可变形细胞的移动性诱导相位分离
Austin Hopkins1, Benjamin Loewe2, Michael Chiang2
1Department of Physics, University of California Santa Barbara, Santa Barbara, CA 93106, USA. austinhopkins@ucsb.edu.
Soft matter
|October 18, 2023
概括
粒子变形性通过增加碰撞持续时间来增强运动性诱导相分离 (MIPS). 软细胞表现出更有效的MIPS和混乱的密集区域,影响生物自我组织.
科学领域:
- 物理 物理学 物理
- 生物物理学的生物物理.
- 软物质物理学 软物质物理学
背景情况:
- 机动性诱导相位分离 (MIPS) 描述了活性物质系统中的自我组织.
- 细胞刚性或可变性是影响细胞行为和相互作用的关键物理参数.
研究的目的:
- 研究粒子变形能力对运动性诱导相位分离 (MIPS) 的影响.
- 了解细胞硬度的变化如何影响相隔生物系统的动态和结构.
主要方法:
- 利用多相场模型来模拟粒子相互作用.
- 量化了粒子变形性和MIPS效率之间的关系.
主要成果:
- 与刚性粒子相比,纯粹排斥性的可变形粒子表现出更有效的MIPS.
- 增加的粒子变形性导致更长的有效碰撞时间.
- 在MIPS过程中形成的密集区域随着粒子变形能力的增加而变得更加混乱.
结论:
- 粒子变形性显著影响MIPS的有效性和特性.
- 这些发现为MIPS的生物相关性及其在细胞自我组织中的作用提供了背景.
- 细胞硬度是理解集体细胞行为和新兴结构的关键因素.
相关概念视频
Cell Motility through Blebbing
1.9K
Blebs are a type of membrane protrusion formed by the internal hydrostatic pressure of the cytoplasm. Blebs are observed in several cell types, including fibroblasts, immune cells, and single-celled organisms like the amoeba. The primary function of blebs is cell locomotion and apoptosis, but they are also found during necrosis and cell division. The life cycle of a bleb comprises an initiation phase followed by the expansion and retraction phases.
Blebbing Through the Matrix
In multicellular...
Blebbing Through the Matrix
In multicellular...
1.9K
Determining the Plane of Cell Division
3.3K
Positioning the cell division plane is a critical step during development and cell differentiation, particularly during mitosis when the plane is essential for determining the size of the two daughter cells. The cell division plane is perpendicular to the plane of chromosome segregation, but different types of organisms have different cell division mechanisms to suit their morphology and function.
Animal cells
In animal cells, the cleavage furrow forms along the plane of cell division...
Animal cells
In animal cells, the cleavage furrow forms along the plane of cell division...
3.3K
Cell Migration
17.0K
Cell migration, the process by which cells move from one location to another, is essential for the proper development and viability of organisms throughout their life. When cells are not able to migrate properly to their ordained locations, various disorders may occur. For example, disruption in cell migration causes chronic inflammatory diseases such as arthritis.
17.0K
Mechanism of Lamellipodia Formation
2.6K
Cells migrating in response to external stimuli form lamellipodia, which are thin membrane protrusions supported by a mesh of linked, branched, or unbranched actin filaments. These actin filaments interact with myosin motor proteins, creating the dynamic actomyosin complex within the cytoskeleton. Contractility, or the ability to generate contractile stress, is inherent to the actomyosin complex. It helps cells detect the stiffness of the surrounding ECM and exert contractile force for...
2.6K
Cytoskeletal Coordination in Cell Migration
4.8K
A migrating cell changes its shape during the cyclic events of attachment and detachment from the substratum and repositions the cell organelles correspondingly. These complex events are orchestrated by the dynamic cytoskeletal network comprising actin filaments, intermediate filaments, and microtubules. Cytoskeletal crosstalk — the direct and indirect communication between the different components — is crucial for this coordination. Direct communication involves various linker...
4.8K
Role of Myosin in Cell Migration
2.3K
Myosins are multimeric motor proteins involved in various cellular processes such as migration, adhesion, and proliferation. Myosin II is the most common type in animal cells, which binds and cross-links actin filaments.
Myosin II is a hexamer comprising two heavy chains with globular heads and coiled-coil tails, two regulatory light chains, and two essential light chains. The ATPase sites on the myosin heads hydrolyze ATP, and the released phosphate generates the force for contraction....
Myosin II is a hexamer comprising two heavy chains with globular heads and coiled-coil tails, two regulatory light chains, and two essential light chains. The ATPase sites on the myosin heads hydrolyze ATP, and the released phosphate generates the force for contraction....
2.3K


