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白细胞介素-(IL)-11/IL-11 受体在骨代谢和稳态中的新作用:从细胞因子到骨细胞因子。

The Emerging Role of Interleukin-(IL)-11/IL-11R in Bone Metabolism and Homeostasis: From Cytokine to Osteokine.

机构信息

Department of Endocrinology and Metabolism, The Affiliated Hospital of Qingdao University, Qingdao, China.

Department of Clinical Laboratory, The Affiliated Hospital of Qingdao University, Qingdao, China.

出版信息

Aging Dis. 2023 Dec 1;14(6):2113-2126. doi: 10.14336/AD.2023.0306.

DOI:10.14336/AD.2023.0306
PMID:37199584
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10676798/
Abstract

Interleukin-(IL)-11 is a cytokine involved in hematopoiesis, cancer metastasis, and inflammation. IL-11 belongs to the IL-6 cytokine family, binding to the complex of receptors glycoprotein gp130 and the ligand-specific-receptor subunits (IL-11Rα or their soluble counterpart sIL-11R). IL-11/IL-11R signaling enhances osteoblast differentiation and bone formation and mitigates osteoclast-induced bone resorption and cancer bone metastasis. Recent studies have shown that systemic and osteoblast/osteocyte-specific IL-11 deficiency leads to reduced bone mass and formation, but also adiposity, glucose intolerance, and insulin resistance. In humans, mutations of IL-11 and the receptor IL-11RA genes are associated with height reduction, osteoarthritis, and craniosynostosis. In this review, we describe the emerging role of IL-11/IL-11R signaling in bone metabolism by targeting osteoblasts, osteoclasts, osteocytes, and bone mineralization. Furthermore, IL-11 promotes osteogenesis and suppresses adipogenesis, thereby influencing the fate of osteoblast/adipocyte differentiation derived from pluripotent mesenchymal stem cells. We have newly identified IL-11 as a bone-derived cytokine that regulates bone metabolism and the link between bone and other organs. Thus, IL-11 is vital in bone homeostasis and could be considered a potential therapeutic strategy.

摘要

白细胞介素-(IL)-11 是一种参与造血、癌症转移和炎症的细胞因子。IL-11 属于 IL-6 细胞因子家族,与糖蛋白 gp130 复合物和配体特异性受体亚基(IL-11Rα 或其可溶性对应物 sIL-11R)结合。IL-11/IL-11R 信号增强成骨细胞分化和骨形成,并减轻破骨细胞诱导的骨吸收和癌症骨转移。最近的研究表明,全身和成骨细胞/成骨细胞特异性 IL-11 缺乏会导致骨量和形成减少,但也会导致肥胖、葡萄糖不耐受和胰岛素抵抗。在人类中,IL-11 和受体 IL-11RA 基因的突变与身高降低、骨关节炎和颅缝早闭有关。在这篇综述中,我们描述了 IL-11/IL-11R 信号通过靶向成骨细胞、破骨细胞、骨细胞和骨矿化在骨代谢中的新作用。此外,IL-11 促进成骨并抑制脂肪生成,从而影响多能间充质干细胞来源的成骨细胞/脂肪细胞分化的命运。我们新确定 IL-11 是一种调节骨代谢和骨与其他器官之间联系的骨源性细胞因子。因此,IL-11 在骨稳态中至关重要,可被视为一种有潜力的治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7be9/10676798/ad89b5d8b74f/AD-14-6-2113-g3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7be9/10676798/882a7e896007/AD-14-6-2113-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7be9/10676798/a72bc7381000/AD-14-6-2113-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7be9/10676798/ad89b5d8b74f/AD-14-6-2113-g3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7be9/10676798/882a7e896007/AD-14-6-2113-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7be9/10676798/a72bc7381000/AD-14-6-2113-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7be9/10676798/ad89b5d8b74f/AD-14-6-2113-g3.jpg

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