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. Author manuscript; available in PMC: 2011 Aug 1.
Published in final edited form as: J Orthop Res. 2010 Aug;28(8):1107–1112. doi: 10.1002/jor.21111

Table 1.

Studied Receptors and Their Binding Growth Factors

Receptorsa Description Growth Factor Concentration in PRP (pg/ml)b Function in Fibroblasts
TGF-β R1 Similar binding affinities, high affinity for TGF-β1, low affinity for TGF-β2, equivalent to TGF-β receptor 2 Various subforms; TGF-β1 enhances fibroblast proliferation and differentiation and acts as stimulus for type I collagen and firbonection production; TGF-β2 more important for embryonic development
TGF-β-R2a TGF-β 9184.0
TGF-β-R3 High affinity for TGF-β1 and TGF-β2
PDGF-R Dimeric receptor in three different conformations (αα, αβ, ββ) PDGF 3192.9 Enhances fibroblast proliferation and collagen synthesis
FGFR Including all splicing variants 48 isoforms FGF Traces Potent stimulus of fibroblast proliferation
VEGF-R1 Binds VEGF-A, thought to modulate VEGF-R2 signaling VEGF 61.6 Expressed in fibroblasts, but role in fibroblast activity still unclear
VEGF-R2 Binds VEGF-A, VEGF-E, VEGF-C; main mediator of VEGF function
VEGF-R3a Binds VEGF-C, VEGF-D; lymphangiogenetic

This table provides a brief summary on the function of the studied receptors and their growth factors. The more interested reader is asked to refer to reviews of the biology of cell signaling (e.g., Refs. 1821,3032,3639).

a

Not studied (see text).

b

100 × 109 platelets/L 18–21.