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脂肪酸转运蛋白(FAT)/CD36在人1型和2型骨骼肌纤维中的亚细胞免疫定位

Subcellular immunolocalisation of fatty acid translocase (FAT)/CD36 in human type-1 and type-2 skeletal muscle fibres.

作者信息

Keizer Hans A, Schaart Gert, Tandon Narenda N, Glatz Jan F C, Luiken Joost J F P

机构信息

Department of Movement Sciences, Maastricht University, P.O. Box 616, 6200 MD, Maastricht, The Netherlands.

出版信息

Histochem Cell Biol. 2004 Feb;121(2):101-7. doi: 10.1007/s00418-003-0615-3. Epub 2004 Jan 23.

Abstract

Limited information exists about the putative role and expression in human skeletal muscle cells of the 88-kDa integral membrane protein fatty acid translocase (FAT), highly homologous to the human leucocyte differentiation factor CD36. Therefore, we investigated in healthy male individuals the muscle (m. vastus lateralis) fibre type specific expression and subcellular localisation of FAT/CD36. For this purpose four different monoclonal antibodies raised against human and mouse FAT/CD36 were used. Acetone or methanol/acetone fixation were tested. Serial cryosections were cut at -20 degrees C, thaw-mounted on uncoated glass slides and air-dried before processing indirect immunofluorescence assays. Images were examined in a Nikon ER800 microscope, digitally captured, processed and analysed by LUCIA laboratory software. Three antibodies showed that FAT/CD36 was: (1) most abundantly expressed in capillary endothelium, (2) colocalised with caveolin-3, which indicates that FAT/CD36 is in the sarcolemma, or its close vicinity, and (3) abundantly expressed in (or in the close vicinity) of the sarcolemma and intracellular structures of type-1 muscle fibres, and much less abundantly in the sarcolemma of type-2 muscle fibres. One of the antibodies raised against mouse CD36 also detected myosin heavy chain 1, which makes it unsuitable in skeletal muscle research. The fixation (acetone or methanol/acetone) was found to be highly important for the result.

摘要

关于88 kDa整合膜蛋白脂肪酸转运蛋白(FAT)在人类骨骼肌细胞中的假定作用和表达情况,目前所知有限,该蛋白与人类白细胞分化因子CD36高度同源。因此,我们在健康男性个体中研究了FAT/CD36在外侧股四头肌中的纤维类型特异性表达和亚细胞定位。为此,我们使用了四种针对人类和小鼠FAT/CD36产生的不同单克隆抗体。测试了丙酮或甲醇/丙酮固定方法。在-20℃下切割连续冰冻切片,解冻后安装在未包被的载玻片上,风干后进行间接免疫荧光测定。在尼康ER800显微镜下检查图像,通过LUCIA实验室软件进行数字捕获、处理和分析。三种抗体显示FAT/CD36:(1)在毛细血管内皮中表达最为丰富;(2)与小窝蛋白-3共定位,这表明FAT/CD36位于肌膜或其附近;(3)在1型肌纤维的肌膜和细胞内结构中(或附近)大量表达,而在2型肌纤维的肌膜中表达较少。一种针对小鼠CD36产生的抗体还检测到肌球蛋白重链1,这使得它不适用于骨骼肌研究。结果发现固定方法(丙酮或甲醇/丙酮)对实验结果非常重要。

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