Department of Clinical Sciences, College of Veterinary Medicine, Cornell University, Ithaca, NY, USA.
Theriogenology. 2012 Jan 15;77(2):356-72. doi: 10.1016/j.theriogenology.2011.08.008. Epub 2011 Sep 14.
Whereas neutrophils are the main phagocytic leukocytes, monocytes and macrophages are actively involved in immunomodulation after infection. Recent studies have demonstrated that neutrophil function is impaired by the state of negative energy balance around parturition, and that cows that develop uterine disease have a greater degree of negative energy balance than healthy cows. The objectives of this study were to compare monocyte gene expression and protein secretion of selected cytokines from calving to 42 d after calving in Holstein cows that did or did not develop uterine disease. Real time quantitative RT-PCR (Tumor necrosis factor-α (TNFα), Interleukin (IL)-1β, IL-6, IL-8 and IL-10) and ELISA (TNFα, IL-1β and IL-8) were used to evaluate cytokine response following in vitro stimulation of blood-derived monocytes with irradiated E. coli. Relative to unstimulated cells, E. coli-stimulated monocytes from cows with metritis had lower gene expression of key pro-inflammatory cytokines than healthy cows from calving to 14 d after calving (TNFα at 0, 7, and 14 d after calving, IL-1β and IL-6 at 7 and 14 d after calving; P < 0.05). There were no significant differences between groups for expression of IL-8 or the anti-inflammatory cytokine IL-10. This was due, in part, to higher gene expression in unstimulated monocytes (TNFα, IL-1β, IL-6 and IL-10) in early lactation from cows with metritis. Expression of mRNA in stimulated cells (relative to housekeeping genes) was lower for TNFα (7 and 14 d postpartum) and for IL-10 (7 and 14 d postpartum) in cows with metritis. Concentration of TNFα was lower in the culture medium of E. coli-stimulated monocytes from cows with metritis than healthy cows at calving and 7 and 21 d after calving (P < 0.05). Circulating cytokine concentrations were not different between groups for IL-8 and were below the limits of detection for TNFα and IL-1β. Cytokine gene expression and production were similar between healthy cows and cows that developed endometritis, diagnosed cytologically at 42 d after calving. We concluded that altered levels of expression and production of pro-inflammatory cytokines postpartum could contribute to impaired inflammatory response and predispose cows to development of metritis.
虽然中性粒细胞是主要的吞噬性白细胞,但单核细胞和巨噬细胞在感染后积极参与免疫调节。最近的研究表明,围分娩期负氮平衡状态会损害中性粒细胞功能,而且发生子宫疾病的奶牛比健康奶牛有更大程度的负氮平衡。本研究的目的是比较产犊后至产后 42 天患或不患子宫疾病的荷斯坦奶牛单核细胞基因表达和选定细胞因子的蛋白分泌。实时定量 RT-PCR(肿瘤坏死因子-α(TNFα)、白细胞介素(IL)-1β、IL-6、IL-8 和 IL-10)和 ELISA(TNFα、IL-1β 和 IL-8)用于评估血源性单核细胞经照射大肠杆菌体外刺激后的细胞因子反应。与未刺激细胞相比,患有子宫炎的奶牛产后至产后 14 天的大肠杆菌刺激单核细胞中关键促炎细胞因子的基因表达低于健康奶牛(产后 0、7 和 14 天的 TNFα、7 和 14 天的 IL-1β 和 IL-6;P<0.05)。两组间 IL-8 或抗炎细胞因子 IL-10 的表达无显着差异。这部分归因于患有子宫炎的奶牛在泌乳早期未刺激单核细胞中更高的基因表达(TNFα、IL-1β、IL-6 和 IL-10)。与管家基因相比,刺激细胞中的 mRNA 表达较低(产后 7 和 14 天的 TNFα 和产后 7 和 14 天的 IL-10)患有子宫炎的奶牛。与健康奶牛相比,患有子宫炎的奶牛大肠杆菌刺激单核细胞培养基中的 TNFα 浓度在产后和产后 7 天和 21 天较低(P<0.05)。对于 IL-8,两组间的循环细胞因子浓度没有差异,并且对于 TNFα 和 IL-1β,浓度低于检测限。健康奶牛和产后 42 天通过细胞学诊断患有子宫内膜炎的奶牛之间的细胞因子基因表达和产生相似。我们得出结论,产后促炎细胞因子表达和产生水平的改变可能导致炎症反应受损,并使奶牛易发生子宫炎。