TY - JOUR
T1 - Cellulose Mesh with Charged Nanocellulose Coatings as a Promising Carrier of Skin and Stem Cells for Regenerative Applications
AU - Pajorova, Julia
AU - Skogberg, Anne
AU - Hadraba, Daniel
AU - Broz, Antonin
AU - Travnickova, Martina
AU - Zikmundova, Marketa
AU - Honkanen, Mari
AU - Hannula, Markus
AU - Lahtinen, Panu
AU - Tomkova, Maria
AU - Bacakova, Lucie
AU - Kallio, Pasi
N1 - Funding Information:
We acknowledge the Light Microscopy Core Facility, IMG ASCR, Prague, Czech Republic, supported by MEYS CR (LM2015062, CZ.02.1.01/0.0/0.0/16_013/0001775), OPPK (CZ.2.16/3.1.00/21547), and MEYS CR (LO1419), for its support with confocal imaging and image analysis presented here. We further acknowledge the IPHYS imaging facility supported by MEYS CR (LM2018129) and CF Nanobiotechnology, Jan Pribyl, supported by MEYS CR (LM2018127). Dr. M. Tomkova acknowledges the International Visegrad Fund (No. 51910646). Ing. Tomas Sopuch, from Holzbecher, spol. s.r.o., is acknowledged for providing the cellulose mesh. Dr. Ivan Kostic and Dr. Milan Beno, from the Slovak Academy of Sciences, are acknowledged for their help with sample preparation and with preliminary imaging on the scanning electron microscope. SEM studies were carried out at Tampere University using facilities provided by the Tampere Microscopy Center. James Morrison, Academic Editor (JamesEdits Academic Editing, Nelson, Marlborough & Tasman, New Zealand), and Robin Healey (Czech Technical University in Prague, Czech Republic) are gratefully acknowledged for their language revision of the manuscript. We also acknowledge Mari Leino (Senior Research Technician, VTT) for TEMPO oxidation of CNFs and Pia Willberg-Keyriläinen (Senior Scientist, VTT) for cationization of CNFs.
Funding Information:
This study was supported by the Grant Agency of Czech Republic (Grant no. 20-01641S), by the Grant Agency of Charles University in Prague (Grant no. 756218), by the Academy of Finland through the WoodBone Project (Grant no. 326399), by the Centre of Excellence in Body-on-Chip Research (Grant no. 336785), and by the Ministry of Education, Youth and Sports of the Czech Republic (MEYS CR) within LQ1604 National Sustainability Program II (BIOCEV-FAR Project). Julia Pajorova received funding (Development of HR capabilities, internationalization, popularization and IP utilization, No. CZ.02.2.69/0.0/0.0/16_028/0006226) for traveling to Finland.
Publisher Copyright:
© 2020 American Chemical Society.
Copyright:
Copyright 2021 Elsevier B.V., All rights reserved.
PY - 2020/12/14
Y1 - 2020/12/14
N2 - Engineering artificial skin constructs is an ongoing challenge. An ideal material for hosting skin cells is still to be discovered. A promising candidate is low-cost cellulose, which is commonly fabricated in the form of a mesh and is applied as a wound dressing. Unfortunately, the structure and the topography of current cellulose meshes are not optimal for cell growth. To enhance the surface structure and the physicochemical properties of a commercially available mesh, we coated the mesh with wood-derived cellulose nanofibrils (CNFs). Three different types of mesh coatings are proposed in this study as a skin cell carrier: positively charged cationic cellulose nanofibrils (cCNFs), negatively charged anionic cellulose nanofibrils (aCNFs), and a combination of these two materials (c+aCNFs). These cell carriers were seeded with normal human dermal fibroblasts (NHDFs) or with human adipose-derived stem cells (ADSCs) to investigate cell adhesion, spreading, morphology, and proliferation. The negatively charged aCNF coating significantly improved the proliferation of both cell types. The positively charged cCNF coating significantly enhanced the adhesion of ADSCs only. The number of NHDFs was similar on the cCNF coatings and on the noncoated pristine cellulose mesh. However, the three-dimensional (3D) structure of the cCNF coating promoted cell survival. The c+aCNF construct proved to combine benefits from both types of CNFs, which means that the c+aCNF cell carrier is a promising candidate for further application in skin tissue engineering.
AB - Engineering artificial skin constructs is an ongoing challenge. An ideal material for hosting skin cells is still to be discovered. A promising candidate is low-cost cellulose, which is commonly fabricated in the form of a mesh and is applied as a wound dressing. Unfortunately, the structure and the topography of current cellulose meshes are not optimal for cell growth. To enhance the surface structure and the physicochemical properties of a commercially available mesh, we coated the mesh with wood-derived cellulose nanofibrils (CNFs). Three different types of mesh coatings are proposed in this study as a skin cell carrier: positively charged cationic cellulose nanofibrils (cCNFs), negatively charged anionic cellulose nanofibrils (aCNFs), and a combination of these two materials (c+aCNFs). These cell carriers were seeded with normal human dermal fibroblasts (NHDFs) or with human adipose-derived stem cells (ADSCs) to investigate cell adhesion, spreading, morphology, and proliferation. The negatively charged aCNF coating significantly improved the proliferation of both cell types. The positively charged cCNF coating significantly enhanced the adhesion of ADSCs only. The number of NHDFs was similar on the cCNF coatings and on the noncoated pristine cellulose mesh. However, the three-dimensional (3D) structure of the cCNF coating promoted cell survival. The c+aCNF construct proved to combine benefits from both types of CNFs, which means that the c+aCNF cell carrier is a promising candidate for further application in skin tissue engineering.
UR - http://www.scopus.com/inward/record.url?scp=85096828872&partnerID=8YFLogxK
U2 - 10.1021/acs.biomac.0c01097
DO - 10.1021/acs.biomac.0c01097
M3 - Article
C2 - 33136375
AN - SCOPUS:85096828872
SN - 1525-7797
VL - 21
SP - 4857
EP - 4870
JO - Biomacromolecules
JF - Biomacromolecules
IS - 12
ER -