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首页> 外文期刊>Journal of Nanjing Medical University >Effects of mature Sertoli cells on allogeneic islets cocultured in vitro
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Effects of mature Sertoli cells on allogeneic islets cocultured in vitro

机译:成熟的支持细胞对异基因胰岛体外共培养的影响

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摘要

Objective: To set up a method for isolation and culture of mature Sertoli cells and to estimate their effects on allogeneic islets cocultured in vitro. Methods: Adult SD rat testicular Sertoli cells were prepared successfully by three-step enzyme digestion. Then they were cocultured respectively with allogeneic islets and activated Wistar rat splenocytes. 24-hour cumulative insulin release and glucose-stimulated insulin secretion test were performed to detect islet function between pure islets culture group and coculture group. Splenocyte proliferation activity was determined by MTT colorimetry assay to observe the inhibition effect of Sertoli cells in different densities. Result : Firstly, in pure islet culture group, the 24-hour cumulative insulin release was gradually decreased in 21-day culture time. Compared to day 3, this change was significant on day 7 (P < 0.05) and on day 10,14,21 (P < 0.01). In contrast, in coculture group, compared to day 3, the 24-hour cumulative insulin release was increased significantly on day 7 (P < 0.01), and then gradually decreased on day 10 and 14, but still higher than that of day 3. It was on day 21 that it began to decrease compared to day 3 (P < 0.05). During the culture time in vitro, the 24-hour cumulative insulin release of islet coculture group was significantly higher than that of pure islets culture group (P < 0.01). In the case of stimulation index (SI), there was a similar tendency as insulin release in the two groups. Secondly, mature Sertoli cells (1 x 10~6/mL) pretreated by 15 grays irradiation could decrease proliferation activity of activated splenocytes compared to that of control group (P < 0.01). This inhibition effect was dose-dependent. Conclusion: Mature Sertoli cells can improve the function and prolong the survival of islet cells cultured in vitro. They can also provide an immune protection to islet cells. The approach described above might be applicable to human islet transplantation as soon as if it is also valid in large animal models.
机译:目的:建立分离培养成熟睾丸支持细胞的方法,并评价其对体外共培养的同种异体胰岛的影响。方法:三步酶消化法成功制备成年SD大鼠睾丸支持细胞。然后将它们分别与同种异体胰岛和活化的Wistar大鼠脾细胞共培养。进行24小时累积胰岛素释放和葡萄糖刺激的胰岛素分泌试验,以检测纯胰岛培养组和共培养组之间的胰岛功能。通过MTT比色法测定脾细胞的增殖活性,观察不同密度对支持细胞的抑制作用。结果:首先,在纯胰岛培养组中,培养21天后24小时累积胰岛素释放逐渐减少。与第3天相比,该变化在第7天(P <0.05)和第10、14、21天(P <0.01)显着。相反,在共培养组中,与第3天相比,第7天的24小时累积胰岛素释放显着增加(P <0.01),然后在第10和14天逐渐下降,但仍高于第3天。与第3天相比,它是在第21天开始减少的(P <0.05)。在体外培养时间中,胰岛共培养组的24小时累积胰岛素释放量明显高于纯胰岛培养组(P <0.01)。就刺激指数(SI)而言,两组的胰岛素释放趋势相似。其次,与对照组相比,经15次灰色辐射预处理的成熟Sertoli细胞(1 x 10〜6 / mL)可能降低活化的脾细胞的增殖活性(P <0.01)。这种抑制作用是剂量依赖性的。结论:成熟的支持细胞可以改善胰岛细胞的功能,延长其存活时间。它们还可以为胰岛细胞提供免疫保护。只要上述方法在大型动物模型中也有效,就可以将其应用于人胰岛移植。

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