Hubrecht Institute and Oncode Institute, Royal Academy of Arts and Science (KNAW) and University Medical Centre Utrecht, Utrecht, Netherlands.
Utrecht University and Princess Maxima Center, Utrecht, Netherlands.
Nat Rev Gastroenterol Hepatol. 2019 Jan;16(1):19-34. doi: 10.1038/s41575-018-0081-y.
The intestinal epithelium withstands continuous mechanical, chemical and biological insults despite its single-layered, simple epithelial structure. The crypt-villus tissue architecture in combination with rapid cell turnover enables the intestine to act both as a barrier and as the primary site of nutrient uptake. Constant tissue replenishment is fuelled by continuously dividing stem cells that reside at the bottom of crypts. These cells are nurtured and protected by specialized epithelial and mesenchymal cells, and together constitute the intestinal stem cell niche. Intestinal stem cells and early progenitor cells compete for limited niche space and, therefore, the ability to retain or regain stemness. Those cells unable to do so differentiate to one of six different mature cell types and move upwards towards the villus, where they are shed into the intestinal lumen after 3-5 days. In this Review, we discuss the signals, cell types and mechanisms that control homeostasis and regeneration in the intestinal epithelium. We investigate how the niche protects and instructs intestinal stem cells, which processes drive differentiation of mature cells and how imbalance in key signalling pathways can cause human disease.
尽管肠道上皮细胞只有单层简单的上皮结构,但它能耐受持续的机械、化学和生物损伤。隐窝-绒毛组织结构加上快速的细胞更替,使肠道既能作为屏障,又能作为营养物质吸收的主要部位。不断分裂的干细胞位于隐窝底部,为持续的组织补充提供动力。这些细胞受到专门的上皮细胞和间充质细胞的滋养和保护,共同构成了肠道干细胞龛。肠道干细胞和早期祖细胞为有限的龛位空间竞争,因此,它们能否保持或恢复干细胞特性。那些不能这样做的细胞分化为六种不同的成熟细胞类型之一,并向上移动到绒毛,在那里它们在 3-5 天后被排入肠腔。在这篇综述中,我们讨论了控制肠道上皮细胞体内平衡和再生的信号、细胞类型和机制。我们研究了龛位如何保护和指导肠道干细胞,哪些过程驱动成熟细胞的分化,以及关键信号通路的失衡如何导致人类疾病。