中国组织工程研究
中國組織工程研究
중국조직공정연구
Journal of Clinical Rehabilitative Tissue Engineering Research
2013年
7期
1168-1173
,共6页
宁斌%丁远景%龚维明%刘海飞%刘勇%王德春%胡有谷
寧斌%丁遠景%龔維明%劉海飛%劉勇%王德春%鬍有穀
저빈%정원경%공유명%류해비%류용%왕덕춘%호유곡
组织构建%软骨组织构建%髓核细胞%退变%微载体%细胞培养%细胞鉴定%立体培养%单层培养%国家自然科学基金%组织构建图片文章
組織構建%軟骨組織構建%髓覈細胞%退變%微載體%細胞培養%細胞鑒定%立體培養%單層培養%國傢自然科學基金%組織構建圖片文章
조직구건%연골조직구건%수핵세포%퇴변%미재체%세포배양%세포감정%입체배양%단층배양%국가자연과학기금%조직구건도편문장
背景:旋转生物反应器是目前应用较多的微载体培养系统.目的:应用微载体旋转立体培养方法对成人退变髓核细胞进行扩增及鉴定.方法:对手术切除的髓核组织进行原代培养,传代后进行单层培养和微载体旋转立体培养的对比,并行苏木精-伊红、Gimsa 染色观察细胞形态,利用电镜观察其超微结构,利用 MTT 比色法检测细胞生长活性.结果与结论:倒置相差显微镜观察培养的细胞符合退变髓核细胞形态,透射电镜下可显示其退变改变.倒置相差显微镜和扫描电镜下观察,可见退变的髓核细胞呈立体状生长,并能够成功甩珠传代.细胞在对数生长期时,微载体培养的细胞的生长活性明显高于单层培养组的细胞.表明微载体旋转立体培养法可以较好的维持细胞表型,对对数生长期髓核细胞的细胞活性具有明显的刺激作用.
揹景:鏇轉生物反應器是目前應用較多的微載體培養繫統.目的:應用微載體鏇轉立體培養方法對成人退變髓覈細胞進行擴增及鑒定.方法:對手術切除的髓覈組織進行原代培養,傳代後進行單層培養和微載體鏇轉立體培養的對比,併行囌木精-伊紅、Gimsa 染色觀察細胞形態,利用電鏡觀察其超微結構,利用 MTT 比色法檢測細胞生長活性.結果與結論:倒置相差顯微鏡觀察培養的細胞符閤退變髓覈細胞形態,透射電鏡下可顯示其退變改變.倒置相差顯微鏡和掃描電鏡下觀察,可見退變的髓覈細胞呈立體狀生長,併能夠成功甩珠傳代.細胞在對數生長期時,微載體培養的細胞的生長活性明顯高于單層培養組的細胞.錶明微載體鏇轉立體培養法可以較好的維持細胞錶型,對對數生長期髓覈細胞的細胞活性具有明顯的刺激作用.
배경:선전생물반응기시목전응용교다적미재체배양계통.목적:응용미재체선전입체배양방법대성인퇴변수핵세포진행확증급감정.방법:대수술절제적수핵조직진행원대배양,전대후진행단층배양화미재체선전입체배양적대비,병행소목정-이홍、Gimsa 염색관찰세포형태,이용전경관찰기초미결구,이용 MTT 비색법검측세포생장활성.결과여결론:도치상차현미경관찰배양적세포부합퇴변수핵세포형태,투사전경하가현시기퇴변개변.도치상차현미경화소묘전경하관찰,가견퇴변적수핵세포정입체상생장,병능구성공솔주전대.세포재대수생장기시,미재체배양적세포적생장활성명현고우단층배양조적세포.표명미재체선전입체배양법가이교호적유지세포표형,대대수생장기수핵세포적세포활성구유명현적자격작용.
@@@@BACKGROUND: Rotating bioreactor is a microcarrier-based stirred culture system that is currently used more often. OBJECTIVE: To culture the adult degenerative nucleus pulposus cells in vitro by a microcarrier-based stirred culture system, and then to amplify and identify the cells. METHODS: Nucleus pulposus specimens taken from patients with disc degenerative diseases were randomly divided into monolayer culture group and micro-carrier culture group. The cel morphology was observed by hematoxylin-eosin staining and Gimsa staining, the microstructure was observed under an electron microscope, cel viability was detected by MTT method. RESULTS AND CONCLUSION: The morphology of degenerative nucleus pulpous cells was identified by inverted phase contrast microscope, and the regression was showed by a transmission electron microscope. The microcarrier cultured cells were observed by an inverted phase contrast microscope and scanning electron microscope showing stereoscopic shape. In the logarithmic growth phase, the growth activity of microcarrier culture cells was significantly higher than that of the cells in monolayer culture. Microcarrier-based stirred culture system can stabilize the cel phenotype, and significantly stimulate the cel ular activity of nucleus pulposus cells in the logarithmic growth phase.