Division of Pediatric Gastroenterology and Nutrition, Xinhua Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai 200092, China.
Shanghai Institute for Pediatric Research, Shanghai 200092, China.
Nutrients. 2023 Jun 7;15(12):2660. doi: 10.3390/nu15122660.
Pediatric intestinal failure (IF) is the reduction in gut function to below the minimum necessary for the absorption of macronutrients and/or water and electrolytes, such that intravenous supplementation is required to maintain health and/or growth. The overall goal in treating IF is to achieve intestinal adaptation; however, the underlying mechanisms have not been fully understood. In this study, by performing single-cell RNA sequencing in pediatric IF patients, we found that decreased Kruppel-Like Factor 4 (KLF4) may serve as the hub gene responsible for the functional deficit in mature enterocytes in IF patients, leading to the downregulation of solute carrier (SLC) family transporters (e.g., SLC7A9) and, consequently, nutrient malabsorption. We also found that inducible KLF4 was highly sensitive to the loss of certain enteral nutrients: in a rodent model of total parenteral nutrition mimicking the deprivation of enteral nutrition, the expression of KLF4 dramatically decreased only at the tip of the villus and not at the bottom of crypts. By using IF patient-derived intestinal organoids and Caco-2 cells as in vitro models, we demonstrated that the supplementation of decanoic acid (DA) could significantly induce the expression of KLF4 along with SLC6A4 and SLC7A9, suggesting that DA may function as a potential therapeutic strategy to promote cell maturation and functional improvement. In summary, this study provides new insights into the mechanism of intestinal adaptation depending on KLF4, and proposed potential strategies for nutritional management using DA.
儿科肠衰竭 (IF) 是指肠道功能下降到不能吸收足够的宏量营养素和/或水和电解质的最低限度,需要静脉补充以维持健康和/或生长。治疗 IF 的总体目标是实现肠道适应;然而,其潜在机制尚未完全了解。在这项研究中,通过对儿科 IF 患者进行单细胞 RNA 测序,我们发现 Kruppel 样因子 4 (KLF4) 的减少可能是 IF 患者成熟肠细胞功能缺陷的关键基因,导致溶质载体 (SLC) 家族转运蛋白 (例如,SLC7A9) 的下调,从而导致营养吸收不良。我们还发现,诱导型 KLF4 对某些肠内营养物质的丢失非常敏感:在模拟肠内营养剥夺的全肠外营养的啮齿动物模型中,KLF4 的表达仅在绒毛尖端而不在隐窝底部急剧下降。通过使用 IF 患者来源的肠类器官和 Caco-2 细胞作为体外模型,我们证明癸酸 (DA) 的补充可以显著诱导 KLF4 以及 SLC6A4 和 SLC7A9 的表达,表明 DA 可能是一种促进细胞成熟和功能改善的潜在治疗策略。总之,这项研究提供了关于 KLF4 依赖的肠道适应机制的新见解,并提出了使用 DA 进行营养管理的潜在策略。