Sharmila C, Williams John W, Reddy P Gopal
Department of Pathobiology, College of Veterinary Medicine Tuskegee University, AL 36088, USA.
Am J Vet Res. 2002 Oct;63(10):1418-22. doi: 10.2460/ajvr.2002.63.1418.
To determine the effect of caprine arthritis-encephalitis virus (CAEV) infection on expression of interleukin-16 (IL-16).
6 goats experimentally infected with CAEV and 6 age-matched healthy uninfected control goats.
Peripheral blood mononuclear cells (PBMCs) and synovial membrane cells from infected and control goats cultured with or without phytohemagglutinin were analyzed for IL-16 mRNA by use of a reverse transcriptase-polymerase chain reaction assay with goat-specific primers, after cloning and sequencing of a 384-bp fragment of the goat IL-16 gene. Synovial fluid, serum, and culture supernatants of PBMCs and synovial cells of control and CAEV-infected goats were analyzed for IL-16 by use of an ELISA.
The 384-bp product was 86% homologous to the corresponding human IL-16 nucleotide sequence. Higher expression of IL-16 mRNA in PBMCs (unstimulated or stimulated with phytohemagglutinin) was detected in samples from CAEV-infected goats, compared with control goats, but the difference was not significant. Synovial membrane cells infected in vitro had higher expression than uninfected control cells. Higher IL-16 concentration was detected in synovial fluid, serum, and culture supernatants of PBMCs of infected goats than in samples from control goats.
infection with CAEV increases expression of IL-16, a proinflammatory and chemotactic cytokine. This cytokine appears to be constitutively expressed at low concentrations in normal uninfected PBMCs and synovial membrane cells. Increased production of IL-16 in CAEV infection may partly be responsible for increased lymphoid cell infiltrations observed in arthritic joints and other tissues of CAEV-infected goats.
确定山羊关节炎-脑炎病毒(CAEV)感染对白细胞介素-16(IL-16)表达的影响。
6只经实验感染CAEV的山羊和6只年龄匹配的未感染健康对照山羊。
在用山羊特异性引物进行逆转录-聚合酶链反应分析之前,先对山羊IL-16基因的一个384bp片段进行克隆和测序,然后分析感染山羊和对照山羊的外周血单个核细胞(PBMCs)以及在有或没有植物血凝素的情况下培养的滑膜细胞中的IL-16 mRNA。使用酶联免疫吸附测定法(ELISA)分析对照山羊和CAEV感染山羊的滑膜液、血清以及PBMCs和滑膜细胞的培养上清液中的IL-16。
384bp产物与相应的人IL-16核苷酸序列具有86%的同源性。与对照山羊相比,在CAEV感染山羊的样本中检测到PBMCs(未刺激或用植物血凝素刺激)中IL-16 mRNA的表达较高,但差异不显著。体外感染的滑膜细胞比未感染的对照细胞表达更高。在感染山羊的滑膜液、血清以及PBMCs的培养上清液中检测到的IL-16浓度高于对照山羊的样本。
CAEV感染增加了促炎和趋化细胞因子IL-16的表达。这种细胞因子似乎在正常未感染的PBMCs和滑膜细胞中以低浓度组成性表达。CAEV感染中IL-16产生的增加可能部分是导致在CAEV感染山羊的关节炎关节和其他组织中观察到的淋巴细胞浸润增加的原因。