Platelet physiology. Platelets are not cells, but rather 1–4 μm anucleated cytoplasmic fragments of megakaryocytes. Platelets contain dense granules and alpha granules. The latter contain adhesion molecules, coagulation and fibrinolytic factors, growth factors, cytokines, antibacterial proteins, and other factors, totaling more than 1000. These factors are released with platelet activation as shown on the schematics. ∗AG – Alpha granules, DG – Dense granules, PDGF – Platelet-derived growth factor, IGF-1 – Insulin-like growth factor-1, TGF-b1 – Transforming growth factor beta-1, CTGF – Connective tissue growth factor, VEGF – Vascular endothelial growth factor, b-FGF – Basic fibroblastic growth factor, EGF – Epidermal growth factor
Platelet-rich plasma proteins
Biologically active proteins released from platelet-rich plasma and their effects on tissue repair |
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Platelet-derived growth factor (PDGF) – fibroblast production, chemotaxis, collagen production |
Insulin-like growth factor-1 (IGF-1) – cell growth, differentiation |
Transforming growth factor beta-1 (TGF-b1) angiogenesis, extracellular matrix formation, cell viability |
Connective tissue growth factor (CTGF) – connective tissue growth |
Vascular endothelial growth factor (VEGF) – new blood vessel growth and anti-apoptosis of blood vessel cells |
Fibroblastic growth factor (b-FGF) – tissue repair, collagen production, myoblast proliferation |
Epidermal growth factor (EGF) – cell recruitment, proliferation, differentiation, promotion of epithelial cells |
![../images/457420_1_En_25_Chapter/457420_1_En_25_Fig2_HTML.png](https://i0.wp.com/aneskey.com/wp-content/uploads/2020/10/457420_1_En_25_Fig2_HTML.png?w=960)
Typical pattern of healing. An initial reaction to injury starts immediately with hemostasis. The inflammatory phase followed by proliferation and then remodeling. The healing of tissue may last more than a year
![../images/457420_1_En_25_Chapter/457420_1_En_25_Fig3_HTML.png](https://i0.wp.com/aneskey.com/wp-content/uploads/2020/10/457420_1_En_25_Fig3_HTML.png?w=960)
Why use platelet-rich plasma (PRP)? The normal or physiologic platelet concentration in blood is 150–450,00 per μL. It is characteristically three to eight times greater in the PRP. Subsequently, the concentration of growth factors and other signaling molecules is significantly higher, which may potentially explain some of the mechanisms of accelerated tissue regeneration with platelet-rich plasma application. PRP seems to produce simultaneous anti-inflammatory and pro-inflammatory effects, which diverge it from corticosteroids, widely used to hold up inflammatory cascade, and from prolotherapy, which typically aggravates inflammatory reaction after its injection
The mechanisms of effects of PRP on repair are complex but appear to resemble a typical pattern of healing, facilitated with PRP (Figs. 25.2 and 25.3). There are a number of factors, producing impact on its effect, including volume of blood used for PRP preparation, PRP concentration, use of anticoagulant during PRP preparation, platelet count, white blood cell (WBC) count, type of injury or disease, PRP equipment used, number of PRP injections, interval between PRP injections, and many others (Table 25.2). The recent studies suggest that the release of PRP growth factors may be dependent on such remote factors and the microbiota and immune status of the host.
Factors influencing platelet-rich plasma effect
Factors affecting PRP injection outcomes |
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Volume of blood used for PRP preparation |
PRP concentration |
Use of anticoagulant |
Pre-procedure platelet count |
WBC count |
Type of injury or disease treated with PRP |
Equipment used in PRP preparation |
Number of PRP injections |
Interval between PRP injections |
Host microbiota |
Host immune status |
Others |
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