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  lüll Receptors, subcellular compartments and the regulation of peripheral B cell  responses: the illuminating state of anergy Clark MR; Tanaka A; Powers SE; Veselits MMol Immunol  2011[Jun]; 48 (11): 1281-6Signals through the B cell antigen receptor (BCR) are necessary but not  sufficient for cellular activation. Co-stimulatory signals must be provided  through other immune recognition receptor systems, such as MHC class II/CD40 and  the toll-like receptor (TLR) 9 that can only productively acquire their ligands  in the processive environment of specialized late endosomes (MHC class II  containing compartment or MIIC). It has long been appreciated that the BCR, by  effectively capturing complex antigens and delivering them to late endosomes, is  the link between activation events on the cell surface and those dependent on  late endosomes. However, it has become increasingly apparent that the BCR also  directs the translocation of MHC class II and TLR9 into the MIIC and that the  endocytic flow of these receptors coincides with that of the BCR. This likely  ensures close apposition of receptor complexes within the MIIC and the efficient  transfer of ligands from the BCR to MHC class II and TLR9. This complex  orchestration of receptor endocytic movement is dependent upon the quality of  signals elicited through the BCR. Failure to activate specific signaling  pathways, such as occurs in anergic B cells, prevents the entry of the BCR and  TLR9 into the MIIC and abrogates TLR9 activation. Like anergy, this block in  endocytic trafficking is rapidly reversible. These findings indicate that  cellular responsiveness can be determined by mechanisms that control the  subcellular location of important immune recognition receptors.|Animals[MESH]|B-Lymphocytes/*immunology[MESH]|CD40 Antigens/immunology[MESH]|Clonal Anergy/*immunology[MESH]|Endocytosis/immunology[MESH]|Endosomes/immunology[MESH]|Genes, MHC Class II/immunology[MESH]|Humans[MESH]|Intracellular Space/*immunology[MESH]|Mice[MESH]|Receptors, Antigen, B-Cell/*immunology[MESH]|Toll-Like Receptor 9/immunology[MESH]|Ubiquitination/immunology[MESH] |