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
28期
4439-4444
,共6页
潘建科%郭柏铭%刘军%张娴%谢辉%郭达
潘建科%郭柏銘%劉軍%張嫻%謝輝%郭達
반건과%곽백명%류군%장한%사휘%곽체
干细胞%骨髓干细胞%龙鳖胶囊%骨髓间充质干细胞%骨关节炎%补肾活血%MTT%细胞增殖%国家自然科学基金
榦細胞%骨髓榦細胞%龍鱉膠囊%骨髓間充質榦細胞%骨關節炎%補腎活血%MTT%細胞增殖%國傢自然科學基金
간세포%골수간세포%룡별효낭%골수간충질간세포%골관절염%보신활혈%MTT%세포증식%국가자연과학기금
背景:临床应用补肾活血中药龙鳖胶囊治疗骨关节炎取得满意的疗效,但其作用机制尚不明确。目的:观察龙鳖胶囊对大鼠骨髓间充质干细胞增殖活性的影响。<br> 方法:采用全骨髓贴壁培养方法分离培养 SD 大鼠骨髓间充质干细胞,倒置显微镜进行形态学观察,流式细胞术检测细胞表面标志表达。用含龙鳖胶囊的完全培养基培养第4代骨髓间充质干细胞,药物质量浓度分为5,1 g/L和250,50,10 mg/L,作用24 h后用 MTT 法测定细胞活力。<br> 结果与结论:原代细胞呈现不规则形状贴壁生长,第2代细胞呈典型的纤维状,第3代细胞呈长纤维状、漩涡式生长。第4代骨髓间充质干细胞的表面分子CD29、CD90呈强阳性表达,CD44呈阳性表达,CD45、CD34呈阴性表达。5 g/L 和1 g/L质量浓度的龙鳖胶囊溶液可促进骨髓间充质干细胞增殖。结果表明龙鳖胶囊可能是通过促进骨髓间充质干细胞的增殖和分化,进而发挥治疗骨关节炎的作用。
揹景:臨床應用補腎活血中藥龍鱉膠囊治療骨關節炎取得滿意的療效,但其作用機製尚不明確。目的:觀察龍鱉膠囊對大鼠骨髓間充質榦細胞增殖活性的影響。<br> 方法:採用全骨髓貼壁培養方法分離培養 SD 大鼠骨髓間充質榦細胞,倒置顯微鏡進行形態學觀察,流式細胞術檢測細胞錶麵標誌錶達。用含龍鱉膠囊的完全培養基培養第4代骨髓間充質榦細胞,藥物質量濃度分為5,1 g/L和250,50,10 mg/L,作用24 h後用 MTT 法測定細胞活力。<br> 結果與結論:原代細胞呈現不規則形狀貼壁生長,第2代細胞呈典型的纖維狀,第3代細胞呈長纖維狀、漩渦式生長。第4代骨髓間充質榦細胞的錶麵分子CD29、CD90呈彊暘性錶達,CD44呈暘性錶達,CD45、CD34呈陰性錶達。5 g/L 和1 g/L質量濃度的龍鱉膠囊溶液可促進骨髓間充質榦細胞增殖。結果錶明龍鱉膠囊可能是通過促進骨髓間充質榦細胞的增殖和分化,進而髮揮治療骨關節炎的作用。
배경:림상응용보신활혈중약룡별효낭치료골관절염취득만의적료효,단기작용궤제상불명학。목적:관찰룡별효낭대대서골수간충질간세포증식활성적영향。<br> 방법:채용전골수첩벽배양방법분리배양 SD 대서골수간충질간세포,도치현미경진행형태학관찰,류식세포술검측세포표면표지표체。용함룡별효낭적완전배양기배양제4대골수간충질간세포,약물질량농도분위5,1 g/L화250,50,10 mg/L,작용24 h후용 MTT 법측정세포활력。<br> 결과여결론:원대세포정현불규칙형상첩벽생장,제2대세포정전형적섬유상,제3대세포정장섬유상、선와식생장。제4대골수간충질간세포적표면분자CD29、CD90정강양성표체,CD44정양성표체,CD45、CD34정음성표체。5 g/L 화1 g/L질량농도적룡별효낭용액가촉진골수간충질간세포증식。결과표명룡별효낭가능시통과촉진골수간충질간세포적증식화분화,진이발휘치료골관절염적작용。
BACKGROUND:Longbie Capsule has satisfactory outcomes in the treatment of osteoarthritis, but its mechanism is stil unclear. <br> OBJECTIVE:To study the effect of Longbie Capsule on proliferation of bone marrow mesenchymal stem cel s. METHODS:The bone marrow mesenchymal stem cel s from SD rats were separated and expanded by whole adherence culture, then subcultured and confirmed by morphological observation and flow cytometry. Passage 4 cel s were cultured in complete media containing 5 g/L, 1 g/L, 250 mg/L, 50 mg/L, 10 mg/L Longbie Capsule, respectively, for 24 hours. Then, MTT assay was used to detect cel viability. <br> RESULTS AND CONCLUSION:The primary cel s were adherent cel s characterized by irregular shape, passage 2 cel s were typical y fibrous-shaped, passage 3 cel s grew in long fibrous and swirl-type shape. Passage 4 cel s were strongly positive for CD29 and CD90, positive for CD44, and negative for CD34 and CD45. 5 g/L and 1 g/L Longbie Capsule promoted the proliferation of bone marrow mesenchymal stem cel s. These findings indicate that Longbie Capsule may promote the proliferation and differentiation of bone marrow mesenchymal stem cel s, thereby playing a therapeutic effect on osteoarthritis.