在MDCK细胞的顶端和底侧内细胞囊泡之间体外微管和运动依赖的融合
M Bomsel1, R Parton, S A Kuznetsov
1European Molecular Biology Laboratory, Heidelberg, Federal Republic of Germany.
Cell
|August 24, 1990
概括
细胞内细胞形成的途径在晚期内体中合并. 在体外复制后,这个过程需要微管和运动蛋白质,如素和素,用于囊泡融合.
科学领域:
- 细胞生物学 细胞生物学
- 分子生物学分子生物学
- 皮质细胞生物学 皮质细胞生物学
背景情况:
- 皮质细胞利用不同的顶端和底侧内细胞突变通路.
- 众所周知,这些通路聚集在细胞内的晚期内体.
- 了解这种趋同对于细胞贩运和功能至关重要.
研究的目的:
- 复制和分析顶和底侧内细胞囊泡与晚期内体的体外融合.
- 确定在无细胞系统中内细胞通路的融合所需的分子要求.
- 研究微管和相关蛋白质在这个过程中的作用.
主要方法:
- 开发一种无细胞检测法,以测量囊泡与晚期内分泌体的融合.
- 利用马丁-达比犬细胞 (MDCK) 来研究表皮内细胞.
- 对微管体依赖蛋白质需求的生物化学分析.
主要成果:
- 在体外复制的内细胞囊泡融合与晚期内体是成功的.
- 发现聚合微管对于这种体外融合过程至关重要.
- 确定了微管结合蛋白,包括素和细胞质二烯,是关键成分.
结论:
- 顶端和底侧内细胞突变途径的融合依赖于微管体依赖的机制.
- 机械化学电机氨酸和氨酸在介导晚期内分泌体的囊泡融合中发挥着重要作用.
- 这种无细胞系统为剖析内细胞通路融合的分子机制提供了有价值的工具.
相关概念视频
Intralumenal Vesicles and Multivesicular Bodies
3.9K
Intraluminal vesicles (ILVs) are small vesicles 50-80 nm in diameter formed during the maturation of early endosomes. A specialized endosome containing numerous ILVs is called a multivesicular body (MVB). ILVs contain internalized molecules such as antigens, nucleic acids, proteins, and metabolites. Some of these molecules are released from the MVBs inside exosomes and are transported to other cells. Other MVBs contain molecules that are retained in the ILVs and are later degraded within the...
3.9K
Fusion of Secretory Vesicles with the Plasma Membrane
15.8K
Proteins and neurotransmitters in secretory vesicles can be released from a cell upon vesicle docking, priming, and fusion with the plasma membrane. Vesicles are docked and primed in preparation for the quick exocytosis of their contents in response to a stimulus. The fusion process is mainly carried out by a SNAP Receptor or SNARE complex, consisting of synaptobrevin, syntaxin-1, and SNAP-25.
In 1993, Jim Rothman proposed that the antiparallel pairing of vesicular and transmembrane SNAREs, or...
In 1993, Jim Rothman proposed that the antiparallel pairing of vesicular and transmembrane SNAREs, or...
15.8K
Microtubule Associated Motor Proteins
9.9K
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...
9.9K
The Movement of Organelles and Vesicles
5.3K
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,...
5.3K
Vesicular Tubular Clusters
2.4K
After budding out from the ER membrane, some COPII vesicles lose their coat and fuse with one another to form larger vesicles and interconnected tubules called vesicular tubular clusters or VTCs. These clusters constitute a compartment at the ER-Golgi interface known as ERGIC (Endoplasmic Reticulum Golgi Intermediate Compartment). The ERGIC is a mobile membrane-bound cargo transport system that sorts proteins secreted from ER and delivers them to the Golgi.
With the help of motor proteins such...
With the help of motor proteins such...
2.4K
Anaphase A and B
4.3K
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...
4.3K


