Analysis of tissue distribution of TNF-α, TNF-α-receptors, and the activating TNF-α-converting enzyme suggests activation of the TNF-α system in the aging intervertebral disc

被引:121
作者
Bachmeier, Beatrice E.
Nerlich, Andreas G.
Weiler, Christoph
Paesold, Gunther
Jochum, Marianne
Boos, Norbert
机构
[1] Univ Munich, Dept Clin Chem & Clin Biochem, D-80336 Munich, Germany
[2] Acad Hosp Munich Bogenhausen, Dept Pathol, D-81925 Munich, Germany
[3] Univ Munich, Inst Pathol, D-80337 Munich, Germany
[4] Univ Zurich, Ctr Spinal Surg, CH-8008 Zurich, Switzerland
来源
SIGNAL TRANSDUCTION PATHWAYS, PT D: INFLAMMATORY SIGNALING PATHWAYS AND NEUROPATHOLOGY | 2007年 / 1096卷
关键词
TNF-alpha; TNF-Rl and TNF-RII; histomorphological; immunohistochemical;
D O I
10.1196/annals.1397.069
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We immunohistochemically analyzed the expression and localization of TNF-alpha, its receptors TNF-RI and -RII, and the TNF-alpha-activating enzyme TACE in human autopsy (n = 63) and surgical (n = 35) lumbar intervertebral disc samples. In parallel, the TNF-alpha-mRiNA was quantified by reverse transcriptase-polymerase chain reaction (RT-PCR). All samples were morphometrically evaluated for the proportion of positively labeled cells in the different anatomical regions of the disc. We detected a significant and comparable expression of all four parameters beginning in young adult age (c. 18 years) and being most extensive in the nucleus pulposus. This level was slightly reduced in older age discs. The annulus fibrosus contained significantly less labeled cells. In accord, the number of TNF-alpha-transcripts was elevated in most cases with immunohistochernical TNF-alpha expression. We provide clear evidence that TNF-ot is expressed in discs of increasing age, which correlates with histomorphological signs of disc degeneration. In consequence, TNF-alpha seems to be activated (by the converting enzyme TACE) and biologically active through its receptors in human lumbar disc tissue.
引用
收藏
页码:44 / 54
页数:11
相关论文
共 24 条
[1]   mRNA expression of cytokines and chemokines in herniated lumbar intervertebral discs [J].
Ahn, SH ;
Cho, YW ;
Ahn, MW ;
Jang, SH ;
Sohn, YK ;
Kim, HS .
SPINE, 2002, 27 (09) :911-917
[2]   Targeting death and decoy receptors of the tumour-necrosis factor superfamily [J].
Ashkenazi, A .
NATURE REVIEWS CANCER, 2002, 2 (06) :420-430
[3]  
Baba H, 1997, EUR J HISTOCHEM, V41, P261
[4]   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
[5]   Discovery of TNF-α as a therapeutic target in rheumatoid arthritis:: preclinical and clinical studies [J].
Feldmann, M ;
Maini, RN .
JOINT BONE SPINE, 2002, 69 (01) :12-18
[6]  
GRONBLAD M, 1994, SPINE, V19, P2744
[7]   Vascular endothelial growth factor (VEGF)-induced angiogenesis in herniated disc resorption [J].
Haro, H ;
Kato, T ;
Komori, H ;
Osada, M ;
Shinomiya, K .
JOURNAL OF ORTHOPAEDIC RESEARCH, 2002, 20 (03) :409-415
[8]   Matrix metalloproteinase-3-dependent generation of a macrophage chemoattractant in a model of herniated disc resorption [J].
Haro, H ;
Crawford, HC ;
Fingleton, B ;
MacDougall, JR ;
Shinomiya, K ;
Spengler, DM ;
Matrisian, LM .
JOURNAL OF CLINICAL INVESTIGATION, 2000, 105 (02) :133-141
[9]   Matrix metalloproteinase-7-dependent release of tumor necrosis factor-α in a model of herniated disc resorption [J].
Haro, H ;
Crawford, HC ;
Fingleton, B ;
Shinomiya, K ;
Spengler, DM ;
Matrisian, LM .
JOURNAL OF CLINICAL INVESTIGATION, 2000, 105 (02) :143-150
[10]  
Heyninck Karen, 2001, Molecular Cell Biology Research Communications, V4, P259, DOI 10.1006/mcbr.2001.0295