M1 macrophage-derived oncostatin M induces osteogenic differentiation of ligamentum flavum cells through the JAK2/STAT3 pathway

被引:4
|
作者
Yang, Jun [1 ,2 ]
Chen, Guanghui [3 ]
Fan, Tianqi [3 ]
Qu, Xiaochen [1 ,2 ,3 ]
机构
[1] Dalian Med Univ, Affiliated Hosp 1, Dept Orthopaed, Dalian, Peoples R China
[2] Dept Orthopaed, Key Lab Mol Mech Repair & Remodeling Orthopaed Dis, Dalian, Peoples R China
[3] Peking Univ Third Hosp, Dept Orthopaed, Beijing, Peoples R China
来源
JOR SPINE | 2024年 / 7卷 / 01期
基金
中国国家自然科学基金;
关键词
JAK2/STAT3; signaling; macrophages; oncostatin M; ossification of the ligamentum flavum; MESENCHYMAL STEM-CELLS; THORACIC OSSIFICATION; MYELOPATHY;
D O I
10.1002/jsp2.1290
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Background: M1 macrophages (M phi s) are involved in osteogenic differentiation of ligamentum flavum (LF) cells and play an important role in heterotopic ossification. However, the mechanism by which M1 M phi s influence osteogenic differentiation of LF cells has not been studied.Methods: The effect of conditioned medium including secretions of M1 M phi s (CM-M1) on LF cells was analyzed by GeneChip profiling and ingenuity pathway analysis (IPA). THP-1 cells were polarized into M1 M phi s and CM-M1 was used to induce LF cells. In addition, LF cells were induced by CM-M1 in the presence of cyclooxygenase 2 (COX-2) inhibitors or oncostatin M (OSM)-neutralizing antibodies. Based on the presence of OSM, knockout of OSMR or GP130 receptors, or addition of the Janus kinase 2 (JAK2) inhibitor AZD1480 or signal transducer and activator of transcription 3 (STAT3) inhibitor Stattic were examined for effects on osteogenic differentiation of LF cells. OSM secretion was quantified by ELISA, while qPCR and western blot were used to evaluate expression of osteogenic genes and receptor and signaling pathway-related proteins, respectively.Results: GeneChip and IPA results indicate that the OSM signaling pathway and its downstream signaling molecules JAK2 and STAT3 are significantly activated. ELISA results indicate that OSM is highly expressed in cells treated with CM-M1 and lowly expressed in cells treated with CM-M1 and a COX-2 inhibitor. Besides, CM-M1 induces osteogenic differentiation of LF cells, which is weakened when COX-2 inhibitors or OSM-neutralizing antibody are added to it. Recombinant OSM could induce osteogenic differentiation of LF cells and upregulate expression of OSMR, GP130, phosphorylated (P)-JAK2, and P-STAT3. Upon knockdown of OSMR or GP130, or the addition of AZD1480 or Stattic, P-JAK2 and P-STAT3 expression were decreased and osteogenic differentiation was reduced.Conclusion: M1 M phi-derived OSM induces osteogenic differentiation of LF cells and the JAK2/STAT3 signaling pathway plays an important role.
引用
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页数:11
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