细胞质actomyosin网络的活跃波动促进了dynein驱动的运输
Takayuki Torisawa1,2, Kei Saito2,3, Ken'ya Furuta4
1Cell Architecture Laboratory, Department of Chromosome Science, National Institute of Genetics, Mishima, Shizuoka 411-8540, Japan.
iScience
|December 24, 2025
概括
像dynein这样的细胞分子电机利用细胞质的波动来实现更快的货物运输. 这项研究揭示了actomyosin网络如何在C. elegans胚胎中积极加速dynein运动蛋白的运动.
科学领域:
- 细胞生物学 细胞生物学
- 生物物理学的生物物理.
- 发展生物学 发展生物学
背景情况:
- 分子电机对于拥挤的细胞环境中的细胞内运输至关重要.
- 细胞质动力学对运动蛋白质效率的确切影响仍然在很大程度上是未知的.
研究的目的:
- 研究细胞质动力学对早期C. elegans胚胎中dynein驱动的运输的影响.
- 阐明了actomyosin网络在调节运动蛋白速率中的作用.
主要方法:
- 在活生生的C. elegans胚胎中观察人工dynein-cargo复合体运输.
- 操纵actomyosin网络活动 (肌化素上调/消耗).
- 在体外测量dynein运动蛋白的力测量.
主要成果:
- 在体内与体外相比,dynein驱动的运输在体内显著更快.
- 由actomyosin网络驱动的细胞质波动加速了dynein的运输.
- 运输速度与肌肉蛋白水平相关,随上调增加,随耗尽减少.
结论:
- 由actomyosin驱动的细胞质波动可以积极加速分子运动运输.
- 迪尼因对波动力的不对称力响应可能有助于提高运输效率.
- 细胞可以利用细胞质动力学来优化拥挤环境中的细胞内运输.
相关概念视频
The Movement of Organelles and Vesicles
6.0K
In eukaryotic cells, cytoskeletal filaments such as actin, microtubules, and intermediate filaments form a mesh-like cytoskeletal network. These filaments serve as tracks for transporting cellular cargo. Specialized motor proteins use the chemical energy stored in adenosine triphosphate (ATP) for this transport. During interphase, microtubules are polarized, with the plus-end towards the cell periphery and the minus-end towards the cell center. Two microtubule-associated motor proteins,...
6.0K
Microtubule Associated Motor Proteins
10.1K
Eukaryotic cells have different motor proteins for transporting various cargo within the cell. These motor proteins differ based on the filament they associate with, the direction they move within the cell, and the type of cargo they transport. Motor proteins that associate with microtubules are known as microtubule-associated motor proteins. There are two families of microtubule-associated motor proteins —Kinesins and Dyneins. Both these proteins assist in the transport of cellular...
10.1K
Mechanism of Ciliary Motion
4.8K
The ciliary structures were first seen in 1647 by Antonie Leeuwenhoek while observing the protozoans. In lower organisms, these appendages are responsible for cell movement, while in higher organisms, these appendages help in the movement of the extracellular fluids within the body cavities.
The cilia are made up of microtubules in a 9+2 arrangement, with nine microtubule doublet ring bundles, surrounding a pair of central singlet microtubule bundles. The doublet microtubule bundles are...
The cilia are made up of microtubules in a 9+2 arrangement, with nine microtubule doublet ring bundles, surrounding a pair of central singlet microtubule bundles. The doublet microtubule bundles are...
4.8K
Adaptability of Cytoskeletal Filaments
5.6K
The cytoskeleton is a complex dynamic structure performing varied functions based on cellular requirements. The adaptability of the individual filaments in the cytoskeleton determines their ability to perform various functions within the cell. It can undergo rapid reorganization during processes like cell division or remain stable for several hours as in the interphase. The adaptability of these filaments depends on stringent regulatory mechanisms. The microfilament and microtubules of the...
5.6K
Cytoskeletal Coordination in Cell Migration
5.4K
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...
5.4K
Anaphase A and B
5.3K
Microtubules form through the end-to-end polymerization of tubulin heterodimers. Kinetochore microtubules originate from the spindle poles, and their plus-ends connect with the kinetochores on sister-chromatids. Ndc80 protein complexes, present on the kinetochore, form low-affinity links with the plus end of these kinetochore microtubules.
Plus-end depolymerization releases tubulin heterodimers from the terminal region of the microtubule. As tubulin subunits are lost, the Ndc80 complexes detach...
Plus-end depolymerization releases tubulin heterodimers from the terminal region of the microtubule. As tubulin subunits are lost, the Ndc80 complexes detach...
5.3K


