Andreev Darja, Kachler Katerina, Liu Mengdan, Chen Zhu, Krishnacoumar Brenda, Ringer Mark, Frey Silke, Krönke Gerhard, Voehringer David, Schett Georg, Bozec Aline
Department of Internal Medicine 3 - Rheumatology and Immunology, Friedrich-Alexander-University (FAU) Erlangen-Nürnberg and Universitätsklinikum Erlangen, Erlangen, Germany.
Deutsches Zentrum für Immuntherapie (DZI), Erlangen, Germany.
Nat Commun. 2024 Feb 5;15(1):1067. doi: 10.1038/s41467-024-45261-8.
Eosinophils are involved in tissue homeostasis. Herein, we unveiled eosinophils as important regulators of bone homeostasis. Eosinophils are localized in proximity to bone-resorbing osteoclasts in the bone marrow. The absence of eosinophils in ΔdblGATA mice results in lower bone mass under steady-state conditions and amplified bone loss upon sex hormone deprivation and inflammatory arthritis. Conversely, increased numbers of eosinophils in IL-5 transgenic mice enhance bone mass under steady-state conditions and protect from hormone- and inflammation- mediated bone loss. Eosinophils strongly inhibit the differentiation and demineralization activity of osteoclasts and lead to profound changes in the transcriptional profile of osteoclasts. This osteoclast-suppressive effect of eosinophils is based on the release of eosinophil peroxidase causing impaired reactive oxygen species and mitogen-activated protein kinase induction in osteoclast precursors. In humans, the number and the activity of eosinophils correlates with bone mass in healthy participants and rheumatoid arthritis patients. Taken together, experimental and human data indicate a regulatory function of eosinophils on bone.
嗜酸性粒细胞参与组织稳态。在此,我们揭示嗜酸性粒细胞是骨稳态的重要调节因子。嗜酸性粒细胞定位于骨髓中与骨吸收破骨细胞相邻的位置。ΔdblGATA小鼠中缺乏嗜酸性粒细胞会导致稳态条件下骨量降低,以及在性激素剥夺和炎性关节炎时骨丢失加剧。相反,IL-5转基因小鼠中嗜酸性粒细胞数量增加会在稳态条件下增加骨量,并防止激素和炎症介导的骨丢失。嗜酸性粒细胞强烈抑制破骨细胞的分化和脱矿质活性,并导致破骨细胞转录谱发生深刻变化。嗜酸性粒细胞的这种破骨细胞抑制作用基于嗜酸性粒细胞过氧化物酶的释放,导致破骨细胞前体中活性氧受损和丝裂原活化蛋白激酶诱导。在人类中,健康参与者和类风湿性关节炎患者的嗜酸性粒细胞数量和活性与骨量相关。综上所述,实验和人类数据表明嗜酸性粒细胞对骨具有调节功能。