The First Clinical Medical College of Lanzhou University, Lanzhou, China.
Department of Endocrinology, The First Hospital of Lanzhou University, Lanzhou, China.
Front Endocrinol (Lausanne). 2021 Sep 27;12:752546. doi: 10.3389/fendo.2021.752546. eCollection 2021.
Osteoporosis is a systemic bone metabolism disease that often causes complications, such as fractures, and increases the risk of death. The nucleotide-binding oligomerization domain-like-receptor family pyrin domain-containing 3 (NLRP3) inflammasome is an intracellular multiprotein complex that regulates the maturation and secretion of Caspase-1 dependent proinflammatory cytokines interleukin (IL)-1β and IL-18, mediates inflammation, and induces pyroptosis. The chronic inflammatory microenvironment induced by aging or estrogen deficiency activates the NLRP3 inflammasome, promotes inflammatory factor production, and enhances the inflammatory response. We summarize the related research and demonstrate that the NLRP3 inflammasome plays a vital role in the pathogenesis of osteoporosis by affecting the differentiation of osteoblasts and osteoclasts. IL-1β and IL-18 can accelerate osteoclast differentiation by expanding inflammatory response, and can also inhibit the expression of osteogenic related proteins or transcription factors. and experiments showed that the overexpression of NLRP3 protein was closely related to aggravated bone resorption and osteogenesis deficiency. In addition, abnormal activation of NLRP3 inflammasome can not only produce inflammation, but also lead to pyroptosis and dysfunction of osteoblasts by upregulating the expression of Caspase-1 and gasdermin D (GSDMD). In conclusion, NLRP3 inflammasome overall not only accelerates bone resorption, but also inhibits bone formation, thus increasing the risk of osteoporosis. Thus, this review highlights the recent studies on the function of NLRP3 inflammasome in osteoporosis, provides information on new strategies for managing osteoporosis, and investigates the ideal therapeutic target to treat osteoporosis.
骨质疏松症是一种全身性骨代谢疾病,常导致骨折等并发症,增加死亡风险。核苷酸结合寡聚化结构域样受体家族富含pyrin 结构域蛋白 3(NLRP3)炎性小体是一种细胞内多蛋白复合物,调节 Caspase-1 依赖性促炎细胞因子白细胞介素(IL)-1β和 IL-18 的成熟和分泌,介导炎症,并诱导细胞焦亡。衰老或雌激素缺乏引起的慢性炎症微环境激活 NLRP3 炎性小体,促进炎症因子的产生,增强炎症反应。我们总结了相关研究,并证明 NLRP3 炎性小体通过影响成骨细胞和破骨细胞的分化,在骨质疏松症的发病机制中起重要作用。IL-1β和 IL-18 通过扩大炎症反应,加速破骨细胞分化,也可以抑制成骨相关蛋白或转录因子的表达。和实验表明,NLRP3 蛋白的过表达与加重的骨吸收和成骨不足密切相关。此外,NLRP3 炎性小体的异常激活不仅可以产生炎症,还可以通过上调 Caspase-1 和 Gasdermin D(GSDMD)的表达,导致成骨细胞的细胞焦亡和功能障碍。总之,NLRP3 炎性小体不仅加速了骨吸收,还抑制了骨形成,从而增加了骨质疏松症的风险。因此,本综述强调了 NLRP3 炎性小体在骨质疏松症中的功能的最新研究,为管理骨质疏松症提供了信息,并探讨了治疗骨质疏松症的理想治疗靶点。