Del Fattore Andrea, Teti Anna
Regenerative Medicine Unit, Ospedale Pediatrico Bambino Gesù, Rome, Italy.
Inflamm Allergy Drug Targets. 2012 Jun;11(3):181-7. doi: 10.2174/187152812800392733.
Osteoimmunology is an interdisciplinary field addressing the interplay between the skeletal and the immune system. A substantial body of evidence demonstrated the existence of two-way regulatory mechanisms that affect both systems, placing them in much closer association to each other than one could ever predict. Inflammatory diseases have long been known to induce alterations in bone metabolism, and inflammatory cytokines play prominent roles in the control of bone resorption, representing communication pathways bridging the two systems. Osteoclasts are particularly linked to the immune cells because they belong to the monocyte/macrophage family, have tight relationships with B and T cells, and differentiate in response to RANKL which is also produced by lymphocytes and regulates lymphopoiesis. Osteoclasts are negatively regulated by cytokines and other factors known for their anti-inflammatory and immune regulatory activity. Finally, they express immune co-receptor typical of immune cells which are indispensable for their differentiation, thus leading to the hypothesis that osteoclasts are immune cells themselves. The underlying principle why an immune cell is required to resorb bone has not yet been elucidated. Data from early literature suggest that the bone matrix could trigger an innate immune response activating giant cells that could destroy large bone areas because of their unique property of resorbing bone extracellularly. Bone resorption could though be prevented by the physical barrier made by osteoblasts and lining cells, whose retraction would be required to give access to osteoclasts when specific pathways signal their precursors to differentiate and mature osteoclasts to reach the uncovered bone surface.
骨免疫学是一个跨学科领域,研究骨骼系统与免疫系统之间的相互作用。大量证据表明,存在影响这两个系统的双向调节机制,使它们之间的联系比人们预期的更为紧密。长期以来,人们已知炎症性疾病会引起骨代谢改变,炎症细胞因子在控制骨吸收中起重要作用,是连接这两个系统的通讯途径。破骨细胞与免疫细胞特别相关,因为它们属于单核细胞/巨噬细胞家族,与B细胞和T细胞关系密切,并对RANKL产生反应而分化,RANKL也由淋巴细胞产生并调节淋巴细胞生成。破骨细胞受到细胞因子和其他以抗炎和免疫调节活性著称的因子的负调控。最后,它们表达免疫细胞典型的免疫共受体,这些共受体对其分化不可或缺,从而导致破骨细胞本身就是免疫细胞的假说。需要免疫细胞来吸收骨的潜在原理尚未阐明。早期文献的数据表明,骨基质可以触发先天性免疫反应,激活巨细胞,由于它们在细胞外吸收骨的独特特性,巨细胞可能会破坏大片骨区域。然而,成骨细胞和衬里细胞形成的物理屏障可以防止骨吸收,当特定途径向破骨细胞前体发出分化信号并使成熟破骨细胞到达未覆盖的骨表面时,成骨细胞和衬里细胞的收缩是破骨细胞接触骨所必需的。