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血清淀粉样蛋白A通过影响骨代谢与股骨头坏死相关。

Serum Amyloid A Correlates With the Osteonecrosis of Femoral Head by Affecting Bone Metabolism.

作者信息

Peng Xiaoyuan, Ma Yiyang, Wang Qiyang, Gao Yanchun, Li Guangyi, Jiang Chenyi, Gao Yun, Feng Yong

机构信息

Department of Orthopedic Surgery, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai, China.

出版信息

Front Pharmacol. 2021 Oct 18;12:767243. doi: 10.3389/fphar.2021.767243. eCollection 2021.

Abstract

Osteonecrosis of femoral head (ONFH) is a progressive hip joint disease without disease-modifying treatment. Lacking understanding of the pathophysiological process of ONFH has become the humper to develop therapeutic approach. Serum amyloid A (SAA) is an acute phase lipophilic protein during inflammation and we found that SAA is increased for the first time in the serum of ONFH patients through proteomic studies and quantitatively verified by ELISA. Treating rBMSCs with SAA inhibited the osteogenic differentiation Wnt/β-catenin signaling pathway deactivation and enhanced the adipogenic differentiation MAPK/PPARγ signaling pathway activation. Finally, bilateral critical-sized calvarial-defect rat model which received SAA treated rBMSCs demonstrated reduction of bone formation when compared to untreated rBMSCs implantation control. Hence, SAA is a vital protein in the physiological process of ONFH and can act as a potential therapeutic target to treat ONFH.

摘要

股骨头坏死(ONFH)是一种没有疾病缓解治疗方法的进行性髋关节疾病。对ONFH病理生理过程缺乏了解已成为开发治疗方法的障碍。血清淀粉样蛋白A(SAA)是炎症期间的一种急性期亲脂性蛋白,我们通过蛋白质组学研究首次发现ONFH患者血清中SAA升高,并通过酶联免疫吸附测定(ELISA)进行了定量验证。用SAA处理大鼠骨髓间充质干细胞(rBMSCs)会抑制成骨分化,使Wnt/β-连环蛋白信号通路失活,并增强脂肪生成,激活丝裂原活化蛋白激酶/过氧化物酶体增殖物激活受体γ(MAPK/PPARγ)信号通路。最后,与未处理的rBMSCs植入对照组相比,接受SAA处理的rBMSCs的双侧临界大小颅骨缺损大鼠模型显示骨形成减少。因此,SAA是ONFH生理过程中的一种重要蛋白质,可作为治疗ONFH的潜在治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6870/8559508/de84badda5ce/fphar-12-767243-g001.jpg

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