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纸质出版:2007
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徐惠成,王延洲,王丹,秦茂林,常青,梁志清,史常旭.肌源性干细胞治疗压力性尿失禁的实验研究[J].陆军军医大学学报(原第三军医大学学报),2007,29(02):101-104.
XU Hui-cheng,WANG Yan-zhou,WANG Dan,QIN Mao-lin,CHANG Qing,LIANG Zhi-qing,SHI Chang-xu.Experimental study of muscle derived-stem cells for treatment of stress urinary incontinence[J].J Amry Med Univ (J Third Mil Med Univ),2007,29(02):101-104.
徐惠成,王延洲,王丹,秦茂林,常青,梁志清,史常旭.肌源性干细胞治疗压力性尿失禁的实验研究[J].陆军军医大学学报(原第三军医大学学报),2007,29(02):101-104. DOI:
XU Hui-cheng,WANG Yan-zhou,WANG Dan,QIN Mao-lin,CHANG Qing,LIANG Zhi-qing,SHI Chang-xu.Experimental study of muscle derived-stem cells for treatment of stress urinary incontinence[J].J Amry Med Univ (J Third Mil Med Univ),2007,29(02):101-104. DOI:
目的 探讨肌源性干细胞(muscle-derived stem cells, MDSCs)移植至压力性尿失禁(stress urinary incontinence, SUI)大鼠近端尿道后体内形态、分布以及尿动力学变化,为压力性尿失禁的干细胞移植治疗提供理论基础。 方法 采用坐骨神经离断法建立压力性尿失禁模型,改良差速贴壁技术分离MDSCs,pEGFP-N1转染作标记,注射至SUI大鼠近端尿道。尿动力学仪检测MDSCs移植后1、2周的漏尿点压力(leak point pressure, LPP)和最大膀胱容量。显微镜观察MDSCs移植后1、3、7、10、14 d荧光细胞的形态和分布。 结果 MDSCs移植后第7、14天,SUI大鼠的LPP均显著提高,移植后2周LPP显著高于移植后1周。在MDSCs移植后第1、3天,细胞保持小圆形和短梭形,局限于注射部位;第7天,一部分移植的MDSCs开始分化,分布范围扩大;第10天,一部分MDSCs分化为平滑肌细胞,部分死亡;第14天,一部分细胞分化为肌纤维,而其余细胞发生变性、死亡。 结论 MDSCs移植后能存活并分化而整合至尿道括约肌,尿道括约肌功能得到改善,提示MDSCs移植可能是治疗压力性尿失禁的有效方法。
Objective To study the differentiation of muscle-derived stem cells (MDSCs) and metergasis of periurethral intrinsic sphincter after MDSCs transplantation into proximal urethra of stress urinary incontinence (SUI) rats. Methods Sciatic nerve transection was used to establish rat model of SUI. MDSCs were isolated by improved preplate technique. After transfected with pEGFP-N1 plasmid
MDSCs were injected into proximal urethra of SUI rats. Urodynamic test was used to measure leak point pressure (LPP) and maximal bladder cap
acity at 1
st
week and 2
nd
week after MDSCs transplantation. On day 1
3
7
10
14 after injection
fluorocytes were observed by fluorescence microscope. Results LPP were significantly increased at 1
st
week and 2
nd
week after MDSCs injection
while LPP at 2
nd
week was significantly higher than that at 1
st
week. On day 1
3 after injection
the cells were small
round and short-fusiform
and distributed around the injected point; On day 7
some high-fluorescence cells were elongated and occupied larger area
but still localized within muscles surrounding urethra; On day 10
some fluorescent cells were long-fusiform and of strong fluorescence
while others lost normal form and were of weakened fluorescence; On day 14
fluorescent cells decreased with weakened fluorescence. Conclusion MDSCs could survive and differentiate after transplanted into proximal urethra of SUI rats and could improve function of sphincter muscle of urethra
suggesting that MDSCs transplantation may be an effective method to treat SUI.
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