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The co-culture of keratinocytes and fibroblasts on a multi-layered polyester nanofibrous membrane enriched with platelet lysate
Blanquer, Andreu ; Filová, Elena ; Jenčová, V. ; Brož, Antonín ; Kuželová Košťáková, E. ; Lisnenko, M. ; Procházková, R. ; Bačáková, Lucie
The prevalence of chronic wounds is increasing due to the population ageing and specific illnesses like diabetes mellitus and vascular diseases. Nanofibrous membranes fabricated using synthetic polymers are promising materials to enhance skin wound healing. PCL and PVA membranes are being studied to be used as scaffolds for skin tissue engineering and hydrogels for controlled drug delivery, respectively. The present study considers the development of a multi-layered membrane made of PCL and PVA loaded with platelet lysate (PL). PCL nanofibers allowed cell adhesion and growth, whereas PVA acted as a hydrogel that releases the bioactive compounds of platelet lysate. The cytocompatibility of the membranes containing PL and without it was demonstrated on two cell types involved in wound healing, i.e. keratinocytes and fibroblasts. Both cell types were able to adhere and proliferate on the membranes. In addition, the membrane containing PL enhanced the proliferation of fibroblasts. A co-culture study was also performed by seeding each cell type on one side of the membrane. The cells were co-cultured for 7 days and the results showed that PL increased the proliferation of cells achieving a monolayer of keratinocytes or fibroblasts on each side of the membrane. Thus, the beneficial effect of PCL-PVA+PL membranes on monocultures and co-cultures of skin cells was demonstrated, and these membranes can be considered potential scaffolds for treatment of chronic wounds.
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Differentiation of mesenchymal stem cells on fibrin assemblies supported by immobilized growth factors FGF2 and VEGF
Musílková, Jana ; Filová, Elena ; Kaplan, Ondřej ; Bačáková, Lucie
Bioartificial heart valves and vascular grafts prepared from decellularized tissues could be recellularized with bone marrow-derived mesenchymal stem cells (MSCs) that are able to differentiate into both smooth muscle cells and endothelial cells. MSCs differentiation is facilitated by sustained release of growth factors. In our study assemblies based on fibrin, fibrin with heparin, fibrin with adsorbed or covalently-immobilized vascular endothelial growth factor A165 (VEGF) or basic fibroblast growth factor (FGF-2) via binding to heparin attached to fibrin have been prepared and were evaluated for their stimulation of MSCs differentiation. We estimated the mRNA expression of endothelial marker CD31 (PECAM1), smooth muscle marker α-actin (ACTA2), osteoblast markers osteocalcin (BGLAP) and alkaline phosphatase (ALP). The gene expression was estimated using RT-PCR on days 1, 7 and 21 after seeding. The cell morphology and viability was evaluated by LIVE/DEAD staining. VEGF, both adsorbed and covalently bound, increased significantly the expression of smooth muscle marker α-actin. The mRNA expression of ACTA2 on day 7 and 21 raised more than 200 times in comparison to control samples (undifferentiated cells before seeding). The ACTA2 gene expression significantly exceeded the expression of all other evaluated genes at all time intervals. Moreover, on day 21, the late smooth muscle marker desmin (DES) was steeply rising in cells cultivated on assemblies containing heparin and covalently bound VEGF. The expression of osteocalcin was minimal. We conclude that fibrin assembly containing covalently bound VEGF is the most convenient for MSCs differentiation towards smooth muscle cells.
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Differentiation of keratinocytes: molecular markers and potential of influencing them in vitro
Ondrúšková, Denisa ; Filová, Elena (advisor) ; Porubská, Bianka (referee)
Keratinocytes are the most abundant skin cells found in epidermis. They are divided into proliferative basal stem cells, which are in close contact with basement membrane and suprabasal differentiating cells. Basal keratinocytes express K5 and K14 keratins and give rise to differentiating layers via delamination or asymmetric division. The firstly formed layer is stratum spinosum that expresses keratins K1 and K10 and involucrin, and, subsequently, it passes into the stratum granulosum, in which cells express loricrin and profilagrin. The last layer of epidermis is the stratum corneum formed by corneocytes that finally desquamate. Keratinocytes participate in the process of skin regeneration and can be isolated and cultivated. Their cultivation can be affected by various factors, such as selection of suitable materiál (nanofibers/gels) and suitable culture media, which can be enriched with growth factors, platelet lysat, vitamins and other substances. When culturing them, it also depends on whether the cells are entirely immersed in medium or growing on liquid/air interface. To approximate in vivo conditions and to study interaction between cell populations, keratinocytes are often cultured in co-cultures with different cells such as fibroblasts, endothelial cells, monocytes and others....
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Vascular and osseous cells in polymer structures for tissue engineering
Filová, Elena ; Bačáková, Lucie (advisor) ; Maxová, Hana (referee) ; Motlík, Jan (referee) ; Kromka, Alexander (referee)
Artificial vascular and bone prostheses are engineered as bioinert, not allowing cell attachment and growth. Our aim was to prepare materials based on natural and synthetic polymers that could modify the surface or create the bulk material of prostheses, and test their bioactivity in vitro. We prepared fibrin assemblies of various thicknesses and evaluated the adhesion, growth and differentiation of endothelial cells (EC) on these layers. We observed increased cell spreading on twodimensional fibrin assemblies and improved cell growth and maturation on thick fibrin gels. Fibrin coated with collagen I, or fibronectin, increased the adhesion area and the proliferation activity of vascular smooth muscle cells (VSMC). Synthetic polymers were based on an inert block copolymer of poly(DL-lactide) and polyethylene oxide (PDLLA-b-PEO) in which 5% or 20% of the PEO chains were grafted with Gly-Arg-Gly-Asp-Ser-Gly oligopeptide, a ligand for cell adhesion receptors. Grafting oligopeptide peptide to the cell non-adhesive copolymer restored adhesion and growth of VSMC, even in a serum-free medium. Synthetic polymers could therefore serve as artificial extracellular matrix analogues for vascular tissue repair and regeneration. Our study with human osteoblast-like MG 63 cells cultured in poly(lactic-co-glycolic acid)...
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Growth of human osteoblasts SaOS2 on titanium modified with nanotubes.
Krýslová, Markéta ; Filová, Elena (advisor) ; Melkes, Barbora (referee)
This work summarizes information about the interactions between osteoblasts and nanostructured materials, which are of growing importance and are highly promising in regard to their application in medicine and in tissue engineering. The number of people with artificial replacements of tissues, such as bones, joints, teeth, cartilage, and tendons increases every year. Titanium and his alloys are extensively used for artificial tissue replacements. Titanium is favourable for its mechanical properties that allow the implant to remain in the place of implantation more than thirty years. For better osseointegration the surface of titanium can be modified with hydroxyapatite, coating with diamond-like carbon or plasma spray coating. Another option is to prepare a layer of nanotubes, which forms nanoroughness on material surface. The nanoroughness in turn improves physical and chemical properties of the material surface. Nanostructured materials mimic the natural bone tissue, support adsorption of specific proteins, improve the biocompatibility of the implants and positively influence cell behaviour, e.g. stimulate the synthesis and suitable conformation of specific molecules for cell adhesion and differentiation.
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Biomimetic modifications of titanium in bone tissue engineering.
Krýslová, Markéta ; Filová, Elena (advisor) ; Rampichová, Michala (referee)
When the big joints like a knee or hip joint are damaged, the solution of this problem is an artificial substitute. The replacement of damaged joints with endoprotesis helps to reduce the pain and to move normally. In the design of the implant is necessary to fulfil all requirements on the properties of the material. The surface of implant is important, because it is directly connected to bone tissue. After implantation, the negative effect include infection, inflammation or release of the implant due to limited osseointegration, may appear. The osseointegration can be improved by modifying the material surface. This thesis is focused on development and evaluation of advanced materials imitating the bone structure, especially nanoroughness and the presence of biomimetic component, such as hydroxyapatite. In this study is evaluated adhesion, proliferation, viability, differentiation, and synthesis of specific proteins of human osteoblasts like Saos-2 on titanium modified with nanotubes and plasma sprayed hydroxyapatite compared with smooth surfaces. Key words: titanium, nanotubes, osteoblasts, hydroxyapatite, nanoroughness
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Natural biomaterials and mesenchymal stem cells in regeneration of spinal cord injury
Kekulová, Kristýna ; Kubinová, Šárka (advisor) ; Krulová, Magdaléna (referee) ; Filová, Elena (referee)
Spinal cord injury is a serious trauma and despite intensive research there is still no effective treatment for patients. The aim of this thesis is to study new possibilities of spinal cord injury therapy in animal models. We have focused on the use of natural materials, stem cells, gene therapy and the possibility of combining these approaches. The effect of extracellular matrix (ECM) based materials prepared by decellularization of porcine spinal cord and porcine urinary bladder on tissue regeneration after acute hemisection of the spinal cord was investigated. Another tested material was a hydrogel based on hyaluronic acid modified with RGD adhesion peptide, which was applied acutely and subacutely into the hemisection lesion. We have shown that both types of biomaterials have positive effect on regeneration of the spinal cord tissue by bridging the lesion and promotion of axonal ingrowth. In addition, ECM hydrogels promote the growth of blood vessels into the lesion site. The combination of hydrogels with mesenchymal stem cells derived from human umbilical cord (hWJ-MSCs) had synergistic effect, but since only a limited number of cells could be incorporated into hydrogels, this effect was not associated with improvement in motor skills. The limitation of ECM hydrogels is their rapid...
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Evaluation of influence of mechanical loading on differentiation of stem cells into smooth muscle cells
Pražák, Šimon ; Filová, Elena (advisor) ; Maxová, Hana (referee)
Cultivation of cells in bioreactors with mechanical load simulates the physiological conditions to which cells in the body are exposed. This technology has been used to induce the differentiation of stem cells from adipose tissue towards the phenotype of vascular smooth muscle cells, which can further serve to form vascular replacements. At present, there is no established strategy for cultivating stem cells while being exposed to mechanical stress. The main aim of this work was therefore to optimize the cultivation strategy and determine the ideal load parameters. Differentiation was analyzed by immunofluorescence of specific smooth muscle cell markers, α-actin and h1-calponin, which were quantified by Western blot. Extracellular matrix production was also detected by immunofluorescence staining. The outcome of this work is the establishment of ideal conditions of cell culture in a bioreactor with mechanical load, during which they differentiate into smooth muscle cells. Three types of scaffolds were used for cultivation; plasma treated glass, fibrin-coated glass and decelularized pericardium. Preliminary results show that smooth muscle differentiation was succesfully induced in human and porcine adipose tissue stem cells. Cells were analyzed after 3 and 7 days of culture. Developing a stem cell...
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Adhesion and growth of adipose tissue-derived stem cells on fibrin assemblies with attached growth factors for tissue engineering of heart valves
Filová, Elena ; Trávníčková, Martina ; Knitlová, Jarmila ; Matějka, Roman ; Kučerová, Johanka ; Riedelová, Zuzana ; Brynda, Eduard ; Bačáková, Lucie
Currently used xenogeneic biological heart valve prostheses are decellularized and crosslinked with glutaraldehyde. These grafts usually undergo degeneration and calcification. Pericardium-based heart valve prostheses, re-seeded with autologous cells, i.e. Adipose tissue-derived cells (ASCs) and endothelial cells, could have longer durability and biocompatibility. In order to improve the adhesion of cells and their ingrowth into decellularized pericardium, various fibrin (Fb) layers were developed, i.e. Fb, Fb with covalently bound heparin (H), Fb with either vascular endothelial growth factor (VEGF) or fibroblast growth factor 2 (FGF) in various concentrations (1 ng/ml, 10 ng/ml, 100 ng/ml) or with both VEGF and FGF (100 ng/ml). Growth factors were attached onto Fb via heparin or were adsorbed. ASCs were seeded on theses layers in a DMEM medium supplemented with 2 % of fetal bovine serum, TGFβ1 and BMP-4 (both 2.5 ng/ml), and with ascorbic acid. Cell adhesion and growth/viability was assessed by counted cell number/MTS evaluation. ASCs were stained for differentiation markers of smooth muscle cells, such as alpha-actin, calponin, and myosin heavy chain. On day 7, ASCs on Fb-H-VEGF layers produced both calponin and alpha-actin. An increased FGF concentration caused reduced calponin staining of ASCs. Lack of heparin in fibrin assemblies with growth factors inhibited the production of both alpha-actin and calponin in ASCs. The highest ASCs density/viability was found on Fb-H-VEGF-FGF layer. The proper formulation of fibrin coatings could be favorable for ASCs growth and differentiation and could subsequently support endothelialization of cardiovascular prostheses with endothelial cells.
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