国际生物医学工程杂志
國際生物醫學工程雜誌
국제생물의학공정잡지
INTERNATIONAL JOURNAL OF BIOMEDICAL ENGINEERING
2010年
3期
142-146,后插3
,共6页
高亭%刘肖珩%薛隆娟%赖怡%曾烨%毛斌%沈阳%黄先亮
高亭%劉肖珩%薛隆娟%賴怡%曾燁%毛斌%瀋暘%黃先亮
고정%류초형%설륭연%뢰이%증엽%모빈%침양%황선량
白细胞介素-8%血管内皮细胞%通透性
白細胞介素-8%血管內皮細胞%通透性
백세포개소-8%혈관내피세포%통투성
Interleukin-8%Vascular endothelial cell%Permeability
目的 研究白细胞介素-8(IL-8)对血管内皮细胞通透性的影响.方法 采用Transwell弥散模型,以标志物漏出法检测IL-8不同浓度、不同作用时间对EA.hy926细胞单层通透性的影响;结晶紫染色法检测细胞形态学改变;透射电镜进行细胞连接形态学观察.结果 IL-8可明显增加血管内皮细胞单层的通透性(P<0.05),呈一定的剂量和时间依赖关系;荧光倒置相差显微镜观察,随着IL-8浓度和作用时间的增加,细胞明显回缩,细胞间隙明显增加;透射电镜实验表明,随着IL-8浓度和作用时间的增加,细胞连接逐渐打开、破坏.结论 IL-8以时间和剂量依赖方式引起血管内皮细胞通透性升高、细胞及细胞连接形态学的改变.
目的 研究白細胞介素-8(IL-8)對血管內皮細胞通透性的影響.方法 採用Transwell瀰散模型,以標誌物漏齣法檢測IL-8不同濃度、不同作用時間對EA.hy926細胞單層通透性的影響;結晶紫染色法檢測細胞形態學改變;透射電鏡進行細胞連接形態學觀察.結果 IL-8可明顯增加血管內皮細胞單層的通透性(P<0.05),呈一定的劑量和時間依賴關繫;熒光倒置相差顯微鏡觀察,隨著IL-8濃度和作用時間的增加,細胞明顯迴縮,細胞間隙明顯增加;透射電鏡實驗錶明,隨著IL-8濃度和作用時間的增加,細胞連接逐漸打開、破壞.結論 IL-8以時間和劑量依賴方式引起血管內皮細胞通透性升高、細胞及細胞連接形態學的改變.
목적 연구백세포개소-8(IL-8)대혈관내피세포통투성적영향.방법 채용Transwell미산모형,이표지물루출법검측IL-8불동농도、불동작용시간대EA.hy926세포단층통투성적영향;결정자염색법검측세포형태학개변;투사전경진행세포련접형태학관찰.결과 IL-8가명현증가혈관내피세포단층적통투성(P<0.05),정일정적제량화시간의뢰관계;형광도치상차현미경관찰,수착IL-8농도화작용시간적증가,세포명현회축,세포간극명현증가;투사전경실험표명,수착IL-8농도화작용시간적증가,세포련접축점타개、파배.결론 IL-8이시간화제량의뢰방식인기혈관내피세포통투성승고、세포급세포련접형태학적개변.
Objective To explore the influence of IL-8 on the permeability of vascular endothelial cells. Methods Vascular endothelial cells were cultured on the inserts of transwell filters. At different times after the addition of IL-8 of different concentration to the upper wells, the alternation of cell permeability was measured. Crystal violet staining was used to observe the morphological change of vascular endothelial cells. Transmission electron microscope was used to observe the morphology of the cell-cell junctions. Results The results demonstrated that IL-8 induced increase in the permeability of vascular endothelial cells in a dose and time dependent manner. Fluorescence inverted microscopic results showed that vascular endothelial cells recovered and the intercellular space increased with the increase of the dose of IL-8 or culture time. TEM observation indicated that the cell-cell junctions were opened and destroyed gradually with the increase of dose or culture time of IL-8. Conclusion IL-8 induces the increase of the permeability of vascular endothelial cells, alters the morphology of vascular endothelial cells, and destroys the cell-cell junctions in a dose and time dependent manner.