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作 者:程庆[1] 刘振湘[1] 尹先来[1] 邓湘东[2] 曹卉[2] 王顺兰[2] 谈顺[3] 白志明[1]
机构地区:[1]海口市人民医院泌尿外科,570208 [2]海口市人民医院中心实验室 [3]海口市人民医院病理科
出 处:《中华实验外科杂志》2012年第12期2416-2418,共3页Chinese Journal of Experimental Surgery
基 金:海南省自然科学基金资助项目(811151)
摘 要:目的观察大鼠骨髓间充质干细胞(BMSCs)经肾包膜下移植对可复性单侧输尿管梗阻模型(R—UUO)大鼠。肾间质纤维化及纤维化过程中炎性反应的影响,探讨包膜下移植的安全性。方法54只4月龄SD大鼠随机分为实验组(R—UUO+MSCs)、对照组(R.UUO+DMEM)、损伤对照组(R-UUO),每组18只,肾包膜下注射法移植后,于3、7、14d随机于每组内取6只大鼠,取患肾。免疫组织化学检测单核/巨噬细胞表面特异性标志抗原(ED-1)表达,Masson染色检测胶原沉积量。结果(1)和对照组(0.000773±0.000380)比较,实验组(0.000384±0.000407)在第14天的ED-1表达水平显著降低(P〈0.05),但胶原沉积量未见改善。(2)与损伤对照组(0.000293±0.000281)比较,对照组(0.000773±0.000380)在第14天时ED-1表达显著增加(P〈0.05),但胶原沉积量未见有显著增加。结论MSCs包膜下移植可抑制肾间质纤维化过程中的巨噬细胞浸润,但短期内不能改善纤维化。包膜下注射短期内有明确损伤,但并未造成纤维化水平加重。Objective To investigate the efficacy and safety of mesenchymal stem cells (MSCs) subcapsular injection in R-UUO model of rats by observing the changes in macrophage infiltration and collagen deposition. Methods A total of 54 S-D rats were randomly divided into three groups ( n = 18 each) , including the MSCs delivered group, DMEM delivered group and R-UUO group. At the day 3, 7 and 14 af- ter subeapsular transplantation of MSCs or vehicle, the 4 I^m thick sections of the kidney were stained with the Masson trichrome technique. Immunohistochemical staining was performed with mouse anti-CD68 anti- body ( ED-1 ). Results ( 1 ) The subeapsular transplantation of MSCs significantly reduced the mean 1.4 of ED-1 expression at 14th day after transplantation ( P 〈 0. 05 ), but didn' t attenuate the collagen deposi- tion; (2) The subcapsular transplantation of MSCs caused a significant rise in ED-1 mean IA as compared with sham-operated group on the 14th day ( P 〈 0.05 ), but didn' t augment the interstitial fibrosis. Con- dusion The subcapsular transplantation of MSCs in R-UUO rats could ameliorate the macrophage infiltra- tion in interstitium, but didn' t improve the interstitial fibrosis within 2 weeks. The subeapsular transplantation of MSCs aggravates inflammation of obstructive nephropathy on the 14th day after transplantation, but doesn't contribute to the interstitial fibrosis.
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