Funaoka Hiroyuki, Kanda Tatsuo, Fujii Hiroshi
DS Pharma Biomedical Co., Ltd., Suita 564-0053, Japan.
Rinsho Byori. 2010 Feb;58(2):162-8.
Fatty acid binding protein (FABP) is one of the intracellular proteins, with a low molecular weight of approximately 15 kDa, that plays important roles in the transportation and metabolism of long-chain fatty acids. FABP family proteins could be used as tissue specific injury marker based on the following characteristics of FABP: (1) a soluble protein in the cytoplasm, (2) high tissue specificity, (3) abundance in the tissue, and (4) low molecular weight. Among the FABP family proteins, intestinal fatty acid-binding protein(I-FABP) is specifically and abundantly present in epithelial cells of the mucosal layer of the small intestinal tissue. I-FABP is also considered to be rapidly released into the circulation just after small intestinal mucosal tissue is injured. Based on this mechanism, many investigators have already reported the relationship between serum I-FABP concentration and small intestinal diseases from early 1990s. Recently, we have succeeded in establishing a sandwich ELISA system for measuring human I-FABP concentration by using the combination of antibodies highly specific to I-FABP. This ELISA system did not show any cross-reactivity with other types of FABP and indicated excellent quantitative characteristics such as reproducibility, dilution linearity, and recovery. Using this ELISA system, we determined that the reference value of serum I-FABP concentration is designated to 2.0 ng/mL or less in the circulation of normal healthy individuals. In considering the clinical potential of serum I-FABP concentration, this sandwich ELISA system may contribute as a tool to perform differential diagnosis of acute abdomen with mucosal damage of the small intestine.
脂肪酸结合蛋白(FABP)是一种细胞内蛋白质,分子量约为15 kDa,在长链脂肪酸的运输和代谢中起重要作用。基于FABP的以下特性,FABP家族蛋白可作为组织特异性损伤标志物:(1)细胞质中的可溶性蛋白;(2)高组织特异性;(3)在组织中含量丰富;(4)分子量低。在FABP家族蛋白中,肠脂肪酸结合蛋白(I-FABP)特异性且大量存在于小肠组织黏膜层的上皮细胞中。I-FABP也被认为在小肠黏膜组织受损后会迅速释放到循环中。基于这一机制,自20世纪90年代初以来,许多研究人员已经报道了血清I-FABP浓度与小肠疾病之间的关系。最近,我们成功建立了一种夹心ELISA系统,通过使用对I-FABP高度特异的抗体组合来测量人I-FABP浓度。该ELISA系统与其他类型的FABP没有任何交叉反应,并显示出优异的定量特性,如重现性、稀释线性和回收率。使用该ELISA系统,我们确定正常健康个体循环中血清I-FABP浓度的参考值设定为2.0 ng/mL或更低。考虑到血清I-FABP浓度的临床潜力,这种夹心ELISA系统可能有助于作为一种工具对小肠黏膜损伤的急腹症进行鉴别诊断。