酸性成纖維細(xì)胞生長(zhǎng)因子對(duì)體外培養(yǎng)肌腱細(xì)胞增殖和量效關(guān)系的影響
發(fā)布時(shí)間:2018-04-03 10:24
本文選題:aFGF 切入點(diǎn):體外培養(yǎng) 出處:《中南大學(xué)》2007年碩士論文
【摘要】: 目的:觀察不同濃度aFGF對(duì)體外培養(yǎng)肌腱細(xì)胞增殖作用的影響。 方法:體外培養(yǎng)乳兔屈趾肌腱細(xì)胞后,取第3代乳兔肌腱細(xì)胞,按細(xì)胞數(shù)約為4×10~3/孔接種在96孔培養(yǎng)板的60孔中,每5孔為一組,在肌腱細(xì)胞相對(duì)同步化后加入aFGF,共分為12組,分別為無(wú)aFGF組(對(duì)照組),0.5ng/ml aFGF組,1.0ng/ml aFGF組,2.0ng/ml aFGF組,5.0ng/ml aFGF組,10ng/ml aFGF組,20ng/ml aFGF組,30ng/mlaFGF組,40ng/ml aFGF組,50ng/ml aFGF組,100g/ml aFGF組,200ng/ml aF GF組。顯微鏡下觀察各組細(xì)胞均進(jìn)入對(duì)數(shù)生長(zhǎng)期時(shí),用噻唑藍(lán)(meth-yl thiazolyl tetrazolium,MTT)法染色,在酶聯(lián)免疫檢測(cè)儀上測(cè)出各孔吸光度(optical density,OD)值,并計(jì)算各組OD均值。 結(jié)果:與對(duì)照組OD均值相比:1.0ng/ml aFGF組,2.0ng/ml aFGF組,5.0ng/ml aFGF組,10ng/ml aFGF組,30ng/ml aFGF組,40ng/mlaFGF組,50ng/ml aFGF,100ng/ml aFGF及200ng/ml aFGF組均有顯著性差異(P<0.05);0.5ng/mlaFGF無(wú)顯著性差異。各組OD均值隨aFGF濃度的增加,先逐漸增大(Ong/ml~20ng/ml),達(dá)到峰值后,,又逐漸下降(20ng/ml~200ng/ml)。 結(jié)論:1.0、2.0、5.0、10、20、30、40、50、100、200ng/ml aFGF組對(duì)肌腱細(xì)胞增殖有明顯作用;0.5ng/ml aFGF組對(duì)肌腱細(xì)胞增殖無(wú)明顯作用。aFGF濃度在Ong/ml~20ng/ml之間時(shí),肌腱細(xì)胞的增殖隨濃度增加呈上升趨勢(shì);在20ng/ml~200ng/ml之間時(shí),肌腱細(xì)胞的增殖隨濃度增加呈下降趨勢(shì)。20ng/ml aFGF是促進(jìn)體外培養(yǎng)乳兔屈趾肌腱細(xì)胞增殖最佳濃度。
[Abstract]:Aim: to observe the effect of different concentrations of aFGF on the proliferation of cultured tendon cells in vitro.Methods: after cultured rabbit flexor digitorum tendon cells in vitro, the third passage of rabbit tendon cells were inoculated into 60 holes of 96 well culture plate according to the number of cells 4 脳 10 ~ 3 / well. The tendon cells were added into aFGF12 groups after the relative synchronization of tendon cells.鍒嗗埆涓烘棤aFGF緇
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