Literature DB >> 27002737

The unfolded protein response in skeletal development and homeostasis.

Keisuke Horiuchi1,2, Takahide Tohmonda3,4, Hideo Morioka3.   

Abstract

Osteoblasts and chondrocytes produce a large number of extracellular matrix proteins to generate and maintain the skeletal system. To cope with their functions as secretory cells, these cells must acquire a considerable capacity for protein synthesis and also the machinery for the quality-control and transport of newly synthesized secreted proteins. The unfolded protein response (UPR) plays a crucial role during the differentiation of these cells to achieve this goal. Unexpectedly, however, studies in the past several years have revealed that the UPR has more extensive functions in skeletal development than was initially assumed, and the UPR critically orchestrates many facets of skeletal development and homeostasis. This review focuses on recent findings on the functions of the UPR in the differentiation of osteoblasts, chondrocytes, and osteoclasts. These findings may have a substantial impact on our understanding of bone metabolism and also on establishing treatments for congenital and acquired skeletal disorders.

Entities:  

Keywords:  ATF6; Chondrocyte; ER stress; IRE1α; Osteoblast; Osteoclast; PERK; Unfolded protein response

Mesh:

Year:  2016        PMID: 27002737     DOI: 10.1007/s00018-016-2178-1

Source DB:  PubMed          Journal:  Cell Mol Life Sci        ISSN: 1420-682X            Impact factor:   9.261


  153 in total

1.  Activation of caspase-12, an endoplastic reticulum (ER) resident caspase, through tumor necrosis factor receptor-associated factor 2-dependent mechanism in response to the ER stress.

Authors:  T Yoneda; K Imaizumi; K Oono; D Yui; F Gomi; T Katayama; M Tohyama
Journal:  J Biol Chem       Date:  2001-01-29       Impact factor: 5.157

Review 2.  Mechanisms of release of nucleotides and integration of their action as P2X- and P2Y-receptor activating molecules.

Authors:  Eduardo R Lazarowski; Richard C Boucher; T Kendall Harden
Journal:  Mol Pharmacol       Date:  2003-10       Impact factor: 4.436

Review 3.  Building strong bones: molecular regulation of the osteoblast lineage.

Authors:  Fanxin Long
Journal:  Nat Rev Mol Cell Biol       Date:  2011-12-22       Impact factor: 94.444

Review 4.  Regulation of osteoblast differentiation by transcription factors.

Authors:  Toshihisa Komori
Journal:  J Cell Biochem       Date:  2006-12-01       Impact factor: 4.429

5.  XBP-1 regulates a subset of endoplasmic reticulum resident chaperone genes in the unfolded protein response.

Authors:  Ann-Hwee Lee; Neal N Iwakoshi; Laurie H Glimcher
Journal:  Mol Cell Biol       Date:  2003-11       Impact factor: 4.272

6.  Signalling mediated by the endoplasmic reticulum stress transducer OASIS is involved in bone formation.

Authors:  Tomohiko Murakami; Atsushi Saito; Shin-ichiro Hino; Shinichi Kondo; Soshi Kanemoto; Kazuyasu Chihara; Hiroshi Sekiya; Kenji Tsumagari; Kimiko Ochiai; Kazuya Yoshinaga; Masahiro Saitoh; Riko Nishimura; Toshiyuki Yoneda; Ikuyo Kou; Tatsuya Furuichi; Shiro Ikegawa; Masahito Ikawa; Masaru Okabe; Akio Wanaka; Kazunori Imaizumi
Journal:  Nat Cell Biol       Date:  2009-09-20       Impact factor: 28.824

7.  Regulated IRE1-dependent decay participates in curtailing immunoglobulin secretion from plasma cells.

Authors:  Sandrine Benhamron; Rivka Hadar; Takao Iwawaky; Jae-Seon So; Ann-Hwee Lee; Boaz Tirosh
Journal:  Eur J Immunol       Date:  2013-12-23       Impact factor: 5.532

8.  The CrebA/Creb3-like transcription factors are major and direct regulators of secretory capacity.

Authors:  Rebecca M Fox; Caitlin D Hanlon; Deborah J Andrew
Journal:  J Cell Biol       Date:  2010-11-01       Impact factor: 10.539

9.  Hypertrophic chondrocytes have a limited capacity to cope with increases in endoplasmic reticulum stress without triggering the unfolded protein response.

Authors:  Louise H W Kung; M Helen Rajpar; Michael D Briggs; Raymond P Boot-Handford
Journal:  J Histochem Cytochem       Date:  2012-08-01       Impact factor: 2.479

10.  ER stress-mediated apoptosis in a new mouse model of osteogenesis imperfecta.

Authors:  Thomas S Lisse; Frank Thiele; Helmut Fuchs; Wolfgang Hans; Gerhard K H Przemeck; Koichiro Abe; Birgit Rathkolb; Leticia Quintanilla-Martinez; Gabriele Hoelzlwimmer; Miep Helfrich; Eckhard Wolf; Stuart H Ralston; Martin Hrabé de Angelis
Journal:  PLoS Genet       Date:  2008-02       Impact factor: 5.917

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  18 in total

1.  Inhibiting the integrated stress response pathway prevents aberrant chondrocyte differentiation thereby alleviating chondrodysplasia.

Authors:  Cheng Wang; Zhijia Tan; Ben Niu; Kwok Yeung Tsang; Andrew Tai; Wilson C W Chan; Rebecca L K Lo; Keith K H Leung; Nelson W F Dung; Nobuyuki Itoh; Michael Q Zhang; Danny Chan; Kathryn Song Eng Cheah
Journal:  Elife       Date:  2018-07-19       Impact factor: 8.140

Review 2.  Transcriptional control of chondrocyte specification and differentiation.

Authors:  Chia-Feng Liu; William E Samsa; Guang Zhou; Véronique Lefebvre
Journal:  Semin Cell Dev Biol       Date:  2016-10-19       Impact factor: 7.727

3.  Phenotypic Spectrum in Osteogenesis Imperfecta Due to Mutations in TMEM38B: Unraveling a Complex Cellular Defect.

Authors:  Emma A Webb; Meena Balasubramanian; Nadja Fratzl-Zelman; Wayne A Cabral; Hannah Titheradge; Atif Alsaedi; Vrinda Saraff; Julie Vogt; Trevor Cole; Susan Stewart; Nicola J Crabtree; Brandi M Sargent; Sonja Gamsjaeger; Eleftherios P Paschalis; Paul Roschger; Klaus Klaushofer; Nick J Shaw; Joan C Marini; Wolfgang Högler
Journal:  J Clin Endocrinol Metab       Date:  2017-06-01       Impact factor: 5.958

4.  Sel1l May Contributes to the Determinants of Neuronal Lineage and Neuronal Maturation Regardless of Hrd1 via Atf6-Sel1l Signaling.

Authors:  Ryo Saito; Seisuke Mimori; Yasunobu Okuma; Koichi Kawada
Journal:  Neurochem Res       Date:  2022-09-08       Impact factor: 4.414

5.  Silencing of both ATF4 and PERK inhibits cell cycle progression and promotes the apoptosis of differentiating chondrocytes.

Authors:  Zhimeng Wu; Meiling Li; Wei Zheng; Qin Hu; Zhi Cheng; Fengjin Guo
Journal:  Int J Mol Med       Date:  2017-05-10       Impact factor: 4.101

6.  ATG5 and ATG7 induced autophagy interplays with UPR via PERK signaling.

Authors:  Wei Zheng; Weiwei Xie; Danyang Yin; Rui Luo; Min Liu; Fengjin Guo
Journal:  Cell Commun Signal       Date:  2019-05-06       Impact factor: 5.712

7.  PERK-mediated translational control is required for collagen secretion in chondrocytes.

Authors:  Satoshi Hisanaga; Masato Miyake; Shusuke Taniuchi; Miho Oyadomari; Masatoshi Morimoto; Ryosuke Sato; Jun Hirose; Hiroshi Mizuta; Seiichi Oyadomari
Journal:  Sci Rep       Date:  2018-01-15       Impact factor: 4.379

8.  Suppressing UPR-dependent overactivation of FGFR3 signaling ameliorates SLC26A2-deficient chondrodysplasias.

Authors:  Chao Zheng; Xisheng Lin; Xiaolong Xu; Cheng Wang; Jinru Zhou; Bo Gao; Jing Fan; Weiguang Lu; Yaqian Hu; Qiang Jie; Zhuojing Luo; Liu Yang
Journal:  EBioMedicine       Date:  2019-01-23       Impact factor: 8.143

Review 9.  New developments in chondrocyte ER stress and related diseases.

Authors:  Michael D Briggs; Ella P Dennis; Helen F Dietmar; Katarzyna A Pirog
Journal:  F1000Res       Date:  2020-04-24

Review 10.  Sledgehammer to Scalpel: Broad Challenges to the Heart and Other Tissues Yield Specific Cellular Responses via Transcriptional Regulation of the ER-Stress Master Regulator ATF6α.

Authors:  Winston T Stauffer; Adrian Arrieta; Erik A Blackwood; Christopher C Glembotski
Journal:  Int J Mol Sci       Date:  2020-02-08       Impact factor: 5.923

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