中国组织工程研究
中國組織工程研究
중국조직공정연구
Journal of Clinical Rehabilitative Tissue Engineering Research
2015年
40期
6515-6519
,共5页
李林格%冯娟%胡斌%寿玺%张春%张瑜%张华
李林格%馮娟%鬍斌%壽璽%張春%張瑜%張華
리림격%풍연%호빈%수새%장춘%장유%장화
实验动物%组织构建实验模型%变应性鼻炎%鼻科学%变态反应性疾病%小鼠%卵清蛋白%炎症反应%细胞因子%Th1/Th2平衡%嗜酸性粒细胞%国家自然科学基金
實驗動物%組織構建實驗模型%變應性鼻炎%鼻科學%變態反應性疾病%小鼠%卵清蛋白%炎癥反應%細胞因子%Th1/Th2平衡%嗜痠性粒細胞%國傢自然科學基金
실험동물%조직구건실험모형%변응성비염%비과학%변태반응성질병%소서%란청단백%염증반응%세포인자%Th1/Th2평형%기산성립세포%국가자연과학기금
背景:变应性鼻炎是指特应性个体接触变应原后,主要由 IgE 介导的介质组胺释放,并有多种免疫活性细胞和细胞因子等参与的鼻黏膜非感染性炎性疾病,与Th1和Th2免疫失衡相关。干扰素γ是Th1细胞分泌的细胞因子,而白细胞介素4是Th2细胞分泌的细胞因子。目的:构建稳定的129Sv小鼠变应性鼻炎模型,为129Sv小鼠为背景来源的基因敲除小鼠构建实验变应性鼻炎模型奠定基础,观察IgE、白细胞介素4和干扰素γ浓度变化。方法:将小鼠24只随机分2组,模型组采用卵清蛋白腹腔注射致敏激发,建立小鼠变应性鼻炎模型,对照组腹腔注射 PBS。建模成功后用取小鼠鼻黏膜染色后评估鼻黏膜嗜酸性粒细胞、浆细胞浸润的病理变化。用ELISA法检测白细胞介素4和干扰素γ细胞因子水平和卵清蛋白特异性IgE抗体浓度。结果与结论:与对照组相比,ELISA法检测显示,模型组血清中卵清蛋白-IgE和白细胞介素4浓度明显升高,干扰素γ浓度显著降低(P <0.05);苏木精-伊红染色显示,模型组纤毛倒伏,黏膜下层浆液腺增生明显,嗜酸性粒细胞、浆细胞浸润较明显。结果证实,实验成功构建实验变应性鼻炎小鼠模型,变应性鼻炎的发病机制与Th1/Th2失衡有关。
揹景:變應性鼻炎是指特應性箇體接觸變應原後,主要由 IgE 介導的介質組胺釋放,併有多種免疫活性細胞和細胞因子等參與的鼻黏膜非感染性炎性疾病,與Th1和Th2免疫失衡相關。榦擾素γ是Th1細胞分泌的細胞因子,而白細胞介素4是Th2細胞分泌的細胞因子。目的:構建穩定的129Sv小鼠變應性鼻炎模型,為129Sv小鼠為揹景來源的基因敲除小鼠構建實驗變應性鼻炎模型奠定基礎,觀察IgE、白細胞介素4和榦擾素γ濃度變化。方法:將小鼠24隻隨機分2組,模型組採用卵清蛋白腹腔註射緻敏激髮,建立小鼠變應性鼻炎模型,對照組腹腔註射 PBS。建模成功後用取小鼠鼻黏膜染色後評估鼻黏膜嗜痠性粒細胞、漿細胞浸潤的病理變化。用ELISA法檢測白細胞介素4和榦擾素γ細胞因子水平和卵清蛋白特異性IgE抗體濃度。結果與結論:與對照組相比,ELISA法檢測顯示,模型組血清中卵清蛋白-IgE和白細胞介素4濃度明顯升高,榦擾素γ濃度顯著降低(P <0.05);囌木精-伊紅染色顯示,模型組纖毛倒伏,黏膜下層漿液腺增生明顯,嗜痠性粒細胞、漿細胞浸潤較明顯。結果證實,實驗成功構建實驗變應性鼻炎小鼠模型,變應性鼻炎的髮病機製與Th1/Th2失衡有關。
배경:변응성비염시지특응성개체접촉변응원후,주요유 IgE 개도적개질조알석방,병유다충면역활성세포화세포인자등삼여적비점막비감염성염성질병,여Th1화Th2면역실형상관。간우소γ시Th1세포분비적세포인자,이백세포개소4시Th2세포분비적세포인자。목적:구건은정적129Sv소서변응성비염모형,위129Sv소서위배경래원적기인고제소서구건실험변응성비염모형전정기출,관찰IgE、백세포개소4화간우소γ농도변화。방법:장소서24지수궤분2조,모형조채용란청단백복강주사치민격발,건립소서변응성비염모형,대조조복강주사 PBS。건모성공후용취소서비점막염색후평고비점막기산성립세포、장세포침윤적병리변화。용ELISA법검측백세포개소4화간우소γ세포인자수평화란청단백특이성IgE항체농도。결과여결론:여대조조상비,ELISA법검측현시,모형조혈청중란청단백-IgE화백세포개소4농도명현승고,간우소γ농도현저강저(P <0.05);소목정-이홍염색현시,모형조섬모도복,점막하층장액선증생명현,기산성립세포、장세포침윤교명현。결과증실,실험성공구건실험변응성비염소서모형,변응성비염적발병궤제여Th1/Th2실형유관。
BACKGROUND:Atopic individuals predispose to alergic rhinitis after contacting with an alergen, which is mainly released by IgE-mediated histamine. Alergic rhinitis is a kind of non-infectious inflammatory disease that involves a variety of immune cels and cytokines and is related to Th1 and Th2 immune imbalance. Interferon γ is a cytokine secreted by Th1 cels, while interleukin-4 is a cytokine secreted by Th2 cels. OBJECTIVE:To establish a stable 129Sv mouse model of alergic rhinitis, so as to lay the foundation of establishing gene knockout 129Sv mouse models of alergic rhinitis, and to observe the concentration variation of IgE, interleukin-4 and interferon γ. METHODS: Twenty-four mice were randomly divided into 2 groups: model and control groups. Mice in the model group were sensitized by intraperitoneal injection of ovalbumin to establish mouse models of alergic rhinitis. Mice in the control group were subjected to intraperitoneal injection of PBS. After successful modeling, pathological changes of nasal eosinophils and plasmocyte infiltration were evaluated by nasal mucosa staining. Interleukin 4 and interferon γ levels and ovalbumin-specific IgE antibody concentration were detected by enzyme-linked immunosorbent assay. RESULTS AND CONCLUSION:Enzyme-linked immunosorbent assay showed that compared with the control group, serum ovalbumin-IgE and interleukin-4 concentrations were significantly increased, and Interferon γ concentration was significantly lower in the model group (P < 0.05). Hematoxylin-eosin staining results showed that cilia lodging and submucosal serous gland hyperplasia, eosinophils and plasmocyte infiltration were obvious. These results confirm that a mouse model of allergic rhinitis was successfully constructed in this study and the pathogenesis of allergic rhinitis was related to Th1/Th2 imbalance.