Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 12 de 12
Filter
Add more filters










Publication year range
1.
Anticancer Res ; 37(6): 3001-3007, 2017 06.
Article in English | MEDLINE | ID: mdl-28551638

ABSTRACT

BACKGROUND: The human melanoma cell line IGR-1 was used for the detection and regulation of both melanotransferrin (MTf) and transferrin receptor 1 (TFRC, CD71). While the function in iron transport of the TFRC is well documented the functional importance of MTf is not yet fully understood. Due to the up-regulation of TFRC by hyaluronan (HA) some components and aspects of CD44 signaling were investigated. MATERIALS AND METHODS: The cell-surface proteins MTf, TFRC and ERBB2 receptor tyrosine kinase 2 (ERBB2) were detected by immunoluminescent technique using different polyclonal and monoclonal antibodies. Ionomycin was used to inhibit ß-catenin/T-cell-specific transcription factor (TCF) association, essential in HA-CD44-ERBB2 signaling. RESULTS: MTf, was found to be resistant to phosphatidylinositol-specific phospholipase C. However, MTf as well as TFRC were sensitive to partial proteolytic degradation by pronase E and trypsin. The expression of MTf was shown to be up-regulated by mannose-6-phosphate and that of TFRC by HA. Ionomycin at 10 µM inhibited TFRC up-regulation. However, at 50 µM it induced a 7.5-fold increase of TFRC concentration. CONCLUSION: Our results suggest that human melanoma cells are able to up-regulate TFRC expression using HA/CD44 signaling. The whole pathway comprises of the sequence: HA/CD44, neural Wiskott-Aldrich syndrome protein (N-WASP), ERBB2, ß-catenin/TCF, c-MYC and TFRC. Since ß-catenin is also known to be a component of wingless/Int-1-Frizzled signaling that also leads to transcriptional c-MYC activation, the pathway found here might be alternatively used by melanoma cells for iron supply, necessary for cell proliferation.


Subject(s)
Antigens, CD/metabolism , Hyaluronan Receptors/metabolism , Melanoma/metabolism , Receptors, Transferrin/metabolism , Ribosomal Proteins/metabolism , Cell Line, Tumor , Humans , Hyaluronic Acid/pharmacology , Mannosephosphates/pharmacology , Signal Transduction/drug effects , Up-Regulation/drug effects
3.
PLoS One ; 9(8): e105403, 2014.
Article in English | MEDLINE | ID: mdl-25148252

ABSTRACT

BACKGROUND: Sialic acids (Sia) represent negative-charged terminal sugars on most glycoproteins and glycolipids on the cell surface of vertebrates. Aberrant expression of tumor associated sialylated carbohydrate epitopes significantly increases during onset of cancer. Since Sia contribute towards cell migration ( =  metastasis) and to chemo- and radiation resistance. Modulation of cellular Sia concentration and composition poses a challenge especially for neuroblastoma therapy, due to the high heterogeneity and therapeutic resistance of these cells. Here we propose that Metabolic Sia Engineering (MSE) is an effective strategy to reduce neuroblastoma progression and metastasis. METHODS: Human neuroblastoma SH-SY5Y cells were treated with synthetic Sia precursors N-propanoyl mannosamine (ManNProp) or N-pentanoyl mannosamine (ManNPent). Total and Polysialic acids (PolySia) were investigated by high performance liquid chromatography. Cell surface polySia were examined by flow-cytometry. Sia precursors treated cells were examined for the migration, invasion and sensitivity towards anticancer drugs and radiation treatment. RESULTS: Treatment of SH-SY5Y cells with ManNProp or ManNPent (referred as MSE) reduced their cell surface sialylation significantly. We found complete absence of polysialylation after treatment of SH-SY5Y cells with ManNPent. Loss of polysialylation results in a reduction of migration and invasion ability of these cells. Furthermore, radiation of Sia-engineered cells completely abolished their migration. In addition, MSE increases the cytotoxicity of anti-cancer drugs, such as 5-fluorouracil or cisplatin. CONCLUSIONS: Metabolic Sia Engineering (MSE) of neuroblastoma cells using modified Sia precursors reduces their sialylation, metastatic potential and increases their sensitivity towards radiation or chemotherapeutics. Therefore, MSE may serve as an effective method to treat neuroblastoma.


Subject(s)
Metabolic Engineering , N-Acetylneuraminic Acid/metabolism , Neuroblastoma/metabolism , Antineoplastic Agents/pharmacology , Cell Line, Tumor , Cell Membrane/metabolism , Cell Movement/drug effects , Drug Resistance, Multiple/drug effects , Flow Cytometry , Hexosamines/metabolism , Hexosamines/pharmacology , Humans , N-Acetylneuraminic Acid/analogs & derivatives , N-Acetylneuraminic Acid/chemistry , N-Acetylneuraminic Acid/pharmacology , Neuroblastoma/drug therapy , Radiation Tolerance/drug effects , Sialic Acids/metabolism , Sialic Acids/pharmacology
4.
Cytometry A ; 83(7): 612-26, 2013 Jul.
Article in English | MEDLINE | ID: mdl-23650268

ABSTRACT

Quantitative determinations of the cell membrane potential of lymphocytes (Wilson et al., J Cell Physiol 1985;125:72-81) and thymocytes (Krasznai et al., J Photochem Photobiol B 1995;28:93-99) using the anionic dye DiBAC4 (3) proved that dye depletion in the extracellular medium as a result of cellular uptake can be negligible over a wide range of cell densities. In contrast, most flow cytometric studies have not verified this condition but rather assumed it from the start. Consequently, the initially prepared extracellular dye concentration has usually been used for the calculation of the Nernst potential of the dye. In this study, however, external dye depletion could be observed in both large IGR-1 and small LCL-HO cells under experimental conditions, which have often been applied routinely in spectrofluorimetry and flow cytometry. The maximum cell density at which dye depletion could be virtually avoided was dependent on cell size and membrane potential and definitely needed to be taken into account to ensure reliable results. In addition, accepted calibration procedures based on the partition of sodium and potassium (Goldman-Hodgkin-Katz equation) or potassium alone (Nernst equation) were performed by flow cytometry on cell suspensions with an appropriately low cell density. The observed extensive lack of concordance between the correspondingly calculated membrane potential and the equilibrium potential of DiBAC4 (3) revealed that these methods require the additional measurement of cation parameters (membrane permeability and/or intracellular concentration). In contrast, due to the linear relation between fluorescence and low DiBAC4 (3) concentrations, the Nernst potential of the dye for totally depolarized cells can be reliably used for calibration with an essentially lower effort and expense.


Subject(s)
Barbiturates/chemistry , Flow Cytometry/methods , Fluorescent Dyes/chemistry , Isoxazoles/chemistry , Membrane Potentials/drug effects , Algorithms , Barbiturates/metabolism , Calcium Ionophores/pharmacology , Calibration , Cell Line , Cell Membrane Permeability , Fluorescent Dyes/metabolism , Gramicidin/pharmacology , Humans , Ionomycin/pharmacology , Isoxazoles/metabolism , Models, Biological , Staining and Labeling/methods
5.
Biol Chem ; 393(8): 777-83, 2012 Aug.
Article in English | MEDLINE | ID: mdl-22944680

ABSTRACT

During the last years, the use of therapeutic glycoproteins has increased strikingly. Glycosylation of recombinant glycoproteins is of major importance in biotechnology, as the glycan composition of recombinant glycoproteins impacts their pharmacological properties. The terminal position of N-linked complex glycans in mammals is typically occupied by sialic acid. The presence of sialic acid is crucial for functionality and affects the half-life of glycoproteins. However, glycoproteins in the bloodstream become desialylated over time and are recognized by the asialoglycoprotein receptors via the exposed galactose and targeted for degradation. Non-natural sialic acid precursors can be used to engineer the glycosylation side chains by biochemically introducing new non-natural terminal sialic acids. Previously, we demonstrated that the physiological precursor of sialic acid (i.e., N-acetylmannosamine) can be substituted by the non-natural precursors N-propanoylmannosamine (ManNProp) or N-pentanoylmannosamine (ManNPent) by their simple application to the cell culture medium. Here, we analyzed the glycosylation of erythropoietin (EPO). By feeding cells with ManNProp or ManNPent, we were able to incorporate N-propanoyl or N-pentanoyl sialic acid in significant amounts into EPO. Using a degradation assay with sialidase, we observed a higher resistance of EPO to sialidase after incorporation of N-propanoyl or N-pentanoyl sialic acid.


Subject(s)
Erythropoietin/chemistry , Erythropoietin/metabolism , N-Acetylneuraminic Acid/analysis , N-Acetylneuraminic Acid/metabolism , Neuraminidase/metabolism , Animals , CHO Cells , Carbohydrate Sequence , Clostridium perfringens/enzymology , Cricetinae , Glycosylation , Hexosamines/metabolism , Humans , Molecular Sequence Data , Recombinant Proteins/chemistry , Recombinant Proteins/metabolism
6.
Arch Biochem Biophys ; 524(1): 56-63, 2012 Aug 01.
Article in English | MEDLINE | ID: mdl-22542522

ABSTRACT

Polysialic acid represents a unique posttranslational modification of the neural cell adhesion molecule (NCAM). It is built as a homopolymer of up to 150 molecules of alpha 2-8-linked sialic acids on N-glycans of the fifth immunoglobulin-like domain of NCAM. Besides its role in cell migration and axonal growth during development, polysialic acids are closely related to tumor malignancy as they are linked to the malignant potential of several tumors, such as undifferentiated neuroblastoma. Polysialic acid expression is significantly more frequent in high-grade tumors than in low-grade tumors. It is synthesized in the Golgi apparatus by the activity of two closely related enzymes, the polysialyltransferases ST8SiaII and ST8SiaIV. Interestingly, polysialylation of tumors is not equally synthesized by both polysialyltransferases. It has been shown that especially the ST8SiaII gene is not expressed in some normal tissue, but is strongly expressed in tumor tissue. Here we summarize some knowledge on the role of polysialic acid in cell migration and tumor progression and present novel evidence that interfering with polysialylation using unnatural sialic acid precursors decreases the migration of neuroblastoma cells.


Subject(s)
Cell Movement , Neural Cell Adhesion Molecules/metabolism , Neuroblastoma/metabolism , Sialic Acids/metabolism , Animals , Gene Expression Regulation, Neoplastic , Humans , Neural Cell Adhesion Molecules/chemistry , Neural Cell Adhesion Molecules/genetics , Neuroblastoma/genetics , Protein Processing, Post-Translational , Sialic Acids/chemistry , Sialic Acids/genetics
7.
Mol Pharm ; 6(2): 407-15, 2009.
Article in English | MEDLINE | ID: mdl-19718794

ABSTRACT

Some Pluronics, particularly F127, are known to stabilize nanospheres and prolong their circulation time in vivo. However, these copolymers of poly(ethylene glycol) (PEG) and poly(propylene glycol) are not biodegradable, and despite the long history, there is no approved commercial product using F127 for parenteral administration until now. Meanwhile, hydroxyethyl starch (HES) is a biodegradable polymer that is currently investigated as a substitute for PEG. In order to produce a fully biodegradable amphiphilic polymer, we esterified different molar masses of HES with lauric acid to get different molar substitutions. These polymers, as well as Pluronic F68 and F127, were used to stabilize poly(lactic-co-glycolic acid) (PLGA) nanospheres prepared by nanoprecipitation. For physicochemical characterization, the particle size, zeta potential, and the thickness of the adsorbed polymer layer were measured. The ability of the polymer coating to prevent the adsorption of human serum albumin (HSA) and fibrinogen (FBG) was evaluated. Finally, the phagocytosis of the stabilized nanospheres by a monocyte macrophage cell line (J774.2) was assessed. Results show that the PLGA nanospheres had an average particle size of 110-140 nm. The thickness of the adsorbed polymer layer increases with the increase in molar mass, and is generally higher for HES laurates than the studied Pluronics. Pluronic F68, F127 as well as the HES laurates with low molar substitution prevented the adsorption of HSA. HES laurates with low molar substitution and F127, but not F68, prevented the adsorption of FBG. The phagocytosis experiments showed that the HES laurates, particularly the one with the highest molar mass, could reduce the uptake of the nanospheres better than F68 and comparable to F127. Finally, these results warrant in vivo experiments to evaluate how the HES laurates can affect the pharmacokinetics and fate of the nanospheres.


Subject(s)
Glycolates/chemistry , Hydroxyethyl Starch Derivatives/chemistry , Nanospheres , Poloxamer/chemistry , Polymers/chemistry , Animals , Cells, Cultured , Humans , Lactic Acid , Macrophages/metabolism , Mice , Phagocytosis , Polyglycolic Acid , Polylactic Acid-Polyglycolic Acid Copolymer , Serum Albumin/metabolism
8.
Cytometry A ; 75(7): 593-608, 2009 Jul.
Article in English | MEDLINE | ID: mdl-19504578

ABSTRACT

The bis-barbituric acid oxonol, DiBAC(4)(3) is used as a standard potentiometric probe in human cells. However, its fluorescence depends not only on membrane potential but also varies with nonpotential related changes in the amount of intracellular free and bound dye. This study demonstrates the influence of different experimental conditions on this nonspecific fluorescence proportion. IGR1 melanoma cells as a model were specifically altered in cell volume and protein content by depolarizing treatments or cell cycle synchronization. Flow cytometry was performed over a wide range of extracellular DiBAC(4)(3) concentrations. Fixation and increase in protein content led to a nonspecifically enhanced fluorescence, while changes in the amount of free intracellular dye as a result of altered cell volume proved to be negligible. To establish a calibration curve using totally depolarized cells, the pore-forming action of gramicidin should be preferred to fixation. Below 100 nM DiBAC(4)(3), the logarithmic relation between cell fluorescence and dye concentration turned into a virtually linear function intersecting with zero. Consequently, calibration can then be confined to determination of the fluorescence of depolarized cells stained with the same concentration as used for the actual measurement of membrane potential. Unexpectedly, quenching of fluorescence occurred in totally depolarized cells at concentrations higher than 6,250 nM. Linearity and quenching could be confirmed by additional experiments on Chinese hamster ovary CHO-K1 and B lymphoblastoid LCL-HO cells.


Subject(s)
Flow Cytometry/methods , Membrane Potentials/physiology , Animals , Barbiturates/pharmacology , CHO Cells , Cell Line , Cell Line, Tumor , Cricetinae , Cricetulus , Fluorescent Dyes/pharmacology , Humans , Isoxazoles/pharmacology , Microscopy, Confocal
9.
Exp Dermatol ; 18(12): 1064-6, 2009 Dec.
Article in English | MEDLINE | ID: mdl-19397696

ABSTRACT

Various glutamate receptors have been described in both keratinocytes and melanocytes. L-Glutamate is the physiological agonist of the glutamate receptor family. The source of this transmitter had not yet been identified. In normal human epidermal keratinocytes (NHEK) and HaCaT-keratinocytes, cell supernatants were sampled in various stages of cell density and the l-glutamate content photometrically determined. The following examination time-points were defined: non-confluent (ca. 33%), subconfluent (ca. 70%) and confluent (90-100%). The L-glutamate concentration originally in the culture medium was 14.7 mg/l (0.1 mm/l). The L-glutamate concentration in the cell supernatant increased in NHEK with increasing cell density: non-confluent 39.9 + or - 4 mg/l, subconfluent 60.6 + or - 15.8 mg/l, confluent 100.7 + or - 33.2 mg/l. A linear increase of L-glutamate concentration was also found for HaCaT cells. The investigations show that keratinocytes are capable of producing and releasing L-glutamate. Thus they are a source of L-glutamate which acts as a transmitter on epidermal glutamate receptors.


Subject(s)
Epidermis/metabolism , Glutamic Acid/metabolism , Keratinocytes/metabolism , Neurotransmitter Agents/metabolism , Cell Count , Cell Line , Culture Media, Conditioned/metabolism , Epidermal Cells , Humans , Receptors, Glutamate/metabolism
10.
J Mol Endocrinol ; 42(3): 249-60, 2009 Mar.
Article in English | MEDLINE | ID: mdl-19060179

ABSTRACT

Retinoic acid (RA) acts as an anti-proliferative and redifferentiation agent in the therapy of thyroid carcinoma. Our previous studies demonstrated that pretreatment of follicular thyroid carcinoma cell lines FTC-133 and FTC-238 resulted in decreased in vitro proliferation rates and reduced tumor cell growth of xenotransplants. In addition to the previous results, we found that RA led to decreased vitality and invasiveness of FTC-133 and FTC-238 cells as they reacted with reduction of intracellular ATP levels and number of migrated cells respectively. However, the molecular mechanisms by which RA mediates these effects are not well understood. Two-dimensional (2D) screening of the proteins related to ATP metabolism and western blot analysis revealed alpha-enolase (ENO1) to be down-regulated in FTC-133 and FTC-238 cells after RA treatment. 2D gel detection and mass spectrometric analysis revealed that ENO1 existed as three separate protein spots of distinct pIs (ENO1-A1-A3). Comparative 2D difference gel electrophoresis analysis of fluorescently labeled protein samples of RA-treated and untreated FTC-133 demonstrated a selective down-regulation of ENO1-A1 which we identified as a phosphoprotein. RA caused the dephosphorylation of ENO1-A1. Both, RA-mediated and specific knock-down of ENO1/MBP-1 resulted in the reduction of MYC oncoprotein, and simultaneously decreased proliferation rates of FTC-133 and FTC-238 cell lines. In summary, the RA-mediated down-regulation of the ENO1 gene products and MYC oncoprotein provides a novel molecular mechanism facilitating the anti-proliferative effect of RA in human thyroid carcinoma cells and suggests new pathways for supportive RA therapies.


Subject(s)
Biomarkers, Tumor/physiology , Cell Movement/drug effects , DNA-Binding Proteins/physiology , Gene Expression Regulation, Neoplastic/drug effects , Phosphopyruvate Hydratase/physiology , Thyroid Neoplasms/metabolism , Tretinoin/pharmacology , Tumor Suppressor Proteins/physiology , Apoptosis/drug effects , Biomarkers, Tumor/metabolism , Blotting, Western , Cell Line, Tumor , Cell Proliferation/drug effects , DNA-Binding Proteins/metabolism , Electrophoresis, Gel, Two-Dimensional , Humans , Phosphopyruvate Hydratase/metabolism , Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization , Thyroid Neoplasms/drug therapy , Tumor Suppressor Proteins/metabolism
11.
Ophthalmic Res ; 38(2): 62-5, 2006.
Article in English | MEDLINE | ID: mdl-16465068

ABSTRACT

High sensitivity of cultured bovine and human lens epithelial cells to unsaturated free fatty acids has been reported in previous papers. Here we show that micromolar concentrations of unsaturated free fatty acids also impair lens cells during organ culturing, a system which resembles the in vivo situation much better than cell cultures do. This added weight to the assumption that fatty acid cytotoxicity might be causally related to senile cataract as well as to cataracts associated with systemic diseases.


Subject(s)
Fatty Acids/toxicity , Lens, Crystalline/drug effects , Animals , Cataract/etiology , Cataract/pathology , Cattle , Lens, Crystalline/ultrastructure , Male , Microscopy, Confocal , Organ Culture Techniques
12.
Exp Dermatol ; 13(8): 512-9, 2004 Aug.
Article in English | MEDLINE | ID: mdl-15265016

ABSTRACT

In the present study, the distribution of ionotropic glutamate receptors of the N-methyl-D-aspartate (NMDA)-receptor type was immunohistochemically demonstrated in healthy human skin (n = 22) and healthy buccal mucosa (n = 20). Moreover, the intracellular calcium concentration of HaCaT-cells and native human keratinocytes were studied under the influence of the selective agonist NMDA and the selective NMDA-antagonist MK-801. Immunohistochemical imaging of NMDA receptors in healthy epidermis showed a positive reaction in the stratum basale, spinosum and granulosum, whereby the greatest expression was observed in the granular layer. In the mucosal preparations, the distribution of NMDA receptors was observed to be equal in all cell layers. In the cell culture (HaCaT-cells), NMDA concentrations between 25 microM and 1 mM resulted in a significant increase in the number of cells showing elevated intracellular calcium concentration. This effect could be significantly reduced by prior application of MK-801 (100 micro M). In supplementary tests on HaCaT-keratinocytes, blockade of the keratinocytic NMDA receptors with MK-801 suppressed the differentiation of the cells (expression of cytokeratin 10). The proliferation of cells was not influenced by NMDA. The investigations showed that glutamate receptors of the NMDA type have an influence on keratinocytic calcium concentration. This appears especially important for the differentiation of keratinocytes.


Subject(s)
Calcium/metabolism , Keratinocytes/metabolism , Receptors, N-Methyl-D-Aspartate/physiology , Cell Differentiation , Cell Line , Cell Proliferation , Cell Survival , Epidermis/metabolism , Flow Cytometry , Humans , Immunohistochemistry , Keratins/biosynthesis , Lasers , Mouth Mucosa/metabolism , N-Methylaspartate/metabolism , Receptors, N-Methyl-D-Aspartate/metabolism , Skin/metabolism , Time Factors
SELECTION OF CITATIONS
SEARCH DETAIL
...