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细胞外 PPM1A 通过 FOXO1A-RUNX2 通路促进强直性脊柱炎成骨细胞分化的矿化。

Extracellular PPM1A promotes mineralization of osteoblasts differentiation in ankylosing spondylitis via the FOXO1A-RUNX2 pathway.

机构信息

Hanyang University Institute for Rheumatology Research (HYIRR), Seoul, Korea.

Department of Translational Medicine, Graduate School of Biomedical Science and Engineering, Hanyang University, Seoul, Korea.

出版信息

J Cell Mol Med. 2023 Mar;27(5):650-658. doi: 10.1111/jcmm.17685. Epub 2023 Feb 9.

Abstract

Protein phosphatase magnesium-dependent 1A (PPM1A), serine/threonine protein phosphatase, in sera level was increased in patients with ankylosing spondylitis (AS). Preosteoblasts were differentiated actively to matured osteoblasts by intracellular PPM1A overexpression. However, it was unclear whether extracellular PPM1A contributes to the excessive bone-forming activity in AS. Here, we confirmed that PPM1A and runt-related transcription factor 2 (RUNX2) were increased in facet joints of AS. During osteoblasts differentiation, exogenous PPM1A treatment showed increased matrix mineralization in AS-osteoprogenitor cells accompanied by induction of RUNX2 and factor forkhead box O1A (FOXO1A) protein expressions. Moreover, upon growth condition, exogenous PPM1A treatment showed an increase in RUNX2 and FOXO1A protein expression and a decrease in phosphorylation at ser256 of FOXO1A protein in AS-osteoprogenitor cells, and positively regulated promoter activity of RUNX2 protein-binding motif. Mechanically, exogenous PPM1A treatment induced the dephosphorylation of transcription factor FOXO1A protein and translocation of FOXO1A protein into the nucleus for RUNX2 upregulation. Taken together, our results suggest that high PPM1A concentration promotes matrix mineralization in AS via the FOXO1A-RUNX2 pathway.

摘要

蛋白磷酸酶镁依赖性 1A(PPM1A),丝氨酸/苏氨酸蛋白磷酸酶,在强直性脊柱炎(AS)患者的血清水平升高。过表达细胞内 PPM1A 可使前成骨细胞向成熟成骨细胞积极分化。然而,细胞外 PPM1A 是否有助于 AS 中过度的成骨活性尚不清楚。在这里,我们证实 PPM1A 和 runt 相关转录因子 2(RUNX2)在 AS 的小关节中增加。在成骨细胞分化过程中,外源性 PPM1A 处理可增加 AS 成骨前体细胞中基质矿化,同时诱导 RUNX2 和叉头框蛋白 O1A(FOXO1A)蛋白的表达。此外,在生长条件下,外源性 PPM1A 处理可增加 AS 成骨前体细胞中 RUNX2 和 FOXO1A 蛋白的表达,并降低 FOXO1A 蛋白丝氨酸 256 的磷酸化,正向调节 RUNX2 蛋白结合基序的启动子活性。在机制上,外源性 PPM1A 处理诱导转录因子 FOXO1A 蛋白去磷酸化,并将 FOXO1A 蛋白转位到细胞核中,从而上调 RUNX2。总之,我们的结果表明,高 PPM1A 浓度通过 FOXO1A-RUNX2 途径促进 AS 中的基质矿化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a768/9983316/12c81fb7c347/JCMM-27-650-g002.jpg

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