Effects of calcium and thrombin on growth factor release from platelet concentrates: Kinetics and regulation of endothelial cell proliferation

被引:107
作者
Martineau, I
Lacoste, E
Gagnon, G [1 ]
机构
[1] Univ Laval, Fac Med Dent, Ste Foy, PQ G1K 7P4, Canada
[2] Univ Laval, Grp Rech Ecol Buccale, Ste Foy, PQ G1K 7P4, Canada
关键词
platelet activation; thrombin; growth factors; endothelial cell; wound healing;
D O I
10.1016/j.biomaterials.2003.11.013
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Platelet concentrates (PCs) constitute new biological mediators used in osseous reconstructive surgery. In this study, we assessed (i) the effects of various concentrations of calcium and thrombin on the kinetics of platelet-derived growth factor (PDGF-BB), transforming growth factor-beta1 (TGF-beta1), basic fibroblast growth factor (bFGF), and vascular endothelial growth factor (VEGF) release by PCs and (ii) the contribution of PC supernatants to endothelial cell proliferation. Our results indicate that high concentrations of calcium (Ca) and thrombin (Thr) trigger an immediate and significant increase in bFGF, TGF-beta1 and PDGF-BB concentrations. Thereafter, PDGF-BB, VEGF and TGF-beta1 levels remained generally constant over a 6-day period while a decrease in bFGF concentrations was noted after 24 h. Lower Ca and Thr concentrations tended to reduce and delay growth factors release from PCs. Endothelial cell proliferation was greatly enhanced with PC supernatants (mean: 20-fold increase). This was especially evident when endothelial cells were treated with supernatants harvested early after PC treatment with high concentrations of Ca and Thr or later after PC treatment with low Ca and Thr concentrations. Additional research aiming to measure the effects of Ca and Thr on bone formation in vivo is needed. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4489 / 4502
页数:14
相关论文
共 59 条
[1]   Investigation of platelet-rich plasma in rabbit cranial defects: A pilot study [J].
Aghaloo, TL ;
Moy, PK ;
Freymiller, EG .
JOURNAL OF ORAL AND MAXILLOFACIAL SURGERY, 2002, 60 (10) :1176-1181
[2]   TIME SEQUENCE OF TISSUE REGENERATION IN HUMAN EXTRACTION WOUNDS [J].
AMLER, MH .
ORAL SURGERY ORAL MEDICINE ORAL PATHOLOGY ORAL RADIOLOGY AND ENDODONTICS, 1969, 27 (03) :309-&
[3]  
Anitua E, 1999, INT J ORAL MAX IMPL, V14, P529
[4]   Release of the angiogenic cytokine vascular endothelial growth factor (VEGF) from platelets: significance for VEGF measurements and cancer biology [J].
Banks, RE ;
Forbes, MA ;
Kinsey, SE ;
Stanley, A ;
Ingham, E ;
Walters, C ;
Selby, PJ .
BRITISH JOURNAL OF CANCER, 1998, 77 (06) :956-964
[5]   GROWTH-FACTORS AND WOUND-HEALING - BIOCHEMICAL-PROPERTIES OF GROWTH-FACTORS AND THEIR RECEPTORS [J].
BENNETT, NT ;
SCHULTZ, GS .
AMERICAN JOURNAL OF SURGERY, 1993, 165 (06) :728-737
[6]   GROWTH-FACTORS AND WOUND-HEALING .2. ROLE IN NORMAL AND CHRONIC WOUND-HEALING [J].
BENNETT, NT ;
SCHULTZ, GS .
AMERICAN JOURNAL OF SURGERY, 1993, 166 (01) :74-81
[7]   Bimodal concentration-dependent effect of thrombin on endothelial cell proliferation and growth factor release in culture [J].
Borrelli, V ;
Sterpetti, AV ;
Coluccia, P ;
Randone, B ;
Cavallaro, A ;
D'Angelo, LS ;
Cucina, A .
JOURNAL OF SURGICAL RESEARCH, 2001, 100 (02) :154-160
[8]   Factors in the fracture microenvironment induce primary osteoblast angiogenic cytokine production [J].
Bouletreau, PJ ;
Warren, SM ;
Spector, JA ;
Steinbrech, DS ;
Mehrara, BJ ;
Longaker, MT .
PLASTIC AND RECONSTRUCTIVE SURGERY, 2002, 110 (01) :139-148
[9]   Impaired myocardial angiogenesis and ischemic cardiomyopathy in mice lacking the vascular endothelial growth factor isoforms VEGF164 and VEGF188 [J].
Carmeliet, P ;
Ng, YS ;
Nuyens, D ;
Theilmeier, G ;
Brusselmans, K ;
Cornelissen, I ;
Ehler, E ;
Kakkar, VV ;
Stalmans, I ;
Mattot, V ;
Perriard, JC ;
Dewerchin, M ;
Flameng, W ;
Nagy, A ;
Lupu, F ;
Moons, L ;
Collen, D ;
D'Amore, PA ;
Shima, DT .
NATURE MEDICINE, 1999, 5 (05) :495-502
[10]   Molecular mechanisms of blood vessel growth [J].
Conway, EM ;
Collen, D ;
Carmeliet, P .
CARDIOVASCULAR RESEARCH, 2001, 49 (03) :507-521