Department of Surgery, University of California, Irvine, Irvine, CA, USA.
Department of Materials Science and Engineering, Sue and Bill Gross Stem Cell Research Center, University of California, Irvine, Irvine, CA, USA.
Xenotransplantation. 2021 May;28(3):e12667. doi: 10.1111/xen.12667. Epub 2021 Jan 12.
Necrostatin-1 (Nec-1) supplementation to tissue culture media on day 3 has recently been shown to augment the insulin content, endocrine cellular composition, and insulin release of pre-weaned porcine islets (PPIs); however, its effects were only examined for the first 7 days of tissue culture. The present study examined whether the addition of Nec-1 on day 3 could further enhance the in vitro development and function of PPIs after 14 days of tissue culture.
PPIs were isolated from 8- to 15-day-old, pre-weaned Yorkshire piglets and cultured in an islet maturation media supplemented with Nec-1 on day 3. The recovery, viability, insulin content, endocrine cellular composition, GLUT2 expression in beta cells, differentiation and proliferation potential, and glucose-stimulated insulin secretion of PPIs were assessed on days 3, 7, and 14 of tissue culture (n = 5 on each day).
Compared with day 7 of tissue culture, islets on day 14 had a lower recovery, GLUT2 expression in beta cells, proliferation capacity of endocrine cells, and glucose-induced insulin stimulation index. Prolonging the culture time to 14 days did not affect islet viability, insulin content, proportion of endocrine cells, and differentiation potential.
The growth-inducing effects of Nec-1 on PPIs were most effective on day 7 of tissue culture when added on day 3. Our findings support existing evidence that the in vitro activities of Nec-1 are short-lived and encourage future studies to explore the use of other novel growth factors during prolonged islet tissue culture.
最近的研究表明,在第 3 天向组织培养液中添加 Necrostatin-1(Nec-1)可以增加未成熟猪胰岛(PPIs)的胰岛素含量、内分泌细胞组成和胰岛素分泌;然而,其作用仅在组织培养的前 7 天进行了检查。本研究探讨了在组织培养 14 天后,第 3 天添加 Nec-1 是否可以进一步增强 PPIs 的体外发育和功能。
从 8-15 天大的未成熟约克夏仔猪中分离出 PPIs,并在第 3 天添加 Nec-1 的胰岛成熟培养基中进行培养。在组织培养的第 3、7 和 14 天(每组 5 个)评估 PPIs 的回收率、活力、胰岛素含量、内分泌细胞组成、β细胞中的 GLUT2 表达、分化和增殖潜能以及葡萄糖刺激的胰岛素分泌。
与组织培养第 7 天相比,第 14 天的胰岛回收率、β细胞中的 GLUT2 表达、内分泌细胞的增殖能力和葡萄糖诱导的胰岛素刺激指数较低。将培养时间延长至 14 天不会影响胰岛活力、胰岛素含量、内分泌细胞的比例和分化潜能。
当在第 3 天添加时,Nec-1 对 PPIs 的促生长作用在组织培养的第 7 天最为有效。我们的研究结果支持现有证据,即 Nec-1 的体外活性是短暂的,并鼓励未来的研究探索在延长胰岛组织培养过程中使用其他新型生长因子。