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The Journal of Immunology, 2004, 172: 2021-2029.
Copyright © 2004 by The American Association of Immunologists

Visualizing the Site and Dynamics of IgG Salvage by the MHC Class I-Related Receptor, FcRn1

Raimund J. Ober*, Cruz Martinez{dagger}, Carlos Vaccaro{dagger}, Jinchun Zhou{dagger} and E. Sally Ward2,*,{dagger}

* Cancer Immunobiology Center and {dagger} Center for Immunology, University of Texas Southwestern Medical Center, Dallas, TX 75390

The MHC class I-related receptor, FcRn, plays a central role in regulating the serum levels of IgG. FcRn is expressed in endothelial cells, suggesting that these cells may be involved in maintaining IgG levels. We have used live cell imaging of FcRn-green fluorescent protein transfected human endothelial cells to analyze the intracellular events that control IgG homeostasis. We show that segregation of FcRn-IgG complexes from unbound IgG occurs in the sorting endosome. FcRn or FcRn-IgG complexes are gradually depleted from sorting endosomes to ultimately generate multivesicular bodies whose contents are destined for lysosomal degradation. In addition, the pathways taken by FcRn and the transferrin receptor overlap, despite distinct mechanisms of ligand uptake. The studies provide a dynamic view of the trafficking of FcRn and its ligand and have relevance to understanding how FcRn functions to maintain IgG homeostasis.




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