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関連する概念動画

Actin Filament Depolymerization01:19

Actin Filament Depolymerization

Actin filaments (F-actin) are composed of actin subunits. The dissociation of actin monomers can occur from either end of F-actin. The rate of dissociation is faster from the minus-end or the pointed end, where the actin subunits exist with a bound ADP, together known as ADP-actin. The depolymerization of F-actin is aided by proteins, including the actin-depolymerizing factor (ADF) and cofilin family of proteins, gelsolin, and glia maturation factor (GMF).
In F-actin, the ADF/cofilin proteins...
Structure of Cadherins01:25

Structure of Cadherins

The cadherins were one of the first cell adhesion molecules discovered; the term “cadherins”   is based on their calcium-dependent adhering properties. The first cadherins discovered on the epithelial, neuronal, and placental cells were named E-cadherin, P-cadherin, and N-cadherin, respectively. These classical cadherins share sequence and structural similarities. Other cadherins, including those involved in cell signaling, are grouped into non-classical cadherins. This diversity of cadherins...
Catenins01:23

Catenins

Catenins are characterized by multiple binding domains and dynamic structures that allow them to function as linker proteins in cell junction complexes. All catenins, except α-catenin, contain a characteristic protein sequence called the armadillo repeat and are therefore also called armadillo proteins.
Catenins in Cell Junctions
Catenins bind to cell adhesion molecules such as cadherins and link them to different cytoskeletal proteins depending on the type of cell junction. At the adherens...
Adherens Junctions01:24

Adherens Junctions

Strong contact points between adjacent cells anchor them to each other, forming tissues. Such anchoring junctions are of two types –  adherens junctions and desmosomes. Adherens junctions are abundant in tissues such as  epithelium and endothelium, forming a continuous zone of adhesion called the adhesion belt. In other tissues, such as  heart muscle, they appear as clusters, linking the cells to produce coordinated heart muscle contraction.
Adherens Junctions are Dynamic
The endothelial cells...
Cadherins in Tissue Organization01:19

Cadherins in Tissue Organization

The cadherins are a superfamily of cell adhesion molecules comprising over 180 variants, with specific tissues expressing a particular combination of cadherin types. Cadherins generally exhibit homophilic binding; i.e., cadherins on one cell bind to cadherins of the same or closely related type on another cell. Thus, cells of the same type have a specific affinity to bind to each other and sort themselves into clusters to form tissues.
Cell Sorting During Development
Cell sorting plays an...
Tension Response at Adherens Junctions01:26

Tension Response at Adherens Junctions

The adherens junctions that anchor cells together are multi-protein complexes that dynamically adapt to mechanical stimuli such as tensile forces and shear stress. Mechanosensory proteins in these junctions can sense such mechanical stimuli and undergo a shift in their conformation, resulting in an altered function — a process called mechanotransduction.
α-Catenin as a Mechanosensory Protein
The α-catenin of adherens junctions is an allosteric protein with three VH (vinculin homology) domains...

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関連する実験動画

Updated: Jul 15, 2026

Bead Aggregation Assays for the Characterization of Putative Cell Adhesion Molecules
08:15

Bead Aggregation Assays for the Characterization of Putative Cell Adhesion Molecules

Published on: October 17, 2014

カデリン-カタニン-アクチン複合体の分解

Soichiro Yamada1, Sabine Pokutta, Frauke Drees

  • 1Department of Molecular and Cellular Physiology, Stanford University School of Medicine, Stanford, CA 94305, USA.

Cell
|December 6, 2005
PubMed
まとめ

E-カデリンのような細胞粘着タンパク質は,β-カタニンとα-カタニン経由でアクチン細胞骨格と結合する. この研究は,アルファ-カタニンがアクチンとカデリン-カタニン複合体を同時に結合しないことを明らかにし,細胞-細胞粘着ダイナミクスの確立されたモデルに挑戦しています.

科学分野:

  • 細胞生物学 細胞生物学
  • 分子生物学と構造生物学について
  • バイオフィジックス 生物物理学

背景:

  • 細胞-細胞結合は組織組織にとって極めて重要です.
  • カデリンは,細胞外相互作用を通じて粘着を媒介する.
  • アクチン細胞骨格との結合は,粘着を安定させると考えられている.

研究 の 目的:

  • アルファ-カタニン,アクチンフィラメント,およびE-カデリン-ベータ-カタニン複合体の間の直接的な相互作用を調査する.
  • カテニンを経由したカデリン-アクチン結合の既存のモデルを検証する.
  • カデリン-カテニン複合体とアクチン細胞骨格の構成要素の動態を分析する.

主な方法:

  • 精製されたタンパク質と隔離された膜を用いたインビトロ結合測定法.
  • 溶液中のタンパク質の相互作用の生体物理学的測定.
  • 光顕微鏡を用いた偏光細胞におけるタンパク質の移動性を生細胞画像化.

主要な成果:

  • アルファ-カテニンは,アクチン繊維とE-カデリン-ベータ-カテニン複合体を同時に結合しません.
  • アクチン結合タンパク質 (ビンキュリン,アルファ-アクチニン) の存在は,同時結合を容易にはしなかった.

さらに関連する動画

Analysis of Cardiomyocyte Development using Immunofluorescence in Embryonic Mouse Heart
10:56

Analysis of Cardiomyocyte Development using Immunofluorescence in Embryonic Mouse Heart

Published on: March 26, 2015

Tuning the Contractility and Deformation Modes of Active Actin-Based Assemblies In Vitro: From Two-Dimensional Active Networks to Liquid Crystal Drops
06:48

Tuning the Contractility and Deformation Modes of Active Actin-Based Assemblies In Vitro: From Two-Dimensional Active Networks to Liquid Crystal Drops

Published on: July 11, 2025

関連する実験動画

Last Updated: Jul 15, 2026

Bead Aggregation Assays for the Characterization of Putative Cell Adhesion Molecules
08:15

Bead Aggregation Assays for the Characterization of Putative Cell Adhesion Molecules

Published on: October 17, 2014

Analysis of Cardiomyocyte Development using Immunofluorescence in Embryonic Mouse Heart
10:56

Analysis of Cardiomyocyte Development using Immunofluorescence in Embryonic Mouse Heart

Published on: March 26, 2015

Tuning the Contractility and Deformation Modes of Active Actin-Based Assemblies In Vitro: From Two-Dimensional Active Networks to Liquid Crystal Drops
06:48

Tuning the Contractility and Deformation Modes of Active Actin-Based Assemblies In Vitro: From Two-Dimensional Active Networks to Liquid Crystal Drops

Published on: July 11, 2025

  • E-カデリン,β-カテニン,アルファ-カテニンの移動性は,アクチンダイナミクスに関係なく,細胞内で類似していました.
  • アクチンおよび関連するタンパク質は,カデリン-カテニン複合体と比較して,より高い運動性を示した.
  • 結論:

    • 直接的なカデリン-カタニン-アクチン結合の確立されたモデルは,直接的な実験的証拠によって支持されていません.
    • カデリン-カテニン複合体とアクチン細胞骨格の間の結合は,これまで考えられていたよりもダイナミックである.
    • これは,細胞粘着におけるカデリン-アクチン相互作用を制御する代替メカニズムまたは規制プロセスを示唆しています.