The Institute for Chemistry, Engineering & Medicine for Human Health (Sarafan ChEM-H), Stanford University, Stanford, California, USA.
Department of Chemical Engineering, Stanford University, Stanford, California, USA; email:
Annu Rev Biochem. 2024 Aug;93(1):447-469. doi: 10.1146/annurev-biochem-092823-113814. Epub 2024 Jul 2.
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.
溶酶体分解和回收脂质和其他生物分子,以在各种营养环境中维持细胞内稳态。溶酶体脂质分解代谢依赖于双(单酰基甘油)磷酸(BMP)的刺激活性,BMP 是一种神秘的脂质,其水平在无数与溶酶体相关的疾病中发生改变。在这里,我们回顾了半个多世纪前 BMP 的发现及其结构特性,这些特性促进了脂质水解酶的激活和它们的共激活因子的募集。我们进一步讨论了目前但仍不完整的 BMP 分解代谢和合成代谢的理解。最后,我们讨论了它在与溶酶体相关的疾病中的作用,以及通过药理学激活和抑制 BMP 合酶来调节其水平的潜力,以治疗性靶向溶酶体贮积症、药物诱导的磷脂沉积病、阿尔茨海默病、帕金森病、额颞叶痴呆、癌症和病毒感染。