lysosomal 功能障碍:连接人类疾病景观中的点
Elisabet Uribe-Carretero1,2,3, Verónica Rey4, Jose Manuel Fuentes1,2,3
1Departamento de Bioquímica y Biología Molecular y Genética, Facultad de Enfermería y Terapia Ocupacional, Universidad de Extremadura, 10003 Caceres, Spain.
Biology
|January 22, 2024
概括
溶酶体,对于细胞降解至关重要,在溶酶体储存障碍 (LSD) 中功能障碍. 研究探索分子洞察力和治疗策略,以改善患者的寿命和生活质量.
科学领域:
- 细胞生物学 细胞生物学
- 分子生物学分子生物学
- 遗传学 是一个遗传学.
背景情况:
- 溶解体是真核细胞中宏分子降解的关键器官.
- 溶解体功能扩展到自,营养感应和细胞内信号传递.
- 溶酶体异常会导致人类病理,称为溶酶体储存障碍 (LSD).
研究的目的:
- 为人类疾病中的溶酶体功能障碍提供分子洞察力.
- 审查最近在了解和治疗LSD方面的进展和突破.
- 探索LSDs的潜在治疗方法.
主要方法:
- 文献综述侧重于溶酶体功能障碍的分子机制.
- 对导致LSDs的遗传和酶性因素的分析.
- 检查针对LSDs的治疗策略.
主要成果:
- 溶解体功能障碍在LSD中是由酶缺乏,激活器问题,修饰器改变或膜蛋白改变引起的.
- 临床表型取决于堆积基质,遗传突变和残留酶活性.
- 目前正在进行的研究重点是提高LSD患者的寿命和生活质量.
结论:
- 在分子水平上了解溶解体功能障碍对于开发有效的LSD疗法至关重要.
- 最近的进展为治疗这些复杂的遗传疾病提供了新的希望.
- 准分子通路有望改善LSD患者的治疗结果.
相关概念视频
Lysosomal Hydrolases
3.8K
Lysosomes are the site for the degradation of macromolecules and biological polymers released during membrane trafficking events such as secretory, endocytic, autophagic, and phagocytic pathways. The membrane-enclosed area of the lysosome, called the lumen, contains hydrolytic enzymes active in an acidic environment. These acid hydrolases are functional at a pH between 4.5 and 5 and are involved in cellular processes such as cell signaling, energy metabolism, restoration of the plasma membrane,...
3.8K
Delivery Pathways to the Lysosome
6.6K
Eukaryotic cells use different mechanisms to eliminate toxic waste obsolete and worn-out substances. Lysosomes play a pivotal role in this, and hence, these substances are carried to the lysosome from other parts of the cell and extracellular space through different pathways. The most elaborately studied pathways to the lysosome are the endocytic pathways.
Endocytosis
In endocytosis, the cell membrane takes up macromolecules and particles from the surrounding medium. Clathrin-mediated...
Endocytosis
In endocytosis, the cell membrane takes up macromolecules and particles from the surrounding medium. Clathrin-mediated...
6.6K
Lysosomes
18.1K
Lysosomes are membrane-enclosed spherical sacs derived from the Golgi apparatus. The most important function of the lysosome is degrading macromolecules and biological polymers that are released during membrane trafficking events such as the secretory, endocytic, autophagic, and phagocytic pathways. The degradation is carried out by several hydrolytic enzymes active in an acidic environment of the lysosomal lumen. These acid hydrolases are involved in cellular processes such as cell signaling,...
18.1K
Inborn Errors of Metabolism
160
Phenylketonuria (PKU) is a protein metabolism disorder characterized by high blood levels of the amino acid phenylalanine. This results from a mutation in the gene responsible for phenylalanine hydroxylase, an enzyme that converts phenylalanine into tyrosine. When this enzyme is deficient, phenylalanine builds up in the blood, leading to symptoms such as vomiting, rashes, seizures, growth deficiency, and severe mental retardation. An early diagnosis and a diet restricting phenylalanine intake...
160
pH Regulation in Cells
6.1K
pH plays a critical role in maintaining normal cellular activities. It helps maintain the structure and function of various proteins, dictates the charge on cellular membranes, and is crucial for metabolic reactions inside the cell. Moreover, cells use the energy from the proton motive force to generate ATP.
Cytosolic pH
Under physiological conditions, the cytosolic pH is slightly more acidic than the extracellular pH. However, cells must prevent further acidification of their cytosol to...
Cytosolic pH
Under physiological conditions, the cytosolic pH is slightly more acidic than the extracellular pH. However, cells must prevent further acidification of their cytosol to...
6.1K
Export of Misfolded Proteins out of the ER
3.6K
After folding, the ER assesses the quality of secretory and membrane proteins. The correctly folded proteins are cleared by the calnexin cycle for transport to their final destination, while misfolded proteins are held back in the ER lumen. The ER chaperones attempt to unfold and refold the misfolded proteins but sometimes fail to achieve the correct native conformation. Such terminally misfolded proteins are then exported to the cytosol by ER-associated degradation or ERAD pathway for...
3.6K


