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建立 SV40 大 T 抗原永生化牦牛瘤胃成纤维细胞系及其对脂多糖的反应。

Establishment of SV40 Large T-Antigen-Immortalized Yak Rumen Fibroblast Cell Line and the Fibroblast Responses to Lipopolysaccharide.

机构信息

Key Laboratory of Low Carbon Culture and Safety Production in Cattle in Sichuan, Animal Nutrition Institute, Sichuan Agricultural University, Chengdu 611130, China.

出版信息

Toxins (Basel). 2023 Aug 31;15(9):537. doi: 10.3390/toxins15090537.

DOI:10.3390/toxins15090537
PMID:37755963
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10537058/
Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79d7/10537058/094e2961830f/toxins-15-00537-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79d7/10537058/9fd63d2be723/toxins-15-00537-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79d7/10537058/5e1373415006/toxins-15-00537-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79d7/10537058/0f5d82427bb6/toxins-15-00537-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79d7/10537058/a7d48a55a5bf/toxins-15-00537-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79d7/10537058/f3403f25345f/toxins-15-00537-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79d7/10537058/094e2961830f/toxins-15-00537-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79d7/10537058/9fd63d2be723/toxins-15-00537-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79d7/10537058/5e1373415006/toxins-15-00537-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79d7/10537058/0f5d82427bb6/toxins-15-00537-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79d7/10537058/a7d48a55a5bf/toxins-15-00537-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79d7/10537058/f3403f25345f/toxins-15-00537-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79d7/10537058/094e2961830f/toxins-15-00537-g006.jpg

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