中国麻风皮肤病杂志
中國痳風皮膚病雜誌
중국마풍피부병잡지
CHINA JOURNAL OF LEPROSY AND SKIN DISEASES
2014年
5期
259-262
,共4页
许莉%段逸群%陈宏翔%曾志良%王辉
許莉%段逸群%陳宏翔%曾誌良%王輝
허리%단일군%진굉상%증지량%왕휘
白念珠菌%雌激素%NLRP3%核因子-κB%白细胞介素- 1β
白唸珠菌%雌激素%NLRP3%覈因子-κB%白細胞介素- 1β
백념주균%자격소%NLRP3%핵인자-κB%백세포개소- 1β
candida albicans%estrogen%NLRP3%nuclear factor-κB%interleukin- 1β
目的:确定雌激素对白念珠菌诱导的小鼠腹腔巨噬细胞NLRP3炎性体基因表达的影响。方法:体外培养小鼠腹腔巨噬细胞,将其分为5组:空白对照组、白念珠菌组、白念珠菌+10-10 mol/L 17β-雌二醇组、白念珠菌+10-9 mol/L 17β-雌二醇组和白念珠菌+10-8 mol/L 17β-雌二醇组。荧光定量PCR检测细胞内NLRP3 mRNA表达;Western Blot检测细胞内NF-κBp65和caspase-1p20的活性;酶联免疫吸附法( ELISA)测定各组细胞培养上清液中白细胞介素-1β( IL-1β)的含量。结果:巨噬细胞在白念珠菌的刺激下,与空白对照组比较细胞内NLRP3 mRNA的表达、NF-κB和caspase-1p20活性和细胞培养上清液中的IL-1β含量均明显升高(P<0.01);加入雌激素干预后,随着雌激素浓度的增高,细胞内NLRP3 mRNA表达、NF-κB和caspase-1p20活性、细胞培养上清液中的IL-1β含量明显低于对照组( P<0.01)。结论:雌激素可能通过抑制NF-κB活性抑制白念珠菌诱导的NLRP3表达、caspase-1的活化和IL-1β的分泌。
目的:確定雌激素對白唸珠菌誘導的小鼠腹腔巨噬細胞NLRP3炎性體基因錶達的影響。方法:體外培養小鼠腹腔巨噬細胞,將其分為5組:空白對照組、白唸珠菌組、白唸珠菌+10-10 mol/L 17β-雌二醇組、白唸珠菌+10-9 mol/L 17β-雌二醇組和白唸珠菌+10-8 mol/L 17β-雌二醇組。熒光定量PCR檢測細胞內NLRP3 mRNA錶達;Western Blot檢測細胞內NF-κBp65和caspase-1p20的活性;酶聯免疫吸附法( ELISA)測定各組細胞培養上清液中白細胞介素-1β( IL-1β)的含量。結果:巨噬細胞在白唸珠菌的刺激下,與空白對照組比較細胞內NLRP3 mRNA的錶達、NF-κB和caspase-1p20活性和細胞培養上清液中的IL-1β含量均明顯升高(P<0.01);加入雌激素榦預後,隨著雌激素濃度的增高,細胞內NLRP3 mRNA錶達、NF-κB和caspase-1p20活性、細胞培養上清液中的IL-1β含量明顯低于對照組( P<0.01)。結論:雌激素可能通過抑製NF-κB活性抑製白唸珠菌誘導的NLRP3錶達、caspase-1的活化和IL-1β的分泌。
목적:학정자격소대백념주균유도적소서복강거서세포NLRP3염성체기인표체적영향。방법:체외배양소서복강거서세포,장기분위5조:공백대조조、백념주균조、백념주균+10-10 mol/L 17β-자이순조、백념주균+10-9 mol/L 17β-자이순조화백념주균+10-8 mol/L 17β-자이순조。형광정량PCR검측세포내NLRP3 mRNA표체;Western Blot검측세포내NF-κBp65화caspase-1p20적활성;매련면역흡부법( ELISA)측정각조세포배양상청액중백세포개소-1β( IL-1β)적함량。결과:거서세포재백념주균적자격하,여공백대조조비교세포내NLRP3 mRNA적표체、NF-κB화caspase-1p20활성화세포배양상청액중적IL-1β함량균명현승고(P<0.01);가입자격소간예후,수착자격소농도적증고,세포내NLRP3 mRNA표체、NF-κB화caspase-1p20활성、세포배양상청액중적IL-1β함량명현저우대조조( P<0.01)。결론:자격소가능통과억제NF-κB활성억제백념주균유도적NLRP3표체、caspase-1적활화화IL-1β적분비。
Objective:To investigate the regulatory effects of estrogen on NLRP3 expression in murine per-itoneal macrophages induced by candida albicans. Methods: Murine peritoneal macrophages were cultured and randomly divided into five groups:blank control group, C. albicans group, C. albicans+10-10 mol/L-17β-estradiol group, C. albicans+10-9 mol/L- 17β-estradiol group and C. albicans+10-8 mol/L-17β-estradiol group.The mRNA expressions of NLRP3 in the cells were determined by real-time PCR. Western blot was per-formed to determine the activities of NF-κB and caspase-1p20. The protein of interleukin-1β( IL-1β) were determined by enzyme-linked immunosorbent assay ( ELISA) . Results: The mRNA expressions of NLRP3, the activities of NF-κB and caspase-1p20 in macrophages and the levels of IL-1β in the supernatant in-creased significantly when compared to the controls ( P<0.01) . After adding estrogen into the cells challenged with C. albicans, the mRNA expressions of NLRP3, the activities of NF-κB and caspase-1p20 in macropha-ges and the levels of IL-1βin the supernatant decreased with the increasing of estrogen concentrations, when compared to the control group (P<0.01). Conclusion: Estrogen can inhibit the expressions of NLRP3, the activation of caspase-1 and the production of pro-inflammatory cytokines IL-1β in macrophages challenged with C. albicans, through inhibiting the activities of NF-κB.