Expression profile of osteoprotegerin, RANK and RANKL genes in the femoral head of patients with avascular necrosis

被引:38
作者
Samara, Stavrouta [1 ]
Dailiana, Zoe [2 ]
Chassanidis, Christos [1 ]
Koromila, Theodora [3 ]
Papatheodorou, Lciukia [2 ]
Malizos, Konstantinos N. [2 ,4 ]
Kollia, Panagoula [3 ]
机构
[1] Univ Thessalia, Fac Med, Lab Med Genet & Cytogenet, Larisa, Greece
[2] Univ Thessalia, Fac Med, Dept Orthopaed Surg, Larisa, Greece
[3] Univ Athens, Fac Biol, Dept Genet & Biotechnol, Athens 15701, Greece
[4] Ctr Res & Technol, Dept Biomed Res & Technol, Thessaly Cereteth, Larissa, Greece
关键词
Avascular necrosis of the bone; Osteoblasts; Osteoclasts; OPG; RANK; RANKL; BONE MORPHOGENETIC PROTEINS; KAPPA-B LIGAND; EXPANSILE SKELETAL HYPERPHOSPHATASIA; RECEPTOR ACTIVATOR; IDIOPATHIC HYPERPHOSPHATASIA; FACTOR-V; OSTEONECROSIS; DENSITY; DISEASE; OSTEOCLASTOGENESIS;
D O I
10.1016/j.yexmp.2013.10.014
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Introduction: Femoral head avascular necrosis (AVN) is a recalcitrant disease of the hip that leads to joint destruction. Osteoprotegerin (OPG), Receptor Activator of Nuclear Factor kappa-B (RANK) and RANK ligand (RANKL) regulate the balance between osteoclasts-osteoblasts. The expression of these genes affects the maturation and function of osteoblasts-osteoclasts and bone remodeling. In this study, we investigated the molecular pathways leading to AVN by studying the expression profile of OPG, RANK and RANKL genes. Material and methods: Quantitative Real Time-PCR was performed for evaluation of OPG, RANK and RANKL expression. Analysis was based on parallel evaluation of mRNA and protein levels in normal/necrotic sites of 42 osteonecrotic femoral heads (FHs). OPG and RANKL protein levels were estimated by western blotting. Results: The OPG mRNA levels were higher (insignificantly) in the necrotic than the normal site (p > 0.05). Although the expression of RANK and RANKL was significantly lower than OPG in both sites, RANK and RANKL mRNA levels were higher in the necrotic part than the normal (p < 0.05). Protein levels of OPG and RANKL showed no remarkable divergence. Conclusions: Our results indicate that differential expression mechanisms for OPG, RANK and RANKL that could play an important role in the progress of bone remodeling in the necrotic area, disturbing bone homeostasis. This finding may have an effect on the resulting bone destruction and the subsequent collapse of the hip joint. (C) 2013 Published by Elsevier Inc.
引用
收藏
页码:9 / 14
页数:6
相关论文
共 39 条
[1]   Osteoprotegerin and its ligand: A new paradigm for regulation of osteoclastogenesis and bone resorption [J].
Aubin, JE ;
Bonnelye, E .
OSTEOPOROSIS INTERNATIONAL, 2000, 11 (11) :905-913
[2]   High quality RNA isolation from tumours with low cellularity and high extracellular matrix component for cDNA microarrays:: application to chondrosarcoma [J].
Baelde, HJ ;
Cleton-Jansen, AM ;
van Beerendonk, H ;
Namba, M ;
Bovée, JVMG ;
Hogendoorn, PCW .
JOURNAL OF CLINICAL PATHOLOGY, 2001, 54 (10) :778-782
[3]   Factor V Leiden and prothrombin gene mutation [J].
Björkman, A ;
Svensson, PJ ;
Hillarp, A ;
Burtscher, IM ;
Rünow, A ;
Benoni, G .
CLINICAL ORTHOPAEDICS AND RELATED RESEARCH, 2004, (425) :168-172
[4]   Associations of serum osteoprotegerin levels with diabetes, stroke, bone density, fractures, and mortality in elderly women [J].
Browner, WS ;
Lui, LY ;
Cummings, SR .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2001, 86 (02) :631-637
[5]   osteoprotegerin-deficient mice develop early onset osteoporosis and arterial calcification [J].
Bucay, N ;
Sarosi, I ;
Dunstan, CR ;
Morony, S ;
Tarpley, J ;
Capparelli, C ;
Scully, S ;
Tan, HL ;
Xu, WL ;
Lacey, DL ;
Boyle, WJ ;
Simonet, WS .
GENES & DEVELOPMENT, 1998, 12 (09) :1260-1268
[6]   Bone morphogenetic proteins, their antagonists, and the skeleton [J].
Canalis, E ;
Economides, AN ;
Gazzerro, E .
ENDOCRINE REVIEWS, 2003, 24 (02) :218-235
[7]   Association of corticosteroids and factor V, prothrombin, and MTHFR gene mutations with avascular osteonecrosis in renal allograft recipients [J].
Celik, A ;
Tekis, D ;
Saglam, F ;
Tunali, S ;
Kabakci, N ;
Ozaksoy, D ;
Manisali, M ;
Ozcan, MA ;
Meral, M ;
Gülay, H ;
Camsari, T .
TRANSPLANTATION PROCEEDINGS, 2006, 38 (02) :512-516
[8]   Bone morphogenetic proteins [J].
Chen, D ;
Zhao, M ;
Mundy, GR .
GROWTH FACTORS, 2004, 22 (04) :233-241
[9]   Osteogenic activity of the fourteen types of human bone morphogenetic proteins (BMPs) [J].
Cheng, HW ;
Jiang, W ;
Phillips, FM ;
Haydon, RC ;
Peng, Y ;
Zhou, L ;
Luu, HH ;
An, NL ;
Breyer, B ;
Vanichakarn, P ;
Szatkowski, JP ;
Park, JY ;
He, TC .
JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME, 2003, 85A (08) :1544-1552
[10]   Idiopathic hyperphosphatasia and TNFRSF11B mutations:: Relationships between phenotype and genotype [J].
Chong, B ;
Hegde, M ;
Fawkner, M ;
Simonet, S ;
Cassinelli, H ;
Coker, M ;
Kanis, J ;
Seidel, J ;
Tau, C ;
Tüysüz, B ;
Yüksel, B ;
Love, D ;
Cundy, T .
JOURNAL OF BONE AND MINERAL RESEARCH, 2003, 18 (12) :2095-2104