中国医药导报
中國醫藥導報
중국의약도보
CHINA MEDICAL HERALD
2015年
1期
4-7
,共4页
张辉%俞诚波%张蓓蓓%叶美华%蔡敏秋%许红苗%林敏丽
張輝%俞誠波%張蓓蓓%葉美華%蔡敏鞦%許紅苗%林敏麗
장휘%유성파%장배배%협미화%채민추%허홍묘%림민려
白色念珠菌%人口腔黏膜上皮角质细胞%细胞凋亡%细胞周期
白色唸珠菌%人口腔黏膜上皮角質細胞%細胞凋亡%細胞週期
백색념주균%인구강점막상피각질세포%세포조망%세포주기
Candida albicans%Human oral mucosal epithelial cells%Apoptosis%Cell cycle
目的:研究白色念珠菌对人口腔黏膜上皮角质细胞的作用机制。方法将培养的口腔黏膜上皮角质细胞分别加入孢子型白色念珠菌(孢子组)和菌丝型白色念珠菌(菌丝组),另将单独培养的口腔黏膜上皮角质细胞作为阴性对照组。比较各组对口腔黏膜上皮角质细胞的黏附作用,并观察白色念珠菌对口腔黏膜上皮角质细胞的凋亡和增殖作用。结果菌丝组黏附指数(7.63±1.39)显著高于孢子组(3.47±1.04),差异有统计学意义(P<0.05);菌丝组凋亡率[(3.49±0.4)%]显著高于孢子组[(2.07±0.15)%]和阴性对照组[(1.98±0.07)%],差异有统计学意义(P<0.05),而孢子组和阴性对照组凋亡率相比差异无统计学意义(P>0.05)。菌丝组G0/G1期细胞比例[(38.17±7.83)%]显著低于孢子组[(49.47±11.41)%]和阴性对照组[(57.71±9.39)%],差异有统计学意义(P <0.05);S期[(8.54±4.03)%]、G2/M期[(20.18±9.59)%]细胞比例上升,且显著高于孢子组[(6.47±2.73)%、(10.71±3.19)%]和阴性对照组[(5.35±2.11)%、(12.38±4.35)%],差异有统计学意义(P<0.05);PI[(42.79±18.73)%]明显高于孢子组[(28.67±8.79)%]和阴性对照组[(26.87±7.64)%],差异有统计学意义(P<0.05),而孢子组和阴性对照组PI相比差异无统计学意义(P>0.05)。结论白色念珠菌能够导致口腔黏膜上皮角质细胞发生凋亡和增殖周期改变。
目的:研究白色唸珠菌對人口腔黏膜上皮角質細胞的作用機製。方法將培養的口腔黏膜上皮角質細胞分彆加入孢子型白色唸珠菌(孢子組)和菌絲型白色唸珠菌(菌絲組),另將單獨培養的口腔黏膜上皮角質細胞作為陰性對照組。比較各組對口腔黏膜上皮角質細胞的黏附作用,併觀察白色唸珠菌對口腔黏膜上皮角質細胞的凋亡和增殖作用。結果菌絲組黏附指數(7.63±1.39)顯著高于孢子組(3.47±1.04),差異有統計學意義(P<0.05);菌絲組凋亡率[(3.49±0.4)%]顯著高于孢子組[(2.07±0.15)%]和陰性對照組[(1.98±0.07)%],差異有統計學意義(P<0.05),而孢子組和陰性對照組凋亡率相比差異無統計學意義(P>0.05)。菌絲組G0/G1期細胞比例[(38.17±7.83)%]顯著低于孢子組[(49.47±11.41)%]和陰性對照組[(57.71±9.39)%],差異有統計學意義(P <0.05);S期[(8.54±4.03)%]、G2/M期[(20.18±9.59)%]細胞比例上升,且顯著高于孢子組[(6.47±2.73)%、(10.71±3.19)%]和陰性對照組[(5.35±2.11)%、(12.38±4.35)%],差異有統計學意義(P<0.05);PI[(42.79±18.73)%]明顯高于孢子組[(28.67±8.79)%]和陰性對照組[(26.87±7.64)%],差異有統計學意義(P<0.05),而孢子組和陰性對照組PI相比差異無統計學意義(P>0.05)。結論白色唸珠菌能夠導緻口腔黏膜上皮角質細胞髮生凋亡和增殖週期改變。
목적:연구백색념주균대인구강점막상피각질세포적작용궤제。방법장배양적구강점막상피각질세포분별가입포자형백색념주균(포자조)화균사형백색념주균(균사조),령장단독배양적구강점막상피각질세포작위음성대조조。비교각조대구강점막상피각질세포적점부작용,병관찰백색념주균대구강점막상피각질세포적조망화증식작용。결과균사조점부지수(7.63±1.39)현저고우포자조(3.47±1.04),차이유통계학의의(P<0.05);균사조조망솔[(3.49±0.4)%]현저고우포자조[(2.07±0.15)%]화음성대조조[(1.98±0.07)%],차이유통계학의의(P<0.05),이포자조화음성대조조조망솔상비차이무통계학의의(P>0.05)。균사조G0/G1기세포비례[(38.17±7.83)%]현저저우포자조[(49.47±11.41)%]화음성대조조[(57.71±9.39)%],차이유통계학의의(P <0.05);S기[(8.54±4.03)%]、G2/M기[(20.18±9.59)%]세포비례상승,차현저고우포자조[(6.47±2.73)%、(10.71±3.19)%]화음성대조조[(5.35±2.11)%、(12.38±4.35)%],차이유통계학의의(P<0.05);PI[(42.79±18.73)%]명현고우포자조[(28.67±8.79)%]화음성대조조[(26.87±7.64)%],차이유통계학의의(P<0.05),이포자조화음성대조조PI상비차이무통계학의의(P>0.05)。결론백색념주균능구도치구강점막상피각질세포발생조망화증식주기개변。
Objective To explore the mechanism of Candida albicans on human buccal epithelial cells. Methods The oral mucosa keratinocyte cultures were added to spore type of Candida albicans (spores group) and hyphae of Candida albicans (mycelium group), oral mucosal epithelial cells cultured alone as negative control group. Compared adhesion effect of oral mucosal epithelial cells in each group, and observed the apoptosis and proliferation of Candida albicans to buccal epithelial cells. Results Adhesion index of mycelium group (7.63±1.39) was significantly higher than spore group (3.47±1.04), with statistically significant difference (P< 0.05); the apoptosis rate [(3.49±0.4)%] was significantly higher than that in spores group [(2.07±0.15)%] and the control group [(1.98±0.07)%], with statistically significant dif-ference (P<0.05), while the spores group and the control group had no significant difference (P>0.05). The proportion of phase G0/G1 in mycelium group [(38.17±7.83)%] was significantly lower than that of spore group [(49.47±11.41)%] and the control group [(57.71±9.39)%], with statistically significant difference (P<0.05);the proportion of phase S [(8.54±4.03)%] and phase G2/M [(20.18±9.59)%] increased, significantly higher than those of the spores group [(6.47±2.73)%, (10.71±3.19)%] and the control group [(5.35±2.11)%, (12.38±4.35)%], with statistically significant difference (P< 0.05);PI [(42.79±18.73)%] was significantly higher than spore group [(28.67±8.79)%] and the control group [(26.87±7.64)%] , with statistically significant difference (P<0.05), while the spores group and the control group had no significant difference (P>0.05). Conclusion Candida albicans can cause oral mucosa keratinocyte apoptosis and proliferation cycle change.