中国组织工程研究
中國組織工程研究
중국조직공정연구
Journal of Clinical Rehabilitative Tissue Engineering Research
2015年
41期
6677-6682
,共6页
干细胞%移植%骨不连%骨髓间充质干细胞%干细胞治疗%微损伤环境
榦細胞%移植%骨不連%骨髓間充質榦細胞%榦細胞治療%微損傷環境
간세포%이식%골불련%골수간충질간세포%간세포치료%미손상배경
Bone Marrow%Mesenchymal Stem Cel Transplantation%Radius%Bone Diseases%Tissue Engineering
背景:骨髓干细胞能够增殖再生,与传统的手术治疗方案结合能明显增强骨不连的治疗效果,具有重要的应用价值。目的:探讨骨髓间充质干细胞在微损伤环境中对骨不连的治疗效果。方法:选取清洁级纯种新西兰大白兔40只,采用随机数字表法分为实验组与对照组,每组20只。按照手术操作流程获取胫骨骨髓,分离培养骨髓间充质干细胞,待细胞增殖到第3代够107数量级时,进行超顺磁氧化铁纳米粒子培养标记。在兔前肢桡骨中段约15 mm处造成骨缺损,骨缺损6周发生骨不连。实验组大白兔将骨髓间充质干细胞与髂骨碎粒一起植入骨缺损处。对照组不进行干细胞移植,于骨缺损处植入髂骨碎粒。术后12周内,观察大白兔骨不连部位大体形态、X射线片、病理学染色结果。结果与结论:实验组术后明显发现骨痂,骨缺损处逐渐修复,直至完全愈合;对照组大白兔骨不连部位没有骨痂,骨髓腔封闭,充填肉芽组织。实验组有增生活跃的软骨组织,碎粒融合,骨缺损处出现类骨质,成骨细胞进行性增加;对照组软骨增生差,有大量死骨,骨粒未融合,没有成骨细胞。实验组桡骨缺损部位X射线显示云雾状影,骨髓腔恢复再通,骨骼塑形好;对照组骨碎粒吸收较少,骨髓腔部分闭塞,骨骼未连接,缺损处硬化。结果显示在局部微损伤环境中,骨髓间充质干细胞能够增殖分化为成骨细胞,修复骨缺损导致的骨不连具有显著效果。
揹景:骨髓榦細胞能夠增殖再生,與傳統的手術治療方案結閤能明顯增彊骨不連的治療效果,具有重要的應用價值。目的:探討骨髓間充質榦細胞在微損傷環境中對骨不連的治療效果。方法:選取清潔級純種新西蘭大白兔40隻,採用隨機數字錶法分為實驗組與對照組,每組20隻。按照手術操作流程穫取脛骨骨髓,分離培養骨髓間充質榦細胞,待細胞增殖到第3代夠107數量級時,進行超順磁氧化鐵納米粒子培養標記。在兔前肢橈骨中段約15 mm處造成骨缺損,骨缺損6週髮生骨不連。實驗組大白兔將骨髓間充質榦細胞與髂骨碎粒一起植入骨缺損處。對照組不進行榦細胞移植,于骨缺損處植入髂骨碎粒。術後12週內,觀察大白兔骨不連部位大體形態、X射線片、病理學染色結果。結果與結論:實驗組術後明顯髮現骨痂,骨缺損處逐漸脩複,直至完全愈閤;對照組大白兔骨不連部位沒有骨痂,骨髓腔封閉,充填肉芽組織。實驗組有增生活躍的軟骨組織,碎粒融閤,骨缺損處齣現類骨質,成骨細胞進行性增加;對照組軟骨增生差,有大量死骨,骨粒未融閤,沒有成骨細胞。實驗組橈骨缺損部位X射線顯示雲霧狀影,骨髓腔恢複再通,骨骼塑形好;對照組骨碎粒吸收較少,骨髓腔部分閉塞,骨骼未連接,缺損處硬化。結果顯示在跼部微損傷環境中,骨髓間充質榦細胞能夠增殖分化為成骨細胞,脩複骨缺損導緻的骨不連具有顯著效果。
배경:골수간세포능구증식재생,여전통적수술치료방안결합능명현증강골불련적치료효과,구유중요적응용개치。목적:탐토골수간충질간세포재미손상배경중대골불련적치료효과。방법:선취청길급순충신서란대백토40지,채용수궤수자표법분위실험조여대조조,매조20지。안조수술조작류정획취경골골수,분리배양골수간충질간세포,대세포증식도제3대구107수량급시,진행초순자양화철납미입자배양표기。재토전지뇨골중단약15 mm처조성골결손,골결손6주발생골불련。실험조대백토장골수간충질간세포여가골쇄립일기식입골결손처。대조조불진행간세포이식,우골결손처식입가골쇄립。술후12주내,관찰대백토골불련부위대체형태、X사선편、병이학염색결과。결과여결론:실험조술후명현발현골가,골결손처축점수복,직지완전유합;대조조대백토골불련부위몰유골가,골수강봉폐,충전육아조직。실험조유증생활약적연골조직,쇄립융합,골결손처출현류골질,성골세포진행성증가;대조조연골증생차,유대량사골,골립미융합,몰유성골세포。실험조뇨골결손부위X사선현시운무상영,골수강회복재통,골격소형호;대조조골쇄립흡수교소,골수강부분폐새,골격미련접,결손처경화。결과현시재국부미손상배경중,골수간충질간세포능구증식분화위성골세포,수복골결손도치적골불련구유현저효과。
BACKGROUND:Bone marrow stem cels combined with traditional surgery regimen can significantly improve the therapeutic effects on bone nonunion, which are considered to have an important application value. OBJECTIVE:To explore therapeutic effect of bone marrow mesenchymal stem cels on bone nonunion under micro-damage environment. METHODS:Forty New Zealand white rabbits were selected and randomized into experimental and control groups, 20 rabbits in each group. Bone marrow of the tibia was extracted to isolate and culture bone marrow mesenchymal stem cels. Passage 3 cels with the order of magnitudes of 107 were labeled by superparamagnetic iron oxide nanoparticles. A 15-mm bone defect was made at the middle of the radius of the rabbit forelimb. Bone nonunion appeared at 6 weeks after bone defects. Bone marrow mesenchymal stem cels combined with iliac particles were implanted into the bone defect of rabbits in the experimental group, and only iliac particles were implanted into the bone defect of rabbits in the control group. Within 12 weeks after implantation, the bone nonunion was observed through gross morphology, X-ray observation, and pathological observation. RESULTS AND CONCLUSION:After implantation, a remarkable calus was found in the experimental group, and the bone defect recovered gradualy until it was completely healed; in the control group, there was no calus, and the bone marrow cavity was closed and ful of granulation tissues. In the experimental group, there were actively proliferated cartilage tissues, bone particles were fused, osteoid structures appeared, and osteoblasts proliferated progressively; in the control group, poor cartilage hyperplasia was found, and there were a large amount of dead bone tissues but no fused bone particles and osteoblasts. In the experimental group, X-ray films on the defected radium showed cloudiness-like shadow, the bone marrow cavity was recanalized, and the skeleton was shaped wel; in the control group, few bone particles were absorbed, the bone marrow cavity was partly recanalized, and the injured bone was not healed with osteosclerosis. These findings indicate that under the micro-damage environment, bone marrow mesenchymal stem cels can differentiate into osteoblasts to repair bone defects-induced bone nonunion.