CAJ | 학술논문

目的：探讨益气与活血中药含药血清对骨髓间充质干细胞( bone marrow mesenchymal stem cells,BMSCs )增殖能力的影响。方法全细胞贴壁培养法获取、纯化BMSCs,体外培养,建立大鼠骨髓间充质干细胞的培养体系,采集空白对照大鼠、益气药、活血药、益气活血中药灌胃大鼠含药血清,用10%浓度以上不同含药血清培养第三代BMSCs,置于37℃,5% CO2培养箱中孵育。用流式细胞术鉴定BMSCs。噻唑基四唑比色法( methyl thiazolyl tetrazolium,MTT)测细胞活性,绘制生长曲线,观察10%益气、活血、益气活血中药含药血清对大鼠骨髓间充质干细胞体外增殖的影响。结果采用全骨髓贴壁法获取的BMSCs,经流式细胞术检测,CD44、CD106呈阳性表达,基本不表达CD45、CD34；MTT法检测结果显示,培养第2、4、5天细胞快速增长,均较前一天增长明显( P <0．05),第6天时活血方血清组与益气活血方血清组细胞增长已呈下降趋势,而其它三组在第6天细胞增长达最大,与前一天比较仍有差异( P<0．05),到第7天呈下降趋势。 BMSCs去除基线增殖率组间比较,培养第2天时,各组间比较虽无差异,但活血方血清组达最大(71．39±4．98%)；第4、6天时,益气活血方组达最大(66．40±1．47%),与其它三组比较P<0．01,活血方血清组次之；培养第6天时,益气方血清组较其它三组大,益气活血方血清组次之,活血方血清组最低。结论全细胞贴壁培养的大鼠骨髓间充质干细胞在细胞形态与表形表达上均具备BMSCs特征；益气活血中药含药血清对培养BMSCs增殖影响最大,活血方含药血清对细胞增殖影响出现最早、益气方含药血清对细胞增殖影响时间最长。
목적：탐토익기여활혈중약함약혈청대골수간충질간세포( bone marrow mesenchymal stem cells,BMSCs )증식능력적영향。방법전세포첩벽배양법획취、순화BMSCs,체외배양,건립대서골수간충질간세포적배양체계,채집공백대조대서、익기약、활혈약、익기활혈중약관위대서함약혈청,용10%농도이상불동함약혈청배양제삼대BMSCs,치우37℃,5% CO2배양상중부육。용류식세포술감정BMSCs。새서기사서비색법( methyl thiazolyl tetrazolium,MTT)측세포활성,회제생장곡선,관찰10%익기、활혈、익기활혈중약함약혈청대대서골수간충질간세포체외증식적영향。결과채용전골수첩벽법획취적BMSCs,경류식세포술검측,CD44、CD106정양성표체,기본불표체CD45、CD34；MTT법검측결과현시,배양제2、4、5천세포쾌속증장,균교전일천증장명현( P <0．05),제6천시활혈방혈청조여익기활혈방혈청조세포증장이정하강추세,이기타삼조재제6천세포증장체최대,여전일천비교잉유차이( P<0．05),도제7천정하강추세。 BMSCs거제기선증식솔조간비교,배양제2천시,각조간비교수무차이,단활혈방혈청조체최대(71．39±4．98%)；제4、6천시,익기활혈방조체최대(66．40±1．47%),여기타삼조비교P<0．01,활혈방혈청조차지；배양제6천시,익기방혈청조교기타삼조대,익기활혈방혈청조차지,활혈방혈청조최저。결론전세포첩벽배양적대서골수간충질간세포재세포형태여표형표체상균구비BMSCs특정；익기활혈중약함약혈청대배양BMSCs증식영향최대,활혈방함약혈청대세포증식영향출현최조、익기방함약혈청대세포증식영향시간최장。
Objective To explore the qi-tonifying and blood-activating Chinese herb serum on pro-liferation of SD rat bone marrow mesenchymal stem cells ( BMSCs) in vitro. Methods Rat BMSCs were i-solated from rat bone marrow and expanded by whole bone marrow adherent culture method in vitro, collect-ed blank serum of rat as control group and serum from qi-tonifying Chinese herb, blood-activating Chinese herb, qi-tonifying & blood-activating Chinese herb gavaged rats. BMSCs of the third generation were cul-tured in vitro with 10% concentrations of these four kinds of medicated serum at 37 ℃ and 5% CO2 incu-bator respectively. Flow cytometry was used for the identification of BMSCs and the proliferation of BMSCs was observed by MTT method and drew the growth curve. Results The BMSCs were obtained by whole bone marrow adherent culture method. The membranes of third generation of BMSCs were positive for CD44 and CD106 and negative for CD45 and CD34 detected by flow cytometry. The results showed that BMSCs grown rapidly compared to the day before it selves to the 2nd, 4th, and 5th days, the difference was signifi-cantly ( P<0. 05 ) . The cell growth of the blood-activating Chinese herb serum group and qi-tonifying &blood-activating Chinese herb serum group showed a downward trend, while the cell growth of the other three groups reached peak on the 6th day, but still had differences compared to the 5th day (P<0. 05), and declined on the 7th day. The removed baseline proliferation rate of BMSCs had no differences comparison a-mong groups at 2nd day, but the removed baseline proliferation rate of BMSCs in blood-activating Chinese herb serum group reached maximum (71. 39 ± 4. 98%), but no differences compared with the other three groups (P>0. 05). Compared with the other three groups, the removed baseline proliferation rate of qi-tonifying & blood-activating Chinese herb serum group was the largest ( 66. 40 ± 1. 47%) ( P<0. 01 ) on the 4th and 6th days, followed by blood-activating Chinese herb serum group. The removed baseline prolifer-ation rate of qi-tonifying Chinese herb serum group was the highest on the 6th day, followed by qi-tonifying&blood-activating Chinese herb serum group and blood-activating Chinese herb serum group. Conclusion BMSCs of SD rat isolation and cultivation by whole bone marrow adherent culture method could steadily express the bone mesenchymal stem cells surface markers and cells morphology. Qi-tonifying&blood-acti-vating Chinese herb serum has the greatest effect on the proliferation of cultured BMSCs; blood-activating Chinese herb serum motivates cell proliferation earliest; qi-tonifying Chinese herb serum has the longest effects on cell proliferation.