Dissection of surface area-dependent lipolysis at a single organelle level

Lipid droplets are dynamic organelles whose size and number signify their role in energy. However, owing to cellular heterogeneity and technological limitations, the relationship between the lipolytic ability and lipid droplet morphology is unclear. Here, we developed a live-cell imaging assay using geometric analysis to quantify cellular lipolysis at a single organelle level, designated imaging lipolysis. Using imaging lipolysis and super-resolution imaging, we found that lipolysis is controlled by both lipase-accessible lipid droplet surface area and lipase activity. Moreover, lipid droplet fusion regulatory proteins CLSTN3β/CIDEs promote lipolysis by increasing the total lipid droplet surface area-to-volume ratio in biophysical regulation. We further identified that brown adipocytes exhibit more efficient lipolysis due to higher lipase activity and a larger lipid droplet surface area-to-volume ratio compared to white adipocytes. Taken together, imaging lipolysis generally enabled single-cell lipase activity measurement and revealed a mechanistic basis for energy-generating brown adipocytes to enforce a multilocular phenotype for lipolysis.

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Publication Details

Journal
Cell Reports
Published
2025-08-01
DOI
https://doi.org/10.1016/j.celrep.2025.116100
Citations
2
Primary Topic
Lipid metabolism and biosynthesis
Type
article
Field-Weighted Citation Impact
2.22

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article

Dissection of surface area-dependent lipolysis at a single organelle level

Yan Liang, Li Xu, Feng‐Jung Chen, Tong‐Jin Zhao et al.
2 citations
Cell Reports
Lipid metabolism and biosynthesis
2.22
article

Dissection of surface area-dependent lipolysis at a single organelle level

Yan Liang, Li Xu, Feng‐Jung Chen, Tong‐Jin Zhao, Xinmeng Che, Jin Wu, Peng Li, Hongyuan Yang, Chengxin Ma, Yuqi Li
article en
2 citations

Abstract

Lipid droplets are dynamic organelles whose size and number signify their role in energy. However, owing to cellular heterogeneity and technological limitations, the relationship between the lipolytic ability and lipid droplet morphology is unclear. Here, we developed a live-cell imaging assay using geometric analysis to quantify cellular lipolysis at a single organelle level, designated imaging lipolysis. Using imaging lipolysis and super-resolution imaging, we found that lipolysis is controlled by both lipase-accessible lipid droplet surface area and lipase activity. Moreover, lipid droplet fusion regulatory proteins CLSTN3β/CIDEs promote lipolysis by increasing the total lipid droplet surface area-to-volume ratio in biophysical regulation. We further identified that brown adipocytes exhibit more efficient lipolysis due to higher lipase activity and a larger lipid droplet surface area-to-volume ratio compared to white adipocytes. Taken together, imaging lipolysis generally enabled single-cell lipase activity measurement and revealed a mechanistic basis for energy-generating brown adipocytes to enforce a multilocular phenotype for lipolysis.

Cell ReportsVol. 44(8)
Fudan University (CN), UNSW Sydney (AU), Center for Life Sciences (CN), The University of Texas Health Science Center at Houston (US), Tsinghua University (CN)
National Natural Science Foundation of China, Fudan University, Shanghai Municipal People's Government, Key Technologies Research and Development Program, National Key Research and Development Program of China
Openalex Percentile: Top 12%
Lipid metabolism and biosynthesis
2.22
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