Literature DB >> 22189477

Gene expression and localization of high-mobility group box chromosomal protein-1 (HMGB-1)in human osteoarthritic cartilage.

Chuji Terada1, Aki Yoshida, Yoshihisa Nasu, Shuji Mori, Yasuko Tomono, Masato Tanaka, Hideo K Takahashi, Masahiro Nishibori, Toshifumi Ozaki, Keiichiro Nishida.   

Abstract

We investigated the expression and localization of high-mobility group box chromosomal protein-1 (HMGB-1) in human osteoarthritic (OA) cartilage in relation to the histopathological grade of cartilage destruction, and examined the role of HMGB-1 in the regulation of proinflammatory cytokine expression in chondrocytes. An immunohistochemical study demonstrated that total HMGB-1-positive cell ratios increase as the Osteoarthritis Research Society International (OARSI) histological grade increased. The population of cytoplasmic HMGB-1-positive chondrocytes was especially increased in the deep layers of higher-grade cartilage. The ratios and localization of receptors for advanced glycation end products (RAGE) expression by chondrocytes in Grade 2, 3, and 4 were significantly higher than those in Grade 1. In vitro stimulation with IL-1β, but not TNFα, significantly upregulated the expression of HMGB-1 mRNA by human OA chondrocytes. Both IL-1β and TNFα promoted the translocation of HMGB-1 from nuclei to cytoplasm. IL-1β and TNFα secretions were stimulated at higher levels of HMGB-1. The results of our study suggest the involvement of HMGB-1 in the pathogenesis of cartilage destruction in OA.

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Year:  2011        PMID: 22189477     DOI: 10.18926/AMO/47262

Source DB:  PubMed          Journal:  Acta Med Okayama        ISSN: 0386-300X            Impact factor:   0.892


  15 in total

1.  Modeling and simulation of the effects of cyclic loading on articular cartilage lesion formation.

Authors:  Xiayi Wang; Bruce P Ayati; Marc J Brouillete; Jason M Graham; Prem S Ramakrishnan; James A Martin
Journal:  Int J Numer Method Biomed Eng       Date:  2014-04-21       Impact factor: 2.747

Review 2.  The danger from within: alarmins in arthritis.

Authors:  Meriam Nefla; Dirk Holzinger; Francis Berenbaum; Claire Jacques
Journal:  Nat Rev Rheumatol       Date:  2016-10-13       Impact factor: 20.543

Review 3.  Inflammation in osteoarthritis: is it time to dampen the alarm(in) in this debilitating disease?

Authors:  M H J van den Bosch
Journal:  Clin Exp Immunol       Date:  2018-11-28       Impact factor: 4.330

Review 4.  Damage-associated molecular patterns in the pathogenesis of osteoarthritis: potentially novel therapeutic targets.

Authors:  John H Rosenberg; Vikrant Rai; Matthew F Dilisio; Devendra K Agrawal
Journal:  Mol Cell Biochem       Date:  2017-05-04       Impact factor: 3.396

5.  Increased expression of damage-associated molecular patterns (DAMPs) in osteoarthritis of human knee joint compared to hip joint.

Authors:  John H Rosenberg; Vikrant Rai; Matthew F Dilisio; Todd D Sekundiak; Devendra K Agrawal
Journal:  Mol Cell Biochem       Date:  2017-06-01       Impact factor: 3.396

6.  Inhibition of HMGB1 suppresses inflammation and catabolism in temporomandibular joint osteoarthritis <em>via</em> NF-κB signaling pathway.

Authors:  Yan Yan Li; Ya Ping Feng; Li Liu; Jin Ke; Xing Long
Journal:  Eur J Histochem       Date:  2022-06-21       Impact factor: 1.966

7.  MicroRNA-142-3p Inhibits Chondrocyte Apoptosis and Inflammation in Osteoarthritis by Targeting HMGB1.

Authors:  Xiuqin Wang; Yanqing Guo; Chunyan Wang; Hong Yu; Xiuxiang Yu; Hongbo Yu
Journal:  Inflammation       Date:  2016-10       Impact factor: 4.092

8.  High Mobility Group Box 1 Protein in Osteoarthritic Knee Tissue and Chondrogenic Progenitor Cells: An Ex Vivo and In Vitro Study.

Authors:  Gunar Wagner; Christoph Lehmann; Christa Bode; Nicolai Miosge; Andrea Schubert
Journal:  Cartilage       Date:  2019-03-26       Impact factor: 4.634

9.  A validated model of the pro- and anti-inflammatory cytokine balancing act in articular cartilage lesion formation.

Authors:  Xiayi Wang; Marc J Brouillette; Bruce P Ayati; James A Martin
Journal:  Front Bioeng Biotechnol       Date:  2015-03-10

10.  Advanced glycation end products induce peroxisome proliferator-activated receptor γ down-regulation-related inflammatory signals in human chondrocytes via Toll-like receptor-4 and receptor for advanced glycation end products.

Authors:  Ying Ju Chen; Meei Ling Sheu; Keh Sung Tsai; Rong Sen Yang; Shing Hwa Liu
Journal:  PLoS One       Date:  2013-06-12       Impact factor: 3.240

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