The Transplant Institute, Sahlgrenska University Hospital, 413 45 Gothenburg, Sweden.
Laboratory for Transplantation and Regenerative Medicine, Institute of Clinical Sciences, Sahlgrenska Academy at the University of Gothenburg, Sahlgrenska Science Park Medicinaregatan 8, 413 90 Gothenburg, Sweden.
Int J Mol Sci. 2019 Jun 27;20(13):3135. doi: 10.3390/ijms20133135.
Advanced preservation injury (PI) after intestinal transplantation has deleterious short- and long-term effects and constitutes a major research topic. Logistics and costs favor rodent studies, whereas clinical translation mandates studies in larger animals or using human material. Despite diverging reports, no direct comparison between the development of intestinal PI in rats, pigs, and humans is available. We compared the development of PI in rat, porcine, and human intestines. Intestinal procurement and cold storage (CS) using histidine-tryptophan-ketoglutarate solution was performed in rats, pigs, and humans. Tissue samples were obtained after 8, 14, and 24 h of CS), and PI was assessed morphologically and at the molecular level (cleaved caspase-3, zonula occludens, claudin-3 and 4, tricellulin, occludin, cytokeratin-8) using immunohistochemistry and Western blot. Intestinal PI developed slower in pigs compared to rats and humans. Tissue injury and apoptosis were significantly higher in rats. Tight junction proteins showed quantitative and qualitative changes differing between species. Significant interspecies differences exist between rats, pigs, and humans regarding intestinal PI progression at tissue and molecular levels. These differences should be taken into account both with regards to study design and the interpretation of findings when relating them to the clinical setting.
先进的保存损伤(PI)在肠移植后具有有害的短期和长期影响,是一个主要的研究课题。物流和成本有利于啮齿动物的研究,而临床转化需要在较大的动物或使用人类材料上进行研究。尽管报告存在分歧,但目前还没有大鼠、猪和人类肠 PI 发展之间的直接比较。我们比较了大鼠、猪和人肠 PI 的发展。在大鼠、猪和人中进行肠采集和用组氨酸-色氨酸-酮戊二酸溶液进行冷保存(CS)。在 CS 后 8、14 和 24 小时获得组织样本,并通过免疫组织化学和 Western blot 评估 PI 在形态和分子水平上(cleaved caspase-3、zonula occludens、claudin-3 和 4、tricellulin、occludin、cytokeratin-8)的发展。与大鼠和人相比,猪的肠 PI 发展较慢。大鼠的组织损伤和细胞凋亡明显更高。紧密连接蛋白在不同物种之间表现出定量和定性的变化。大鼠、猪和人之间在组织和分子水平上的肠 PI 进展存在显著的种间差异。在将这些发现与临床环境相关联时,应考虑到这些差异在研究设计和结果解释方面的影响。