Antohe F, Popov D, Radulescu L, Simionescu N, Börchers T, Spener F, Simionescu M
Institute of Cellular Biology and Pathology Nicolae Simionescu, Bucharest, Romania.
Eur J Cell Biol. 1998 Jun;76(2):102-9. doi: 10.1016/S0171-9335(98)80022-8.
Due to their hydrophobic nature, free fatty acids require carriers for transport across and within the cells. The endothelial layer is the first barrier to be traversed by the fatty acids, from the plasma to the underlying cells and tissues. We tried to find out whether cytosolic fatty acid-binding proteins (FABPs) are present in the endothelium of large vessels (aortic endothelial cells) and small vessels (myocardial capillaries) using the following experimental approaches: (i) loading the delipidated aortic endothelial cell (EC) homogenate and the heart cytosolic proteins and membrane proteins with [14C]palmitate or [14C]oleate, respectively, followed by autoradiographic detection of electrophoretically separated bands; (ii) detection by immunoprecipitation of heart-type FABP (H-FABP) using an affinity-purified antibody raised against bovine H-FABP (anti-H-FABP), and (iii) localization of FABP by indirect immunofluorescence and gold-immunocytochemistry applied to cultured EC and to thick and thin frozen sections of mouse heart. The results showed that: (i) within the EC homogenate proteins that express affinity for [14C]palmitate have an apparent Mr of 15000, and 40000-45000, that correspond as molecular mass to cytosolic and membrane FABPs, respectively. Similar affinity was found by incubation with [14C]oleate, that binds to a protein of Mr 15000 in the heart cytosol, and to a 40-45 kDa protein in the membrane fraction; (ii) anti-H-FABP immunoprecipitated specifically a cytosolic 15 kDa peptide (H-FABP); (iii) by indirect immunofluorescence, cytosolic H-FABP was localized on heart microvessels and myocytes and also in cultured aortic EC where intense spotted fluorescence characteristic for cytosolic antigens was present; (iv) by immunocytochemistry, H-FABP was detected in the EC cytoplasm, and in close proximity to the cytoplasmic aspect of plasmalemma and vesicle membranes. Together the data attest the presence of the 15 kDa, heart-type FABP in the endothelium of aorta and heart microvessels.
由于其疏水性,游离脂肪酸需要载体才能在细胞间穿梭并进入细胞内部。从血浆到其下方的细胞和组织,内皮层是脂肪酸穿越的第一道屏障。我们试图通过以下实验方法来确定大血管(主动脉内皮细胞)和小血管(心肌毛细血管)的内皮中是否存在胞质脂肪酸结合蛋白(FABP):(i)分别用[14C]棕榈酸酯或[14C]油酸酯加载脱脂的主动脉内皮细胞(EC)匀浆、心脏胞质蛋白和膜蛋白,然后通过放射自显影检测电泳分离的条带;(ii)使用针对牛心脏型FABP(H-FABP)制备的亲和纯化抗体(抗H-FABP)通过免疫沉淀法检测心脏型FABP(H-FABP);(iii)通过间接免疫荧光和金免疫细胞化学法对培养的EC以及小鼠心脏的厚、薄冰冻切片进行FABP定位。结果表明:(i)在EC匀浆中,对[14C]棕榈酸酯具有亲和力的蛋白质的表观分子量为15000和40000 - 45000,其分子量分别对应于胞质FABP和膜FABP。用[14C]油酸酯孵育也发现了类似的亲和力,[14C]油酸酯与心脏胞质中分子量为15000的一种蛋白质以及膜组分中40 - 45 kDa的一种蛋白质结合;(ii)抗H-FABP特异性免疫沉淀出一种胞质15 kDa肽(H-FABP);(iii)通过间接免疫荧光,胞质H-FABP定位于心脏微血管和心肌细胞上,也存在于培养的主动脉EC中,其中存在胞质抗原特有的强烈斑点荧光;(iv)通过免疫细胞化学法,在EC细胞质中以及靠近质膜和囊泡膜的细胞质一侧检测到H-FABP。这些数据共同证明了15 kDa心脏型FABP存在于主动脉和心脏微血管的内皮中。