Vomund Anthony N, Zinselmeyer Bernd H, Hughes Jing, Calderon Boris, Valderrama Carolina, Ferris Stephen T, Wan Xiaoxiao, Kanekura Kohsuke, Carrero Javier A, Urano Fumihiko, Unanue Emil R
Division of Immunobiology, Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110;
Division of Endocrinology, Metabolism and Lipid Research, Department of Internal Medicine, Washington University School of Medicine, St. Louis, MO 63110.
Proc Natl Acad Sci U S A. 2015 Oct 6;112(40):E5496-502. doi: 10.1073/pnas.1515954112. Epub 2015 Aug 31.
Beta cells from nondiabetic mice transfer secretory vesicles to phagocytic cells. The passage was shown in culture studies where the transfer was probed with CD4 T cells reactive to insulin peptides. Two sets of vesicles were transferred, one containing insulin and another containing catabolites of insulin. The passage required live beta cells in a close cell contact interaction with the phagocytes. It was increased by high glucose concentration and required mobilization of intracellular Ca2+. Live images of beta cell-phagocyte interactions documented the intimacy of the membrane contact and the passage of the granules. The passage was found in beta cells isolated from islets of young nonobese diabetic (NOD) mice and nondiabetic mice as well as from nondiabetic humans. Ultrastructural analysis showed intraislet phagocytes containing vesicles having the distinct morphology of dense-core granules. These findings document a process whereby the contents of secretory granules become available to the immune system.
来自非糖尿病小鼠的β细胞将分泌囊泡转移至吞噬细胞。这一过程在培养研究中得到证实,研究中用对胰岛素肽有反应的CD4 T细胞探测了这种转移。转移了两组囊泡,一组含有胰岛素,另一组含有胰岛素分解代谢产物。这一过程需要活的β细胞与吞噬细胞进行紧密的细胞接触相互作用。高葡萄糖浓度可增强该过程,且需要细胞内Ca2+的动员。β细胞与吞噬细胞相互作用的实时图像记录了膜接触的紧密程度以及颗粒的转移。在从年轻的非肥胖糖尿病(NOD)小鼠和非糖尿病小鼠的胰岛以及非糖尿病人类分离出的β细胞中均发现了这种转移。超微结构分析显示胰岛内的吞噬细胞含有具有致密核心颗粒独特形态的囊泡。这些发现证明了一个过程,通过该过程分泌颗粒的内容物可被免疫系统利用。