基因敲除
促炎细胞因子
免疫印迹
免疫组织化学
脂多糖
肿瘤坏死因子α
NF-κB
NFKB1型
分子生物学
污渍
化学
炎症
生物
免疫学
细胞凋亡
基因
转录因子
生物化学
作者
Yong‐Wei Fu,Lu Li,Xiao‐Qian Wang,Yi Zhou,Lifang Zhu,Youmin Mei,Yan Xu
出处
期刊:Oral Diseases
[Wiley]
日期:2020-10-22
卷期号:27 (6): 1487-1497
被引量:5
摘要
Experiments were performed to evaluate CYLD expression in human gingival tissue samples and to examine the effects of CYLD on inflammatory responses in lipopolysaccharide (LPS)- or TNF-α-stimulated human gingival fibroblasts (HGFs).Immunohistochemistry for CYLD and p65 expression was performed with healthy and inflamed gingival tissue samples. siRNA was used to knock down the expression of CYLD in HGFs. Upon LPS or TNF-α stimulation, NF-κB activation was detected in control and CYLD-knockdown HGFs. RT-PCR was applied to determine gene expression. Western blot analyses were employed to assess protein expression. Immunofluorescence staining was carried out to evaluate the nuclear translocation of p65.Immunohistochemical staining showed the expression of CYLD in human gingival tissues. In addition, CYLD protein expression was reduced in inflamed gingival tissue samples compared with healthy tissue samples. CYLD knockdown greatly enhanced the mRNA expression of proinflammatory cytokines in LPS- or TNF-α-stimulated HGFs. Furthermore, knocking down CYLD expression increased LPS-stimulated NF-κB activation in HGFs. Unexpectedly, CYLD knockdown did not affect TNF-α-induced NF-κB activation.Our results suggest that CYLD participates in periodontal inflammatory responses by negatively regulating LPS-induced NF-κB signalling.
科研通智能强力驱动
Strongly Powered by AbleSci AI