Resveratrol could reverse the expression of SIRT1 and MMP-1 in vitro

被引:21
作者
Wu, J. W. [1 ]
Wang, J. J. [2 ]
Chen, J. B. [1 ]
Huang, Y. L. [1 ]
Wang, H. [1 ]
Liu, G. H. [1 ]
Li, L. F. [3 ]
Kang, M. [1 ]
Wang, X. G. [1 ]
Cai, H. H. [1 ]
机构
[1] HuiZhou Municipal Cent Hosp, Dept Spine Surg, Huizhou, Guangdong, Peoples R China
[2] HuiZhou Municipal Cent Hosp, Dept Ophthalmol, Huizhou, Guangdong, Peoples R China
[3] HuiZhou Municipal Cent Hosp, Dept Emergency, Huizhou, Guangdong, Peoples R China
关键词
Resveratrol; SIRT1; MMP-1; Immunohistochemistry; Intervertebral disc nucleus pulposus; NUCLEUS PULPOSUS; MATRIX; CHONDROCYTES; SURVIVAL; PATHWAY; CELLS;
D O I
10.4238/2015.October.16.5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Intervertebral disc degeneration is the main cause of lumbago disease, in which the extracellular matrix structure and moisture in the nucleus pulposus is lost continuously. In this study, we aimed to detect differential expression of silence mating type information regulation 2 homolog 1 (SIRT1) and matrix metalloproteinase-1 (MMP-1) in human intervertebral disc nucleus pulposus cells and to explore the effects of SIRT1 and MMP-1 on the development of the intervertebral disc degeneration. Intervertebral disc nucleus pulposus specimens from 41 patients who underwent lumbar protrusion resection at HuiZhou Municipal Central Hospital, during the period from October 2011 to December 2013, were studied in comparison with 23 control cases from patients who underwent fractured lumbar resection. In degenerated human intervertebral disc nucleus pulposus cells, the expression of SIRT1 is decreased and MMP-1 is increased compared with that of the control cells. Resveratrol could reverse these effects, thereby increasing the expression of SIRT1 (0.87 +/- 0.07 vs 0.54 +/- 0.04), Coll2 alpha 1 (0.90 +/- 0.08 vs 0.38 +/- 0.01), and aggrecan (0.69 +/- 0.07 vs 0.42 +/- 0.05) and decreasing the expression of MMP-1 (0.61 +/- 0.03 vs 0.93 +/- 0.08). These results suggest that resveratrol could possibly reverse the process of intervertebral disc degeneration and thus could be applied as a potential drug for the disease.
引用
收藏
页码:12386 / 12393
页数:8
相关论文
共 29 条
[1]
The potential and limitations of a cell-seeded collagen/hyaluronan scaffold to engineer an intervertebral disc-like matrix [J].
Alini, M ;
Li, W ;
Markovic, P ;
Aebi, M ;
Spiro, RC ;
Roughley, PJ .
SPINE, 2003, 28 (05) :446-453
[2]
Implementation of a Guideline for Low Back Pain Management in Primary Care A Cost-Effectiveness Analysis [J].
Becker, Annette ;
Held, Heiko ;
Redaelli, Marcus ;
Chenot, Jean F. ;
Leonhardt, Corinna ;
Keller, Stefan ;
Baum, Erika ;
Pfingsten, Michael ;
Hildebrandt, Jan ;
Basler, Heinz-Dieter ;
Kochen, Michael M. ;
Donner-Banzhoff, Norbert ;
Strauch, Konstantin .
SPINE, 2012, 37 (08) :701-710
[3]
Boileau C, 2011, ARTHRITIS RES THER, V9, P121
[4]
Pathology and possible mechanisms of nervous system response to disc degeneration [J].
Brisby, H .
JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME, 2006, 88A :68-71
[5]
Chen G, 2011, DANG DAI YI XUE, V16, P46
[6]
The intervertebral disc: From pathophysiology to tissue engineering [J].
Clouet, Johann ;
Vinatier, Claire ;
Merceron, Christophe ;
Pot-Vaucel, Marianne ;
Hamel, Olivier ;
Weiss, Pierre ;
Grimandi, Gael ;
Guicheux, Jerome .
JOINT BONE SPINE, 2009, 76 (06) :614-618
[7]
Aging Genes: The Sirtuin Story Unravels [J].
Couzin-Frankel, Jennifer .
SCIENCE, 2011, 334 (6060) :1194-1198
[8]
The Sir2 family of protein deacetylases [J].
Denu, JM .
CURRENT OPINION IN CHEMICAL BIOLOGY, 2005, 9 (05) :431-440
[9]
SirT1 Enhances Survival of Human Osteoarthritic Chondrocytes by Repressing Protein Tyrosine Phosphatase 1B and Activating the Insulin-like Growth Factor Receptor Pathway [J].
Gagarina, Viktoria ;
Gabay, Odile ;
Dvir-Ginzberg, Mona ;
Lee, Eun Jin ;
Brady, Jillian K. ;
Quon, Michael J. ;
Hall, David J. .
ARTHRITIS AND RHEUMATISM, 2010, 62 (05) :1383-1392
[10]
Early histologic changes in lower lumbar discs and facet joints and their correlation [J].
Gries, NC ;
Berlemann, U ;
Moore, RJ ;
Vernon-Roberts, B .
EUROPEAN SPINE JOURNAL, 2000, 9 (01) :23-29