线粒体
生物
细胞生物学
背景(考古学)
肝小叶
磷酸化
营养感应
氧化磷酸化
蛋白质组学
生物化学
信号转导
基因
内分泌学
古生物学
作者
Sun Woo Sophie Kang,Rory P. Cunningham,Colin B. Miller,Lauryn A. Brown,Constance M. Cultraro,Adam Harned,Kedar Narayan,Jonathan M. Hernandez,Lisa M. Jenkins,Alexei Lobanov,Maggie Cam,Natalie Porat‐Shliom
标识
DOI:10.1038/s41467-024-45751-9
摘要
In the liver, mitochondria are exposed to different concentrations of nutrients due to their spatial positioning across the periportal and pericentral axis. How the mitochondria sense and integrate these signals to respond and maintain homeostasis is not known. Here, we combine intravital microscopy, spatial proteomics, and functional assessment to investigate mitochondrial heterogeneity in the context of liver zonation. We find that periportal and pericentral mitochondria are morphologically and functionally distinct; beta-oxidation is elevated in periportal regions, while lipid synthesis is predominant in the pericentral mitochondria. In addition, comparative phosphoproteomics reveals spatially distinct patterns of mitochondrial composition and potential regulation via phosphorylation. Acute pharmacological modulation of nutrient sensing through AMPK and mTOR shifts mitochondrial phenotypes in the periportal and pericentral regions, linking nutrient gradients across the lobule and mitochondrial heterogeneity. This study highlights the role of protein phosphorylation in mitochondrial structure, function, and overall homeostasis in hepatic metabolic zonation. These findings have important implications for liver physiology and disease.
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