Department of Orthopedics, Washington University School of Medicine, St. Louis, Missouri, USA. faccior@ wustl.edu
Ann N Y Acad Sci. 2010 Mar;1192:124-30. doi: 10.1111/j.1749-6632.2009.05217.x.
Identifying common signaling pathways to bone and immune system may lead to better therapeutic approaches in diseases such as inflammatory arthritis. In this context, PLCgamma2 seems to be a promising target. PLCgamma2 modulates bone homeostasis by affecting osteoclast recruitment and function. Via its catalytic activity and the adapter domains, PLCgamma2 controls RANKL and alphavbeta3 integrin-dependent signaling pathways in the resorbing cell. Thus, mice lacking PLCgamma2 are osteopetrotic. PLCgamma2 also regulates neutrophil degranulation after beta2 integrin-dependent attachment. Indeed PLCgamma2(-/-) mice are protected from K/BxN serum transfer arthritis, which is known to require neutrophil activation. These studies position PLCgamma2 as a critical regulator of the cellular and molecular mechanisms occurring in bone and immune cells during autoimmune inflammation.
确定与骨骼和免疫系统相关的共同信号通路可能会为炎性关节炎等疾病带来更好的治疗方法。在这种情况下,PLCγ2 似乎是一个很有前途的靶点。PLCγ2 通过影响破骨细胞的募集和功能来调节骨稳态。通过其催化活性和衔接结构域,PLCγ2 控制着破骨细胞中 RANKL 和 αvβ3 整合素依赖性信号通路。因此,缺乏 PLCγ2 的小鼠出现了严重的骨质增生。PLCγ2 还调节β2 整合素依赖性附着后中性粒细胞的脱颗粒作用。事实上,PLCγ2(-/-) 小鼠对 K/BxN 血清转移关节炎具有保护作用,而该关节炎已知需要中性粒细胞的激活。这些研究将 PLCγ2 定位为在自身免疫性炎症过程中发生在骨骼和免疫细胞中的细胞和分子机制的关键调节因子。