Jove
Visualize
お問い合わせ
JoVE
x logofacebook logolinkedin logoyoutube logo
JoVEについて
概要リーダーシップブログJoVEヘルプセンター
著者向け
出版プロセス編集委員会範囲と方針査読よくある質問投稿
図書館員向け
推薦の声購読アクセスリソース図書館諮問委員会よくある質問
研究
JoVE JournalMethods CollectionsJoVE Encyclopedia of Experimentsアーカイブ
教育
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab Manual教員リソースセンター教員サイト
利用規約
プライバシーポリシー
ポリシー

関連する概念動画

The Cell Cycle Control System01:28

The Cell Cycle Control System

2.9K
The cell cycle regulation directs how a cell proceeds from one phase to the next and begins mitosis. The cell cycle control system includes intracellular regulatory molecules and external triggers. They provide "stop" or "advance" signals and operate at specific cell cycle stages termed checkpoints to ensure that a particular process is completed before the cell advances to the next phase.
Cyclins and cyclin-dependent kinases (Cdks) are the primary cell cycle regulators and...
2.9K
The Spindle Assembly Checkpoint02:19

The Spindle Assembly Checkpoint

3.2K
The spindle assembly checkpoint is a molecular surveillance mechanism ensuring the fidelity of chromosome segregation during anaphase. The checkpoint monitors the completion of all the prerequisite steps before chromosome segregation to determine whether the segregation process should proceed or be delayed.
Many proteins function together to control the spindle assembly checkpoint. Mutations affecting these proteins may allow cells to proceed into anaphase prematurely, resulting in the...
3.2K
M-Cdk Drives Transition Into Mitosis02:15

M-Cdk Drives Transition Into Mitosis

5.6K
Checkpoints throughout the cell cycle serve as safeguards and gatekeepers, allowing the cell cycle to progress in favorable conditions and slow or halt it in problematic ones. This regulation is known as the cell cycle control system.
Cyclin-dependent kinases, or Cdks, work in concert with cyclins to control cell cycle transitions. M-Cdk, a complex of Cdk1 bound to M cyclin, is a well-known example of this coordinated control that drives the transition from the G2 to the M phase.
M cyclin...
5.6K
Molecular Factors Affecting Cell Division01:27

Molecular Factors Affecting Cell Division

3.1K
Several external and internal factors influence the initiation and inhibition of cell division. For instance, the death of nearby cells or the release of human growth hormone (hGH) promotes cell division. In contrast, lack of hGH or crowding of cells can inhibit cell division.
Several proteins function as internal regulators to ensure each cell cycle stage is completed faithfully before proceeding to the next. Regulator molecules may act directly or influence the activity or production of other...
3.1K
Separation of Sister Chromatids02:17

Separation of Sister Chromatids

3.6K
At the transition from prophase to metaphase, there is a reduction in cohesion along the chromosomal arms, resulting in the resolution of sister chromatids. However, residual cohesin connections remain to hold the sister chromatids together until the transition from metaphase to anaphase. The residual connection prevents any premature separation of sister chromatids, blocking the risks of aneuploidy within the daughter cells.
At the onset of anaphase, separase, a proteolytic enzyme, is...
3.6K
Cells Coordinate Growth and Proliferation02:36

Cells Coordinate Growth and Proliferation

4.5K
Cell size is a significant factor impacting cellular design, function, and fitness. There exists some internal coordination by which cells double their masses before division, thus, achieving homeostasis. Coordination between cell growth and proliferation depends on the checkpoints in between cell cycle phases. Loss of coordination or failure in the checkpoint mechanism can drive the cell to uncontrolled growth and loss of cellular function. Like dividing cells that coordinate cellular growth,...
4.5K

こちらも読む

関連記事

共著者、ジャーナル、引用グラフによってこの研究に関連する記事。

並び替え
Same author

Endogenous p21 levels protect genomic stability by suppressing both excess and restrained nascent DNA syntheses.

Science advances·2025
Same author

All roads lead to mitosis: A common requirement for DNA replication stress-dependent and -independent killing of BRCA-deficient cells.

Mutation research. Reviews in mutation research·2025
Same author

Improving therapeutic strategies for triple-negative breast cancer: synergistic effects of DKC1 inhibition and paclitaxel.

Expert opinion on therapeutic targets·2025
Same author

Versatile enhancement of the killing potential of anti-cancer agents achieved by peptide mimetics of the PCNA interface towards specialized DNA polymerases.

Cell death & disease·2025
Same author

Buenos Aires Breast Cancer Symposium 2024: bridging basic and clinical research in breast cancer.

Medicina·2025
Same author

Conserved cysteine-switches for redox sensing operate in the cyclin-dependent kinase inhibitor p21(CIP/KIP) protein family.

Free radical biology & medicine·2024

関連する実験動画

Updated: Jun 29, 2025

Live Cell Imaging to Assess the Dynamics of Metaphase Timing and Cell Fate Following Mitotic Spindle Perturbations
07:14

Live Cell Imaging to Assess the Dynamics of Metaphase Timing and Cell Fate Following Mitotic Spindle Perturbations

Published on: September 20, 2019

8.2K

細胞 の 運命 を 決定 する ミト 的な ストップ 時計

Agustina P Bertolin1, Vanesa Gottifredi2

  • 1The Francis Crick Institute, London, UK.

Science (New York, N.Y.)
|March 28, 2024
PubMed
まとめ

損傷した細胞の拡散を防ぐには 細胞分裂のタイミングを監視することが重要です この監視メカニズムは ゲノムの安定性と細胞の健康を保証します

科学分野:

  • 細胞生物学
  • 遺伝学
  • 分子生物学

背景:

  • ゲノム不安定を防ぐには 細胞循環の調節が不可欠です
  • 細胞分裂の誤りは 損傷した細胞の蓄積につながります
  • ミトスのタイミングは 細胞サイクルにおける重要なチェックポイントです

研究 の 目的:

  • 損傷した細胞の増殖を防止するミトスのタイミングの役割を調査する.
  • 細胞が細胞分裂の誤りを監視し 修正するメカニズムを理解する.
  • 癌のような病気のミトス・タイム・デフェクトの 影響を調べるため

主な方法:

  • 活細胞画像を用いて 線維細胞の進行をリアルタイムで監視した.
  • 遺伝子スクリーニングを用い ミトスのタイミングの重要なレギュレータを特定した.
  • タンパク質の相互作用と翻訳後の改変を分析するために生化学的測定を行った.

主要な成果:

  • ミトーシスの持続時間を 監視する新しい経路を発見しました
  • この経路の欠陥が 細胞死と血管新生を増加させることが示されました
  • 特定された特定のタンパク質は,異常なミトスのタイミングを感知し,それに反応する.

さらに関連する動画

Long-term Live-cell Imaging to Assess Cell Fate in Response to Paclitaxel
08:29

Long-term Live-cell Imaging to Assess Cell Fate in Response to Paclitaxel

Published on: May 14, 2018

9.9K
Live Cell Imaging of Chromosome Segregation During Mitosis
06:39

Live Cell Imaging of Chromosome Segregation During Mitosis

Published on: March 14, 2018

9.3K

関連する実験動画

Last Updated: Jun 29, 2025

Live Cell Imaging to Assess the Dynamics of Metaphase Timing and Cell Fate Following Mitotic Spindle Perturbations
07:14

Live Cell Imaging to Assess the Dynamics of Metaphase Timing and Cell Fate Following Mitotic Spindle Perturbations

Published on: September 20, 2019

8.2K
Long-term Live-cell Imaging to Assess Cell Fate in Response to Paclitaxel
08:29

Long-term Live-cell Imaging to Assess Cell Fate in Response to Paclitaxel

Published on: May 14, 2018

9.9K
Live Cell Imaging of Chromosome Segregation During Mitosis
06:39

Live Cell Imaging of Chromosome Segregation During Mitosis

Published on: March 14, 2018

9.3K

結論:

  • 細胞の完全性を維持するための基本的なメカニズムである.
  • ミトスタイミングの制御不良は 遺伝的不安定性と病気の発生に寄与する.
  • ミトスのタイミング経路をターゲットにすることで,がん治療の治療戦略を提供することができます.