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Wyszukujesz frazę "osteoblasts" wg kryterium: Temat


Tytuł:
The adhesion and growth of human osteoblast-like MG 63 cells in cultures on titanium modified with gold microparticles and polyethylene imine)
Autorzy:
Parizek, M.
Base, T.
Hruby, M.
Lisa, V.
Bacakova, L.
Powiązania:
https://bibliotekanauki.pl/articles/284730.pdf
Data publikacji:
2012
Wydawca:
Akademia Górniczo-Hutnicza im. Stanisława Staszica w Krakowie. Polskie Towarzystwo Biominerałów
Tematy:
osteoblasts
cells
titanium
Opis:
Metallic materials are indispensable for construction of surgical implants, particularly those designed for load-bearing application, such as the bone-anchoring parts of big joint replacements. For good osteointegration, long-term function, durability and also mechanical and chemical resistance of the implant, the physical and chemical properties of the material surface are of a great importance. These properties can be favorably influenced by coating the bone-anchoring parts of the implants with appropriate biocompatible and bioactive films. Therefore, in this study, we have investigated the adhesion and growth of human osteoblast-like MG 63 cells in cultures on titanium substrates coated with films made of gold microparticles and/or poly(ethylene imine) (PEI). Gold microparticles were chosen for good biocompatibility of gold and absence of its cytotoxicity, which has been proved by numerous studies performed in vitro and in vivo [1,2]. When deposited on the material surface, these microparticles provide this surface with microstructure, which has been reported to enhance the osteogenic differentiation of bone-derived cells. On the other hand, the material surface microroughness has dual effect on the cell adhesion, spreading and proliferation - some studies reported the enhancement, other the reduction of these events (for a review, see [3,4]). This suggests that not only the size of the microscale irregularities, but also their shape should be taken into account. Therefore, in our study, gold microparticles were used in the form of plates or polyhedral crystals [5]. These microparticles were deposited on square samples of Ti (1x1 cm, thickness 1 mm) and annealed with a hydrogen flame. As for PEI, this polymer has been used as precursor base layer for further functionalization of metallic substrates, particularly with polyelectrolyte multilayer films [6] or biomolecules such as gelatin, hyaluronan or chitosan [7,8]. Other reason for the PEI deposition was creation of an intermediate layer which would compensate the differences in mechanical properties (e.g., hardness, toughness, specific weight) between a metallic implant and bone tissue. PEI was deposited either on pure or on gold microparticle-coated Ti samples. The materials were sterilized with 70% ethanol (1 hour), inserted into 24-well polystyrene plates (well diameter 1.5 cm; TPP, Switzerland) and seeded with human osteoblast-like MG 63 cells (30 000 cells/well, i.e. 17 000 cells/cm2). Each well contained 1.5 ml of a medium DMEM with 10% of fetal bovine serum and 40 /jg/ml of gentamicin. On days 1, 3 and 7 after seeding, the cell number and morphology were evaluated. For evaluating the cell number, the cells were trypsinized and counted in Bürker hemocytometer. For evaluating the cell morphology, i.e. the cell shape and the size of cell spreading area, the cells were fixed with 70% ethanol (-20°C, 10 min) and stained with a combination of fluorescence dyes Texas Red C2-maleimide, which stains the cell membrane and cytoplasm, and Hoechst #33342, which stains the cell nuclei. The microphotographs of cells were taken using an Olympus IX 51 microscope equipped with a DP 70 digital camera, and the cell spreading area was measured on these pictures using a software Atlas (Tescan, Brno, Czech Rep.) One day after seeding, the highest number of initially adhered cells was found on the surface modified by gold polyhedral crystals. This trend was the same on days 3 and 7 after seeding (FIG.1,2). However, the cell number on Ti modified with gold plates was significantly lower than on Ti with polyhedral crystals. Nevertheless, the numbers of cells on Ti samples coated with gold microparticles without PEI were significantly higher than on PEI-coated samples. Also the cell spreading areas were significantly larger on the samples without PEI. The cells on the samples without PEI were mostly polygonal, while the cells on PEI-coated samples were of star-like appearance, i.e. with multiple long protrusions (FIG.2). This is in accordance with findings published by other authors, documenting cytotoxic effects of PEI, particularly that of a high molecular weight [6], which was also used in our study (m.w. 750 kDa). Nevertheless, this cytotoxicity was considerably reduced by further functionalization of PEI with biomolecules, such as gelatin, hyaluronan or chitosan [7,8]. Thus, it can be concluded that the modification of titanium plates by gold microparticles supported the adhesion and growth of MG 63 cells. In this context, the polyhedral crystals were more advantageous than plates. The effects of PEI coatings on cell behavior need further investigation.
Źródło:
Engineering of Biomaterials; 2012, 15, no. 116-117 spec. iss.; 149-150
1429-7248
Pojawia się w:
Engineering of Biomaterials
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Adhesion and growth of human osteoblast-like MG 63 cells on titanium and stainless steel samples developed for constructing bone implants
Autorzy:
Stranavova, L.
Bacakova, M.
Bacakova, L.
Fencl, J.
Powiązania:
https://bibliotekanauki.pl/articles/284428.pdf
Data publikacji:
2011
Wydawca:
Akademia Górniczo-Hutnicza im. Stanisława Staszica w Krakowie. Polskie Towarzystwo Biominerałów
Tematy:
osteoblasts
biomaterials
implants
Opis:
Titanium and stainless steel are strong, corrosion - resistant and biocompatible metals. Thanks to their remarkable properties, they have been in use for a long time in clinical medicine, mainly for constructing and replacing large joints, in particular the bone-anchoring parts, e.g. cups and stems, and also for fabricating orthopaedic screws and splints. In the Czech Republic, these devices are produced by Beznoska Ltd., and are clinically applied in the Orthopaedic Clinic, Bulovka Faculty Hospital in Prague. This study has investigated the biocompatibility of samples made of pure titanium (according to quality standard ISO 5832-2 ) and corrosion-resistant steel (quality standards ISO 5832-1 and AISI 316L), obtained from Beznoska. In addition to Fe, the steel samples contained C (max. 0.025 wt. %), Si (0.6 wt. %), Mn (1.7 wt. %), P( max. 0.025 wt. %), S(max. 0.003 wt. %), Cr (17.5 wt. %), Ni (13.5 wt. %), Mo (2.8 wt. %), and Cu (max. 0.1 wt. %). The materials were used in the form of square samples (9x9 mm or 30x30 mm, thickness 1 mm ). Both Ti and steel samples were grinded with SiO2. The surface of the steel samples was then treated by polishing with Al2O3 paste (grain size up to 1 μm), while the surface of the Ti samples, i.e. a material not suitable for polishing, was finished by brushing using another type of Al2O3 paste with slightly larger grains. Thus, the surface of the steel samples was finally smoother and glossy, while the Ti surface was rougher and matted. For the in vitro biocompatibility tests, human osteoblast-like MG 63 cells (European Collection of Cell Cultures, Salisbury, UK) were used. The smaller samples (9 x 9 mm) were inserted into polystyrene 2 4-well cell culture plates (TPP, Trasadingen, Switzerland; well diameter 1.5 cm). Each well contained 25000 cells (approx. 14150 cells / cm 2 ) and 1.5 ml of Dulbecco’s Modified Eagle Minimum Essential Medium (DMEM; Sigma, USA, Cat. No. 10270-106) supplemented with 10 % foetal bovine serum (FBS; Gibco, Cat. No. 10270-106) and gentamicin (40 μg/ml, LEK, Slovenia). These samples were used for evaluating the size of the cell spreading area (day 1), and for evaluating cell shape and cell viability (days 1, 4 and 7 after seeding). The size o f the cell spreading area was measured using Atlas Software (Tescan Ltd., Brno, Czech Republic). The viability of the cells was determined by the LIVE/DEAD viability cytotoxicity kit for mammalian cells (Invitrogen, Molecular Probes, USA). The larger samples (30x30 mm) were inserted into GAMA polystyrene dishes (diameter 5 cm; GAMA Group Joint- Stock Company, Ceske Budejovice, Czech Republic) and seeded with 300000 cells/dish (approx. 15300 cells/cm 2) suspended in 9 ml of the above mentioned culture medium. These samples were used for evaluating the cell number on days 1, 4 and 7 after seeding, using a Beckman Vi- CELL XR Cell Analyser automatic cell counter. The results indicated that the number of initially adhering cells on day 1 after seeding was significantly lower on the titanium (5320±390 cells/cm2) and on the stainless steel ( 4110±370 cells/cm 2) than on the control polystyrene culture dishes (7740±350 cells/cm2). However, on day 4 after seeding, the cell population density on both metallic materials studied here became significantly higher than on the control polystyrene dishes (75200±2 890 cells/cm2 on Ti and 90870 ±2350 cells/cm2 on steel vs. 56440±1180 cells/cm2 on polystrene). This suggests faster cell proliferation on both metallic materials than on polystyrene. At the same time, the cell number on the stainless steel samples was significantly higher than on the Ti samples. On day 7, the differences in number of adhered cells on both studied metals and on the control polystyrene substrate was on an average similar (from 328780±680 cells/cm2 to 362200 ±760 cells/cm2). The cell viability on all tested materials was almost 100 % in all culture intervals. The morphology of the cells on the studied materials was similar to the morphology of the adhered cells on the control polystyrene dishes, i.e. the cells were mostly flat and polygonal, and the size of their cell spreading areas w as similar on all tested materials. The cells were distributed homogeneously on the entire material surface, and on day 4 they started to form confluent cell layers (FIG. (1). It can be concluded that the tests of biocompatibility confirmed that the titanium and the stainless steel promoted the adhesion and growth of bone - derived cells, and thus these materials are promising for construction of bone implants and for their good integration with the surrounding bone tissue. Further studies on osteogenic cell differentiation, potential immune activation and the response of the bone cells to growth factors, including bone morphogenetic protein, are in progress.
Źródło:
Engineering of Biomaterials; 2011, 14, no. 109-111 spec. iss.; 10-11
1429-7248
Pojawia się w:
Engineering of Biomaterials
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
CNTs alter the biocompatibility of PAN-derived CNFs
Autorzy:
Benko, A.
Kolecka, B.
Nocuń, M.
Menaszek, E.
Błażewicz, M.
Powiązania:
https://bibliotekanauki.pl/articles/284816.pdf
Data publikacji:
2017
Wydawca:
Akademia Górniczo-Hutnicza im. Stanisława Staszica w Krakowie. Polskie Towarzystwo Biominerałów
Tematy:
CNTs
biocompatibility
osteoblasts
Źródło:
Engineering of Biomaterials; 2017, 20, no. 143 spec. iss.; 71
1429-7248
Pojawia się w:
Engineering of Biomaterials
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Fullerene-titanium (C60/Ti) composites cause no DNA damage response in human osteoblast-like MG 63 cells
Autorzy:
Kopova, I.
Bacakova, L.
Vacik, J.
Lavrentiev, V.
Powiązania:
https://bibliotekanauki.pl/articles/284970.pdf
Data publikacji:
2010
Wydawca:
Akademia Górniczo-Hutnicza im. Stanisława Staszica w Krakowie. Polskie Towarzystwo Biominerałów
Tematy:
fullerenes
composites
human osteoblasts
Opis:
Fullerenes (C60) and fullerene-based composites are considered as promising substrates for biological cell colonization. It might be mainly due to their nanostructure, resembling the nanoarchitecture of the natural extracellular matrix. Thin films of binary C60/Ti composites with various concentrations of Ti ranging from 25% (i.e., 25 Ti atoms and 75 C60 molecules) to 70% were deposited on microscopic glass coverslips in micro-patterned form through a metallic mask, and were tested for their potential use in bone tissue engineering. It is known that fullerenes and their derivatives can cause cytotoxic injury, cell death or inhibition of cell growth. These effects are based mainly on the reactivity of fullerenes, which may weaken with time due to the oxidization and polymerization of fullerenes in an air atmosphere. We therefore tested the dependence between the age of C60/Ti composites (i.e., from one week to one year) and the level of DNA damage of human osteoblast-like MG 63 cells in cultures on these materials. The DNA damage was analyzed by immunofluorescence staining of markers of DNA damage response, such as phosphorylation of histone H2AX and focal recruitment of p53-binding protein. As positive control to markers of DNA damage response was used 7 days long treatment with 2,5 mM Thymidine. We also monitored the proliferation and morphological changes of the cells. After 7 days of cultivation, we observe no cytotoxic morphological changes, such as enlarged cells or cytosolic vacuole formation, which are signs of cell senescence, and no increased induction of cell death. In addition, there was no increased level of DNA damage response on the C60/Ti composites (FIG.1). We also found no significant differences in cell population densities and no increased level of DNA damage among various Ti concentrations (FIG.1). Moreover, there was no effect of the age of the C60/Ti composites on the cell population densities or on the DNA damage response (FIG.1). These results suggest that fullerenes in combination with Ti do not cause cytotoxic injury and this material could be used in bone tissue engineering.
Źródło:
Engineering of Biomaterials; 2010, 13, no. 99-101; 109-110
1429-7248
Pojawia się w:
Engineering of Biomaterials
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Adhesion, growth and differentiation of human osteoblast-like cells on thermally oxidized Ti and TiNb substrates
Autorzy:
Bacakova, L.
Vandrovcova, M.
Jirka, I.
Novotna, K.
Stary, V.
Powiązania:
https://bibliotekanauki.pl/articles/285115.pdf
Data publikacji:
2013
Wydawca:
Akademia Górniczo-Hutnicza im. Stanisława Staszica w Krakowie. Polskie Towarzystwo Biominerałów
Tematy:
osteoblasts
substrates
metallic materials
Opis:
Metallic materials are essential for construction of load-bearing bone implants, such as replacements of hip, knee and other joints. For these applications, modern materials used in advanced tissue engineering, e.g. resorbable porous or fibrous polymeric and ceramic scaffolds are mechanically insufficient, even if these materials enable the ingrowth of bone cells and bone tissue formation. Therefore, searching for new metallic materials and their surface modifications improving their biocompatibility and osseointegration is still desirable. As first metallic materials for bone implantation, AISI 316L stainless steel and Co-Cr alloys were used. In the 1950’s, the Ti-6Al-4V alloy was developed. These materials are still frequently used for construction of implants because of their relatively low price [1]. However, these materials are biomechanically incompatible with the bone tissue, because their Young’s modulus is markedly higher (110-220 GPa) than that of the bone (10-40 GPa). Implants with high stiffness take over a considerable part of load from the bone. This phenomenon, referred as “stress-shielding effect”, can then cause the bone resorption and loosening of the implant [1]. Also chemical compositions of the mentioned metallic materials limit their biocompatibility, because they contain harmful elements as V, Al, Co and Cr, which can act as cytotoxic, catabolic, immunogenic or even carcinogenic agents [2,3], and can also cause serious neurological problems [4]. Due to these adverse reactions, new types of Ti-alloys have been developed, namely low-rigidity β-type Ti alloys, containing non-toxic and non-allergenic elements (Nb, Ta, Zr etc.) and having good mechanical properties and workability [4,5]. The goal of this study was to evaluate the adhesion, growth and differentiation of osteoblast-like MG-63 and Saos-2 cells on titanium-niobium alloys after their surface modification by thermal oxidation at two different temperatures (165°C and 600°C). Pure titanium (treated at 165°C and 600°C) and polystyrene culture dishes (PS) were used as control materials. Possible immune activation of the cells was tested by the levels of TNF-alpha secreted to the cell culture media by murine macrophage-like RAW 264.7 cells cultured on the tested materials. On samples treated at 165°C, the number of initially adhered MG-63 and Saos-2 cells was on an average higher on TiNb than on Ti or PS. On day 3 after seeding, the trend of the cell numbers remained similar, with the highest cell density found on TiNb. Similar results were obtained on samples treated at 600°C, where the difference in cell number between TiNb and Ti samples became more apparent. This cell behavior could be attributed to a less negative zeta potential on TiNb samples. In samples treated at 165°C, the zeta potential of TiNb surfaces was on the average less negative than on Ti surfaces, but this difference was not significant. However, in samples treated at 600°C, this difference became much more pronounced, which was probably due to the formation of T-Nb2O5 phase on the surface of the TiNb samples. This phase was of a crystalline structure, while at 165°C, the structure of Nb2O5 was amorphous. In addition, both Ti and TiNb samples treated at 600°C contained rutile, while the samples treated at 165°C contained anatase in their surface layer. It has been shown that rutile films deposited on PEEK enhanced the adhesion and growth of osteoblasts more than anatase films [6]. This phenomenon was explained by an increase in the material surface wettability, and particularly to the presence of –OH- groups on the rutile films. The expression of collagen I and osteocalcin, i.e. an early and late marker of osteogenic cell differentiation, respectively, was higher on Ti than on TiNb samples, and this difference was more apparent in samples treated at 165°C. At the same time, no considerable immune activation of the cells on all tested samples was found. The production of TNF-α by RAW 264.7 cells was very low in comparison with cells grown in the presence of bacterial lipopolysaccharide, and also significantly lower than on untreated samples. These results indicate that TiNb substrates increased the proliferation of human bone cells, while pure Ti rather supported the cell differentiation. The effect on cell proliferation was more apparent in samples treated at the higher temperature (600°C), while the effect on cell differentiation was more pronounced at the lower temperature (165°C). None of the tested samples induce significant cell proinflammatory activation. Thus, all tested samples are suitable as carriers for bone cells; only an appropriate application (i.e., requiring either proliferation or quick differentiation of osteogenic cells) should be selected.
Źródło:
Engineering of Biomaterials; 2013, 16, no. 122-123 spec. iss.; 75-76
1429-7248
Pojawia się w:
Engineering of Biomaterials
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Chitosan/β-1,3-glucan/HA bone scaffold possesses osteopromotive properties in vitro
Autorzy:
Przekora, A.
Ginalska, G.
Powiązania:
https://bibliotekanauki.pl/articles/284166.pdf
Data publikacji:
2016
Wydawca:
Akademia Górniczo-Hutnicza im. Stanisława Staszica w Krakowie. Polskie Towarzystwo Biominerałów
Tematy:
osteoblasts
osteopromotive properties
biomaterials
Źródło:
Engineering of Biomaterials; 2016, 19, 138; 51
1429-7248
Pojawia się w:
Engineering of Biomaterials
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Tetraspanin CD151 mediates communication between PC3 prostate cancer cells and osteoblasts
Autorzy:
Grudowska, Alicja
Czaplińska, Dominika
Polom, Wojciech
Matuszewski, Marcin
Sądej, Rafał
Składanowski, Andrzej
Powiązania:
https://bibliotekanauki.pl/articles/1038698.pdf
Data publikacji:
2017
Wydawca:
Polskie Towarzystwo Biochemiczne
Tematy:
CD151
prostate cancer
osteoblasts
Opis:
Invasion and migration of cancer cells are crucial for the formation of secondary lesions. These require activation of signalling cascades modulated by the number of regulatory molecules. One such molecule is CD151, a member of evolutionary conserved tetraspanin family. CD151 is involved in cell adhesion, motility and cancer progression due to formation of complexes with laminin-binding integrins and regulation of growth factor receptors function (e.g. HGFR, TGFβR, EGFR). Recent studies point to correlation between CD151 expression and high tumour grade in prostate cancer (PCa). Herein, we investigated a possible role of CD151 in communication between PC3 cancer cells and either cancer-associated fibroblasts (CAFs) or osteoblasts, an interplay which is significant for metastasis. The analysis showed that although CAFs strongly enhanced both migration and invasion of PC3 prostate cancer cells, the effect was not dependent on CD151. On the other hand, CD151 was found to promote 3D migration as well as invasive growth in response to osteoblasts-secreted growth factors. Obtained data revealed that knockdown of CD151 abolished activation of pro-migratory/pro-survival kinases (i.e FAK, Src, HSP27) triggered by osteoblasts, along with expression of matrix metalloproteinase-13. This suggests that CD151 participates in communication between PC3 cells and bone microenvironment and the process can be considered as a significant step of PCa progression and metastasis.
Źródło:
Acta Biochimica Polonica; 2017, 64, 1; 135-141
0001-527X
Pojawia się w:
Acta Biochimica Polonica
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Growth and osteogenic differentiation of human osteoblast-like cells on nanofibrous scaffolds loaded with diamond nanoparticles: improvement or impairment?
Autorzy:
Musilkova, J.
Stankova, L.
Potocky, S.
Kromka, A.
Stranska, D.
Bacakova, L.
Powiązania:
https://bibliotekanauki.pl/articles/285888.pdf
Data publikacji:
2016
Wydawca:
Akademia Górniczo-Hutnicza im. Stanisława Staszica w Krakowie. Polskie Towarzystwo Biominerałów
Tematy:
nanofibrous scaffold
diamond nanoparticles
human osteoblasts
Źródło:
Engineering of Biomaterials; 2016, 19, 138; 32
1429-7248
Pojawia się w:
Engineering of Biomaterials
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Biocomatibility study of BOC polymer mesh enriched with HAp and TCP covered by PCL fibres
Autorzy:
Menaszek, E.
Ścisłowska-Czarnecka, A.
Draczyński, Z.
Bogun, M.
Stodolak-Zych, E.
Powiązania:
https://bibliotekanauki.pl/articles/286223.pdf
Data publikacji:
2012
Wydawca:
Akademia Górniczo-Hutnicza im. Stanisława Staszica w Krakowie. Polskie Towarzystwo Biominerałów
Tematy:
polymer mesh
HAp
TCP
osteoblasts NHOst
Opis:
The study was conducted in order to determine the biocomatibility of polimer mesh based on BOC and enriched with HAp or TCP coverd by PCL sub-micrometric fibres. Human osteoblast cell line NHOst was cultured in standard conditions on disk-shaped polymer samples. Interactions between materials and cells were examined through microscopic observation of cells' adhesion and morphology, and tests of viability/proliferation and cytotoxicity. The study proved the biocompatibility of all examined materials, though the surface of TCP enriched polymer didn't promote the adhesion of cells.
Źródło:
Engineering of Biomaterials; 2012, 15, no. 116-117 spec. iss.; 151-152
1429-7248
Pojawia się w:
Engineering of Biomaterials
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Effect of polylactide modification with β-TCP and lecithin on the properties of the material as a substrate for osteoblasts
Autorzy:
Olkowski, R.
Stefanek, A.
Kaszczewski, P.
Ciach, T.
Lewandowska-Szumieł, M.
Kalaszczyńska, I.
Powiązania:
https://bibliotekanauki.pl/articles/285423.pdf
Data publikacji:
2015
Wydawca:
Akademia Górniczo-Hutnicza im. Stanisława Staszica w Krakowie. Polskie Towarzystwo Biominerałów
Tematy:
polylactide
lecithin
osteoblasts
scaffold
bone tissue engineering
Opis:
Polylactide (PLLA) containing β-TCP is biodegradable composite and an attractive biomaterial for bone tissue engineering, however, hydrophobicity of PLLA based composites is major limitation for their use as scaffolds for cell culture. In our study lecithin was used to improve hydrophilicity and cytocompatibility of PLLA/ β-TCP composite. Thin films of PLLA, PLLA/ β-TCP and PLLA/β-TCP/lecithin were manufactured by solvent-casting technique. Comparative analysis of all types of films was performed. Addition of β-TCP did not change hydrophilicity of PLLA. The hydrophilicity of PLLA/β-TCP/lecithin increased in comparison to PLLA and PLLA/β-TCP. Degradation of PLLA/β-TCP composite surpassed the degradation of PLLA while addition of lecithin diminished the degradation of composite. The cytocompatibility of composites were studied in 7 day long in vitro assay. Human bone derived cells were seeded on all tested surfaces. Cell viability was estimated by Live/Dead fluorescent staining and Alamar Blue test. Surprisingly, although lecithin addition improved hydrophilicity of the PLLA-based composite, adhesion and proliferation of human bone derived cells were markedly hampered on PLLA/β-TCP/lecithin in comparison to PLLA and PLLA/β-TCP. Despite positive effect we found of lecithin addition on hydrophilicity and stability of PLLA-based composite, its effect on cell attachment and proliferation is negative. Hence, incorporation of lecithin did not improve properties of PLLA/β-TCP/lecithin composite intended for bone tissue regeneration.
Źródło:
Engineering of Biomaterials; 2015, 18, 131; 8-11
1429-7248
Pojawia się w:
Engineering of Biomaterials
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Artificial extracellular matrices of collagen fibrils and lactoferrin as coatings to enhance osteoblast behavior
Autorzy:
Vandorovcova, M.
Bacakova, L.
Dubruel, P.
Douglas, T. E. L.
Powiązania:
https://bibliotekanauki.pl/articles/284321.pdf
Data publikacji:
2012
Wydawca:
Akademia Górniczo-Hutnicza im. Stanisława Staszica w Krakowie. Polskie Towarzystwo Biominerałów
Tematy:
coating
collagen
osteoblasts
proliferation
extracellular matrix
lactoferrin
Opis:
Lactoferrin, a glycoprotein found in milk, has stimulated osteoblast proliferation and differentiation, but has remained relatively unexplored as a biomaterial component. In this study, artificial extracellular matrices consisting of fibrils of collagen type I containing lactoferrin were used as coatings for the biocompatible polymer poly(lactic-co-glycolic acid) (PLGA). The numbers of cells, their viability and proliferation rate were evaluated in various time intervals. Additionally, cell initial spreading area on day 1 was measured. The results show that lactoferrin accelerates fibril-logenesis, leads to increased osteoblast cell numbers 1 and 3 days post-seeding, and encourages their proliferation in each of the tested time intervals.
Źródło:
Engineering of Biomaterials; 2012, 15, no. 116-117 spec. iss.; 132-134
1429-7248
Pojawia się w:
Engineering of Biomaterials
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Oddziaływanie powłok hydroksyapatytowych wytworzonych różnymi metodami na Ti3P na aktywność biologiczną osteoblastów linii Saos-2
Effects of HAp produced by different methods on Ti3P surface layer on biological activity of osteoblasts Soas-2 line
Autorzy:
Zajączkowska, A.
Mróz, W.
Stoch, A.
Długoń, E.
Borowski, T.
Wierzchoń, T.
Czarnowska, E.
Powiązania:
https://bibliotekanauki.pl/articles/284621.pdf
Data publikacji:
2008
Wydawca:
Akademia Górniczo-Hutnicza im. Stanisława Staszica w Krakowie. Polskie Towarzystwo Biominerałów
Tematy:
osteoblasty
hydroksyapatyt
aktywność biologiczna
osteoblasts
hydroxyapatite
biological activity
Źródło:
Engineering of Biomaterials; 2008, 11, no. 77-80; 96-98
1429-7248
Pojawia się w:
Engineering of Biomaterials
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Proliferacja osteoblastów Saos-2 oraz komórek endotelialnych EA.hy 926 na polerowanych i piaskowanych powierzchniach stopów tytanu Ti6Al4V i Ti6Al7Nb
Proliferation of human osteoblast-like cells Saos-2 and human endothelial cells EA.hy 929 on polished and sandblasted surfaces of titanium alloys Ti6Al4V and Ti6Al7Nb
Autorzy:
Walkowiak-Przybyło, M.
Walczyńska, M.
Komorowski, P.
Klimek, L.
Walkowiak, B.
Powiązania:
https://bibliotekanauki.pl/articles/285427.pdf
Data publikacji:
2011
Wydawca:
Akademia Górniczo-Hutnicza im. Stanisława Staszica w Krakowie. Polskie Towarzystwo Biominerałów
Tematy:
osteoblasty
stopy tytanu
proliferacja
osteoblasts
titanium alloys
proliferation
Źródło:
Engineering of Biomaterials; 2011, 14, no. 109-111 spec. iss.; 39-41
1429-7248
Pojawia się w:
Engineering of Biomaterials
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Odpowiedź biologiczna osteoblastów linii Soas-2 inkubowanych na warstwie Ti3P+(Ti-Ni) implantowanej jonami wapnia
Biological response of osteoblast Saos-2 line to calcium ions implanted surface layer Ti3P+(Ti-Ni) type
Autorzy:
Zajączkowska, A.
Borowski, T.
Rajchel, B.
Wierzchoń, T.
Czarnowska, E.
Powiązania:
https://bibliotekanauki.pl/articles/283905.pdf
Data publikacji:
2008
Wydawca:
Akademia Górniczo-Hutnicza im. Stanisława Staszica w Krakowie. Polskie Towarzystwo Biominerałów
Tematy:
osteoblasty
biomateriały tytanowe
implanty
osteoblasts
titanium biomaterials
implants
Źródło:
Engineering of Biomaterials; 2008, 11, no. 77-80; 99-101
1429-7248
Pojawia się w:
Engineering of Biomaterials
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
A comparative study of the effects of genistein, estradiol and raloxifene on the murine skeletal system
Autorzy:
Śliwiński, Leszek
Folwarczna, Joanna
Nowińska, Barbara
Cegieła, Urszula
Pytlik, Maria
Kaczmarczyk-Sedlak, Ilona
Trzeciak, Hanna
Trzeciak, Henryk
Powiązania:
https://bibliotekanauki.pl/articles/1040583.pdf
Data publikacji:
2009
Wydawca:
Polskie Towarzystwo Biochemiczne
Tematy:
bone mechanical properties
estradiol
osteoclasts
bone mineralization
osteoblasts
genistein
raloxifene
Opis:
Genistein, a major phytoestrogen of soy, is considered a potential drug for prevention and treatment of postmenopausal osteoporosis. The aim of the present study was to compare the effects of genistein, estradiol and raloxifene on the skeletal system in vivo and in vitro. Genistein (5 mg/kg), estradiol (0.1 mg/kg) or raloxifene hydrochloride (5 mg/kg) were administered daily by a stomach tube to mature ovariectomized Wistar rats for 4 weeks. Bone mass, mineral and calcium content, macrometric parameters and mechanical properties were examined. Also the effects of genistein, estradiol and raloxifene (10-9-10-7 M) on the formation of osteoclasts from neonatal mouse bone marrow cells and the activity of osteoblasts isolated from neonatal mouse calvariae were compared. In vivo, estrogen deficiency resulted in the impairment of bone mineralization and bone mechanical properties. Raloxifene but not estradiol or genistein improved bone mineralization. Estradiol fully normalized the bone mechanical properties, whereas genistein augmented the deleterious effect of estrogen-deficiency on bone strength. In vitro, genistein, estradiol and raloxifene inhibited osteoclast formation from mouse bone marrow cells, decreasing the ratio of RANKL mRNA to osteoprotegerin mRNA expression in osteoblasts. Genistein, but not estradiol or raloxifene, decreased the ratio of alkaline phosphatase mRNA to ectonucleotide pyrophosphatase phosphodiesterase 1 mRNA expression in osteoblasts. This difference may explain the lack of genistein effect on bone mineralization observed in ovariectomized rats in the in vivo study. Concluding, our experiments demonstrated profound differences between the activities of genistein, estradiol and raloxifene towards the osseous tissue in experimental conditions.
Źródło:
Acta Biochimica Polonica; 2009, 56, 2; 261-270
0001-527X
Pojawia się w:
Acta Biochimica Polonica
Dostawca treści:
Biblioteka Nauki
Artykuł

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