Author:
Jara Carlos Poblete,Wang Ou,do Prado Thais Paulino,Ismail Ayman,Fabian Frank Marco,Li Han,Velloso Licio A.,Carlson Mark A.,Burgess William,Lei Yuguo,Velander William H.,Araújo Eliana P.
Abstract
AbstractPlasma fibrinogen (F1) and fibronectin (pFN) polymerize to form a fibrin clot that is both a hemostatic and provisional matrix for wound healing. About 90% of plasma F1 has a homodimeric pair of γ chains (γγF1) and 10% has a heterodimeric pair of γ and more acidic γ’ chains (γγ’F1). We have synthesized a novel fibrin matrix exclusively from a 1:1 (molar ratio) complex of γγ’F1 and pFN in the presence of highly active thrombin and recombinant Factor XIII (rFXIIIa). In this matrix, the fibrin nanofibers were wrapped with periodic 200-300 nm wide pFN nanobands (termed γγ’F1:pFN fibrin). In contrast, fibrin made from 1:1 mixture of γγF1 and pFN formed a sporadic distribution of “pFN droplets” (termed γγF1 +pFN fibrin). The γγ’F1:pFN fibrin enhanced the adhesion of primary human umbilical vein endothelium cells (HUVECs) relative to the γγF1+FN fibrin. Three dimensional (3D) culturing showed that the γγ’F1:pFN complex fibrin matrix enhanced the proliferation of both HUVECs and primary human fibroblasts. HUVECs in the 3D γγ’F1:pFN fibrin exhibited a starkly enhanced vascular morphogenesis while an apoptotic growth profile was observed in the γγF1 +pFN fibrin. Relative to γγF1 +pFN fibrin, mouse dermal wounds that were sealed by γγ’F1:pFN fibrin exhibited accelerated and enhanced healing. This study suggests that a 3D pFN nano-array presented on a fibrin matrix can promote wound healing.
Publisher
Cold Spring Harbor Laboratory
Cited by
1 articles.
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