双(单酰基甘油)-磷酸假说:从溶酶体功能到治疗途径

IF 12.1 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Annual review of biochemistry Pub Date : 2024-04-11 DOI:10.1146/annurev-biochem-092823-113814
Uche N. Medoh, Monther Abu-Remaileh
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引用次数: 0

摘要

溶酶体分解和回收脂质及其他生物分子,以维持细胞在不同营养环境中的平衡。溶酶体脂质分解依赖于磷酸二(单酰基甘油)酯(BMP)的刺激活性,这是一种神秘的脂质,其水平在无数溶酶体相关疾病中都会发生改变。在此,我们回顾了半个多世纪前发现的 BMP 及其结构特性,这些特性促进了脂质水解酶的活化及其辅助激活剂的招募。我们进一步讨论了目前对 BMP 分解代谢和合成代谢的不完全理解。最后,我们讨论了 BMP 在溶酶体相关疾病中的作用,以及通过药物激活和抑制 BMP 合成酶来调节其水平,从而治疗溶酶体贮积症、药物诱导的磷脂病、阿尔茨海默病、帕金森病、额颞叶痴呆症、癌症和病毒感染的可能性。
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The Bis(monoacylglycero)-phosphate Hypothesis: From Lysosomal Function to Therapeutic Avenues
Lysosomes catabolize and recycle lipids and other biological molecules to maintain cellular homeostasis in diverse nutrient environments. Lysosomal lipid catabolism relies on the stimulatory activity of bis(monoacylglycero)phosphate (BMP), an enigmatic lipid whose levels are altered across myriad lysosome-associated diseases. Here, we review the discovery of BMP over half a century ago and its structural properties that facilitate the activation of lipid hydrolases and recruitment of their coactivators. We further discuss the current, yet incomplete, understanding of BMP catabolism and anabolism. To conclude, we discuss its role in lysosome-associated diseases and the potential for modulating its levels by pharmacologically activating and inhibiting the BMP synthase to therapeutically target lysosomal storage disorders, drug-induced phospholipidosis, Alzheimer's disease, Parkinson's disease, frontotemporal dementia, cancer, and viral infection.
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来源期刊
Annual review of biochemistry
Annual review of biochemistry 生物-生化与分子生物学
CiteScore
33.90
自引率
0.00%
发文量
31
期刊介绍: The Annual Review of Biochemistry, in publication since 1932, sets the standard for review articles in biological chemistry and molecular biology. Since its inception, these volumes have served as an indispensable resource for both the practicing biochemist and students of biochemistry.
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