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靶向磷脂酶PLAG-15通过溶酶体相关基因促进健康衰老。

Targeting phospholipase PLAG-15 promotes healthy aging in via lysosomal-related genes.

作者信息

van der Rijt Sanne, Molenaars Marte, Kamble Rashmi, Li Weisha, Schomakers Bauke V, Dane Adrie D, Denis Simone W, van Weeghel Michel, Vaz Frédéric M, Tammaro Alessandra, Janssens Georges E, Gao Arwen W, Houtkooper Riekelt H

机构信息

Laboratory Genetic Metabolic Diseases, Department of Laboratory Medicine, Amsterdam UMC Location University of Amsterdam, Meibergdreef 9, Amsterdam, the Netherlands.

Pathology Research Laboratory, Amsterdam UMC Location University of Amsterdam, Meibergdreef 9, Amsterdam, the Netherlands.

出版信息

iScience. 2025 Jun 16;28(7):112880. doi: 10.1016/j.isci.2025.112880. eCollection 2025 Jul 18.

Abstract

Complex lipid metabolism plays a crucial role in regulating aging. We recently discovered that the phospholipid bis(monoacylglycero)phosphate (BMP) increases in aged human muscles and many mouse tissues. The phospholipase PLA2G15 is reportedly involved in BMP synthesis, however, its specific role in aging remains unknown. To elucidate the role of PLA2G15 in aging, we used as a model. When silencing , the predicted worm orthologue of we observed improved healthspan and lifespan extension. Semi-targeted lipidomics highlighted that instead of changes related to BMP, RNAi led to lower levels of lysophosphatidic acid, lysophosphatidylcholine, and lysophosphatidylethanolamine. Transcriptome-guided epistasis experiments identified that the lifespan extension of RNAi worms is regulated by transcription factors and , and lysosomal vitamin B12 transporter (human , , and respectively). Overall, we conclude that targeting phospholipid remodeling through could be a promising strategy to promote healthy aging.

摘要

复杂的脂质代谢在调节衰老过程中起着至关重要的作用。我们最近发现,磷脂双(单酰甘油)磷酸酯(BMP)在老年人肌肉和许多小鼠组织中有所增加。据报道,磷脂酶PLA2G15参与BMP的合成,然而,其在衰老中的具体作用仍不清楚。为了阐明PLA2G15在衰老中的作用,我们以[具体模型]作为模型。当沉默[具体基因](预测的线虫直系同源基因)时,我们观察到健康寿命得到改善,寿命延长。半靶向脂质组学强调,与BMP相关的变化不同,[具体基因]RNA干扰导致溶血磷脂酸、溶血磷脂酰胆碱和溶血磷脂酰乙醇胺水平降低。转录组引导的上位性实验确定,[具体基因]RNA干扰线虫的寿命延长受转录因子[具体转录因子1]和[具体转录因子2]以及溶酶体维生素B12转运蛋白[具体转运蛋白](分别对应人类[具体基因1]、[具体基因2]和[具体基因3])调节。总体而言,我们得出结论,通过[具体基因]靶向磷脂重塑可能是促进健康衰老的一种有前景的策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ab8/12246578/ef468d4366b6/fx1.jpg

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