Layer-by-layer assembled nanocoatings of human platelet's lysate and marine-origin polysaccharides trigger pro-angiogenic behaviour

last updated: 2014-11-12
ProjectComplexiTE :: publications list
TitleLayer-by-layer assembled nanocoatings of human platelet's lysate and marine-origin polysaccharides trigger pro-angiogenic behaviour
Publication TypeConference Abstract -ISI Web of Science Indexed
Year of Publication2014
AuthorsOliveira S. M., Pirraco R. P., Marques A. P., Reis R. L., and Mano J. F.

Introduction: Several growth factors (GFs) participate in the regulation of cell proliferation, migration, differentiation and apoptosis. GFs such as VEGF-A and FGF-b are essential to trigger the angiogenic cascade that is crucial for the subsequent steps of new tissue formation.1 Human Platelet lysate (hPL) has been used as an autologous source of GFs.2 Herein, we investigated whether marine-origin polysaccharides are able to attract and stabilize pro-angiogenic GFs from PL and activate endothelial cells by providing pro-angiogenic cues.

Materials and methods: κ-, ι-, λ-carrageenan (Car), alginate, chitosan and heparin were purchased from Sigma-Aldrich. Human PL was obtained as described elsewhere3. The interaction of mentioned the polyelectrolytes (PEs) with PL was assessed by QCM-D (Q-sense). The thickness of the nanocoatings was measured by ellipsometry and VEGF-A and FGF-b binding quantified by ELISA (Peportech). Human umbilical vein endothelial cells (HUVECs) were cultured in M199 culture media supplemented with 20%FBS and ECGS. Cells were seeded on 48-well-plates previously modified with the nanocoatings prepared by Layer-by-Layer assembling, i.e. by the alternating deposition of each of the mentioned PE with diluted PL (1, 3 and 6 bilayers), in the absence of ECGS and with 10% serum. The effect of the VEGF-A and bFGF on HUVECs was assessed in cultures established with 150 or 200 nM of FGF/VEGF Receptor Tyrosine Kinase Inhibitor (Santa Cruz Biotechnology).

Results: The thickness of nanocoatings varied between 30 and 45 and the GFs binding was quantified. The more sulfated PE’s, heparin/PL and k-Car/PL, were able to induce the formation of tube-like structures after 20 hours of culture (Figure 1). An increase of tube-length was observed with increasing number of bilayers. When the binding of the angiogenic GFs to the VEGF/FGF receptors is inhibited, the formation of tube-like structures is reduced or does not occur, depending on the concentration of the inhibitor.

The cells were able to proliferate on the nanocoatings that have induced tube-like structures formation, especially on ι-carrageenan/PL. However with proliferation slowed down in absence of ECGS, tube-like structures can be observed after 4 days in culture.

Discussion and conclusions: Nanocoatings composed by sulfated marine-origin polysaccharides and hPL bio-activate endothelial cells inducing the formation of tube-like structures. The formation of the tube-like structures, which depended on the PE and number of bilayers, was achieved after 20 hours of incubation and was mediated by the VEGF/FGF. The combination of hPL with these PEs may be an efficient and simple method to introduce pro-angiogenic cues in any 2D/3D cell-material interface and improve tissue regeneration. Acknowledgments: FCT is gratefully acknowledged for fellowships of S.M.O. (SFRH/BD/70107/2010).

Disclosure: The authors have noting to disclose.
1. Varkey M, et al. Expert Opin Drug Deliv. 1,19-36, 2004.
2. Italiano JE, et al. Blood. 111:1227–1233, 2008.
3. Santo EV, et al. Journal of Controlled Release. 162, 19-27. 2012.

JournalJournal of Tissue Engineering and Regenerative Medicine
Conference NameTERMIS-EU 2014
Date Published2014-06-09
Conference LocationGenova, Italy
KeywordsAngiogenesis, endothelial cells, FGF, HUVECs, layer-by-layer, sulfated polysaccharides, tube-like structures, VEGF
Peer reviewedno

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