Platelet-released growth factors can accelerate tenocyte proliferation and activate the anti-oxidant response element

被引:64
作者
Tohidnezhad, M. [1 ]
Varoga, D. [2 ]
Wruck, C. J. [1 ]
Brandenburg, L. O. [1 ]
Seekamp, A. [2 ]
Shakibaei, M. [3 ]
Soenmez, T. T. [4 ]
Pufe, Thomas [1 ]
Lippross, S. [2 ]
机构
[1] Rhein Westfal TH Aachen, Dept Anat & Cell Biol, D-52074 Aachen, Germany
[2] Univ Hosp Schleswig Holstein, Dept Trauma Surg, D-24105 Kiel, Germany
[3] Univ Munich, Inst Anat, Musculoskeletal Res Grp, D-80336 Munich, Germany
[4] Rhein Westfal TH Aachen, Dept Operat Dent & Plast Facial Surg, D-52074 Aachen, Germany
关键词
PRP; PRGF; Tenocyte; Nrf-2; RAT ACHILLES-TENDON; RICH PLASMA; BRAIN-INJURY; IN-VITRO; CELLS; BONE; TENOMODULIN; CULTURE; NRF2; CONCENTRATE;
D O I
10.1007/s00418-011-0808-0
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Little is know about the pathophysiology of acute and degenerative tendon injuries. Although most lesions are uncomplicated, treatment is long and unsatisfactory in a considerable number of cases. Besides the common growth factors that were shown to be relevant for tendon integrity more recently protection against oxidative stress was shown to promote tendon healing. To improve tendon regeneration, many have advocated the use of platelet-rich plasma (PRP), a thrombocyte concentrate that can serve as an autologous source of growth factors. In this study, we investigated the effect of platelet-released growth factors (PRGF) on tenocytes. Tenocytes were isolated from the Achilles tendon of postnatal rats. Tenocyte cell cultures were stimulated with PRGF. We used a CyQuant assay and WST assay to analyse tendon cell growth and viability in different concentrations of PRGF. Migration and proliferation of cells grown in PRGF were assessed by a scratch test. A dual-luciferase assay was used to demonstrate the activation of the anti-oxidant response element (ARE) in tenocytes. A positive effect of PRGF could be shown on tendon cell growth and migratory capacity. PRGF activated the Nrf2-ARE pathway in a dose-dependent manner. Here, we provide evidence of a biological effect of PRGF on tenocytes by the promotion of tenocyte growth and activation of the Nrf2-ARE pathway. This is a novel aspect of the action of platelet concentrates on tendon growth.
引用
收藏
页码:453 / 460
页数:8
相关论文
共 45 条
[1]   Autologous preparations rich in growth factors promote proliferation and induce VEGF and HGF production by human tendon cells in culture [J].
Anitua, E ;
Andía, I ;
Sanchez, M ;
Azofra, J ;
Zalduendo, MD ;
de la Fuente, M ;
Nurden, P ;
Nurden, AT .
JOURNAL OF ORTHOPAEDIC RESEARCH, 2005, 23 (02) :281-286
[2]   Platelet concentrate injection improves Achilles tendon repair in rats [J].
Aspenberg, P ;
Virchenko, O .
ACTA ORTHOPAEDICA SCANDINAVICA, 2004, 75 (01) :93-99
[3]   Antibacterial effect of autologous platelet gel enriched with growth factors and other active substances -: An in vitro study [J].
Bielecki, T. M. ;
Gazdzik, T. S. ;
Arendt, J. ;
Szczepanski, T. ;
Krol, W. ;
Wielkoszynski, T. .
JOURNAL OF BONE AND JOINT SURGERY-BRITISH VOLUME, 2007, 89B (03) :417-420
[4]   Nrf2 is essential for protection against acute pulmonary injury in mice [J].
Chan, KM ;
Kan, YW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (22) :12731-12736
[5]   Autologous growth factors versus autogenous graft for anterior cervical interbody fusion: an in vivo caprine model Laboratory investigation [J].
Cunningham, Bryan W. ;
Sefter, John C. ;
Hu, Nianbin ;
McAfee, Paul C. .
JOURNAL OF NEUROSURGERY-SPINE, 2010, 13 (02) :216-223
[6]  
de Vos RJ, 2010, BR J SPORTS MED
[7]   Tenomodulin is necessary for tenocyte proliferation and tendon maturation [J].
Docheva, D ;
Hunziker, EB ;
Fässler, R ;
Brandau, O .
MOLECULAR AND CELLULAR BIOLOGY, 2005, 25 (02) :699-705
[8]  
Froum SJ, 2002, INT J PERIODONT REST, V22, P45
[9]   Effects of fibrin sealant protein concentrate with and without platelet-released growth factors on bony healing of cortical mandibular defects - An experimental study in minipigs [J].
Fuerst, G ;
Gruber, R ;
Tangl, S ;
Sanroman, F ;
Watzek, G .
CLINICAL ORAL IMPLANTS RESEARCH, 2004, 15 (03) :301-307
[10]  
Goel DP, 2009, CAN J SURG, V52, P467