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分泌型簇蛋白通过抑制 ERK1/2 信号通路抑制骨髓间充质干细胞的成骨细胞分化。

Secreted Clusterin protein inhibits osteoblast differentiation of bone marrow mesenchymal stem cells by suppressing ERK1/2 signaling pathway.

机构信息

Biological Sciences Department, College of Science, King Faisal University, Hofuf, Saudi Arabia; Endocrine Research (KMEB), Department of Endocrinology, Odense University Hospital and University of Southern Denmark, Odense, Denmark.

Biological Sciences Department, College of Science, King Faisal University, Hofuf, Saudi Arabia.

出版信息

Bone. 2018 May;110:221-229. doi: 10.1016/j.bone.2018.02.018. Epub 2018 Feb 21.

Abstract

Secreted Clusterin (sCLU, also known as Apolipoprotein J) is an anti-apoptotic glycoprotein involved in the regulation of cell proliferation, lipid transport, extracellular tissue remodeling and apoptosis. sCLU is expressed and secreted by mouse bone marrow-derived skeletal (stromal or mesenchymal) stem cells (mBMSCs), but its functional role in MSC biology is not known. In this study, we demonstrated that Clusterin mRNA expression and protein secretion in conditioned medium increased during adipocyte differentiation and decreased during osteoblast differentiation of mBMSCs. Treatment of mBMSC cultures with recombinant sCLU protein increased cell proliferation and exerted an inhibitory effect on the osteoblast differentiation while stimulated adipocyte differentiation in a dose-dependent manner. siRNA-mediated silencing of Clu expression in mBMSCs reduced adipocyte differentiation and stimulated osteoblast differentiation of mBMSCs. Furthermore, the inhibitory effect of sCLU on the osteoblast differentiation of mBMSCs was mediated by the suppression of extracellular signal-regulated kinase (ERK1/2) phosphorylation. In conclusion, we identified sCLU as a regulator of mBMSCs lineage commitment to osteoblasts versus adipocytes through a mechanism mediated by ERK1/2 signaling. Inhibiting sCLU is a possible therapeutic approach for enhancing osteoblast differentiation and consequently bone formation.

摘要

分泌型簇集蛋白(sCLU,也称为载脂蛋白 J)是一种抗凋亡糖蛋白,参与细胞增殖、脂质转运、细胞外组织重塑和细胞凋亡的调控。sCLU 由鼠骨髓来源的骨骼(基质或间充质)干细胞(mBMSCs)表达和分泌,但它在 MSC 生物学中的功能作用尚不清楚。在这项研究中,我们证明了在 mBMSCs 的脂肪细胞分化过程中,Clusterin mRNA 表达和条件培养基中的蛋白分泌增加,而在成骨细胞分化过程中则减少。重组 sCLU 蛋白处理 mBMSC 培养物可增加细胞增殖,并以剂量依赖性方式对成骨细胞分化产生抑制作用,同时刺激脂肪细胞分化。mBMSCs 中 Clu 表达的 siRNA 沉默减少了脂肪细胞分化并刺激了 mBMSCs 的成骨细胞分化。此外,sCLU 对 mBMSCs 成骨细胞分化的抑制作用是通过抑制细胞外信号调节激酶(ERK1/2)磷酸化来介导的。总之,我们确定 sCLU 是通过 ERK1/2 信号转导介导的机制调节 mBMSCs 向成骨细胞与脂肪细胞的谱系定向的调节剂。抑制 sCLU 可能是增强成骨细胞分化从而促进骨形成的一种治疗方法。

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