Literature DB >> 16278806

Expression of receptors for putative anabolic growth factors in human intervertebral disc: implications for repair and regeneration of the disc.

Christine L Le Maitre1, Stephen M A Richardson, Pauline Baird, Anthony J Freemont, Judith A Hoyland.   

Abstract

Low back pain (LBP) is a common, debilitating and economically important disorder. Current evidence implicates loss of intervertebral disc (IVD) matrix consequent upon 'degeneration' as a major cause of LBP. Degeneration of the IVD involves increases in degradative enzymes and decreases in the extracellular matrix (ECM) component in a process that is controlled by a range of cytokines and growth factors. Studies have suggested using anabolic growth factors to regenerate the normal matrix of the IVD, hence restoring disc height and reversing degenerative disc disease. However, for such therapies to be successful it is vital that the target cells (i.e. the disc cells) express the appropriate receptors. This immunohistochemical study has for the first time investigated the expression and localization of four potentially beneficial growth factor receptors (i.e. TGFbetaRII, BMPRII, FGFR3 and IGFRI) in non-degenerate and degenerate human IVDs. Receptor expression was quantified across regions of the normal and degenerate disc and showed that cells of the nucleus pulposus (NP) and inner annulus fibrosus (IAF) expressed significantly higher levels of the four growth factor receptors investigated. There were no significant differences between the four growth factor expression in non-degenerate and degenerate biopsies. However, expression of TGFbetaRII, FGFR3 and IGFRI, but not BMP RII, were observed in the ingrowing blood vessels that characterize part of the disease aetiology. In conclusion, this study has demonstrated the expression of the four growth factor receptors at similar levels in the chondrocyte-like cells of the NP and IAF in both non-degenerate and degenerate discs, implicating a role in normal disc homeostasis and suggesting that the application of these growth factors to the degenerate human IVD would stimulate matrix production. However, the expression of some of the growth factor receptors on ingrowing blood vessels might be problematic in a therapeutic approach. Copyright 2005 Pathological Society of Great Britain and Ireland.

Entities:  

Mesh:

Substances:

Year:  2005        PMID: 16278806     DOI: 10.1002/path.1862

Source DB:  PubMed          Journal:  J Pathol        ISSN: 0022-3417            Impact factor:   7.996


  33 in total

1.  Aquaporin expression in the human intervertebral disc.

Authors:  S M Richardson; R Knowles; D Marples; J A Hoyland; A Mobasheri
Journal:  J Mol Histol       Date:  2008-02-06       Impact factor: 2.611

2.  Different Expression of Extracellular Matrix Genes : Primary vs. Recurrent Disc Herniation.

Authors:  Sung-Uk Kuh; Young-Min Kwon; Dong-Kyu Chin; Keun-Su Kim; Byung-Ho Jin; Yong-Eun Cho
Journal:  J Korean Neurosurg Soc       Date:  2010-01-31

3.  Role of growth differentiation factor-5 and bone morphogenetic protein type II receptor in the development of lumbar intervertebral disc degeneration.

Authors:  Yi-Fan Li; Xian-Zhong Tang; Chao-Ge Liang; Yao-Ming Hui; Yun-Han Ji; Wei Xu; WenJun Qiu; Li-Ming Cheng
Journal:  Int J Clin Exp Pathol       Date:  2015-01-01

4.  Identifying molecular phenotype of nucleus pulposus cells in human intervertebral disc with aging and degeneration.

Authors:  Xinyan Tang; Liufang Jing; William J Richardson; Robert E Isaacs; Robert D Fitch; Christopher R Brown; Melissa M Erickson; Lori A Setton; Jun Chen
Journal:  J Orthop Res       Date:  2016-04-13       Impact factor: 3.494

Review 5.  Cell and molecular biology of intervertebral disc degeneration: current understanding and implications for potential therapeutic strategies.

Authors:  S Z Wang; Y F Rui; J Lu; C Wang
Journal:  Cell Prolif       Date:  2014-08-11       Impact factor: 6.831

6.  PDGF, bFGF and IGF-I stimulate the proliferation of intervertebral disc cells in vitro via the activation of the ERK and Akt signaling pathways.

Authors:  Harris Pratsinis; Dimitris Kletsas
Journal:  Eur Spine J       Date:  2007-09-01       Impact factor: 3.134

Review 7.  An understanding of intervertebral disc development, maturation and cell phenotype provides clues to direct cell-based tissue regeneration therapies for disc degeneration.

Authors:  Ricardo Rodrigues-Pinto; Stephen M Richardson; Judith A Hoyland
Journal:  Eur Spine J       Date:  2014-04-29       Impact factor: 3.134

8.  Multiplex Epigenome Editing of Dorsal Root Ganglion Neuron Receptors Abolishes Redundant Interleukin 6, Tumor Necrosis Factor Alpha, and Interleukin 1β Signaling by the Degenerative Intervertebral Disc.

Authors:  Joshua D Stover; Niloofar Farhang; Brandon Lawrence; Robby D Bowles
Journal:  Hum Gene Ther       Date:  2019-06-11       Impact factor: 5.695

9.  Expression of cartilage-derived morphogenetic protein in human intervertebral discs and its effect on matrix synthesis in degenerate human nucleus pulposus cells.

Authors:  Christine L Le Maitre; Anthony J Freemont; Judith A Hoyland
Journal:  Arthritis Res Ther       Date:  2009-09-15       Impact factor: 5.156

Review 10.  Biologic treatment of mild and moderate intervertebral disc degeneration.

Authors:  Elias S Vasiliadis; Spyros G Pneumaticos; Demitrios S Evangelopoulos; Athanasios G Papavassiliou
Journal:  Mol Med       Date:  2014-09-18       Impact factor: 6.354

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.