The effects of necrostatin-1 on the in vitro development and function of young porcine islets over 14-day prolonged tissue culture

被引:4
作者
Lau, Hien [1 ]
Corrales, Nicole [1 ]
Rodriguez, Samuel [1 ]
Park, Soomin [1 ]
Mohammadi, Mohammadreza [2 ,3 ]
Li, Shiri [1 ]
Alexander, Michael [1 ]
Lakey, Jonathan R. T. [1 ,3 ]
机构
[1] Univ Calif Irvine, Dept Surg, Irvine, CA 92717 USA
[2] Univ Calif Irvine, Dept Mat Sci & Engn, Sue & Bill Gross Stem Cell Res Ctr, Irvine, CA USA
[3] Univ Calif Irvine, Dept Biomed Engn, Irvine, CA USA
关键词
diabetes; islet culture; islet development; islet function; necrostatin-1; porcine islets; BETA-CELL PROLIFERATION; DEATH; XENOTRANSPLANTATION; NEUROGENIN3; EXPRESSION; INSULIN;
D O I
10.1111/xen.12667
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: 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. Methods: 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). Results: 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. Conclusion: 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.
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