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首页> 外文期刊>The journal of obstetrics and gynaecology research >Improved nude mouse models for green fluorescence human endometriosis.
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Improved nude mouse models for green fluorescence human endometriosis.

机译:用于绿色荧光人类子宫内膜异位症的改良裸鼠模型。

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摘要

AIM: To establish an improved noninvasive fluorescent animal model for endometriosis. MATERIAL AND METHODS: Adenovirus encoding enhanced green fluorescent protein (Ad-eGFP) was used to transfect primary culture endometrial glandular cells and stromal cells (purified cell transfection and mixed injection, Group 1) as well as endometrial fragments (tissues transfection and injection, Group 2). Transfection results were compared between the cells and tissues in vitro. The GFP-transfected cells suspension of Group 1 or endometrial fragments of Group 2, with similar weight, were injected into nude mice subcutaneously and noninvasively observed every 5 days until day 15 (Subgroup 1, N = 5), day 20 (Subgroup 2, N = 5) or day 25 (Subgroup 3, N =11). The positive rates and duration times of the fluorescent lesions were calculated. RESULTS: After 18 h of incubation, glandular cells and stromal cells all had higher GFP-positive rates. In vivo imaging showed that the GFP positive rates of Group 1 were significantly higher than those of Group 2. The fluorescent-positive durations of Groups 1 and 2 were 23.636 +/- 4.523 days and 5.909 +/- 5.394 days, respectively (P < 0.001). In vivo analysis demonstrated that on days 15, 20, and 25, there were more typical lesions and fluorescent-positive lesions formed in Group 1 and that the lesion weight in Group 1 was greater. The structures of the lesions were all identified as human origin. CONCLUSION: A noninvasive animal model for endometriosis created by subcutaneous injection of an Ad-eGFP-transfected endometrial glandular and stromal cells suspension had higher a positive rate, longer duration time of fluorescent imaging and greater lesion weight.
机译:目的:建立子宫内膜异位症的改良无创荧光动物模型。材料和方法:使用编码增强型绿色荧光蛋白(Ad-eGFP)的腺病毒转染原代培养的子宫内膜腺细胞和基质细胞(纯化的细胞转染和混合注射,组1)以及子宫内膜片段(组织转染和注射,组1)。 2)。在体外比较细胞和组织的转染结果。将第1组的GFP转染的细胞悬液或第2组的子宫内膜片段以相似的重量皮下注射到裸鼠中,每5天观察一次,直到第15天(第1组,N = 5),第20天(第2组,第2天) N = 5)或第25天(子组3,N = 11)。计算出荧光损伤的阳性率和持续时间。结果:孵育18 h后,腺细胞和基质细胞均具有较高的GFP阳性率。体内成像显示,第1组的GFP阳性率显着高于第2组。第1和第2组的荧光阳性持续时间分别为23.636 +/- 4.523天和5.909 +/- 5.394天(P < 0.001)。体内分析表明,在第15、20和25天,第1组中形成了更多的典型病变和荧光阳性病变,而第1组中的病变重量更大。病变的结构都被确定为人类起源。结论:通过皮下注射Ad-eGFP转染的子宫内膜腺和基质细胞悬液建立的子宫内膜异位症非侵入性动物模型具有更高的阳性率,更长的荧光成像持续时间和更大的病变重量。

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