线粒体功能障碍和非传染性疾病的危险因素:从基本概念到未来的前景
Ganna Nevoit1, Gediminas Jarusevicius2, Maksim Potyazhenko3
1Laboratory of Population Studies, Cardiology Institute, Lithuanian University of Health Sciences, 44307 Kaunas, Lithuania.
Diseases (Basel, Switzerland)
|November 26, 2024
概括
线粒体功能障碍 (MD) 是非传染性疾病 (NCD) 的核心. 了解NCD风险因素如何导致MD对于开发针对线粒体的新预防和治疗策略至关重要.
科学领域:
- 生物医学科学 生物医学科学
- 病理生理学 病理生理学
- 临床医学 临床医学
背景情况:
- 非传染性疾病 (NCD) 是一个重大的全球健康挑战.
- 线粒体功能障碍 (MD) 越来越被认为是NCD发展和进展的关键因素.
- 连接NCD风险因素与MD的确切机制仍然不完全理解.
研究的目的:
- 综合审查关于MD在NCD发病过程中的作用的文献.
- 阐明NCD风险因素诱导MD的病因路径.
- 在临床医学中更新对MD的当前理解.
主要方法:
- 广泛的文献搜索和现有科学数据的系统分析.
- 专注于了解NCD风险因素与MD之间的关系.
- 基于科学证据的理论概念开发.
主要成果:
- 提出了一个理论框架,详细说明了NCD风险因素如何导致MD.
- 该审查强调MD是器官功能障碍和NCDs共患病的常见途径.
- 提出了"NCD连续"的概念,反映了MD和NCD的终身进展.
结论:
- 线粒体功能障碍 (MD) 是器官功能障碍和NCD并发症的基础统一机制.
- 预防MD需要识别和减轻其致病因素.
- 线粒体是NCD管理的有希望的治疗点.
相关概念视频
Mitochondria
11.1K
Mitochondria are eukaryotic cellular organelles that are known to produce energy through a process called oxidative phosphorylation. Besides their primary function, mitochondria are involved in various cellular processes, including cell growth, differentiation, signaling, metabolism, and senescence. Age-related changes cause a decline in mitochondrial quality and integrity due to increased mitochondrial mutations and oxidative damage. Thus, aging can severely impact mitochondrial functions,...
11.1K
Electron Transport Chain: Complex I and II
11.7K
The mitochondrial electron transport chain (ETC) is the main energy generation system in the eukaryotic cells. However, mitochondria also produce cytotoxic reactive oxygen species (ROS) due to the large electron flow during oxidative phosphorylation. While Complex I is one of the primary sources of superoxide radicals, ROS production by Complex II is uncommon and may only be observed in cancer cells with mutated complexes.
ROS generation is regulated and maintained at moderate levels necessary...
ROS generation is regulated and maintained at moderate levels necessary...
11.7K
Mitochondrial Membranes
8.7K
A single mitochondrion is a bean-shaped organelle enclosed by a double-membrane system. The outer membrane of mitochondria is smooth and contains many porins - the integral membrane transporters. Porins enable free diffusion of ions and small uncharged molecules through the outer mitochondrial membrane but limit the transport of molecules larger than 5000 Daltons. Further, the outer mitochondrial membrane forms a unique structure called membrane contact sites with other subcellular organelles,...
8.7K
Translocation of Proteins into the Mitochondria
3.0K
Mitochondrial precursors are translocated to the internal subcompartments via independent mechanisms involving distinct protein machineries called translocases.
Sorting of outer membrane proteins:
Mitochondrial outer membrane proteins are of two types: the transmembrane, beta-barrel porins, and the membrane-anchored, alpha-helical proteins. Beta-barrel porin precursors are translocated by the TOM complex and inserted into the outer mitochondrial membrane by the SAM complex. In contrast,...
Sorting of outer membrane proteins:
Mitochondrial outer membrane proteins are of two types: the transmembrane, beta-barrel porins, and the membrane-anchored, alpha-helical proteins. Beta-barrel porin precursors are translocated by the TOM complex and inserted into the outer mitochondrial membrane by the SAM complex. In contrast,...
3.0K
Factors Affecting Illness
4.2K
When a person's physical, emotional, intellectual, social development or spiritual functioning is compromised, this deviation from a healthy normal state is called illness. Illness creates stress that in turn harms individuals. Irritation, anger, denial, hopelessness, and fear are behavioral and emotional changes an individual experiences in the phases of illness. A variety of factors influence a person's health and well-being.
For instance, risk factors are connected to illness,...
For instance, risk factors are connected to illness,...
4.2K
Animal Mitochondrial Genetics
7.5K
Among all the organelles in an animal cell, only mitochondria have their own independent genomes. Animal mitochondrial DNA is a double-stranded, closed-circular molecule with around 20,000 base pairs. Mitochondrial DNA is unique in that one of its two strands, the heavy, or H, -strand is guanine rich, whereas the complementary strand is cytosine rich and called the light, or L, -strand. Compared to nuclear DNA, mitochondrial DNA has a very low percentage of non-coding regions and is marked by...
7.5K


