溶酶体储存障碍:从生物学到临床,参考印度
Jayesh Sheth1, Aadhira Nair1, Babban Jee2
1FRIGE's Institute of Human Genetics, FRIGE House, Jodhpur Gam Road, Satellite, Ahmedabad 380015, India.
The Lancet regional health. Southeast Asia
|June 29, 2023
概括
溶酶体储存障碍 (LSDs) 是由基质积累引起的遗传疾病. 本综述考察了印度的LSD,重点关注其分子谱,流行病学和印度人口的预防策略.
科学领域:
- 遗传学和分子生物学
- 代谢障碍 代谢障碍 代谢障碍
- 公共卫生基因组学
背景情况:
- 溶酶体储存障碍 (LSD) 是一组超过70种遗传代谢疾病.
- 这些疾病是由影响 lysosomal 酶的遗传变异引起的,导致基质积累.
- 越来越多的认识和诊断工具凸显了LSD的重要性,特别是在印度等多样化的人口中.
研究的目的:
- 审查印度人口中LSDs的频谱.
- 了解印度LSDs的分子流行病学和基因型-表型相关性.
- 在印度背景下讨论LSD的预防策略.
主要方法:
- 对印度LSD的现有文献和数据进行了全面的审查.
- 分析印度医学研究理事会 (ICMR) 和卫生研究部 (DHR) 工作组 (成立于2015) 的研究结果.
- 专注于分子谱,常见的LSD,创始变体和流行病学数据.
主要成果:
- 在印度普遍存在的常见LSD的识别.
- 对几个存储障碍的分子谱和创始变体的表征.
- 关于全国各地各种LSDs负担和分布的数据.
结论:
- 由于印度人口异质,印度可能有高频率的LSDs.
- 了解分子流行病学对于有针对性的查和管理至关重要.
- 制定适合印度人口的有效预防策略至关重要.
相关概念视频
Lysosomal Hydrolases
3.9K
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,...
3.9K
Inborn Errors of Metabolism
206
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...
206
Protein Import into the Peroxisomes
3.6K
Cells contain membrane-bound organelles called peroxisomes that oxidize organic molecules by transferring hydrogen atoms to oxygen, producing hydrogen peroxide. Peroxisomes enzymatically convert the released hydrogen peroxide into water and oxygen.
Peroxisomal Protein Import:
Peroxisomes lack the genetic machinery required to code for their own proteins. Hence, most peroxisomal membrane, lumenal and transmembrane proteins are synthesized in the cytoplasm or ER and transported to the peroxisome...
Peroxisomal Protein Import:
Peroxisomes lack the genetic machinery required to code for their own proteins. Hence, most peroxisomal membrane, lumenal and transmembrane proteins are synthesized in the cytoplasm or ER and transported to the peroxisome...
3.6K
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
Fungal Phylum Microsporidia
43
Microsporidia are a group of obligate intracellular fungi that were initially classified as protists but were later reclassified based on phylogenetic, molecular, and structural evidence linking them to the Chytridiomycota. These unicellular, non-motile organisms are highly specialized parasites that infect a wide range of animal hosts, including humans. They have evolved extensive genomic and metabolic reductions, making them highly dependent on their hosts for survival.Morphology and Genomic...
43
ER Retrieval Pathway
3.9K
In the secretory pathway, vesicles transport proteins from one cellular compartment to another in forward transport to deliver the protein to its correct location. Occasionally, misfolded proteins and incorrect proteins escape their original compartments, and a retrieval pathway is used to return the escaped proteins to their original compartment.
The ER uses many checkpoints to prevent the entry of incorrectly folded or a resident protein as cargo onto a transport vesicle. These mechanisms...
The ER uses many checkpoints to prevent the entry of incorrectly folded or a resident protein as cargo onto a transport vesicle. These mechanisms...
3.9K


