Department of Medicine, Division of Hematology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Cell Metab. 2013 Mar 5;17(3):343-52. doi: 10.1016/j.cmet.2013.01.013. Epub 2013 Feb 14.
Sorting of endocytic ligands and receptors is critical for diverse cellular processes. The physiological significance of endosomal sorting proteins in vertebrates, however, remains largely unknown. Here we report that sorting nexin 3 (Snx3) facilitates the recycling of transferrin receptor (Tfrc) and thus is required for the proper delivery of iron to erythroid progenitors. Snx3 is highly expressed in vertebrate hematopoietic tissues. Silencing of Snx3 results in anemia and hemoglobin defects in vertebrates due to impaired transferrin (Tf)-mediated iron uptake and its accumulation in early endosomes. This impaired iron assimilation can be complemented with non-Tf iron chelates. We show that Snx3 and Vps35, a component of the retromer, interact with Tfrc to sort it to the recycling endosomes. Our findings uncover a role of Snx3 in regulating Tfrc recycling, iron homeostasis, and erythropoiesis. Thus, the identification of Snx3 provides a genetic tool for exploring erythropoiesis and disorders of iron metabolism.
内吞配体和受体的分拣对于各种细胞过程至关重要。然而,脊椎动物内体分拣蛋白的生理意义在很大程度上仍不清楚。在这里,我们报告分拣连接蛋白 3(Snx3)促进转铁蛋白受体(Tfrc)的回收,因此是将铁正确递送至红系祖细胞所必需的。Snx3 在脊椎动物造血组织中高度表达。Snx3 的沉默会导致脊椎动物贫血和血红蛋白缺陷,因为转铁蛋白(Tf)介导的铁摄取受损,其在早期内体中积累。这种铁吸收不良可以用非 Tf 铁螯合剂来补充。我们表明,Snx3 和 Vps35(一种逆行体的组成部分)与 Tfrc 相互作用,将其分拣到再循环内体。我们的发现揭示了 Snx3 在调节 Tfrc 回收、铁稳态和红细胞生成中的作用。因此,Snx3 的鉴定为探索红细胞生成和铁代谢紊乱提供了遗传工具。