Davidson Jessica W, Jain Raghav, Kizzar Thomas, Geoghegan Gisela, Nesbitt Daniel J, Cavanagh Amy, Abe Akira, Nyame Kwamina, Hunger Andrea, Chao Xiaojuan, James Isabella, Walesewicz Helaina, Baldwin Dominique A, Wade Gina, Michorowska Sylwia, Verma Rakesh, Schueler Kathryn, Hinkovska-Galcheva Vania, Shishkova Evgenia, Ding Wen-Xing, Coon Joshua J, Shayman James A, Abu-Remaileh Monther, Simcox Judith A
Department of Biochemistry, University of Wisconsin-Madison, Madison, WI 53706, USA.
Department of Biochemistry, University of Wisconsin-Madison, Madison, WI 53706, USA; Howard Hughes Medical Institute, Department of Biochemistry, University of Wisconsin-Madison, Madison, WI 53706, USA.
Cell Metab. 2025 Jun 3;37(6):1413-1425.e6. doi: 10.1016/j.cmet.2025.04.015. Epub 2025 May 14.
Cold exposure is a selective environmental stress that elicits a rapid metabolic shift to maintain energy homeostasis. In response to cold exposure, the liver rewires the metabolic state, shifting from glucose to lipid catabolism. By probing the liver lipids in cold exposure, we observed that the lysosomal bis(monoacylglycero)phosphate (BMP) lipids were rapidly increased during cold exposure. BMP lipid changes occurred independently of lysosomal abundance but were dependent on the lysosomal transcriptional regulator transcription factor EB (TFEB). Knockdown of Tfeb in hepatocytes decreased BMP lipid levels and led to cold intolerance in mice. We assessed TFEB-binding sites of lysosomal genes and determined that the phospholipase a2 group XV (PLA2G15) regulates BMP lipid catabolism. Decreasing Pla2g15 levels in mice increased BMP lipids, ablated the cold-induced rise in BMP lipids, and improved cold tolerance. Mutation of the catalytic site of PLA2G15 ablated the BMP lipid breakdown. Together, our studies uncover TFEB regulation of BMP lipids through PLA2G15 catabolism.
冷暴露是一种选择性环境应激,会引发快速的代谢转变以维持能量稳态。作为对冷暴露的反应,肝脏会重新调整代谢状态,从葡萄糖分解代谢转变为脂质分解代谢。通过探究冷暴露期间的肝脏脂质,我们观察到溶酶体双(单酰甘油)磷酸酯(BMP)脂质在冷暴露期间迅速增加。BMP脂质的变化独立于溶酶体丰度发生,但依赖于溶酶体转录调节因子转录因子EB(TFEB)。在肝细胞中敲低Tfeb会降低BMP脂质水平,并导致小鼠对寒冷不耐受。我们评估了溶酶体基因的TFEB结合位点,并确定磷脂酶a2第XV组(PLA2G15)调节BMP脂质分解代谢。降低小鼠体内的Pla2g15水平会增加BMP脂质,消除冷诱导的BMP脂质升高,并提高耐寒性。PLA2G15催化位点的突变消除了BMP脂质的分解。总之,我们的研究揭示了TFEB通过PLA2G15分解代谢对BMP脂质的调节作用。