中华医学杂志
中華醫學雜誌
중화의학잡지
National Medical Journal of China
2011年
30期
2135-2138
,共4页
曹朴%薛建新%贾瑞鹏%许露伟%李文成%钱铭%陈波%薄成佳
曹樸%薛建新%賈瑞鵬%許露偉%李文成%錢銘%陳波%薄成佳
조박%설건신%가서붕%허로위%리문성%전명%진파%박성가
精索扭转%再灌注损伤%干细胞%细胞移植%增强型绿色荧光蛋白
精索扭轉%再灌註損傷%榦細胞%細胞移植%增彊型綠色熒光蛋白
정색뉴전%재관주손상%간세포%세포이식%증강형록색형광단백
Spermatic cord torison%Reperfusion injury%Stem cells%Cell transplantation%Enhanced green fluorescent protein
目的 探讨内皮祖细胞(EPC)移植对睾丸扭转复位后生精功能的影响.方法 获取大鼠骨髓源性EPC,采用携带增强型绿色荧光蛋白的重组腺病毒(Ad-eGFP)转染EPC.将大鼠分3组,每组各6只.假手术组:左侧睾丸未扭转;缺血再灌注损伤(IRI)组:睾丸扭转复位后经股静脉注射1 ml生理盐水;EPC组:睾丸扭转复位后注射1 ml EPC悬液(EPC数为1.0×106个).另外对3只睾丸扭转复位后大鼠进行Ad-eGFP转染后的EPC移植.术后5 d,观察移植EPC的归巢特征,并检测各组睾丸组织病理变化以及凋亡细胞/生精小管情况.结果 重复感染倍数(MOI)=50时,Ad-eGFP对EPC的转染效率>73.7%.Ad-eGFP EPC移植后5 d,可在左侧睾丸组织中发现绿色荧光细胞.假手术组生精细胞结构正常,凋亡细胞/生精小管为0.09±0.02.IRI组生精细胞稀少,凋亡细胞/生精小管为2.82 ±0.81.EPC组生精上皮较IRI组显著增厚,EPC组凋亡细胞/生精小管为0.32±0.09,低于IRI组,差异有统计学意义(P<0.01).结论 EPC移植可改善睾丸扭转导致的生精功能障碍,对生精细胞产生保护作用.
目的 探討內皮祖細胞(EPC)移植對睪汍扭轉複位後生精功能的影響.方法 穫取大鼠骨髓源性EPC,採用攜帶增彊型綠色熒光蛋白的重組腺病毒(Ad-eGFP)轉染EPC.將大鼠分3組,每組各6隻.假手術組:左側睪汍未扭轉;缺血再灌註損傷(IRI)組:睪汍扭轉複位後經股靜脈註射1 ml生理鹽水;EPC組:睪汍扭轉複位後註射1 ml EPC懸液(EPC數為1.0×106箇).另外對3隻睪汍扭轉複位後大鼠進行Ad-eGFP轉染後的EPC移植.術後5 d,觀察移植EPC的歸巢特徵,併檢測各組睪汍組織病理變化以及凋亡細胞/生精小管情況.結果 重複感染倍數(MOI)=50時,Ad-eGFP對EPC的轉染效率>73.7%.Ad-eGFP EPC移植後5 d,可在左側睪汍組織中髮現綠色熒光細胞.假手術組生精細胞結構正常,凋亡細胞/生精小管為0.09±0.02.IRI組生精細胞稀少,凋亡細胞/生精小管為2.82 ±0.81.EPC組生精上皮較IRI組顯著增厚,EPC組凋亡細胞/生精小管為0.32±0.09,低于IRI組,差異有統計學意義(P<0.01).結論 EPC移植可改善睪汍扭轉導緻的生精功能障礙,對生精細胞產生保護作用.
목적 탐토내피조세포(EPC)이식대고환뉴전복위후생정공능적영향.방법 획취대서골수원성EPC,채용휴대증강형록색형광단백적중조선병독(Ad-eGFP)전염EPC.장대서분3조,매조각6지.가수술조:좌측고환미뉴전;결혈재관주손상(IRI)조:고환뉴전복위후경고정맥주사1 ml생리염수;EPC조:고환뉴전복위후주사1 ml EPC현액(EPC수위1.0×106개).령외대3지고환뉴전복위후대서진행Ad-eGFP전염후적EPC이식.술후5 d,관찰이식EPC적귀소특정,병검측각조고환조직병리변화이급조망세포/생정소관정황.결과 중복감염배수(MOI)=50시,Ad-eGFP대EPC적전염효솔>73.7%.Ad-eGFP EPC이식후5 d,가재좌측고환조직중발현록색형광세포.가수술조생정세포결구정상,조망세포/생정소관위0.09±0.02.IRI조생정세포희소,조망세포/생정소관위2.82 ±0.81.EPC조생정상피교IRI조현저증후,EPC조조망세포/생정소관위0.32±0.09,저우IRI조,차이유통계학의의(P<0.01).결론 EPC이식가개선고환뉴전도치적생정공능장애,대생정세포산생보호작용.
Objective To investigate the effects of transplanted endothelial progenitor cells (EPCs) on the spermatogenic functions in testicular detorsion. Methods Bone-marrow-derived EPCs were obtained from rats and transfected by enhanced green fluorescent protein adenovirus (Ad-eGFP). The rats were divided into 3 groups (n=6 each). In the sham group, left testis was not twisted. In the ischemia reperfusion injury (IRI) group, 1 ml saline was injected into the femoral vein of each rat after testicular detorsion. In the EPCs group, 1 ml EPCs suspension (1.0×106 EPCs) was injected into each rat after testicular detorsion. The Ad-eGFP transfected EPCs were injected into the 3 additional rats of testicular torsion-detorsion. At Day 5 post-transplantation, the characteristics of transplanted EPCs homing were detected. And the pathological changes and apoptotic cells/seminiferous tubules in left testis were examined. ResultsWhen the value of multiplication of infection (MOI) was at 50, the transfection rate of EPCs by Ad-eGFP exceeded 73.7%. At Day 5 post-treatment, the cells exhibiting green fluorescence were detected in left testis. The germ cells in rats of the sham group were normal. And the ratio of apoptotic cells to seminiferous tubules was 0.09±0.02. The germ cells in rats of the IRI group were much fewer. And the ratio of apoptotic cells to seminiferous tubules was 2.82±0.81. As compared with the IRI group, seminiferous epithelium was thicker in the EPCs group. And the ratio of apoptotic cells to seminiferous tubules was 0.32±0.09 in the EPCs group. It was much smaller than that in the IRI group. There was significant difference (P<0.01). Conclusion The transplantation of EPCs is effective for treating the spermatogenic dysfunctions caused by testicular torsion so as to greatly enhance the spermatogenic functions.