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未折叠蛋白反应的增强会增加核因子κB受体活化因子配体(RANKL)的表达。

Elevation of the unfolded protein response increases RANKL expression.

作者信息

Iyer Srividhya, Melendez-Suchi Christian, Han Li, Baldini Giulia, Almeida Maria, Jilka Robert L

机构信息

Department of Orthopaedic Surgery University of Arkansas Medical Sciences Little Rock AR USA.

Division of Endocrinology and Metabolism Center for Osteoporosis and Metabolic Bone Diseases University of Arkansas Medical Sciences Little Rock AR USA.

出版信息

FASEB Bioadv. 2020 Jan 31;2(4):207-218. doi: 10.1096/fba.2019-00032. eCollection 2020 Apr.

Abstract

Increased production of the osteoclastogenic cytokine RANKL is a common feature of pathologic bone loss, but the underlying cause of this increase is poorly understood. The unfolded protein response (UPR) is activated in response to accumulation of misfolded proteins in the endoplasmic reticulum (ER). Failure to resolve misfolding results in excess UPR signaling that stimulates cytokine production and cell death. We therefore investigated whether RANKL is one of the cytokines stimulated in response to elevated UPR in bone cells. Pharmacologic induction of UPR with tunicamycin (Tm)-stimulated RANKL expression in cultures of primary osteoblastic cells and in osteoblast and osteocyte cell lines. Pharmacologic inhibition of the UPR blunted Tm-induced RANKL production. Silencing Edem1 or Sel1l, proteins that aid in degradation of misfolded proteins, also induced UPR and increased RANKL mRNA. Moreover, Tm or hypoxia increased RANKL and bone resorption in cultures of neonatal murine calvaria. Administration of Tm to adult mice caused dilation of ER in osteoblasts and osteocytes, elevated the UPR, and increased RANKL expression and osteoclast number. These findings support the hypothesis that excessive UPR signaling stimulates the expression of RANKL by osteoblasts and osteocytes, and thereby facilitates excessive bone resorption and bone loss in pathologic conditions.

摘要

破骨细胞生成细胞因子RANKL的产量增加是病理性骨质流失的一个常见特征,但这种增加的根本原因尚不清楚。未折叠蛋白反应(UPR)在内质网(ER)中错误折叠蛋白积累时被激活。未能解决错误折叠会导致过量的UPR信号传导,从而刺激细胞因子产生和细胞死亡。因此,我们研究了RANKL是否是骨细胞中因UPR升高而被刺激产生的细胞因子之一。用衣霉素(Tm)对UPR进行药理学诱导,可刺激原代成骨细胞培养物以及成骨细胞和成骨细胞系中的RANKL表达。对UPR进行药理学抑制可减弱Tm诱导的RANKL产生。沉默有助于错误折叠蛋白降解的Edem1或Sel1l蛋白也会诱导UPR并增加RANKL mRNA。此外,Tm或缺氧会增加新生小鼠颅骨培养物中的RANKL和骨吸收。给成年小鼠注射Tm会导致成骨细胞和成骨细胞中ER扩张,UPR升高,并增加RANKL表达和破骨细胞数量。这些发现支持了这样一种假设,即过量的UPR信号传导会刺激成骨细胞和成骨细胞表达RANKL,从而在病理条件下促进过度的骨吸收和骨质流失。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/507b/7133738/5c1b824edc30/FBA2-2-207-g001.jpg

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