病毒诱导的细胞融合和突触形成
1Division of Infection and Immunity, UCL, London, UK. maorong.xie@ucl.ac.uk.
Results and problems in cell differentiation
|November 23, 2023
概括
许多病毒使用融合蛋白来感染细胞并形成合成细胞 (多核巨细胞). 本综述总结了病毒诱导的细胞融合机制及其在病毒传播中的作用.
科学领域:
- 病毒学 病毒学
- 细胞生物学 细胞生物学
- 免疫学 免疫学 免疫学
背景情况:
- 包裹病毒利用病毒融合蛋白通过膜融合进入宿主细胞.
- 许多病毒,包裹和非包裹,可以诱导细胞细胞融合,形成合成细胞或多核巨细胞 (MGCs).
- 病毒诱导的细胞融合在哺乳动物中很普遍,可能促进病毒的传播,克服细胞进入障碍和抗体逃逸.
研究的目的:
- 审查当前对病毒诱导的细胞融合和突触形成的理解.
- 突出病毒融合蛋白在细胞进入和细胞融合中的重要性.
- 讨论细胞融合对病毒传播的潜在优势.
主要方法:
- 对病毒诱导的细胞融合研究的文献综述.
- 分析病毒融合蛋白及其作用.
- 简要介绍已知的结合细胞形成的机制和影响.
主要成果:
- 病毒融合蛋白是病毒进入和细胞-细胞融合的关键媒介.
- 合成细胞形成是各种病毒感染中常见的现象.
- 细胞融合为病毒提供了潜在的好处,包括增强传播和免疫逃避.
结论:
- 病毒诱导的细胞融合是病毒病原学的重要,但尚未完全理解的方面.
- 进一步研究病毒诱导的细胞融合的分子机制是有必要的.
- 了解这些机制可能会揭示抗病毒疗法的新点.
相关概念视频
Fusion of Secretory Vesicles with the Plasma Membrane
11.1K
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...
11.1K
SNAREs and Membrane Fusion
10.9K
Once a transport vesicle has recognized its target organelle, the vesicular membrane needs to fuse with the target membrane to unload the cargo. Transmembrane proteins called SNAREs present on organelle membranes and their vesicles, mediate vesicle fusion.
SNAREs exist in pairs that symmetrically interact and catalyze the fusion of the lipid bilayers in vesicle and target organelle. v-SNARE in the vesicle membrane are single polypeptide chains that bind to a complementary t-SNARE, composed of 2...
SNAREs exist in pairs that symmetrically interact and catalyze the fusion of the lipid bilayers in vesicle and target organelle. v-SNARE in the vesicle membrane are single polypeptide chains that bind to a complementary t-SNARE, composed of 2...
10.9K
Viral Recombination
23.5K
Cells are sometimes infected by more than one virus at once. When two viruses disassemble to expose their genomes for replication in the same cell, similar regions of their genomes can pair together and exchange sequences in a process called recombination. Alternatively, viruses with segmented genomes can swap segments in a process called reassortment.
23.5K
Vesicular Tubular Clusters
2.5K
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...
2.5K
Intracellular Movement of Viruses and Bacteria
2.8K
Intracellular bacteria and viruses often comprise a group of highly infectious pathogens that can cause several diseases. Bacterial pathogens include those belonging to the genus Rickettsia responsible for conditions such as rocky mountain spotted fever and the Mediterranean spotted fever; Chlamydia, a genus responsible for a sexually transmitted disease; Coxiella burnetii, an agent responsible for Q fever. Viral pathogens include vaccinia—a poxvirus, and herpes simplex virus—a...
2.8K
Intralumenal Vesicles and Multivesicular Bodies
3.5K
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...
3.5K


