中国血液流变学杂志
中國血液流變學雜誌
중국혈액류변학잡지
CHINESE JOURNAL OF HEMORHEOLOGY
2014年
2期
195-198,202
,共5页
侯率%杨姝%王元元%吕回%车玉琴
侯率%楊姝%王元元%呂迴%車玉琴
후솔%양주%왕원원%려회%차옥금
锯叶棕提取物%胶质瘤细胞%凋亡%PI3K/Akt信号转导通路
鋸葉棕提取物%膠質瘤細胞%凋亡%PI3K/Akt信號轉導通路
거협종제취물%효질류세포%조망%PI3K/Akt신호전도통로
saw palmetto extract%glioma cell%apoptosis%PI3K/Akt Signal Transduction Pathways
目的:通过锯叶棕提取物对人脑胶质瘤细胞的干预,观察人脑胶质瘤细胞中细胞凋亡和PI3K蛋白表达的变化。方法体外培养U251细胞,应用锯叶棕提取物进行预处理,应用TUNEL法检测细胞凋亡,应用Western Blot法检测PI3K蛋白表达水平的变化。结果TUNEL法染色检测锯叶棕提取物对人脑胶质瘤细胞凋亡的影响,24 h与48 h均可见TUNEL阳性反应细胞即凋亡细胞,胞体缩小,形态不规则,胞核固缩浓染,呈棕黄色或棕褐色;1.5μL/mL组48 h与24 h比较,凋亡数量显著增多(P<0.01);对照组24 h与48 h偶见凋亡细胞,2.0μL/mL组与1.5μL/mL组比较,凋亡率增大(P<0.01)。用Western blot法检测锯叶棕提取物对人脑胶质瘤细胞PI3K蛋白表达的影响,锯叶棕提取物预处理U251细胞与对照组比较, PI3K蛋白表达水平显著降低(P<0.01)。结论锯叶棕提取物能诱导人脑胶质瘤细胞凋亡;锯叶棕提取物诱导人脑胶质瘤细胞凋亡的机制可能是通过阻断PI3K/Akt信号转导通路。
目的:通過鋸葉棕提取物對人腦膠質瘤細胞的榦預,觀察人腦膠質瘤細胞中細胞凋亡和PI3K蛋白錶達的變化。方法體外培養U251細胞,應用鋸葉棕提取物進行預處理,應用TUNEL法檢測細胞凋亡,應用Western Blot法檢測PI3K蛋白錶達水平的變化。結果TUNEL法染色檢測鋸葉棕提取物對人腦膠質瘤細胞凋亡的影響,24 h與48 h均可見TUNEL暘性反應細胞即凋亡細胞,胞體縮小,形態不規則,胞覈固縮濃染,呈棕黃色或棕褐色;1.5μL/mL組48 h與24 h比較,凋亡數量顯著增多(P<0.01);對照組24 h與48 h偶見凋亡細胞,2.0μL/mL組與1.5μL/mL組比較,凋亡率增大(P<0.01)。用Western blot法檢測鋸葉棕提取物對人腦膠質瘤細胞PI3K蛋白錶達的影響,鋸葉棕提取物預處理U251細胞與對照組比較, PI3K蛋白錶達水平顯著降低(P<0.01)。結論鋸葉棕提取物能誘導人腦膠質瘤細胞凋亡;鋸葉棕提取物誘導人腦膠質瘤細胞凋亡的機製可能是通過阻斷PI3K/Akt信號轉導通路。
목적:통과거협종제취물대인뇌효질류세포적간예,관찰인뇌효질류세포중세포조망화PI3K단백표체적변화。방법체외배양U251세포,응용거협종제취물진행예처리,응용TUNEL법검측세포조망,응용Western Blot법검측PI3K단백표체수평적변화。결과TUNEL법염색검측거협종제취물대인뇌효질류세포조망적영향,24 h여48 h균가견TUNEL양성반응세포즉조망세포,포체축소,형태불규칙,포핵고축농염,정종황색혹종갈색;1.5μL/mL조48 h여24 h비교,조망수량현저증다(P<0.01);대조조24 h여48 h우견조망세포,2.0μL/mL조여1.5μL/mL조비교,조망솔증대(P<0.01)。용Western blot법검측거협종제취물대인뇌효질류세포PI3K단백표체적영향,거협종제취물예처리U251세포여대조조비교, PI3K단백표체수평현저강저(P<0.01)。결론거협종제취물능유도인뇌효질류세포조망;거협종제취물유도인뇌효질류세포조망적궤제가능시통과조단PI3K/Akt신호전도통로。
Objective To observe the effect of saw palmetto extract on glioma cell apoptosis and the influence of PI3K in glioma cells through the intervention of saw palmetto on glioma cell. Methods U251 cells are cultured in vitro, pre-treatment with saw palmetto extract, to detect the cell apoptosis by TUNEL method, to detect the changes of the expression of PI3K by Western blot. Results 1.TUNEL method staining to detect the effect of saw palmetto extract on glioma cell apoptosis. (1)Both 24 h and 48 h time point see TUNEL positive cells (apoptotic cells), cell body narrow, irregular, nucleus condensation stain, showed brown yellow or brown, 48 h and 24 h compare, the number of apoptotic cells significantly increased in 1.5μL/mL group (P<0.01);(2)24 h and 48 h time point occasionally see apoptotic cells in the control group, the same time 1.5μL/mL and 2.0μL/mL group, number of apoptotic cells significantly increased (P<0.01). 2.The effect of saw palmetto extract on glioma cell of expression of PI3K protein by Wersten Blot method. Saw palmetto preconditioning, compared with control group, expression of PI3K protein levels were significantly decreased (P<0.01). Conclusion Saw palmetto extract induced apoptosis in glioma cells. Saw Palmetto by blocking PI3K/Akt Signal Transduction Pathways can induce the glioma cell apoptosis.