Suppr超能文献

荧光波动分析显示,LDL 受体受膜胆固醇调节。

The LDL receptor is regulated by membrane cholesterol as revealed by fluorescence fluctuation analysis.

机构信息

Department of Chemistry, Faculty of Science, McGill University, Montreal, Canada.

Department of Physics, Faculty of Science, McGill University, Montreal, Canada.

出版信息

Biophys J. 2023 Sep 19;122(18):3783-3797. doi: 10.1016/j.bpj.2023.08.005. Epub 2023 Aug 9.

Abstract

Membrane cholesterol-rich domains have been shown to be important for regulating a range of membrane protein activities. Low-density lipoprotein receptor (LDLR)-mediated internalization of cholesterol-rich LDL particles is tightly regulated by feedback mechanisms involving intracellular sterol sensors. Since LDLR plays a role in maintaining cellular cholesterol homeostasis, we explore the role that membrane domains may have in regulating LDLR activity. We expressed a fluorescent LDLR-mEGFP construct in HEK293T cells and imaged the unligated receptor or bound to an LDL/DiI fluorescent ligand using total internal reflection fluorescence microscopy. We studied the receptor's spatiotemporal dynamics using fluorescence fluctuation analysis methods. Image cross correlation spectroscopy reveals a lower LDL-to-LDLR binding fraction when membrane cholesterol concentrations are augmented using cholesterol esterase, and a higher binding fraction when the cells are treated with methyl-β-cyclodextrin) to lower membrane cholesterol. This suggests that LDLR's ability to metabolize LDL particles is negatively correlated to membrane cholesterol concentrations. We then tested if a change in activity is accompanied by a change in membrane localization. Image mean-square displacement analysis reveals that unligated LDLR-mEGFP and ligated LDLR-mEGFP/LDL-DiI constructs are transiently confined on the cell membrane, and the size of their confinement domains increases with augmented cholesterol concentrations. Receptor diffusion within the domains and their domain-escape probabilities decrease upon treatment with methyl-β-cyclodextrin, consistent with a change in receptor populations to more confined domains, likely clathrin-coated pits. We propose a feedback model to account for regulation of LDLR within the cell membrane: when membrane cholesterol concentrations are high, LDLR is sequestered in cholesterol-rich domains. These LDLR populations are attenuated in their efficacy to bind and internalize LDL. However, when membrane cholesterol levels drop, LDL has a higher binding affinity to its receptor and the LDLR transits to nascent clathrin-coated domains, where it diffuses at a slower rate while awaiting internalization.

摘要

膜胆固醇丰富的区域被证明对调节一系列膜蛋白的活性非常重要。富含胆固醇的 LDL 颗粒通过涉及细胞内固醇传感器的反馈机制进行 LDLR 介导的内化。由于 LDLR 在维持细胞胆固醇稳态中发挥作用,我们探索了膜结构域在调节 LDLR 活性方面可能发挥的作用。我们在 HEK293T 细胞中表达了荧光 LDLR-mEGFP 构建体,并使用全内反射荧光显微镜对未连接的受体或与 LDL/DiI 荧光配体结合的受体进行成像。我们使用荧光波动分析方法研究了受体的时空动力学。图像互相关谱分析显示,在用胆固醇酯酶增加膜胆固醇浓度时,LDL 与 LDLR 的结合分数较低,而在用甲基-β-环糊精处理以降低膜胆固醇时,结合分数较高。这表明 LDLR 代谢 LDL 颗粒的能力与膜胆固醇浓度呈负相关。然后,我们测试了活性的变化是否伴随着膜定位的变化。图像均方根位移分析表明,未连接的 LDLR-mEGFP 和连接的 LDLR-mEGFP/LDL-DiI 构建体在细胞膜上短暂受限,其受限域的大小随胆固醇浓度的增加而增加。用甲基-β-环糊精处理后,受体在域内的扩散及其域逃逸概率降低,这与受体群体向更受限的域的变化一致,可能是网格蛋白包被的陷窝。我们提出了一个反馈模型来解释 LDLR 在细胞膜内的调节:当膜胆固醇浓度较高时,LDLR 被隔离在富含胆固醇的区域。这些 LDLR 群体在结合和内化 LDL 的效力上受到抑制。然而,当膜胆固醇水平下降时,LDL 与受体的结合亲和力增加,LDLR 转移到新生的网格蛋白包被的区域,在那里它以较慢的速度扩散,同时等待内化。

相似文献

引用本文的文献

本文引用的文献

3
Cholesterol in LDL receptor recycling and degradation.LDL 受体循环和降解中的胆固醇。
Clin Chim Acta. 2020 Jan;500:81-86. doi: 10.1016/j.cca.2019.09.022. Epub 2019 Nov 23.
5
The imaging FCS diffusion law in the presence of multiple diffusive modes.存在多种扩散模式时的成像 FCS 扩散定律。
Methods. 2018 May 1;140-141:140-150. doi: 10.1016/j.ymeth.2017.11.016. Epub 2017 Dec 5.
7

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验