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Dendritic Cells at the Osteo‐Immune Interface: Implications for Inflammation‐Induced Bone Loss
Author(s) -
Alnaeeli Mawadda,
Park Jaekweon,
Mahamed Deeqa,
Penninger Joseph M,
Teng YenTung A
Publication year - 2007
Publication title -
journal of bone and mineral research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.882
H-Index - 241
eISSN - 1523-4681
pISSN - 0884-0431
DOI - 10.1359/jbmr.070314
Subject(s) - inflammation , immune system , osteoimmunology , immunology , medicine , receptor , activator (genetics) , rankl
Within the past decade, the critical roles of T cells and T cell–mediated immunity in inflammation‐induced osteoclastogenesis and subsequent bone loss have been extensively studied, thereby establishing the new paradigm of osteoimmunology. Therefore, dendritic cells (DCs), the most potent antigen‐presenting cells, responsible for activation of naïve T cells and orchestration of the immune response, became critically situated at the osteo‐immune interface. Today, emerging new evidence suggests that DC may be directly involved in inflammation‐induced osteoclastogenesis and bone loss, by acting as osteoclast (OC) precursors that can further develop into DC‐derived OCs (DDOC) under inflammatory conditions. These findings have tremendous implications, because in addition to DC's important roles in regulating innate and adaptive immunity, a direct contribution by these cells to inflammation‐induced bone loss may provide a promising therapeutic target not only for controlling inflammation but also for modulating bone destruction.

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