Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), Illkirch, France; Institut National de la Santé et de la Recherche Médicale (INSERM) U1258, Illkirch, France; Centre National de Recherche Scientifique (CNRS) UMR7104, Illkirch, France; Université de Strasbourg, Illkirch, France.
Nantes Université, CHU Nantes, Inserm, TENS, The Enteric Nervous System in Gut and Brain Diseases, IMAD, Nantes, France.
Cell Mol Gastroenterol Hepatol. 2023;15(6):1443-1461. doi: 10.1016/j.jcmgh.2023.02.013. Epub 2023 Feb 28.
BACKGROUND & AIMS: Enteroendocrine cells (EECs) and their hormones are essential regulators of whole-body energy homeostasis. EECs sense luminal nutrients and microbial metabolites and subsequently secrete various hormones acting locally or at a distance. Impaired development of EECs during embryogenesis is life-threatening in newborn mice and humans due to compromised nutrient absorption. However, the physiological importance of the EEC system in adult mice has yet to be directedly studied. Herein, we aimed to determine the long-term consequences of a total loss of EECs in healthy adults on energy metabolism, intestinal transcriptome, and microbiota.
We depleted intestinal EECs by tamoxifen treatment of adult Neurog3; Villin-CreER male mice. We studied intestinal cell differentiation, food efficiency, lipid absorption, microbiota composition, fecal metabolites, and transcriptomic responses in the proximal and distal small intestines of mice lacking EECs. We also determined the high-fat diet-induced transcriptomic changes in sorted Neurog3 EECs.
Induction of EEC deficiency in adults is not life-threatening unless fed with a high-fat diet. Under a standard chow diet, mice lose 10% of weight due to impaired food efficiency. Blood concentrations of cholesterol, triglycerides, and free fatty acids are reduced, and lipid absorption is impaired and delayed in the distal small intestine. Genes controlling lipogenesis, carbohydrate metabolism, and neoglucogenesis are upregulated. Microbiota composition is rapidly altered after EECs depletion and is characterized by decreased α-diversity. Bacteroides and Lactobacillus were progressively enriched, whereas Lachnospiraceae declined without impacting fecal short-chain fatty acid concentrations.
EECs are dispensable for survival in adult male mice under a standard chow diet. The absence of EECs impairs intestinal lipid absorption, leading to transcriptomic and metabolic adaptations and remodeling of the gut microbiota.
肠内分泌细胞(EECs)及其激素是全身能量稳态的重要调节因子。EEC 能够感知腔内分泌物和微生物代谢物,随后分泌各种局部或远距离作用的激素。由于营养吸收受损,胚胎发生过程中 EEC 发育不良会对新生小鼠和人类的生命造成威胁。然而,EEC 系统在成年小鼠中的生理重要性尚未被直接研究。在此,我们旨在确定健康成年小鼠中 EEC 完全缺失对能量代谢、肠道转录组和微生物群的长期影响。
我们通过使用他莫昔芬处理成年 Neurog3;Villin-CreER 雄性小鼠来耗尽肠道 EEC。我们研究了缺乏 EEC 的小鼠的肠道细胞分化、食物效率、脂质吸收、微生物群组成、粪便代谢物和近端及远端小肠的转录组反应。我们还确定了在分离的 Neurog3 EEC 中高脂肪饮食诱导的转录组变化。
除非给予高脂肪饮食,否则成年期 EEC 缺失不会危及生命。在标准饲料饮食下,由于食物效率降低,小鼠体重减轻 10%。胆固醇、甘油三酯和游离脂肪酸的血液浓度降低,远端小肠的脂质吸收受损且延迟。控制脂肪生成、碳水化合物代谢和新生糖生成的基因上调。EEC 耗竭后,微生物群组成迅速改变,特征是 α-多样性降低。拟杆菌属和乳杆菌属逐渐富集,而lachnospiraceae 减少而不影响粪便短链脂肪酸浓度。
在标准饲料饮食下,EEC 对于成年雄性小鼠的生存不是必需的。EEC 的缺失会损害肠道脂质吸收,导致转录组和代谢适应以及肠道微生物群的重塑。