异型,与Tconvs.不同.
  • 激活的Tregs,但不是Tconvs或非激活的Tregs,在TCR刺激时显示了ICOS和PD-L1的优先表达.
  • PD-L1阻断降低了Treg抑制功能,但没有影响FOXP3表达.

结论:

  • Tregs具有独特的异构体谱,包括特定的FOXP3异构体.
  • 这种独特的曲目在多克隆TCR刺激后变得更加明显.
  • 异形表达在Treg功能和免疫调节中起着重要作用.