Key Laboratory of Low Carbon Culture and Safety Production in Cattle in Sichuan, Animal Nutrition Institute, Sichuan Agricultural University, Chengdu 611130, China.
Toxins (Basel). 2023 Aug 31;15(9):537. doi: 10.3390/toxins15090537.
The yak lives in harsh alpine environments and the rumen plays a crucial role in the digestive system. Rumen-associated cells have unique adaptations and functions. The yak rumen fibroblast cell line (SV40T-YFB) was immortalized by introducing simian virus 40 large T antigen (SV40T) by lentivirus-mediated transfection. Further, we have reported the effects of lipopolysaccharide (LPS) of different concentrations on cell proliferation, extracellular matrix (ECM), and proinflammatory mediators in SV40T-YFB. The results showed that the immortalized yak rumen fibroblast cell lines were identified as fibroblasts that presented oval nuclei, a fusiform shape, and positive vimentin and SV40T staining after stable passage. Chromosome karyotype analysis showed diploid characteristics of yak (n = 60). LPS at different concentrations inhibited cell viability in a dose-dependent manner. SV40T-YFB treated with LPS increased mRNA expression levels of matrix metalloproteinases (MMP-2 and MMP-9), inflammatory cytokines (TNF-α, IL-1β, IL-6), and urokinase-type plasminogen activator system components (uPA, uPAR). LPS inhibits the expression of tissue inhibitors of metalloproteinases (TIMP-1 and TIMP-2), plasminogen activator inhibitor-2 (PAI-2), fibronectin (FN), anti-inflammatory factor IL-10, and collagen I (COL I) in SV40T-YFB. Overall, these results suggest that LPS inhibits cell proliferation and induces ECM degradation and inflammatory response in SV40T-YFB.
牦牛生活在恶劣的高山环境中,瘤胃在消化系统中起着至关重要的作用。瘤胃相关细胞具有独特的适应性和功能。通过慢病毒介导的转染将猿猴病毒 40 大 T 抗原 (SV40T) 引入牦牛瘤胃成纤维细胞系 (SV40T-YFB) 中使其永生化。此外,我们还报道了不同浓度的脂多糖 (LPS) 对 SV40T-YFB 细胞增殖、细胞外基质 (ECM) 和促炎介质的影响。结果表明,稳定传代后的永生化牦牛瘤胃成纤维细胞系鉴定为成纤维细胞,呈椭圆形核,梭形,波形蛋白和 SV40T 染色阳性。染色体核型分析显示牦牛具有二倍体特征 (n = 60)。不同浓度的 LPS 呈剂量依赖性抑制细胞活力。用 LPS 处理的 SV40T-YFB 增加了基质金属蛋白酶 (MMP-2 和 MMP-9)、炎症细胞因子 (TNF-α、IL-1β、IL-6) 和尿激酶型纤溶酶原激活系统成分 (uPA、uPAR) 的 mRNA 表达水平。LPS 抑制 SV40T-YFB 中组织金属蛋白酶抑制剂 (TIMP-1 和 TIMP-2)、纤溶酶原激活物抑制剂-2 (PAI-2)、纤维连接蛋白 (FN)、抗炎因子 IL-10 和胶原蛋白 I (COL I) 的表达。总体而言,这些结果表明 LPS 抑制 SV40T-YFB 中的细胞增殖,并诱导 ECM 降解和炎症反应。