de Bruin T, de Rooster H, van Bree H, Cox E
Department of Diagnostic Imaging of Domestic Animals, Faculty of Veterinary Medicine, Ghent University, Salisburylaan 133, 9820 Merelbeke, Belgium.
Vet Immunol Immunopathol. 2005 Dec 15;108(3-4):387-97. doi: 10.1016/j.vetimm.2005.06.013. Epub 2005 Aug 15.
The objective of this study was to examine and compare the presence of interleukin (IL)-8 mRNA in canine stifle osteoarthritis (OA) differing in etiopathogenesis. Synovial fluid (SF) samples were collected from 24 clinically normal stifle joints and 46 diseased stifle joints (32 stifle joints with cranial cruciate ligament rupture (CCLR), 2 joints with CCLR and patella luxation (PL), 7 joints with medial PL and 5 joints with primary OA). The samples were centrifuged to collect synovial fluid cells for RNA extraction. Reverse transcription polymerase chain reaction (RT-PCR) was performed to obtain cDNA from all samples. Canine IL-8 mRNA expression was determined using real time PCR. Synovial fluid glass smears were made of all samples and coloured with H&E for differential cell counts. All stifle joints were radiographed and graded for the severity of OA. Sixty-one percent (28/46) of the samples from canine stifle OA had IL-8 mRNA expression in contrast to 4% (1/24) in the control stifle joints. This difference in prevalence is highly significant. There were no statistically significant pairwise differences among the mean ranks of the various OA groups for the absolute amount of IL-8 mRNA expression. Neither was there a link between the severity of OA (determined by radiographic evaluation) and the presence of IL-8 in the SF nor any significant difference in the absolute amount of IL-8 between the different OA grades. No statistical difference was found in differential cell counts between IL-8-positive and -negative SF samples. IL-8 cannot be used as a specific joint disease marker since IL-8 expression is found in OA differing in etiopathogenesis. It might, however, relate to the ongoing inflammation within the joint.
本研究的目的是检测和比较不同病因发病机制的犬膝关节骨关节炎(OA)中白细胞介素(IL)-8 mRNA的存在情况。从24个临床正常的膝关节和46个患病膝关节(32个前交叉韧带断裂(CCLR)的膝关节、2个CCLR合并髌骨脱位(PL)的关节、7个内侧PL关节和5个原发性OA关节)采集滑液(SF)样本。将样本离心以收集滑液细胞用于RNA提取。进行逆转录聚合酶链反应(RT-PCR)以从所有样本中获得cDNA。使用实时PCR测定犬IL-8 mRNA表达。对所有样本制作滑液玻璃涂片并用苏木精和伊红染色以进行细胞分类计数。对所有膝关节进行X线摄影并对OA严重程度进行分级。犬膝关节OA样本中有61%(28/46)表达IL-8 mRNA,而对照膝关节中为4%(1/24)。这种患病率差异具有高度显著性。不同OA组IL-8 mRNA表达绝对量的平均秩次之间没有统计学上的显著两两差异。OA严重程度(通过X线评估确定)与SF中IL-8的存在之间也没有关联,不同OA分级之间IL-8的绝对量也没有显著差异。IL-8阳性和阴性SF样本的细胞分类计数没有统计学差异。由于在不同病因发病机制的OA中均发现IL-8表达,因此IL-8不能用作特定的关节疾病标志物。然而,它可能与关节内正在进行的炎症有关。