牛皮中的细胞外囊泡:从致病源到治疗中的可能作用
Marco Iuliano1, Lorenzo Grimaldi1, Paolo Rosa1,2
1Department of Medico-Surgical Sciences and Biotechnologies, Sapienza University of Rome - Polo Pontino, Latina, Italy.
Frontiers in immunology
|June 3, 2024
概括
牛皮涉及免疫细胞释放炎症信号. 细胞外囊泡 (EVs) 在这种慢性皮肤和关节疾病中发挥着关键作用,为新疗法和生物标志物提供了潜力.
科学领域:
- 免疫学 免疫学 免疫学
- 皮肤病学 皮肤病学
- 细胞生物学 细胞生物学
背景情况:
- 牛皮是一种慢性炎症状况,影响皮肤和关节.
- 它涉及一种与特定细胞类型和炎症媒介的免疫反应的改变.
- 关键的介导体包括IL-17,IL-23,IL-22和TNF-α,导致皮肤变化,如帕拉基拉托斯.
研究的目的:
- 审查细胞外囊泡 (EVs) 在牛皮病原发生中的作用.
- 要总结EVs在牛皮中对细胞微环境的调节.
- 讨论EVs用于牛皮治疗和生物标志物发现的生物技术应用.
主要方法:
- 文献综述总结了关于EV和牛皮的当前研究.
- 对涉及EVs在牛皮的炎症级联中的分子机制的分析.
- 探索电动汽车作为治疗交付系统和诊断生物标记物的潜力.
主要成果:
- 电动体参与细胞间通信,驱动牛皮病原体.
- 它们充当炎症媒介的载体,影响疾病的微环境.
- 电动汽车为向抗炎治疗和新生物标志物识别提供了机会.
结论:
- 细胞外囊泡是牛皮病变的关键参与者.
- 电动车为开发创新的治疗策略和牛皮的诊断工具提供了有希望的途径.
- 对EV生物学和功能的进一步研究可以促进牛皮的治疗.
相关概念视频
Overview of Exosomes
2.7K
Exosomes are stable, lipid bilayer-enclosed vesicles capable of crossing biological barriers. They can carry a wide range of molecules required for intercellular communication. Once exosomes are released from the cell where they originated, they enter a recipient cell through various pathways such as fusion, receptor-mediated endocytosis, macropinocytosis, and phagocytosis.
Stahl et al. discovered exosomes in 1983, but the exosomes were initially considered waste products released from the...
Stahl et al. discovered exosomes in 1983, but the exosomes were initially considered waste products released from the...
2.7K
Clinical Applications of Epidermal Stem Cells
2.7K
Epidermal stem cells (EpiSCs) are mainly located at the basal layer of the epidermis. These cells repair minor injuries of the skin and replace dead skin cells. However, EpiSCs’ cannot heal severe wounds such as major burns or those from diabetes or hereditary disorders. In such cases, culturing the epidermal stem cells from the patient is possible and has yielded successful treatment options, such as laboratory-grown skin grafts. These grafts are synthesized using a patient’s own...
2.7K
T Cell Types and Functions
1.0K
When T cells with CD4 markers are activated, they give rise to two types of effector cells: helper T cells and regulatory T cells. Meanwhile, T cells with CD8 markers differentiate into effector cytotoxic T cells. The differentiation of CD4 T cells into helper T cell subsets, such as Th1, Th2, and Th17 cells, is dependent on the antigen type, antigen-presenting cell, and regulatory cytokines.
Th1 cells stimulate dendritic cells to express necessary co-stimulatory molecules on their surfaces for...
Th1 cells stimulate dendritic cells to express necessary co-stimulatory molecules on their surfaces for...
1.0K
Overview of Secretory Vesicles
8.5K
Secretory vesicles, also known as dense core vesicles (DCVs), are membrane-bound vesicles that transport secretory proteins, such as hormones or neurotransmitters. Regulated secretory vesicles transport proteins from the trans-Golgi network to the exterior of the cell. Proteins present in regulated secretory vesicles are required to be rapidly exocytosed in large amounts upon a specific stimulus.
Various proteins regulate the aggregation of molecules inside the secretory vesicles. Chromogranins...
Various proteins regulate the aggregation of molecules inside the secretory vesicles. Chromogranins...
8.5K
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
EPS and iPS Cells in Disease Research
2.8K
Embryonic and induced pluripotent stem cells are excellent models for disease research because of their ability to self-renew and differentiate into most cell types. Somatic cells from a patient are isolated and reprogrammed into induced pluripotent stem cells or iPSCs. These iPSCs are later differentiated into the desired cell type, which mirrors the diseased cell of the patient. In this way, disease models have been created for investigating diseases such as Down syndrome, type I diabetes,...
2.8K


