实用医学杂志
實用醫學雜誌
실용의학잡지
THE JOURNAL OF PRACTICAL MEDICINE
2015年
8期
1222-1225
,共4页
王亚楠%陆平%黄筱慧%田晨光%孙丽君%窦倩%谭丽%王武亮%毛跟红
王亞楠%陸平%黃篠慧%田晨光%孫麗君%竇倩%譚麗%王武亮%毛跟紅
왕아남%륙평%황소혜%전신광%손려군%두천%담려%왕무량%모근홍
人胚胎干细胞%细胞分化%胰岛素%磷脂酰肌醇3激酶抑制剂
人胚胎榦細胞%細胞分化%胰島素%燐脂酰肌醇3激酶抑製劑
인배태간세포%세포분화%이도소%린지선기순3격매억제제
Human embryonic stem cells%Cell differentiation%Insulin%Phosphoinositide-3-kinase inhibitor
目的:探讨磷脂酰肌醇3激酶抑制剂 LY294002对人胚胎干细胞定向分化为成熟胰岛素分泌细胞的影响。方法:体外通过5个阶段诱导人胚胎干细胞定向分化为胰岛素分泌细胞。分别给予尼克酰胺+B27(B27组)为对照组和尼克酰胺+ LY294002(LY组)为实验组诱导胰岛素分泌细胞的成熟。显微镜下观察各阶段细胞形态变化,免疫荧光染色鉴定胰岛素、c-肽、生长抑素和胰高血糖素的表达。结果:第5阶段诱导14 d LY组胰岛素单染阳性率与B27组无统计学差别(P﹥0.05),但生长抑素和胰高血糖素单染阳性率,胰岛素/生长抑素共染率均低于B27组(P﹤0.05)。结论:在无血清培养体系下,磷脂酰肌醇3激酶抑制剂LY294002能够诱导人胚胎干细胞分化为更加成熟的胰岛素分泌细胞。
目的:探討燐脂酰肌醇3激酶抑製劑 LY294002對人胚胎榦細胞定嚮分化為成熟胰島素分泌細胞的影響。方法:體外通過5箇階段誘導人胚胎榦細胞定嚮分化為胰島素分泌細胞。分彆給予尼剋酰胺+B27(B27組)為對照組和尼剋酰胺+ LY294002(LY組)為實驗組誘導胰島素分泌細胞的成熟。顯微鏡下觀察各階段細胞形態變化,免疫熒光染色鑒定胰島素、c-肽、生長抑素和胰高血糖素的錶達。結果:第5階段誘導14 d LY組胰島素單染暘性率與B27組無統計學差彆(P﹥0.05),但生長抑素和胰高血糖素單染暘性率,胰島素/生長抑素共染率均低于B27組(P﹤0.05)。結論:在無血清培養體繫下,燐脂酰肌醇3激酶抑製劑LY294002能夠誘導人胚胎榦細胞分化為更加成熟的胰島素分泌細胞。
목적:탐토린지선기순3격매억제제 LY294002대인배태간세포정향분화위성숙이도소분비세포적영향。방법:체외통과5개계단유도인배태간세포정향분화위이도소분비세포。분별급여니극선알+B27(B27조)위대조조화니극선알+ LY294002(LY조)위실험조유도이도소분비세포적성숙。현미경하관찰각계단세포형태변화,면역형광염색감정이도소、c-태、생장억소화이고혈당소적표체。결과:제5계단유도14 d LY조이도소단염양성솔여B27조무통계학차별(P﹥0.05),단생장억소화이고혈당소단염양성솔,이도소/생장억소공염솔균저우B27조(P﹤0.05)。결론:재무혈청배양체계하,린지선기순3격매억제제LY294002능구유도인배태간세포분화위경가성숙적이도소분비세포。
Objective To investigate the effect of phosphoinositide-3-kinase inhibitor LY294002 on the differentiation of human embryonic stem cells (HESC) into more mature insulin-producing cells. Methods HESCs were induced to differentiate into insulin-producing cells through five stages. Nicotinamide and B27 (group B27), nicotinamide and LY294002 (group LY) were used to induce the nesting positive cells into mature insulin-producing cells. The morphological change of each stage was observed under microscope , and expressions of insulin, c-peptide, somatostatin and glucagon were identified by immunofluorescence staining. Results After 14 days in stage 5 , there was no significant difference in rate of insulin positive cells between group LY and group B27 (P﹥0.05), but rates of somatostatin and glucagon positive cells in group LY were lower than those in group B27(P﹤0.05). Furthermore, the co-stained rate of somatostatin and insulin in group LY was also lower than that in group B27 (P﹤0.05). Conclusion HESCs can be induced to differentiate into more mature insulin-producing cells by phosphoinositide-3-kinase inhibitor LY294002 in serum-free culture medium.