CNC-bZIP protein NFE2L1 regulates osteoclast differentiation in antioxidant-dependent and independent manners

Fine-tuning of osteoclast differentiation (OD) and bone remodeling is crucial for bone homeostasis. Dissecting the mechanisms regulating osteoclastogenesis is fundamental to understanding the pathogenesis of various bone disorders including osteoporosis and arthritis. Nuclear factor erythroid 2-rela...

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Autores principales: Zhiyuan Liu, Huihui Wang, Yongyong Hou, Yang Yang, Jingkun Jia, Jinzhi Wu, Zhuo Zuo, Tianchang Gao, Suping Ren, Yiying Bian, Shengnan Liu, Jingqi Fu, Yongxin Sun, Jiliang Li, Masayuki Yamamoto, Qiang Zhang, Yuanyuan Xu, Jingbo Pi
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Lenguaje:EN
Publicado: Elsevier 2021
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spelling oai:doaj.org-article:12524d37aec54ad8b4d35691e0ff07022021-11-10T04:25:42ZCNC-bZIP protein NFE2L1 regulates osteoclast differentiation in antioxidant-dependent and independent manners2213-231710.1016/j.redox.2021.102180https://doaj.org/article/12524d37aec54ad8b4d35691e0ff07022021-12-01T00:00:00Zhttp://www.sciencedirect.com/science/article/pii/S2213231721003402https://doaj.org/toc/2213-2317Fine-tuning of osteoclast differentiation (OD) and bone remodeling is crucial for bone homeostasis. Dissecting the mechanisms regulating osteoclastogenesis is fundamental to understanding the pathogenesis of various bone disorders including osteoporosis and arthritis. Nuclear factor erythroid 2-related factor 1 (NFE2L1, also known as NRF1), which belongs to the CNC-bZIP family of transcription factors, orchestrates a variety of physiological processes and stress responses. While Nfe2l1 gene may be transcribed into multiple alternatively spliced isoforms, the biological function of the different isoforms of NFE2L1 in bone metabolism, osteoclastogenesis in particular, has not been reported. Here we demonstrate that knockout of all isoforms of Nfe2l1 transcripts specifically in the myeloid lineage in mice [Nfe2l1(M)-KO] results in increased activity of osteoclasts, decreased bone mass and worsening of osteoporosis induced by ovariectomy and aging. In comparison, LysM-Cre-mediated Nfe2l1 deletion has no significant effect on the osteoblast and osteocytes. Mechanistic investigations using bone marrow cells and RAW 264.7 cells revealed that deficiency of Nfe2l1 leads to accelerated and elevated OD, which is attributed, at least in part, to enhanced accumulation of ROS in the early stage of OD and expression of nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1α (Nfatc1/α). In addition, NFE2L1 regulates the transcription of multiple antioxidant genes and Nfatc1/α and OD in an isoform-specific manner. While long isoforms of NFE2L1 function as accelerators of induction of Nfatc1/α and antioxidant genes and OD, the short isoform NFE2L1-453 serves as a brake that keeps the long isoforms’ accelerator effects in check. These findings provide a novel insight into the regulatory roles of NFE2L1 in osteoclastogenesis and highlight that NFE2L1 is essential in regulating bone remodeling and thus may be a valuable therapeutic target for bone disorders.Zhiyuan LiuHuihui WangYongyong HouYang YangJingkun JiaJinzhi WuZhuo ZuoTianchang GaoSuping RenYiying BianShengnan LiuJingqi FuYongxin SunJiliang LiMasayuki YamamotoQiang ZhangYuanyuan XuJingbo PiElsevierarticleNFE2L1ROSNFATc1OsteoclastOsteoporosisOsteoclastogenesisMedicine (General)R5-920Biology (General)QH301-705.5ENRedox Biology, Vol 48, Iss , Pp 102180- (2021)
institution DOAJ
collection DOAJ
language EN
topic NFE2L1
ROS
NFATc1
Osteoclast
Osteoporosis
Osteoclastogenesis
Medicine (General)
R5-920
Biology (General)
QH301-705.5
spellingShingle NFE2L1
ROS
NFATc1
Osteoclast
Osteoporosis
Osteoclastogenesis
Medicine (General)
R5-920
Biology (General)
QH301-705.5
Zhiyuan Liu
Huihui Wang
Yongyong Hou
Yang Yang
Jingkun Jia
Jinzhi Wu
Zhuo Zuo
Tianchang Gao
Suping Ren
Yiying Bian
Shengnan Liu
Jingqi Fu
Yongxin Sun
Jiliang Li
Masayuki Yamamoto
Qiang Zhang
Yuanyuan Xu
Jingbo Pi
CNC-bZIP protein NFE2L1 regulates osteoclast differentiation in antioxidant-dependent and independent manners
description Fine-tuning of osteoclast differentiation (OD) and bone remodeling is crucial for bone homeostasis. Dissecting the mechanisms regulating osteoclastogenesis is fundamental to understanding the pathogenesis of various bone disorders including osteoporosis and arthritis. Nuclear factor erythroid 2-related factor 1 (NFE2L1, also known as NRF1), which belongs to the CNC-bZIP family of transcription factors, orchestrates a variety of physiological processes and stress responses. While Nfe2l1 gene may be transcribed into multiple alternatively spliced isoforms, the biological function of the different isoforms of NFE2L1 in bone metabolism, osteoclastogenesis in particular, has not been reported. Here we demonstrate that knockout of all isoforms of Nfe2l1 transcripts specifically in the myeloid lineage in mice [Nfe2l1(M)-KO] results in increased activity of osteoclasts, decreased bone mass and worsening of osteoporosis induced by ovariectomy and aging. In comparison, LysM-Cre-mediated Nfe2l1 deletion has no significant effect on the osteoblast and osteocytes. Mechanistic investigations using bone marrow cells and RAW 264.7 cells revealed that deficiency of Nfe2l1 leads to accelerated and elevated OD, which is attributed, at least in part, to enhanced accumulation of ROS in the early stage of OD and expression of nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1α (Nfatc1/α). In addition, NFE2L1 regulates the transcription of multiple antioxidant genes and Nfatc1/α and OD in an isoform-specific manner. While long isoforms of NFE2L1 function as accelerators of induction of Nfatc1/α and antioxidant genes and OD, the short isoform NFE2L1-453 serves as a brake that keeps the long isoforms’ accelerator effects in check. These findings provide a novel insight into the regulatory roles of NFE2L1 in osteoclastogenesis and highlight that NFE2L1 is essential in regulating bone remodeling and thus may be a valuable therapeutic target for bone disorders.
format article
author Zhiyuan Liu
Huihui Wang
Yongyong Hou
Yang Yang
Jingkun Jia
Jinzhi Wu
Zhuo Zuo
Tianchang Gao
Suping Ren
Yiying Bian
Shengnan Liu
Jingqi Fu
Yongxin Sun
Jiliang Li
Masayuki Yamamoto
Qiang Zhang
Yuanyuan Xu
Jingbo Pi
author_facet Zhiyuan Liu
Huihui Wang
Yongyong Hou
Yang Yang
Jingkun Jia
Jinzhi Wu
Zhuo Zuo
Tianchang Gao
Suping Ren
Yiying Bian
Shengnan Liu
Jingqi Fu
Yongxin Sun
Jiliang Li
Masayuki Yamamoto
Qiang Zhang
Yuanyuan Xu
Jingbo Pi
author_sort Zhiyuan Liu
title CNC-bZIP protein NFE2L1 regulates osteoclast differentiation in antioxidant-dependent and independent manners
title_short CNC-bZIP protein NFE2L1 regulates osteoclast differentiation in antioxidant-dependent and independent manners
title_full CNC-bZIP protein NFE2L1 regulates osteoclast differentiation in antioxidant-dependent and independent manners
title_fullStr CNC-bZIP protein NFE2L1 regulates osteoclast differentiation in antioxidant-dependent and independent manners
title_full_unstemmed CNC-bZIP protein NFE2L1 regulates osteoclast differentiation in antioxidant-dependent and independent manners
title_sort cnc-bzip protein nfe2l1 regulates osteoclast differentiation in antioxidant-dependent and independent manners
publisher Elsevier
publishDate 2021
url https://doaj.org/article/12524d37aec54ad8b4d35691e0ff0702
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