克拉贝病
生物
白质营养不良
中枢神经系统
神经系统
疾病
生物标志物
表型
尼曼-皮克病
基因
神经科学
遗传学
病理
医学
作者
Husam B. R. Alabed,Ambra Del Grosso,Valeria Bellani,Lorena Urbanelli,Sara Carpi,Miriam De Sarlo,Lorenzo Bertocci,Laura Colagiorgio,Sandra Buratta,Luca Scaccini,Debora N Mancini,Ilaria Tonazzini,Marco Cecchini,Carla Emiliani,Roberto Maria Pellegrino
出处
期刊:Biomolecules
[MDPI AG]
日期:2023-10-23
卷期号:13 (10): 1562-1562
摘要
Krabbe disease is a rare neurodegenerative disease with an autosomal recessive character caused by a mutation in the GALC gene. The mutation leads to an accumulation of psychosine and a subsequent degeneration of oligodendrocytes and Schwann cells. Psychosine is the main biomarker of the disease. The Twitcher mouse is the most commonly used animal model to study Krabbe disease. Although there are many references to this model in the literature, the lipidomic study of nervous system tissues in the Twitcher model has received little attention. This study focuses on the comparison of the lipid profiles of four nervous system tissues (brain, cerebellum, spinal cord, and sciatic nerve) in the Twitcher mouse compared to the wild-type mouse. Altogether, approximately 230 molecular species belonging to 19 lipid classes were annotated and quantified. A comparison at the levels of class, molecular species, and lipid building blocks showed significant differences between the two groups, particularly in the sciatic nerve. The in-depth study of the lipid phenotype made it possible to hypothesize the genes and enzymes involved in the changes. The integration of metabolic data with genetic data may be useful from a systems biology perspective to gain a better understanding of the molecular basis of the disease.
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