蚌埠医学院学报
蚌埠醫學院學報
방부의학원학보
Journal of Bengbu Medical College
2015年
11期
1473-1476
,共4页
轮状病毒%核因子κB%γ-干扰素%肠道外感染%BALB/C乳鼠%蛋白质印迹法%免疫组织化学
輪狀病毒%覈因子κB%γ-榦擾素%腸道外感染%BALB/C乳鼠%蛋白質印跡法%免疫組織化學
륜상병독%핵인자κB%γ-간우소%장도외감염%BALB/C유서%단백질인적법%면역조직화학
rotavirus%nuclear factor κB%interferon-γ%extraintestinal infection%BALB/C suckling mouse%Western blot%immunohistochemistry
目的::检测肝脏核因子( NF)-κB的表达,评估γ-干扰素( IFN-γ)对乳鼠感染轮状病毒( RV)后的作用。方法:将乳鼠分为肠道外感染对照组、IFN-γ大小剂量干预组。腹腔注射RV建立2日龄RV肠道外感染模型。用大小剂量(2μg,0.2μg) IFN-γ在BALB/C乳鼠背部皮下注射3 d。模型建立后第5天取材,观察肝脏病理组织学变化,蛋白质印迹法和免疫组织化学法检测肝脏NF-κB表达。结果:IFN-γ小剂量干预组乳鼠肝脏病理损伤评分较肠道外感染对照组差异无统计学意义( P>0.05)。 IFN-γ大剂量干预组乳鼠肝脏病理损伤评分均较肠道外感染对照组和IFN-γ小剂量干预组明显增高(P<0.01)。蛋白质印迹法和免疫组织化学法显示IFN-γ大小剂量干预组NF-κB表达随IFN-γ剂量的增加而增加(P<0.01)。结论:IFN-γ能刺激NF-κB的表达。肝脏的病理损伤与NF-κB在肝脏的表达量相关。
目的::檢測肝髒覈因子( NF)-κB的錶達,評估γ-榦擾素( IFN-γ)對乳鼠感染輪狀病毒( RV)後的作用。方法:將乳鼠分為腸道外感染對照組、IFN-γ大小劑量榦預組。腹腔註射RV建立2日齡RV腸道外感染模型。用大小劑量(2μg,0.2μg) IFN-γ在BALB/C乳鼠揹部皮下註射3 d。模型建立後第5天取材,觀察肝髒病理組織學變化,蛋白質印跡法和免疫組織化學法檢測肝髒NF-κB錶達。結果:IFN-γ小劑量榦預組乳鼠肝髒病理損傷評分較腸道外感染對照組差異無統計學意義( P>0.05)。 IFN-γ大劑量榦預組乳鼠肝髒病理損傷評分均較腸道外感染對照組和IFN-γ小劑量榦預組明顯增高(P<0.01)。蛋白質印跡法和免疫組織化學法顯示IFN-γ大小劑量榦預組NF-κB錶達隨IFN-γ劑量的增加而增加(P<0.01)。結論:IFN-γ能刺激NF-κB的錶達。肝髒的病理損傷與NF-κB在肝髒的錶達量相關。
목적::검측간장핵인자( NF)-κB적표체,평고γ-간우소( IFN-γ)대유서감염륜상병독( RV)후적작용。방법:장유서분위장도외감염대조조、IFN-γ대소제량간예조。복강주사RV건립2일령RV장도외감염모형。용대소제량(2μg,0.2μg) IFN-γ재BALB/C유서배부피하주사3 d。모형건립후제5천취재,관찰간장병리조직학변화,단백질인적법화면역조직화학법검측간장NF-κB표체。결과:IFN-γ소제량간예조유서간장병리손상평분교장도외감염대조조차이무통계학의의( P>0.05)。 IFN-γ대제량간예조유서간장병리손상평분균교장도외감염대조조화IFN-γ소제량간예조명현증고(P<0.01)。단백질인적법화면역조직화학법현시IFN-γ대소제량간예조NF-κB표체수IFN-γ제량적증가이증가(P<0.01)。결론:IFN-γ능자격NF-κB적표체。간장적병리손상여NF-κB재간장적표체량상관。
Objective:To explore the expression of hepatic NF-κB for evaluating the effects of IFN-γon suckling mouse with rotavirus ( RV) infection. Methods:The suckling mouse were divided into the control group,high and low-dose IFN-γgroups. The extraintestinal rotavirus infection model of 2-day-old suckling mouse was established by intraperitoneal injection of rotavirus. The 2 μg and 0. 2 μg IFN-γ were injected subcutaneously into the back of BALB/C suckling mouse for 3 days. The pathological changes and expressions of NF-κB detected by Western blot and immunohistochemistry in liver were observed after 5 days of model establishment. Results:The difference of the score of liver pathological damage between low-dose IFN-γgroup and control group was not statistically significant( P>0. 05). The score of liver pathological damage in high-dose IFN-γgroup was significantly higher than that in control group and low-dose IFN-γ group(P<0. 01). Western blotting and immunohistochemistry results showed that the expression of NF-κB increased with the dose increasing of IFN-γ(P<0. 01). Conclusions:IFN-γ can stimulate the expression of NF-κB. The pathological damage of the liver was correlated with the expression of NF-κB.