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Expression of scavenger receptor class B type 1 (SR-BI) promotes microvillar channel formation and selective cholesteryl ester transport in a heterologous reconstituted system

机译:表达的清道夫受体B类1型(SR-BI)促进 微绒毛通道形成与选择性胆固醇酯 在异源重组系统中运输

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摘要

In the “selective” cholesteryl ester (CE) uptake process, surface-associated lipoproteins [high density lipoprotein (HDL) and low density lipoprotein] are trapped in the space formed between closely apposed surface microvilli (microvillar channels) in hormone-stimulated steroidogenic cells. This is the same location where an HDL receptor (SR-BI) is found. In the current study, we sought to understand the relationship between SR-BI and selective CE uptake in a heterologous insect cell system. Sf9 (Spodoptera frugiperda) cells overexpressing recombinant SR-BI were examined for (i) SR-BI protein by Western blot analysis and light or electron immunomicroscopy, and (ii) selective lipoprotein CE uptake by the use of radiolabeled or fluorescent (BODIPY-CE)-labeled HDL. Noninfected or infected control Sf9 cells do not express SR-BI, show microvillar channels, or internalize CEs. An unexpected finding was the induction of a complex channel system in Sf9 cells expressing SR-BI. SR-BI-expressing cells showed many cell surface double-membraned channels, immunogold SR-BI, apolipoprotein (HDL) labeling of the channels, and high levels of selective HDL-CE uptake. Thus, double-membraned channels can be induced by expression of recombinant SR-BI in a heterologous system, and these specialized structures facilitate both the binding of HDL and selective HDL-CE uptake.
机译:在“选择性”胆固醇酯(CE)吸收过程中,与表面相关的脂蛋白[高密度脂蛋白(HDL)和低密度脂蛋白]被困在激素刺激的类固醇生成细胞中紧密并置的表面微绒毛(微绒毛通道)之间形成的空间中。在找到HDL受体(SR-BI)的位置相同。在当前的研究中,我们试图了解异源昆虫细胞系统中SR-BI与选择性摄取CE之间的关系。检查过表达重组SR-BI的Sf9(Spodoptera frugiperda)细胞是否(i)通过蛋白质印迹分析和光或电子免疫显微镜检查SR-BI蛋白,以及(ii)通过使用放射性标记或荧光(BODIPY-CE)选择性摄取脂蛋白CE )标记的HDL。未感染或感染的对照Sf9细胞不表达SR-BI,显示微绒毛通道或使CE内在化。意外的发现是在表达SR-BI的Sf9细胞中诱导了复杂的通道系统。表达SR-BI的细胞显示出许多细胞表面双膜通道,免疫金SR-BI,通道的载脂蛋白(HDL)标记以及高水平的选择性HDL-CE摄取。因此,可通过在异源系统中表达重组SR-BI来诱导双膜通道,并且这些专门的结构有助于HDL的结合和选择性HDL-CE的摄取。

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