Annual Review of Immunology Volume 24 2006 - download pdf or read online

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Extra info for Annual Review of Immunology Volume 24 2006

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ANRV270-IY24-02 Figure 4 A model for the cellular interactions linking T cell immunity and bone homeostasis. Pathogenic stimuli or self antigens are phagocytosed and presented to naive T cells by DCs. T cells provide activating signals to DCs through CD40L and in return receive optimal activating and costimulatory signals through MHC:TCR and B7:CD28 interactions, respectively. The activated T cells are induced to express TRANCE, which provides further activating and survival signals to the DCs.

Caspases and nitric oxide broadly regulate dendritic cell maturation and surface expression of class II MHC proteins. Proc. Natl. Acad. Sci. USA 101:17783–88 101. Santambrogio L, Potolicchio I, Fessler SP, Wong SH, Raposo G, Strominger JL. 2005. Involvement of caspase-cleaved and intact adaptor protein 1 complex in endosomal remodeling in maturing dendritic cells. Nat. Immunol. 6:1020–28 102. Krensky AM, Clayberger C, Reiss CS, Strominger JL, Burakoff SJ. 1982. Specificity of OKT4+ cytotoxic T lymphocyte clones.

Walsh et al. Bone Cells OBs are derived from a mesenchymal progenitor cell that is multipotential and can also differentiate into marrow stromal cells and adipocytes (4) (Figure 3). The signals that regulate the decision of mesenchymal progenitor cells to form OBs are not fully understood. However, a number of critical paracrine signals and transcription factors have been identified. These include the transcription factors Runx2 and osterix, which when absent prevent OB formation, and members of the bone morphogenetic protein (BMP) family (5–7), which initiate the signals for OB differentiation.

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