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牙槽骨丧失的骨免疫学

The osteoimmunology of alveolar bone loss.

作者信息

Tompkins Kevin A

机构信息

a Research Unit of Mineralized Tissue, Faculty of Dentistry , Chulalongkorn University , Bangkok , Thailand.

出版信息

Connect Tissue Res. 2016;57(2):69-90. doi: 10.3109/03008207.2016.1140152. Epub 2016 Mar 7.

Abstract

The mineralized structure of bone undergoes constant remodeling by the balanced actions of bone-producing osteoblasts and bone-resorbing osteoclasts (OCLs). Physiologic bone remodeling occurs in response to the body's need to respond to changes in electrolyte levels, or mechanical forces on bone. There are many pathological conditions, however, that cause an imbalance between bone production and resorption due to excessive OCL action that results in net bone loss. Situations involving chronic or acute inflammation are often associated with net bone loss, and research into understanding the mechanisms regulating this bone loss has led to the development of the field of osteoimmunology. It is now evident that the skeletal and immune systems are functionally linked and share common cells and signaling molecules. This review discusses the signaling system of immune cells and cytokines regulating aberrant OCL differentiation and activity. The role of these cells and cytokines in the bone loss occurring in periodontal disease (PD) (chronic inflammation) and orthodontic tooth movement (OTM) (acute inflammation) is then described. The review finishes with an exploration of the emerging role of Notch signaling in the development of the immune cells and OCLs that are involved in osteoimmunological bone loss and the research into Notch signaling in OTM and PD.

摘要

骨的矿化结构通过成骨细胞生成骨和破骨细胞(OCLs)吸收骨的平衡作用而不断重塑。生理性骨重塑是机体对电解质水平变化或骨所受机械力作出反应的需要。然而,存在许多病理状况,由于破骨细胞过度作用导致骨生成与吸收失衡,进而造成净骨丢失。涉及慢性或急性炎症的情况常与净骨丢失相关,对调节这种骨丢失机制的研究推动了骨免疫学领域的发展。现在很明显,骨骼系统和免疫系统在功能上相互关联,共享共同的细胞和信号分子。本综述讨论了调节异常破骨细胞分化和活性的免疫细胞和细胞因子的信号系统。然后描述了这些细胞和细胞因子在牙周病(PD)(慢性炎症)和正畸牙移动(OTM)(急性炎症)中发生的骨丢失中的作用。综述最后探讨了Notch信号在参与骨免疫学骨丢失的免疫细胞和破骨细胞发育中的新作用,以及对正畸牙移动和牙周病中Notch信号的研究。

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