Abstract

The wound healing is a complex process wherein inflammation, proliferation and regeneration evolve according to a spatio‐temporal pattern from the activation of coagulation cascade to the formation of a plug clot including fibrin matrix, blood‐borne cells and cytokines/growth factors. Creating environments conducive to tissue repair, the haemoderivatives are commonly proposed for the treatment of hard‐to‐heal wounds. Here, we explored in vitro the intrinsic regenerative potentialities of a leucocyte‐ and platelet‐rich fibrin product, known as CPL‐MB, defining the stemness grade of cells sprouting from the haemoderivative. Using highly concentrated serum‐based medium to simulate wound conditions, we isolated fibroblast‐like cells (CPL‐CMCs) adhering to plastic and showing stable in vitro propagation, heterogeneous stem cell expression pattern, endothelial adhesive properties and immunomodulatory profile. Due to their blood derivation and expression of CXCR4, CPL‐CMCs have been suggested to be immature cells circulating in peripheral blood at quiescent state until activation by both coagulation event and inflammatory stimuli such as stromal‐derived factor 1/SDF1. Expressing integrins (CD49f, CD103), vascular adhesion molecules (CD106, CD166), endoglin (CD105) and remodelling matrix enzymes (MMP2, MMP9, MMP13), they showed a transendothelial migratory potential besides multipotency. Taken together, our data suggested that a standardized, reliable and economically feasible blood product such as CPL‐MB functions as an artificial stem cell niche that, under permissive conditions, originate ex vivo immature cells that could be useful for autologous stem cell‐based therapies.

Highlights

  • Over the last three decades, the enormous progress in cell processing technology has enhanced a general shift from heterologous to autologous stem cell-based therapies

  • Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine

  • A growing body of evidence demonstrates that the contribution of L-PRF to in vivo angiogenesis and vasculogenesis at injury site is mediated by intrinsically carried haematopoietic stem cells (HSCs) (CD34+) and endothelial progenitor cells (EPCs) (CD34+/VEGR-2+/CD133+) [10]

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Summary

Introduction

Over the last three decades, the enormous progress in cell processing technology has enhanced a general shift from heterologous to autologous stem cell-based therapies. In the prospect of having biomaterials and bioactive surgical additives with predictable outcome in regenerative medicine, several techniques have been developed to process peripheral blood and to obtain products useful for controlling inflammation and enforcing the physiological events of haemostasis and wound healing [1,2,3,4]. Depending on their contents of platelets, leucocytes and fibrin architecture, they are commonly classified into four families: (i) pure platelet-rich plasma (P-PRP, in liquid or gel form); (ii) leucocyte- and platelet-rich plasma As the discovery of multipotent stem cells in L-PRF products could have important implications for the future of regenerative medicine confirming (i) the active role of the haemoderivatives in the so-called in vivo guided regeneration and (ii) the development of a standardized method to extract autologous stem cells, in this study, a leucocyte–platelet-concentrated membrane, prepared according to the Caloprisco protocol [10] and called CLP-MB, has been cultured in vitro to characterize the stemness grade of sprouted cells under permissive conditions

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