University of Kentucky, Maxwell H. Gluck Equine Research Center, Lexington, KY 40546, United States.
University of Kentucky, Maxwell H. Gluck Equine Research Center, Lexington, KY 40546, United States.
Vet Immunol Immunopathol. 2020 Jul;225:110058. doi: 10.1016/j.vetimm.2020.110058. Epub 2020 May 11.
While the use of lipopolysaccharide (LPS) to induce inflammation has been well described in the horse, the object of this study was to evaluate the effect of repeated intra-articular LPS injections and determine whether this method may be of use to assess changes in gene expression related to inflammation. Six mixed breed horses were utilized for this study, with three horses aged 10-17 years (older group) and three horses aged 3 years (younger group). One milliliter of phosphate-buffered saline containing 3 μg of LPS from Escherichia coli O111:B4 was aseptically injected into either the radiocarpal or front fetlock joint a total of four times, with at least two weeks between each injection and a different joint injected each time. Serum for protein concentration quantification and whole blood for expression analysis of 20 different genes were collected before each injection, as well as at multiple times post-injection. Statistical analysis was performed using analysis of variance (one-way and two-way) (P < 0.05). All horses experienced minimal or non-weight bearing lameness at 4-6 hours post-LPS injection, which generally improved by 24 h and resolved by 48 h. Multiple genes exhibited significantly differential expression when compared to both the pre-injection and sham injection time points, including CD14, TLR4, MMP1, MMP9, IL-1β, IL1RN, IL-10, ALOX5AP, IL-8, TNFα, CCL8, IGF1, and PTGS2. Additionally, multiple genes exhibited increased expression in horses where the radiocarpal joint was injected when compared to the fetlock joint, as well as in younger horses compared to older horses. Serum concentrations of serum amyloid A (SAA) were negative prior to injection while all horses demonstrated an increase by 9 h post-injection, which often remained until at least 144 h. Attempts to measure in vivo serum cytokine levels using a multiplex assay were not successful and believed to be due to the lower limits of detection for the assays. The measurement of mRNA expression of pro- and anti-inflammatory genes provide sensitive and rapid information regarding the inflammatory response to an acute, localized stimulus, although care must be taken when selecting target joints or age groups of horses as the transcriptional response may vary based on these choices.
虽然脂多糖 (LPS) 诱导炎症的作用在马中已有很好的描述,但本研究的目的是评估重复关节内 LPS 注射的效果,并确定这种方法是否可用于评估与炎症相关的基因表达变化。本研究使用了 6 匹混合品种马,其中 3 匹马年龄为 10-17 岁(老年组),3 匹马年龄为 3 岁(年轻组)。无菌条件下,将含有 3μg 大肠杆菌 O111:B4 LPS 的 1 毫升磷酸盐缓冲盐水分别注入桡腕关节或前跗关节,总共 4 次,每次注射之间至少间隔 2 周,每次注射不同的关节。在每次注射前以及注射后多个时间点采集血清以定量蛋白质浓度,并采集全血以分析 20 个不同基因的表达。使用方差分析(单向和双向)(P<0.05)进行统计分析。所有马在 LPS 注射后 4-6 小时均出现轻微或非负重性跛行,通常在 24 小时内改善,48 小时内消失。与注射前和假注射时间点相比,多个基因的表达明显不同,包括 CD14、TLR4、MMP1、MMP9、IL-1β、IL1RN、IL-10、ALOX5AP、IL-8、TNFα、CCL8、IGF1 和 PTGS2。此外,与跗关节相比,桡腕关节注射的马以及年轻马的多个基因表达增加。注射前血清淀粉样蛋白 A (SAA) 浓度为阴性,而所有马在注射后 9 小时均出现升高,直到至少 144 小时仍保持升高。尝试使用多重分析测定法测量体内细胞因子水平未成功,据信这是由于测定法的检测下限所致。对促炎和抗炎基因的 mRNA 表达进行测量可提供关于急性局部刺激引起的炎症反应的敏感且快速的信息,但是在选择靶关节或马的年龄组时必须小心,因为转录反应可能因这些选择而有所不同。