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
49期
8468-8473
,共6页
张卫东%章方彪%史宏灿%谭荣邦%叶钢%李广宇%潘枢%孙飞
張衛東%章方彪%史宏燦%譚榮邦%葉鋼%李廣宇%潘樞%孫飛
장위동%장방표%사굉찬%담영방%협강%리엄우%반추%손비
干细胞%骨髓干细胞%骨髓间充质干细胞%红细胞裂解液%细胞培养%分离纯化%细胞增殖%细胞生物学%国家自然科学基金%干细胞图片文章
榦細胞%骨髓榦細胞%骨髓間充質榦細胞%紅細胞裂解液%細胞培養%分離純化%細胞增殖%細胞生物學%國傢自然科學基金%榦細胞圖片文章
간세포%골수간세포%골수간충질간세포%홍세포렬해액%세포배양%분리순화%세포증식%세포생물학%국가자연과학기금%간세포도편문장
背景:有研究向骨髓液中加入红细胞裂解液来提高分离纯化骨髓间充质干细胞的效率,以期获得纯度高、数量多的骨髓间充质干细胞。<br> 目的:进一步验证红细胞裂解液法体外分离纯化兔骨髓间充质干细胞的增殖特性,并对其进行细胞生物学鉴定。<br> 方法:使用红细胞裂解液提取含有兔骨髓间充质干细胞的骨髓悬混液,于4,7,10,13 d记录比较原代细胞的生长相对数量;观察传代细胞的生长情况,绘出 P2、P3、P4及P5代细胞的生长曲线,比较各代细胞的增殖特点;倒置相差显微镜观察细胞的形态,细胞免疫荧光及流式细胞仪检测所获得细胞的CD44、CD34表面抗原的表达情况。<br> 结果与结论:红细胞裂解液法所获得的兔骨髓间充质干细胞为均一规则的以梭形为主的贴壁细胞,其胞核胞核均质、核仁明显、胞浆丰富,且CD44抗原表达阳性、CD34抗原表达阴性;原代细胞生长曲线呈类“S”型;P4代细胞具有较好的增殖活性,其生长速度、所获取的细胞数量均优于其他代数细胞。说明红细胞裂解液法可以在体外较好的培养出骨髓间充质干细胞,其P4代细胞是骨髓间充质干细胞增殖能力最强的一代细胞。
揹景:有研究嚮骨髓液中加入紅細胞裂解液來提高分離純化骨髓間充質榦細胞的效率,以期穫得純度高、數量多的骨髓間充質榦細胞。<br> 目的:進一步驗證紅細胞裂解液法體外分離純化兔骨髓間充質榦細胞的增殖特性,併對其進行細胞生物學鑒定。<br> 方法:使用紅細胞裂解液提取含有兔骨髓間充質榦細胞的骨髓懸混液,于4,7,10,13 d記錄比較原代細胞的生長相對數量;觀察傳代細胞的生長情況,繪齣 P2、P3、P4及P5代細胞的生長麯線,比較各代細胞的增殖特點;倒置相差顯微鏡觀察細胞的形態,細胞免疫熒光及流式細胞儀檢測所穫得細胞的CD44、CD34錶麵抗原的錶達情況。<br> 結果與結論:紅細胞裂解液法所穫得的兔骨髓間充質榦細胞為均一規則的以梭形為主的貼壁細胞,其胞覈胞覈均質、覈仁明顯、胞漿豐富,且CD44抗原錶達暘性、CD34抗原錶達陰性;原代細胞生長麯線呈類“S”型;P4代細胞具有較好的增殖活性,其生長速度、所穫取的細胞數量均優于其他代數細胞。說明紅細胞裂解液法可以在體外較好的培養齣骨髓間充質榦細胞,其P4代細胞是骨髓間充質榦細胞增殖能力最彊的一代細胞。
배경:유연구향골수액중가입홍세포렬해액래제고분리순화골수간충질간세포적효솔,이기획득순도고、수량다적골수간충질간세포。<br> 목적:진일보험증홍세포렬해액법체외분리순화토골수간충질간세포적증식특성,병대기진행세포생물학감정。<br> 방법:사용홍세포렬해액제취함유토골수간충질간세포적골수현혼액,우4,7,10,13 d기록비교원대세포적생장상대수량;관찰전대세포적생장정황,회출 P2、P3、P4급P5대세포적생장곡선,비교각대세포적증식특점;도치상차현미경관찰세포적형태,세포면역형광급류식세포의검측소획득세포적CD44、CD34표면항원적표체정황。<br> 결과여결론:홍세포렬해액법소획득적토골수간충질간세포위균일규칙적이사형위주적첩벽세포,기포핵포핵균질、핵인명현、포장봉부,차CD44항원표체양성、CD34항원표체음성;원대세포생장곡선정류“S”형;P4대세포구유교호적증식활성,기생장속도、소획취적세포수량균우우기타대수세포。설명홍세포렬해액법가이재체외교호적배양출골수간충질간세포,기P4대세포시골수간충질간세포증식능력최강적일대세포。
BACKGROUND:Some studies have demonstrated that red blood celllysate added into the bone marrow can increase the efficiency of isolating and purifying mesenchymal stem cells, in order to obtain high-purity and high-quantity bone marrow mesenchymal stem cells. <br> OBJECTIVE:To isolate and culture bone marrow mesenchymal stem cells of rabbit with red blood celllysis in vitro for exploring proliferation characteristics and performing the biological identification of cells. <br> METHODS:Bone marrow suspension was col ected by puncturing the tibia with medul o-puncture needle. Red blood celllysis was added to the bone marrow suspension, and bone marrow mesenchymal stem cells were isolated and cultured. Numbers of primary cells were recorded at 4, 7, 10, and 13 days later And Growth curves of the cells at passages 2-5 were drawn for comparison of proliferative characteristics. Inverted phase contrast microscope was used to observe the morphological changes of cells. CD34, CD44 antigens of bone marrow mesenchymal stem cells were identified by flow cytometry and immunity fluorescence. <br> RESULTS AND CONCLUSION:The adherent bone marrow mesenchymal stem cells mainly showed s spindle shape, with homogeneous nuclei, prominent nucleoli, and rich cytoplasm, which were positive for CD44 antigen and negative for CD34 antigen. The primary cells exhibited an“S”shape. Passage 4 cells had a better proliferative ability, rapider growth and more counting of cells as compared with other generations. These findings indicate that red blood celllysis method is a feasible ways of culturing bone marrow mesenchymal stem cells 0 in vitro, and passage 4 cells have the strongest proliferation capacity.