Department of Cell Biology, Duke University, Durham, NC 27710, USA; Department of Pharmacology and Cancer Biology, Duke University, Durham, NC 27710, USA.
Department of Cell Biology, Duke University, Durham, NC 27710, USA.
Dev Cell. 2019 Oct 7;51(1):7-20.e6. doi: 10.1016/j.devcel.2019.08.001. Epub 2019 Aug 29.
The guts of neonatal mammals and stomachless fish have a limited capacity for luminal protein digestion, which allows oral acquisition of antibodies and antigens. However, how dietary protein is absorbed during critical developmental stages when the gut is still immature is unknown. Here, we show that specialized intestinal cells, which we call lysosome-rich enterocytes (LREs), internalize dietary protein via receptor-mediated and fluid-phase endocytosis for intracellular digestion and trans-cellular transport. In LREs, we identify a conserved endocytic machinery, composed of the scavenger receptor complex Cubilin/Amnionless and Dab2, that is required for protein uptake by LREs and for growth and survival of larval zebrafish. Moreover, impairing LRE function in suckling mice, via conditional deletion of Dab2, leads to stunted growth and severe protein malnutrition reminiscent of kwashiorkor, a devastating human malnutrition syndrome. These findings identify digestive functions and conserved molecular mechanisms in LREs that are crucial for vertebrate growth and survival.
新生哺乳动物和无胃鱼的肠道对腔蛋白消化的能力有限,这使得它们可以通过口服获得抗体和抗原。然而,当肠道尚未成熟的关键发育阶段,肠道是如何吸收膳食蛋白的还不得而知。在这里,我们表明,我们称之为富含溶酶体的肠细胞(LRE)的专门肠细胞通过受体介导的和液相内吞作用内化膳食蛋白,进行细胞内消化和细胞间转运。在 LRE 中,我们鉴定出一种保守的内吞作用机制,由拾荒受体复合物 Cubilin/Amnionless 和 Dab2 组成,该机制对于 LRE 摄取蛋白质以及斑马鱼幼虫的生长和存活是必需的。此外,通过条件性敲除 Dab2 来破坏哺乳期小鼠的 LRE 功能,会导致生长迟缓以及严重的蛋白质营养不良,类似于 kwashiorkor(一种严重的人类营养不良综合征)。这些发现确定了 LRE 中的消化功能和保守的分子机制,这些功能和机制对于脊椎动物的生长和存活至关重要。