Pyroptotic macrophages induce disruption of glutamate metabolism in periodontal ligament stem cells contributing to their compromised osteogenic potential

上睑下垂 牙周膜干细胞 细胞生物学 化学 巨噬细胞 牙周纤维 生物 炎症 免疫学 炎症体 生物化学 体外 医学 牙科 碱性磷酸酶
作者
Lijuan Sun,Huan Qu,Fa‐Ming Chen,Bei‐Min Tian,Rui‐Xin Wu,Yuan Yin,Jie‐Kang Zou,Hai‐Hua Sun,Xuan Li,Fa‐Ming Chen
出处
期刊:Cell Proliferation [Wiley]
标识
DOI:10.1111/cpr.13663
摘要

Abstract Macrophage pyroptosis is of key importance to host defence against pathogen infections and may participate in the progression and recovery of periodontitis. However, the role of pyroptotic macrophages in regulating periodontal ligament stem cells (PDLSCs), the main cell source for periodontium renewal, remains unclear. First, we found that macrophage pyroptosis were enriched in gingiva tissues from periodontitis patients compared with those of healthy people through immunofluorescence. Then the effects of pyroptotic macrophages on the PDLSC osteogenic differentiation were investigated in a conditioned medium (CM)‐based coculture system in vitro. CM derived from pyroptotic macrophages inhibited the osteogenic differentiation‐related gene and protein levels, ALP activity and mineralized nodule formation of PDLSCs. The osteogenic inhibition of CM was alleviated when pyroptosis was inhibited by VX765. Further, untargeted metabolomics showed that glutamate limitation may be the underlying mechanism. However, exogenous glutamate supplementation aggravated the CM‐inhibited osteogenic differentiation of PDLSCs. Moreover, CM increased extracellular glutamate and decreased intracellular glutamate levels of PDLSCs, and enhanced the gene and protein expression levels of system x c − (a cystine/glutamate antiporter). After adding cystine to CM‐based incubation, the compromised osteogenic potency of PDLSCs was rescued. Our data suggest that macrophage pyroptosis is related to the inflammatory lesions of periodontitis. Either pharmacological inhibition of macrophage pyroptosis or nutritional supplements to PDLSCs, can rescue the compromised osteogenic potency caused by pyroptotic macrophages.
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