中华泌尿外科杂志
中華泌尿外科雜誌
중화비뇨외과잡지
CHINESE JOURNAL OF UROLOGY
2011年
4期
244-248
,共5页
黄世勇%朱绍兴%苏一鸣%蔡鹏%朱德胜%方荣金
黃世勇%硃紹興%囌一鳴%蔡鵬%硃德勝%方榮金
황세용%주소흥%소일명%채붕%주덕성%방영금
神经生长因子%间质干细胞%骨髓%糖尿病%大鼠
神經生長因子%間質榦細胞%骨髓%糖尿病%大鼠
신경생장인자%간질간세포%골수%당뇨병%대서
Nerve growth factor%Mesenchymal stem cells%Bone marrow%Diabetes mellitus%Rats
目的 将转入神经生长因子(NGF)的大鼠骨髓间充质干细胞(MSC)移植于糖尿病大鼠膀胱平滑肌组织内,观察MSC在膀胱组织内的存活和NGF基因的表达情况.方法 糖尿病组(30只)大鼠按链脲佐菌素(STZ)60 mg/kg行单次腹腔注射,对照组(15只)腹腔注射等体积的柠檬酸缓冲液.实验分组:对照组(正常大鼠膀胱)、发病组(糖尿病大鼠膀胱)、治疗组(糖尿病大鼠膀胱内移植转染NGF基因的MSC).溴苷法示踪NGF基因修饰的MSC在大鼠膀胱内的存活情况;RTPCR、ELISA法检测NGF基因在糖尿病大鼠膀胱内的表达情况.结果 单次腹腔注射STZ造模成功,8周后血糖仍处高位.NGF基因修饰的大鼠MSC移植入糖尿病大鼠膀胱内4周仍存活.ELISA检测结果显示对照组、发病组、治疗组大鼠膀胱NGF蛋白含量分别为(114±3)、(70±2)、(110±2)pg/ml,RT-PCR检测mRNA表达量分别为0.183±0.004、0.032±0.139、0.130±0.165.发病组与对照组相比NGF表达下降(P<0.05),治疗组与发病组相比NGF表达上升(P<0.05).结论转入NGF基因的大鼠MSC能在糖尿病大鼠膀胱中存活并稳定表达.
目的 將轉入神經生長因子(NGF)的大鼠骨髓間充質榦細胞(MSC)移植于糖尿病大鼠膀胱平滑肌組織內,觀察MSC在膀胱組織內的存活和NGF基因的錶達情況.方法 糖尿病組(30隻)大鼠按鏈脲佐菌素(STZ)60 mg/kg行單次腹腔註射,對照組(15隻)腹腔註射等體積的檸檬痠緩遲液.實驗分組:對照組(正常大鼠膀胱)、髮病組(糖尿病大鼠膀胱)、治療組(糖尿病大鼠膀胱內移植轉染NGF基因的MSC).溴苷法示蹤NGF基因脩飾的MSC在大鼠膀胱內的存活情況;RTPCR、ELISA法檢測NGF基因在糖尿病大鼠膀胱內的錶達情況.結果 單次腹腔註射STZ造模成功,8週後血糖仍處高位.NGF基因脩飾的大鼠MSC移植入糖尿病大鼠膀胱內4週仍存活.ELISA檢測結果顯示對照組、髮病組、治療組大鼠膀胱NGF蛋白含量分彆為(114±3)、(70±2)、(110±2)pg/ml,RT-PCR檢測mRNA錶達量分彆為0.183±0.004、0.032±0.139、0.130±0.165.髮病組與對照組相比NGF錶達下降(P<0.05),治療組與髮病組相比NGF錶達上升(P<0.05).結論轉入NGF基因的大鼠MSC能在糖尿病大鼠膀胱中存活併穩定錶達.
목적 장전입신경생장인자(NGF)적대서골수간충질간세포(MSC)이식우당뇨병대서방광평활기조직내,관찰MSC재방광조직내적존활화NGF기인적표체정황.방법 당뇨병조(30지)대서안련뇨좌균소(STZ)60 mg/kg행단차복강주사,대조조(15지)복강주사등체적적저몽산완충액.실험분조:대조조(정상대서방광)、발병조(당뇨병대서방광)、치료조(당뇨병대서방광내이식전염NGF기인적MSC).추감법시종NGF기인수식적MSC재대서방광내적존활정황;RTPCR、ELISA법검측NGF기인재당뇨병대서방광내적표체정황.결과 단차복강주사STZ조모성공,8주후혈당잉처고위.NGF기인수식적대서MSC이식입당뇨병대서방광내4주잉존활.ELISA검측결과현시대조조、발병조、치료조대서방광NGF단백함량분별위(114±3)、(70±2)、(110±2)pg/ml,RT-PCR검측mRNA표체량분별위0.183±0.004、0.032±0.139、0.130±0.165.발병조여대조조상비NGF표체하강(P<0.05),치료조여발병조상비NGF표체상승(P<0.05).결론전입NGF기인적대서MSC능재당뇨병대서방광중존활병은정표체.
Objective To confirm that rat bone marrow mesenchymal stem cells (MSC) transfected with nerve growth factor (NGF) gene in the bladder tissue of diabetic rats bladder tissues can survive and stably express NGF. Methods A diabetic rat model was constructed. The BrdU-labelled MSC transfected with NGF gene were transplanted into the diabetic rats bladder tissues. BrdUlabelled immunohistochemistry was used to observe the growth of MSC transfected with NGF gene in the diabetic rats bladder tissues. The expression of NGF mRNA and protein were checked by RT-PCR and ELISA. Results A diabetic rat model was successfully built by a single intraperitoneal injectionof STZ. The blood glucose was still high after 8 weeks. NGF gene modified MSC could be detected in the bladder of diabetic rats by BrdU-labelled immunohistochemistry. The concentration of NGF in the control group, disease group and treatment group were ( 114 ± 3), ( 70 ± 2), ( 110 ± 2) pg/ml by ELISA and mRNA quantity by RT-PCR were 0. 183±0. 004, 0. 032±0. 139, 0. 130±0. 165, respectively. Compared with the control group, the expression of NGF gene was decreased (P<0. 05) in the incidence group. The expression of NGF gene was increased (P<0. 05) in the treatment group compared with the disease group. Conclusions The NGF gene-modified MSC could survive in diabetic rats bladder tissues. The NGF gene in MSC could stably express in diabetic rats bladder tissues.