van Rossum Maartje, van Asten Fons J, Rofina Jaime, Lenstra Johannes A, Benson Merrill D, Gruys Erik
Department of Pathology, Faculty of Veterinary Medicine, Utrecht University, Yalelaan 1, P.O. Box 80.158, 3508 TD Utrecht, The Netherlands.
Amyloid. 2004 Mar;11(1):38-43. doi: 10.1080/13506120410001676836.
Feline amyloidosis is an uncommon disorder caused by deposits of amyloid in a variety of organs. Most frequently encountered types are amyloid derived of pancreatic islet amyloid polypeptide (AIAPP) in older cats and of the apolipoprotein, apo-serum amyloid A (AA) in Abyssinian/Somali (Aby) and Siamese/Oriental (Siam) cats occurring at a relatively young age. For the AA protein of the Aby, Siam and domestic shorthair cat (DSH) breed different amino acid sequences have been described. It is not yet clear, however, whether the tendency to develop AA amyloidosis in Aby and Siam is associated with specific apoSAA protein sequences and whether this is breed specific. In this study, DNA from one Siam and two DSH cats revealed on Southern blot three bands suggesting at least three genes or gene clusters. The SAA cDNAs of hepatic mRNA from three Abys, five Siams and five DSHs were amplified by RT-PCR, cloned and sequenced. Siams and Abys had limited SAA sequence variability. All five Siams, three of which were positive for amyloid, had the amyloidogenic Siam SAA and the amyloidogenic Aby SAA sequence. Two of the Abys, both with amyloid, had the amyloidogenic Aby SAA sequence. The third Aby, without amyloid, missed its amyloidogenic sequence. The SAA sequences of the DSHs found in the present preliminary survey, suggested a possible tendency for more variability, whereas the amyloidogenic Siam as well as the amyloidogenic Aby sequence were found once. Up to five different sequences were found in a single animal. All five DSHs, moreover, had a specific sequence lacking in the Siams and Abys. The present results, especially those of the Siams, favor that in addition to the occurrence of amyloid associated SAA genes other factors such as infections and inflammatory processes are involved in the development of phenotypical amyloidosis.
猫淀粉样变性是一种由淀粉样物质在多种器官沉积引起的罕见疾病。最常见的类型是老年猫中源自胰岛淀粉样多肽(AIAPP)的淀粉样物质,以及在阿比西尼亚/索马里(Aby)和暹罗/东方(Siam)猫中相对年轻时出现的载脂蛋白血清淀粉样蛋白A(AA)。对于Aby、Siam和家猫短毛猫(DSH)品种的AA蛋白,已经描述了不同的氨基酸序列。然而,目前尚不清楚Aby和Siam中发生AA淀粉样变性的倾向是否与特定的载脂蛋白SAA蛋白序列相关,以及这是否具有品种特异性。在本研究中,一只暹罗猫和两只DSH猫的DNA在Southern印迹上显示出三条带,表明至少有三个基因或基因簇。通过RT-PCR扩增、克隆和测序了三只Aby、五只Siam和五只DSH肝脏mRNA的SAA cDNA。Siam和Aby的SAA序列变异性有限。所有五只Siam,其中三只淀粉样变性呈阳性,具有致淀粉样变性的Siam SAA和致淀粉样变性的Aby SAA序列。两只Aby,均有淀粉样变性,具有致淀粉样变性的Aby SAA序列。第三只Aby没有淀粉样变性,缺失了其致淀粉样变性序列。在本次初步调查中发现的DSH的SAA序列表明可能存在更大变异性的倾向,而致淀粉样变性的Siam以及致淀粉样变性的Aby序列仅出现一次。在单个动物中发现了多达五个不同的序列。此外,所有五只DSH都有一个Siam和Aby所没有的特定序列。目前的结果,尤其是Siam的结果,支持除了与淀粉样变性相关的SAA基因的出现外,其他因素如感染和炎症过程也参与了表型淀粉样变性的发展。