中国组织工程研究与临床康复
中國組織工程研究與臨床康複
중국조직공정연구여림상강복
JOURNAL OF CLINICAL REHABILITATIVE TISSUE ENGINEERING RESEARCH
2011年
19期
3567-3570
,共4页
陈昊强%史光军%许评%吴晓平
陳昊彊%史光軍%許評%吳曉平
진호강%사광군%허평%오효평
胰岛移植%胰腺导管干细胞%葡萄糖浓度%胰岛素%分泌量
胰島移植%胰腺導管榦細胞%葡萄糖濃度%胰島素%分泌量
이도이식%이선도관간세포%포도당농도%이도소%분비량
背景:葡萄糖是胰腺导管干细胞分化的重要因素之一,与分化后胰岛素分泌细胞数量及分泌能力相关.目的:对比不同浓度葡萄糖诱导下,胰腺导管干细胞分化后细胞的胰岛素分泌能力.方法:使用胶原酶Ⅴ及Ficoll-400分离及纯化Wistar大鼠胰腺上皮细胞,获取胰腺导管干细胞,将干细胞分为10组,体外培养、增殖及分化形成胰岛素分泌细胞.各组在含有不同浓度葡萄糖的培养基中进行分化.采用免疫荧光染色法鉴定胰腺导管干细胞,光化学发光法检测分化出的胰岛素分泌细胞的胰岛素分泌量.结果与结论:葡萄糖浓度为20.6,25.6,30.6 mmol/L组细胞的刺激指数高于其他组(P < 0.05),但这3组两两比较差异无显著性意义(P > 0.05).葡萄糖浓度为15.6,20.6,25.6 mmol/L组细胞胰岛素分泌量高于其他组(P < 0.05),但这3组两两比较差异无显著性意义(P > 0.05).提示胰腺导管干细胞分化为胰岛素分泌细胞实验中,当分化时培养液所含葡萄糖浓度为20.6~25.6 mmol/L时,所得细胞胰岛素分泌能力最强.
揹景:葡萄糖是胰腺導管榦細胞分化的重要因素之一,與分化後胰島素分泌細胞數量及分泌能力相關.目的:對比不同濃度葡萄糖誘導下,胰腺導管榦細胞分化後細胞的胰島素分泌能力.方法:使用膠原酶Ⅴ及Ficoll-400分離及純化Wistar大鼠胰腺上皮細胞,穫取胰腺導管榦細胞,將榦細胞分為10組,體外培養、增殖及分化形成胰島素分泌細胞.各組在含有不同濃度葡萄糖的培養基中進行分化.採用免疫熒光染色法鑒定胰腺導管榦細胞,光化學髮光法檢測分化齣的胰島素分泌細胞的胰島素分泌量.結果與結論:葡萄糖濃度為20.6,25.6,30.6 mmol/L組細胞的刺激指數高于其他組(P < 0.05),但這3組兩兩比較差異無顯著性意義(P > 0.05).葡萄糖濃度為15.6,20.6,25.6 mmol/L組細胞胰島素分泌量高于其他組(P < 0.05),但這3組兩兩比較差異無顯著性意義(P > 0.05).提示胰腺導管榦細胞分化為胰島素分泌細胞實驗中,噹分化時培養液所含葡萄糖濃度為20.6~25.6 mmol/L時,所得細胞胰島素分泌能力最彊.
배경:포도당시이선도관간세포분화적중요인소지일,여분화후이도소분비세포수량급분비능력상관.목적:대비불동농도포도당유도하,이선도관간세포분화후세포적이도소분비능력.방법:사용효원매Ⅴ급Ficoll-400분리급순화Wistar대서이선상피세포,획취이선도관간세포,장간세포분위10조,체외배양、증식급분화형성이도소분비세포.각조재함유불동농도포도당적배양기중진행분화.채용면역형광염색법감정이선도관간세포,광화학발광법검측분화출적이도소분비세포적이도소분비량.결과여결론:포도당농도위20.6,25.6,30.6 mmol/L조세포적자격지수고우기타조(P < 0.05),단저3조량량비교차이무현저성의의(P > 0.05).포도당농도위15.6,20.6,25.6 mmol/L조세포이도소분비량고우기타조(P < 0.05),단저3조량량비교차이무현저성의의(P > 0.05).제시이선도관간세포분화위이도소분비세포실험중,당분화시배양액소함포도당농도위20.6~25.6 mmol/L시,소득세포이도소분비능력최강.
BACKGROUND: Glucose is an important factor on differentiation of pancreatic duct stem cells, it relates to the quantity and secretion function of insulin-producing cells after differentiation.OBJECTIVE: To compare the insulin secretion capacity of the differentiated rat pancreatic stem cells induced by various glucose concentrations.METHODS: Rat stem cells were isolated and purified from pancreatic duct cells using collagenase V and Ficoll-400. These stem cells were randomly divided into 10 groups. Every group was induced to culture, proliferate, differentiate and form insulin- producing cells in vitro. The differentiation of all groups was performed in medium with different concentrations of glucose. The immunofluorescence staining was used to identify the pancreatic duct stem cells. The electrochemical luminescence method was used to detect the insulin release from stem cell differentiated islets.RESULTS AND CONCLUSION: The stimulation index of glucose 20.6, 25.6, 30.6 mmol/L groups was higher than that in other groups (P < 0.05), but there was no difference between each two groups among these three groups (P > 0.05). The insulin releasing of glucose 15.6, 20.6, 25.6 groups was higher than that in other groups (P < 0.05), but there was no difference between each two groups among these three groups (P > 0.05). The best insulin secretion capacity of insulin-producing cells can be gained by controlling concentration of glucose as 20.6-25.6 mmol/L when pancreatic duct stem cells differentiated into insulin-producing cells.