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活细胞中荧光固醇的内吞作用和膜分布的时空分析。

Spatiotemporal analysis of endocytosis and membrane distribution of fluorescent sterols in living cells.

作者信息

Wüstner Daniel, Faergeman Nils J

机构信息

Department of Biochemistry and Molecular Biology, University of Southern Denmark, Campusvej 55, 5230, Odense M, Denmark.

出版信息

Histochem Cell Biol. 2008 Nov;130(5):891-908. doi: 10.1007/s00418-008-0488-6. Epub 2008 Sep 12.

Abstract

Distribution and dynamics of cholesterol in the plasma membrane as well as internalization pathways for sterol from the cell surface are of great cell biological interest. Here, UV-sensitive wide field microscopy of the intrinsically fluorescent sterols, dehydroergosterol (DHE) and cholestatrienol (CTL) combined with advanced image analysis were used to study spatiotemporal sterol distribution in living macrophages, adipocytes and fibroblasts. Sterol endocytosis was directly visualized by time-lapse imaging and noise-robust tracking revealing confined motion of DHE containing vesicles in close proximity to the cell membrane. Spatial surface intensity patterns of DHE as well as that of the lipid marker DiIC12 being assessed by statistical image analysis persisted over several minutes in cells having a constant overall curvature. Sites of sterol endocytosis appeared indistinguishable from other regions of the cell surface, and endocytosis contributed by 62% to total sterol uptake in J774 cells. DHE co-localized with fluorescent transferrin (Tf) in vesicles right after onset of endocytosis and in deepened surface patches of energy depleted cells. Surface caveolae labeled with GFP-tagged caveolin were not particularly enriched in DHE or CTL. Some sterol co-localized with internalized caveolin suggesting that caveolar endocytosis contributes to vesicular sterol uptake. These findings demonstrate that plasma membrane sterol is internalized by several endocytic pathways. Sterol endocytosis does not require formation of microscopically resolvable sterol clusters or enrichment of sterol in surface caveolae.

摘要

胆固醇在质膜中的分布和动态变化,以及细胞表面甾醇的内化途径,是细胞生物学领域极为关注的问题。在此,利用对紫外线敏感的宽场显微镜观察固有荧光甾醇、脱氢麦角固醇(DHE)和胆甾三烯醇(CTL),并结合先进的图像分析技术,研究活巨噬细胞、脂肪细胞和成纤维细胞中甾醇的时空分布。通过延时成像和抗噪声跟踪直接观察甾醇内吞作用,揭示了含DHE的囊泡在靠近细胞膜处的受限运动。通过统计图像分析评估的DHE以及脂质标记物DiIC12的空间表面强度模式,在具有恒定整体曲率的细胞中持续数分钟。甾醇内吞位点与细胞表面的其他区域似乎并无差异,在J774细胞中,内吞作用对总甾醇摄取的贡献为62%。内吞作用开始后,DHE立即与荧光转铁蛋白(Tf)在囊泡中共定位,并在能量耗尽细胞加深的表面斑块中共定位。用绿色荧光蛋白标记的小窝蛋白标记的表面小窝,在DHE或CTL中并未特别富集。一些甾醇与内化的小窝蛋白共定位,表明小窝内吞作用有助于囊泡甾醇摄取。这些发现表明,质膜甾醇通过多种内吞途径内化。甾醇内吞作用不需要形成显微镜下可分辨的甾醇簇,也不需要甾醇在表面小窝中富集。

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