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天花板培养芯片揭示了脂肪细胞去分化过程中脂滴的动态运输和肌动蛋白重构。

Ceiling culture chip reveals dynamic lipid droplet transport during adipocyte dedifferentiation actin remodeling.

机构信息

Department of Mechanical Engineering, Korea Advanced Institute of Science and Technology, Daejeon, Republic of Korea.

Graduate School of Medical Science and Engineering, Korea Advanced Institute of Science and Engineering, Daejeon, Republic of Korea.

出版信息

Lab Chip. 2022 Oct 11;22(20):3920-3932. doi: 10.1039/d2lc00428c.

Abstract

Adipocyte dedifferentiation has recently gained attention as a process underpinning adipocyte plasticity; however, a lack of suitable experimental platforms has hampered studies into the underlying mechanisms. Here, we developed a microscope-mountable ceiling culture chip that provides a stable yet tunable culture environment for long-term live-imaging of dedifferentiating adipocytes. A detailed spatiotemporal analysis of mature adipocyte dedifferentiation utilizing the culture platform and Cre-recombinase tracers revealed the involvement of dynamic actin remodeling for lipid droplet (LD) secretion during adipocyte dedifferentiation. Additionally, Hippo, Hedgehog, and PPARγ signaling pathways were identified as potent regulators of adipocyte dedifferentiation. Contrary to the belief that adult adipocytes are relatively static, we show that adipocytes are very dynamic, relying on actin-driven mechanical forces to execute LD extrusion and intercellular LD transfer processes.

摘要

脂肪细胞去分化最近作为支撑脂肪细胞可塑性的过程受到关注;然而,缺乏合适的实验平台阻碍了对潜在机制的研究。在这里,我们开发了一种可安装在显微镜上的天花板培养芯片,为长期活细胞成像提供了稳定但可调节的培养环境。利用该培养平台和 Cre 重组酶示踪剂对成熟脂肪细胞去分化的详细时空分析表明,脂肪细胞去分化过程中脂滴(LD)分泌涉及动态肌动蛋白重塑。此外,还确定了 Hippo、Hedgehog 和 PPARγ 信号通路是脂肪细胞去分化的有力调节因子。与认为成体脂肪细胞相对静止的观点相反,我们表明脂肪细胞非常活跃,依赖肌动蛋白驱动的机械力来执行 LD 挤出和细胞间 LD 转移过程。

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