中华皮肤科杂志
中華皮膚科雜誌
중화피부과잡지
Chinese Journal of Dermatology
2011年
3期
199-201
,共3页
王倩%李红文%宫璀璀%吴景兰
王倩%李紅文%宮璀璀%吳景蘭
왕천%리홍문%궁최최%오경란
角蛋白细胞%细胞增殖%细胞分化%细胞,培养的%鳄梨油%橄榄油
角蛋白細胞%細胞增殖%細胞分化%細胞,培養的%鱷梨油%橄欖油
각단백세포%세포증식%세포분화%세포,배양적%악리유%감람유
Keratinocytes%Cell proliferation%Cell differentiation%Cells,cultured%Avocado oil%Olive oil
目的 探讨天然植物鳄梨油和橄榄油对HaCaT细胞系增殖及分化的影响.方法 将培养的HaCaT细胞分为鳄梨油组、橄榄油组及对照组.应用MTT实验确定鳄梨油和橄榄油对HaCaT细胞的适用剂量.以免疫细胞化学、免疫斑点印迹技术分别检测各组HaCaT细胞的c-myc原癌基因(c-myc)、有丝分裂原激活蛋白激酶(MAPK)、NF-κB、丝聚蛋白、内披蛋白、角蛋白10的表达.结果 对照组c-myc、MAPK、NF-κB免疫化学反应的扫描灰度均值(GSM)分别为101.9±8.9、91.4±5.1、94.3±7.0,鳄梨油组分别为131.4±6.6、136.3±4.5、134.3±5.2,与对照组比较均显著增加(P<0.05);橄榄油组分别为121.1±4.5、107.9±7.3、106.4±5.4,与对照组比较均亦显著增加(P<0.05);而鳄梨油组与橄榄油组相比,前者各项GSM均高于后者(P<0.05).鳄梨油组和橄榄油组丝聚蛋白、内披蛋白、角蛋白10免疫化学反应的GSM均高于对照组(P<0.05);而鳄梨油组与橄榄油组相比,后者均高于前者(P<0.05).此外,各组各项免疫斑点印迹的GSM与免疫细胞化学的GSM数据基本相符,在鳄梨油组两者呈显著正相关,r=0.94,P<0.01;在橄榄油组两者也呈现显著正相关,r=0.97,P<0.01.结论 一定浓度鳄梨油和橄榄油,尤其是鳄梨油对HaCaT细胞可呈现显著的促生长、增殖效应;橄榄油和鳄梨油,尤其橄榄油对HaCaT细胞可呈现显著的促分化效应.
目的 探討天然植物鱷梨油和橄欖油對HaCaT細胞繫增殖及分化的影響.方法 將培養的HaCaT細胞分為鱷梨油組、橄欖油組及對照組.應用MTT實驗確定鱷梨油和橄欖油對HaCaT細胞的適用劑量.以免疫細胞化學、免疫斑點印跡技術分彆檢測各組HaCaT細胞的c-myc原癌基因(c-myc)、有絲分裂原激活蛋白激酶(MAPK)、NF-κB、絲聚蛋白、內披蛋白、角蛋白10的錶達.結果 對照組c-myc、MAPK、NF-κB免疫化學反應的掃描灰度均值(GSM)分彆為101.9±8.9、91.4±5.1、94.3±7.0,鱷梨油組分彆為131.4±6.6、136.3±4.5、134.3±5.2,與對照組比較均顯著增加(P<0.05);橄欖油組分彆為121.1±4.5、107.9±7.3、106.4±5.4,與對照組比較均亦顯著增加(P<0.05);而鱷梨油組與橄欖油組相比,前者各項GSM均高于後者(P<0.05).鱷梨油組和橄欖油組絲聚蛋白、內披蛋白、角蛋白10免疫化學反應的GSM均高于對照組(P<0.05);而鱷梨油組與橄欖油組相比,後者均高于前者(P<0.05).此外,各組各項免疫斑點印跡的GSM與免疫細胞化學的GSM數據基本相符,在鱷梨油組兩者呈顯著正相關,r=0.94,P<0.01;在橄欖油組兩者也呈現顯著正相關,r=0.97,P<0.01.結論 一定濃度鱷梨油和橄欖油,尤其是鱷梨油對HaCaT細胞可呈現顯著的促生長、增殖效應;橄欖油和鱷梨油,尤其橄欖油對HaCaT細胞可呈現顯著的促分化效應.
목적 탐토천연식물악리유화감람유대HaCaT세포계증식급분화적영향.방법 장배양적HaCaT세포분위악리유조、감람유조급대조조.응용MTT실험학정악리유화감람유대HaCaT세포적괄용제량.이면역세포화학、면역반점인적기술분별검측각조HaCaT세포적c-myc원암기인(c-myc)、유사분렬원격활단백격매(MAPK)、NF-κB、사취단백、내피단백、각단백10적표체.결과 대조조c-myc、MAPK、NF-κB면역화학반응적소묘회도균치(GSM)분별위101.9±8.9、91.4±5.1、94.3±7.0,악리유조분별위131.4±6.6、136.3±4.5、134.3±5.2,여대조조비교균현저증가(P<0.05);감람유조분별위121.1±4.5、107.9±7.3、106.4±5.4,여대조조비교균역현저증가(P<0.05);이악리유조여감람유조상비,전자각항GSM균고우후자(P<0.05).악리유조화감람유조사취단백、내피단백、각단백10면역화학반응적GSM균고우대조조(P<0.05);이악리유조여감람유조상비,후자균고우전자(P<0.05).차외,각조각항면역반점인적적GSM여면역세포화학적GSM수거기본상부,재악리유조량자정현저정상관,r=0.94,P<0.01;재감람유조량자야정현현저정상관,r=0.97,P<0.01.결론 일정농도악리유화감람유,우기시악리유대HaCaT세포가정현현저적촉생장、증식효응;감람유화악리유,우기감람유대HaCaT세포가정현현저적촉분화효응.
Objective To explore the effects of natural avocado oil and olive oil on the proliferation and differentiation of HaCaT cells. Methods MTT assay was performed to determine the optimal work concentration of avocado oil and olive oil. Cultured HaCaT cells were divided into 3 groups, i.e., avocado oil group treated with avocado oil of 3% (v/v), olive oil group treated with olive oil of 3% (v/v), and control group without any treatment. Immunocytochemistry and immuno-dot-blot method were used to detect the expressions of c-myc, mitogen-activated protein kinase ( MAPK ), nuclear factor ( NF)-κB, filaggrin, involucrin and keratin10 in HaCaT cells. Results As immunocytochemistry showed, the mean grey values (staining intensity) of c-myc,MAPK, and NF-κB in HaCaT cells were 131.4 ± 6.6,136.3 ± 4.5 and 134.3 ± 5.2 respectively in the avocado oil group, 121.1 ± 4.5, 107.9 ± 7.3 and 106.4 ± 5.4 respectively in the olive oil group, significantly higher than that in the control group (101.9 ± 8.9,91.4 ± 5.1 and 94.3 ± 7.0, respectively, all P< 0.05), and the avocado oil group was higher than the olive oil group in all the above parameters (all P < 0.05). Increased expressions of filaggrin, involucrin and keratin 10 were observed in the avocado oil group and olive oil group compared with the control group (all P< 0.05), and in the olive oil group than in the avocado oil group (all P< 0.05).The mean grey values of these proteins obtained by immunocytochemisty were significantly correlated with those obtained by immuno-dot-blot method in avocado oil group (r = 0.94, P < 0.01 ) and olive oil group (r=0.97, P < 0.01 ). Conclusions Certain concentrations of avocado oil and olive oil can promote the proliferation and differentiation of HaCaT cells; avocado oil is more capable to accelerate their growth and proliferation, and olive oil to enhance their differentiation.