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作 者:时炳正[1] 徐志媛[1] 杜晓岩[1] 杜建宇[1] 范龙坤[2] 毕焕京[3] 廖立[3] 金岩[3]
机构地区:[1]佳木斯大学口腔医学院,黑龙江佳木斯154007 [2]沧州市中心医院口腔颌面外科 [3]第四军医大学口腔医学院组织工程中心
出 处:《口腔医学研究》2013年第2期111-116,共6页Journal of Oral Science Research
基 金:国家基础研究项目(973项目)(2010CB944800、2011CB964700);黑龙江省研究生创新科研项目(YJSCX2012-359HLJ);佳木斯大学重大项目培育基金项目(SZP2001-001)
摘 要:目的:探索DNA酶Ⅰ处理后骨髓间充质干细胞降低急性肺栓塞的发生。方法:体外培养小鼠骨髓间充质干细胞。C57小鼠分PBS注射组、10U/mL DNaseⅠ-PBS注射组、正常BMSCs注射组、DNaseⅠ处理后BMSCs注射组。PBS注射组与正常BMSCs注射组尾静脉注射PBS或临界致死剂量的BMSCs,脏器组织学检测,PBS注射组对照,观察急性死亡率;比较正常BMSCs与DNaseⅠ处理后BMSCs体外增殖、分化能力和悬液中细胞聚集状态;DNaseⅠ处理后BMSCs注射组注射DNaseⅠ处理后3×106个BMSCs 5ml/kg观察急性死亡率。结果:PBS注射组相比正常BMSCs注射组急性死亡率为60%、心肺异常、肺血管内异染物质,急性肺栓塞;DNaseⅠ预处理不影响BMSCs体外增殖分化能力;DNaseⅠ处理BMSCs较正常BMSCs聚集成团细胞比例显著下降。DNaseⅠ处理后BMSCs注射组的急性死亡率为23.3%,与正常BMSCs注射组比较差异显著。结论:DNaseⅠ预处理不影响BM-SCs的生物学特性并能抑制单细胞聚集降低静脉注射BMSCs所导致的急性肺栓塞。Objective: To investigate a novel method to reduce the occurrence of pulmonary embolism after BMSCs injection by using DNase I pretreatment. Methods: Mouse BMSCs were isolated, cultured and purified to the 3rd generation in vitro. C57BL/6 mice were divided into 4 groups: PBS injection group, 10U/ml DNase I-PBS injec- tion group, BMSCs injection group and DNase I pretreated BMSCs injection group. Acute death rate were calculated and different organs of dead mice were examined by histological analysis. Proliferation and differentiation ability a- long with aggregation status in cell suspension of BMSCs before and after DNase I treatment were detected in vitro. Result: The acute death rate of BMSCs injection group was 40% lower than PBS injection group, and histological examination revealed cardiopneumatic abnormality. Some deeply stained masses were found in pulmonic vessel. DNase I pretreatment did not affect the proliferation and differentiation ability of BMMSCs in vitro, but the propor- tion of aggregated cells declined significantly. The acute death rate of DNase I pretreated BMSCs injection group was 23.3%, which was significantly lower than BMSCs injection group. Conclution: DNase I pretreatment would not af- fect the biological character of BMSCs but could inhibit single cell aggregation.
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