CAJ | 학술논문

目的建屯三维血管瘤血管生成体外培养模型.方法将10例新鲜的增殖期血管瘤组织块置于纤维蛋白凝胶中以双层夹心法建屯三维血管瘤血管生成体外培养模型.于血管新生后3 d加入平阳霉素(PYM.1×102mg/L)做干预实验.镜下观察新生血管情况,SP免疫组织化学法检测第Ⅷ因子相关抗原(FⅧR-Ag)、透射电镜观察内皮细胞超微结构鉴定新生血管.结果血管瘤组织培养4～7 d后芽生出细小m管,至第8～10大长成枝丫状血管样结构,第11～14天之后血管样结构生长渐缓停滞萎缩.PYM作用1一2 d后血管样结构很快萎缩.组织周边新生树枝状结构经鉴定为血管内皮细胞.结论该模型部分程度上可代表血管生成、萎缩的过程,但细小血管样结构的芽生时间不等,萎缩较快,与体内血管瘤血管仍有一定区别.
목적 건둔삼유혈관류혈관생성체외배양모형.방법 장10례신선적증식기혈관류조직괴치우섬유단백응효중이쌍층협심법건둔삼유혈관류혈관생성체외배양모형.우혈관신생후3 d가입평양매소(PYM.1×102mg/L)주간예실험.경하관찰신생혈관정황,SP면역조직화학법검측제Ⅷ인자상관항원(FⅧR-Ag)、투사전경관찰내피세포초미결구감정신생혈관.결과 혈관류조직배양4～7 d후아생출세소m관,지제8～10대장성지아상혈관양결구,제11～14천지후혈관양결구생장점완정체위축.PYM작용1일2 d후혈관양결구흔쾌위축.조직주변신생수지상결구경감정위혈관내피세포.결론 해모형부분정도상가대표혈관생성、위축적과정,단세소혈관양결구적아생시간불등,위축교쾌,여체내혈관류혈관잉유일정구별.
Objective To create a three dimension(3D) in vitro model for angiogenesis of he-mangioma and to make initial use of the model. Methods A small fragment of hemangioma biopsy is em- bedded in fibrin gel in a well of culture plates and incubated in a serum-free, buffered-sah, minimal medi-um to set up the three-dimesnsion(3D) in vitro model for angiogenesis of hemangioma. The model is cul-tured in the culture box of 5% CO2,37℃ and saturated humidity. And pingyannycin as an interference factor is used to observe its effect of blood vessels. We observed the model by photics microscope and fluo-rescence microscope and HE staining. Results In the model ,a complex network of microvessels grows out from the 3 tissue fragments from the day 4th to 7th day after culture,and on the 8th to 10th day after cul-ture a compact network of microvessels come into being and micmvessels furcating and crossoverring,then tending to be stationary. Microvessels grow slowly to stagnate on the llth to 14th day after culture. The compact network around the tissue fragment was confirmed to be blood vessels by immunohistochemistry and electron microscopy. Micmvessels grow fastly to stagnate after 1 day to 2 day putting pingyangmycin in- to the model. The expression of the factor Ⅷ associated antigen was positive in the microvessels analyzed by SP immunohistochemistry. The cells in the microvessels were the vascular endothelial cells observed by transmission electron. Conclusion This model represented the in vivo status of hemangioma partly and could be an acceptable model for in vitro study. However, it has the disadvantages of unstable growth rate and regression time. Therefore,this model can not fully reflect the in vivo human hemangioma and further study needs to be carried out for establishing better model for investigation.