Wyss Institute for Biologically Inspired Engineering at Harvard University, Boston, MA 02115, USA.
Department of Bioengineering and iBB - Institute for Bioengineering and Biosciences, Instituto Superior Técnico, Universidade de Lisboa, Lisboa, Portugal.
Cell Death Dis. 2018 Feb 14;9(2):223. doi: 10.1038/s41419-018-0304-8.
Studies on human intestinal injury induced by acute exposure to γ-radiation commonly rely on use of animal models because culture systems do not faithfully mimic human intestinal physiology. Here we used a human Gut-on-a-Chip (Gut Chip) microfluidic device lined by human intestinal epithelial cells and vascular endothelial cells to model radiation injury and assess the efficacy of radiation countermeasure drugs in vitro. Exposure of the Gut Chip to γ-radiation resulted in increased generation of reactive oxygen species, cytotoxicity, apoptosis, and DNA fragmentation, as well as villus blunting, disruption of tight junctions, and compromise of intestinal barrier integrity. In contrast, pre-treatment with a potential prophylactic radiation countermeasure drug, dimethyloxaloylglycine (DMOG), significantly suppressed all of these injury responses. Thus, the human Gut Chip may serve as an in vitro platform for studying radiation-induced cell death and associate gastrointestinal acute syndrome, in addition to screening of novel radio-protective medical countermeasure drugs.
研究人类肠道急性 γ 辐射损伤通常依赖于动物模型,因为培养系统不能真实地模拟人类肠道生理学。在这里,我们使用一种人类肠道芯片(Gut Chip)微流控装置,其由人类肠道上皮细胞和血管内皮细胞排列,用于模拟辐射损伤,并在体外评估辐射防护药物的疗效。将 Gut Chip 暴露于 γ 辐射会导致活性氧生成增加、细胞毒性、细胞凋亡和 DNA 片段化,以及绒毛变钝、紧密连接破坏和肠道屏障完整性受损。相比之下,预先用一种有潜力的预防辐射的药物二甲基草酰甘氨酸(DMOG)处理,可以显著抑制所有这些损伤反应。因此,人类肠道芯片可能成为一种体外平台,用于研究辐射诱导的细胞死亡和相关的胃肠道急性综合征,以及筛选新型放射性防护药物。