| Literature DB >> 26324934 |
Anthony N Vomund1, Bernd H Zinselmeyer1, Jing Hughes1, Boris Calderon1, Carolina Valderrama1, Stephen T Ferris1, Xiaoxiao Wan1, Kohsuke Kanekura2, Javier A Carrero1, Fumihiko Urano3, Emil R Unanue4.
Abstract
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.Entities:
Keywords: autoimmune diabetes; autoimmunity; insulin reactivity; insulin-reactive T cells
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Year: 2015 PMID: 26324934 PMCID: PMC4603448 DOI: 10.1073/pnas.1515954112
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205