Jove
Visualize
联系我们
JoVE
x logofacebook logolinkedin logoyoutube logo
关于 JoVE
概览领导团队博客JoVE 帮助中心
作者
出版流程编辑委员会范围与政策同行评审常见问题投稿
图书馆员
用户评价订阅访问资源图书馆顾问委员会常见问题
研究
JoVE JournalMethods CollectionsJoVE Encyclopedia of Experiments存档
教育
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab Manual教师资源中心教师网站
使用条款与条件
隐私政策
政策

相关概念视频

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
The Cell Cycle Control System01:28

The Cell Cycle Control System

2.8K
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...
2.8K
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
Inhibition of Cdk Activity02:34

Inhibition of Cdk Activity

4.7K
The orderly progression of the cell cycle depends on the activation of Cdk protein by binding to its cyclin partner. However, the cell cycle must be restricted when undergoing abnormal changes. Most cancers correlate to the deregulated cell cycle, and since Cdks are a central component of the cell cycle, Cdk inhibitors are extensively studied to develop anticancer agents. For instance, cyclin D associates with several Cdks, such as Cdk 4/6, to form an active complex. The cyclin D-Cdk4/6 complex...
4.7K

您也可能阅读

相关文章

通过共同作者、期刊和引用图与本文相关的文章。

排序
Same author

Optimal experiment design for practical parameter identifiability and model discrimination.

Mathematical biosciences·2026
Same author

Galvanin (TMEM154) is an electric-field sensor for directed cell migration.

Cell·2026
Same author

Modeling Collective Cell Migration in a Data-Rich Age: Challenges and Opportunities for Data-Driven Modeling.

Cold Spring Harbor perspectives in biology·2026
Same author

A likelihood-based Bayesian inference framework for the calibration of and selection between stochastic velocity-jump models.

Journal of the Royal Society, Interface·2026
Same author

Epigenetic control of microglial developmental milestones from proliferative progenitors to efficient phagocytes.

Research square·2026
Same author

Collective transitions from orbiting to matrix invasion in three-dimensional multicellular spheroids.

Nature physics·2026
Same journal

Tau protein differentially affects Piezo1 and Kir2.1 channels in brain capillary endothelial cells.

Biophysical journal·2026
Same journal

Emergent Intercellular Junction Stability during Cyclic Tissue Loading.

Biophysical journal·2026
Same journal

Enhanced-Sampling Simulations Reveal Distinct Intermediates in SARS-CoV-2 FSE Pseudoknot Interconversion.

Biophysical journal·2026
Same journal

Structure-based simulations of the full Flock House virus capsid reveal pathways and energetics of an infection-critical peptide externalization event.

Biophysical journal·2026
Same journal

Quantifying the Peripheral Surface Information Entropy from Conformational Ensembles of Globular Protein-Peptide Complexes.

Biophysical journal·2026
Same journal

Anisotropic unbinding and location-dependent hovering of a kinesin motor head over microtubule.

Biophysical journal·2026
查看所有相关文章

相关实验视频

Updated: Jun 27, 2025

Analysis of Cell Cycle Position in Mammalian Cells
12:19

Analysis of Cell Cycle Position in Mammalian Cells

Published on: January 21, 2012

60.4K

通过组织拥挤量化细胞循环调节的量化.

Carles Falcó1, Daniel J Cohen2, José A Carrillo1

  • 1Mathematical Institute, University of Oxford, Oxford, United Kingdom.

Biophysical journal
|May 8, 2024
PubMed
概括
此摘要是机器生成的。

细胞感知组织密度,并相应地调整它们的分裂速率,从而影响细胞迁移. 这项研究量化了拥挤如何影响组织扩张期间的细胞循环阶段.

更多相关视频

Measuring Cell Cycle Progression Kinetics with Metabolic Labeling and Flow Cytometry
11:23

Measuring Cell Cycle Progression Kinetics with Metabolic Labeling and Flow Cytometry

Published on: May 22, 2012

21.1K
Temporal Tracking of Cell Cycle Progression Using Flow Cytometry without the Need for Synchronization
08:52

Temporal Tracking of Cell Cycle Progression Using Flow Cytometry without the Need for Synchronization

Published on: August 16, 2015

19.2K

相关实验视频

Last Updated: Jun 27, 2025

Analysis of Cell Cycle Position in Mammalian Cells
12:19

Analysis of Cell Cycle Position in Mammalian Cells

Published on: January 21, 2012

60.4K
Measuring Cell Cycle Progression Kinetics with Metabolic Labeling and Flow Cytometry
11:23

Measuring Cell Cycle Progression Kinetics with Metabolic Labeling and Flow Cytometry

Published on: May 22, 2012

21.1K
Temporal Tracking of Cell Cycle Progression Using Flow Cytometry without the Need for Synchronization
08:52

Temporal Tracking of Cell Cycle Progression Using Flow Cytometry without the Need for Synchronization

Published on: August 16, 2015

19.2K

科学领域:

  • 细胞生物学 细胞生物学
  • 生物物理学的生物物理.
  • 数学建模的数学建模

背景情况:

  • 细胞增殖和迁移对于发育和组织修复至关重要.
  • 机械力和组织拥挤影响细胞分裂速度.
  • 细胞循环调节对细胞迁移的确切影响尚不清楚.

研究的目的:

  • 开发一个最小连续模型,整合细胞迁移和细胞周期动态.
  • 量化组织拥挤对不同细胞周期阶段细胞增殖的影响.
  • 阐明密度依赖的增殖和细胞迁移模式之间的关系.

主要方法:

  • 细胞迁移的最小连续模型与细胞周期动态.
  • 参数估计的贝叶斯推理.
  • 对表皮组织扩张的实验数据的分析.

主要成果:

  • 该模型展示了在G1和S/G2/M阶段细胞周期进展的密度依赖调节.
  • 细胞周期阶段持续时间和局部组织密度之间的量化关系.
  • 模型预测与细胞循环调节和迁移的实验观测保持一致.

结论:

  • 细胞根据局部组织密度动态调整增殖率.
  • 密度感应机制为集体细胞迁移提供了机械洞察力.
  • 该研究提供了一个系统的框架,用于在组织动态的背景下分析细胞周期数据.