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関連する概念動画

Assembly of Signaling Complexes01:30

Assembly of Signaling Complexes

Multiprotein signaling complexes are formed in a dynamic process involving protein-protein interactions at the cytoplasmic domain of transmembrane receptors or enzymatic and non-enzymatic proteins associated with the receptor. These complexes ensure the activation and propagation of intracellular signals that regulate cell functions.
Interaction domains in cell signaling
Interaction domains recognize exposed features of their binding partners containing post-translationally modified sequences,...
Immunoglobulin-like Cell Adhesion Molecules01:31

Immunoglobulin-like Cell Adhesion Molecules

Immunoglobulin-like cell adhesion molecules or Ig-CAMs are a versatile group of cell surface glycoproteins belonging to the immunoglobulin protein superfamily. Ig-CAMs possess the characteristic immunoglobulin protein domains and other domains such as the fibronectin type III domain. The Ig domains are glycosylated to varying degrees in different Ig-CAMs.
Ig-CAMs exhibit either homophilic binding (to other Ig-CAMs) or heterophilic binding (to other ligands such as integrins). While most Ig-CAMs...
Antigens Involved in Adaptive Immunity01:26

Antigens Involved in Adaptive Immunity

An antigen is any substance the immune system identifies as foreign and potentially harmful to the body, prompting an immune response. Antigens have two functional properties: immunogenicity and reactivity. Immunogenicity is the ability of an antigen to stimulate a specific immune response. At the same time, reactivity describes the antigen's ability to react with the cells and antibodies produced in response to it.
Complete Antigens
Complete antigens possess both immunogenicity and reactivity.
T Cell Activation and Clonal Selection01:22

T Cell Activation and Clonal Selection

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.
Naive T cells that have not yet encountered an antigen express two primary CD...
Cytotoxic T Cells-mediated Immune Response01:27

Cytotoxic T Cells-mediated Immune Response

Cytotoxic T cells are a vital component of the immune system. They have the remarkable ability to identify and target antigens on infected or abnormal cells. These antigens often originate from intracellular pathogens such as viruses or abnormal proteins cancer cells produce.
Immunological surveillance is the ability of immune cells to monitor and eliminate infected cells with intracellular pathogens, neoplastically transformed cells, and cells with non-self antigens. Cytotoxic T cells and NK...
B Cell Activation and Differentiation01:24

B Cell Activation and Differentiation

The adaptive immune response, a sophisticated defense mechanism, relies on the activation and differentiation of B lymphocytes, or B cells. These processes enable our bodies to mount a tailored response against specific pathogens such as bacteria, free virus particles, toxins, and parasites.
When naive B cells encounter a specific antigen that can bind to the B cell receptor (BCR) on their surface, they undergo sensitization to respond to the antigen's presence. Sensitization begins with...

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関連する実験動画

Updated: May 11, 2026

Real-time Live Imaging of T-cell Signaling Complex Formation
10:31

Real-time Live Imaging of T-cell Signaling Complex Formation

Published on: June 23, 2013

人間のCTLA-4/B7-2複合体による共刺激の構造的基礎

J C Schwartz1, X Zhang, A A Fedorov

  • 1[1] Department of Microbiology and Immunology, [2] These authors contributed equally to this work.

Nature
|March 30, 2001
PubMed
まとめ

CTLA-4 (細胞毒性Tリンパ球関連タンパク質4) とB7-2の相互作用の構造は,T細胞の反応がどのように調節されているかを明らかにします. この発見は,免疫調節と潜在的な治療目標についての洞察を提供します.

科学分野:

  • 免疫学 免疫学とは
  • 構造生物学 構造生物学とは
  • 分子医学は分子医学である.

背景:

  • T細胞の活動は,CD28およびCTLA-4受容体からの共刺激信号に依存しています.
  • CD28の関与はT細胞を刺激し,CTLA-4の関与は反応を弱める.
  • CTLA-4とCD28経路は,自己免疫疾患,移植拒絶,がん免疫療法における主要な標的である.

研究 の 目的:

  • CTLA-4とB7-2の相互作用の構造的基礎を解明する.
  • これらの受容体/リガンド複合体の細胞表面組織を理解するために.
  • T細胞の信号調節のための分子モデルを提供すること.

主な方法:

  • 人間のB7-2受容体結合ドメインと複合したヒトCTLA-4ジメルの3.2-Å解像度の結晶構造を決定した.

主要な成果:

  • 構造は,CTLA-4とB7-2の異常な二分化を示し,二分界面から離れているリガンド結合部位を示した.
  • 双価CTLA-4とB7-2ジメルの交互の配置が観察され,拡張ネットワークを形成した.
  • このネットワークは,免疫学的シナプス内の分子組織のモデルを示唆しています.

結論:

さらに関連する動画

Visualizing the Actin and Microtubule Cytoskeletons at the B-cell Immune Synapse Using Stimulated Emission Depletion (STED) Microscopy
11:00

Visualizing the Actin and Microtubule Cytoskeletons at the B-cell Immune Synapse Using Stimulated Emission Depletion (STED) Microscopy

Published on: April 9, 2018

Use of Single Chain MHC Technology to Investigate Co-agonism in Human CD8+ T Cell Activation
12:09

Use of Single Chain MHC Technology to Investigate Co-agonism in Human CD8+ T Cell Activation

Published on: February 28, 2019

関連する実験動画

Last Updated: May 11, 2026

Real-time Live Imaging of T-cell Signaling Complex Formation
10:31

Real-time Live Imaging of T-cell Signaling Complex Formation

Published on: June 23, 2013

Visualizing the Actin and Microtubule Cytoskeletons at the B-cell Immune Synapse Using Stimulated Emission Depletion (STED) Microscopy
11:00

Visualizing the Actin and Microtubule Cytoskeletons at the B-cell Immune Synapse Using Stimulated Emission Depletion (STED) Microscopy

Published on: April 9, 2018

Use of Single Chain MHC Technology to Investigate Co-agonism in Human CD8+ T Cell Activation
12:09

Use of Single Chain MHC Technology to Investigate Co-agonism in Human CD8+ T Cell Activation

Published on: February 28, 2019

  • CTLA-4/B7-2ネットワーク構造は,免疫シナプスにおける周期的組織のモデルを提供します.
  • この構造は,二次元細胞表面受容体のユニークなシグナル伝達機構を示唆しています.
  • この相互作用を理解することは,標的型免疫療法の開発に不可欠です.