Immunomorphological analysis of RAGE receptor expression and NF-κB activation in tissue samples from normal and degenerated intervertebral discs of various ages

被引:79
作者
Nerlich, Andreas G.
Bachmeier, Beatrice E.
Schleicher, Erwin
Rohrbach, Helmut
Paesold, Guenther
Boos, Norbert
机构
[1] Acad Hosp, Inst Pathol, Dept Pathol, D-81925 Munich, Germany
[2] Univ Munich, Dept Clin Chem Clin Biochem, D-80336 Munich, Germany
[3] Univ Tubingen, Dept Internal Med, D-72076 Tubingen, Germany
[4] Univ Zurich, Ctr Spinal Surg, CH-8008 Balgrist, Switzerland
来源
SIGNAL TRANSDUCTION PATHWAYS, PT D: INFLAMMATORY SIGNALING PATHWAYS AND NEUROPATHOLOGY | 2007年 / 1096卷
关键词
metalloproteinases; MMPs; pathomechanisms; carboxymethyl-lysine; CML;
D O I
10.1196/annals.1397.090
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
We immunohistochemically investigated the pattern of RAGE expression and NF kappa B translocation into the nucleus in 43 complete cross-sections of human lumbar intervertebral discs (neonatal-85 years) and compared this with the carboxymethyl-lysine (CML) modification of proteins as a marker for oxidative stress. No significant expression of RAGE, no obvious activation of NF-kappa B, and no deposition of CML-modified proteins were seen in fetal, juvenile, and young adolescent discs (until age of 13 years). In adults, 25-50% of nucleus pulposus cells were labeled for RAGE and activated NF-kappa B, which correlated well with the occurrence and extent of CML staining in the pericellular matrix. In the annulus fibrosus significantly lower values were seen than in the nucleus pulposus. In consequence, we provide evidence for activation of the NF-kappa B system in intervertebral discs in vivo, which correlates with accumulated oxidative stress and increases in age and disc degeneration. Oxidative stress (as monitored by CML modifications) may lead to RAGE activation and NF-kappa B translocation.
引用
收藏
页码:239 / 248
页数:10
相关论文
共 14 条
[1]
Classification of age-related changes in lumbar intervertebral discs [J].
Boos, N ;
Weissbach, S ;
Rohrbach, H ;
Weiler, C ;
Spratt, KF ;
Nerlich, AG .
SPINE, 2002, 27 (23) :2631-2644
[2]
SPINE UPDATE - AGING AND DEGENERATION OF THE HUMAN INTERVERTEBRAL DISC [J].
BUCKWALTER, JA .
SPINE, 1995, 20 (11) :1307-1314
[3]
COLLAGEN IN THE AGING HUMAN INTERVERTEBRAL-DISK - AN INCREASE IN COVALENTLY BOUND FLUOROPHORES AND CHROMOPHORES [J].
HORMEL, SE ;
EYRE, DR .
BIOCHIMICA ET BIOPHYSICA ACTA, 1991, 1078 (02) :243-250
[4]
HISTOCHEMICAL AND ULTRASTRUCTURAL OBSERVATIONS ON BROWN DEGENERATION OF HUMAN INTERVERTEBRAL-DISK [J].
ISHII, T ;
TSUJI, H ;
SANO, A ;
KATOH, Y ;
MATSUI, H ;
TERAHATA, N .
JOURNAL OF ORTHOPAEDIC RESEARCH, 1991, 9 (01) :78-90
[5]
Nε-(carboxymethyl)lysine adducts of proteins are ligands for receptor for advanced glycation end products that activate cell signaling pathways and modulate gene expression [J].
Kislinger, T ;
Fu, CF ;
Huber, B ;
Qu, W ;
Taguchi, A ;
Yan, SD ;
Hofmann, M ;
Yan, SF ;
Pischetsrieder, M ;
Stern, D ;
Schmidt, AM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (44) :31740-31749
[6]
The economic burden of back pain in the UK [J].
Maniadakis, N ;
Gray, A .
PAIN, 2000, 84 (01) :95-103
[7]
1997 Volvo Award winner in basic science studies - Immunohistologic markers for age-related changes of human lumbar intervertebral discs [J].
Nerlich, AG ;
Schleicher, ED ;
Boos, N .
SPINE, 1997, 22 (24) :2781-2795
[8]
Expression of fibronectin and TGF-β1 mRNA and protein suggest altered regulation of extracellular matrix in degenerated disc tissue [J].
Nerlich, AG ;
Bachmeier, BE ;
Boos, N .
EUROPEAN SPINE JOURNAL, 2005, 14 (01) :17-26
[9]
DEGENERATION AND THE CHEMICAL-COMPOSITION OF THE HUMAN LUMBAR INTERVERTEBRAL-DISK [J].
PEARCE, RH ;
GRIMMER, BJ ;
ADAMS, ME .
JOURNAL OF ORTHOPAEDIC RESEARCH, 1987, 5 (02) :198-205
[10]
1991 VOLVO AWARD IN BASIC SCIENCES - COLLAGEN TYPES AROUND THE CELLS OF THE INTERVERTEBRAL-DISK AND CARTILAGE END PLATE - AN IMMUNOLOCALIZATION STUDY [J].
ROBERTS, S ;
MENAGE, J ;
DUANCE, V ;
WOTTON, S ;
AYAD, S .
SPINE, 1991, 16 (09) :1030-1038