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1.
Article in English | MEDLINE | ID: mdl-38623703

ABSTRACT

Plastic pollution in aquatic ecosystems has become a significant problem especially microplastics which can encapsulate into the skeletons of organisms that produce calcium carbonates, such as foraminifera, molluscs and corals. The encapsulation of microplastics into precipitated aragonite, which in nature builds the coral skeleton, has not yet been studied. It is also not known how the dissolved organic matter, to which microplastics are constantly exposed in aquatic ecosystems, affects the encapsulation of microplastics into aragonite and how such microplastics affect the mechanical properties of aragonite. We performed aragonite precipitation experiments in artificial seawater in the presence of polystyrene (PS) and polyethylene (PE) microspheres, untreated and treated with humic acid (HA). The results showed that the efficiency of encapsulating PE and PE-HA microspheres in aragonite was higher than that for PS and PS-HA microspheres. The mechanical properties of resulting aragonite changed after the encapsulation of microplastic particles. A decrease in the hardness and indentation modulus of the aragonite samples was observed, and the most substantial effect occurred in the case of PE-HA microspheres encapsulation. These findings raise concerns about possible changes in the mechanical properties of the exoskeleton and endoskeleton of calcifying marine organisms such as corals and molluscs due to the incorporation of pristine microplastics and microplastics exposed to dissolved organic matter.

2.
J Cell Physiol ; 226(7): 1771-9, 2011 Jul.
Article in English | MEDLINE | ID: mdl-21506109

ABSTRACT

Chondrocyte cell death can contribute to cartilage degeneration in articular diseases, such as osteoarthritis (OA). Sulforaphane (SFN), a natural compound derived from cruciferous aliment, is well known as an anti-carcinogen, but according to recent evidence it also shows cytoprotective effects on a variety of non-tumoral cells. Therefore we have tested the ability of SFN to protect chondrocytes from cell death in vitro. Treatment of growing monolayer cultures of human C-28/I2 chondrocytes with SFN in the low micro-molecular range for a few days, reduced cell growth without affecting cell survival or inducing apoptosis. However it decreased cell death in C-28/I2 chondrocytes exposed to stimuli previously reported to promptly trigger apoptosis, that is, the cytokine tumor necrosis factor-α (TNF) plus cycloheximide (CHX) or the polyamine analogue N(1),N(11)-diethylnorspermine (DENSPM) plus CHX. In particular pre-treatment with SFN reduced effector and initiator caspase activities and the associated activation of JNK kinases. SFN exerted a cytoprotective action even versus H(2)O(2) , which differently from the previous stimuli induced cell death without producing an evident caspase activation. SFN pre-treatment also prevented caspase activation in three-dimensional micromass cultures of OA chondrocytes stimulated with growth-related oncogene α (GROα), a pro-apoptotic chemokine. The suppression of caspase activation in micromasses appeared to be related to the inhibition of p38 MAPK phosphorylation. In conclusion, the present work shows that low micro-molecular SFN concentrations exert pro-survival and anti-apoptotic actions and influence signaling pathways in a variety of experimental conditions employing chondrocyte cell lines and OA chondrocytes treated with a range of death stimuli.


Subject(s)
Apoptosis/drug effects , Chondrocytes/drug effects , Thiocyanates/pharmacology , Caspases/metabolism , Cell Proliferation/drug effects , Cells, Cultured , Chemokine CXCL1/toxicity , Chondrocytes/pathology , Cycloheximide/toxicity , Cytoprotection , Dose-Response Relationship, Drug , Humans , Hydrogen Peroxide/toxicity , Isothiocyanates , JNK Mitogen-Activated Protein Kinases/metabolism , Phosphorylation , Spermine/analogs & derivatives , Spermine/toxicity , Sulfoxides , Time Factors , Tumor Necrosis Factor-alpha/toxicity , p38 Mitogen-Activated Protein Kinases/metabolism
3.
J Surg Res ; 164(1): e27-35, 2010 Nov.
Article in English | MEDLINE | ID: mdl-20828747

ABSTRACT

The objective of this study was to investigate how long-term cardioplegia/reperfusion affects cardiac nitric oxide synthase 3 (NOS3). To this aim, rat hearts were mounted in a perfusion apparatus and equilibrated with a modified Krebs-Henseleit solution (KH). The hearts were then arrested by soaking them in cold St. Thomas Hospital II solution (STH) for 5, 7, and 15 h. Reperfusion was performed by low-flow cold STH delivering for 1 h followed by 15-min aerobic normothermic KH perfusion. Cardioplegia preserved the amount of NOS3 irrespective of the duration of the cardiac arrest. NOS3 content was also unaffected by reperfusion following 5 and 7 h of cardioplegia. On the contrary, reperfusion performed after 15 h of cardioplegia caused a marked reduction in the amount of NOS3 protein, in both endothelial and cardiac muscle cells, and NOS activity. The involvement of intracellular proteolysis as a cause of reduction in NOS3 cardiac level was then investigated by delivering 0.1 mmol/L of either calpain I and II inhibitors or 0.05 mmol/L leupeptin during heart reperfusion. Only the treatment with leupeptin preserved NOS3, indicating that lysosomal proteases rather then cytoplasmic calpains were mainly responsible for the cleavage of this enzyme. The observed decrease in GSH/GSSG ratio and activation of JNK in the reperfused heart suggested that proteolysis could be triggered by reactive oxygen species.


Subject(s)
Cysteine Proteinase Inhibitors/pharmacology , Heart Arrest, Induced/methods , Leupeptins/pharmacology , Myocardial Reperfusion Injury/drug therapy , Myocardial Reperfusion Injury/metabolism , Nitric Oxide Synthase Type III/metabolism , Animals , Glutathione/metabolism , Glutathione Disulfide/metabolism , Male , Microscopy, Electron, Transmission , Myocardial Reperfusion Injury/pathology , Myocardium/enzymology , Myocardium/pathology , Myocardium/ultrastructure , Nitric Oxide/metabolism , Oxidative Stress/drug effects , Oxidative Stress/physiology , Rats , Rats, Wistar , Time Factors
4.
J Cell Physiol ; 219(1): 109-16, 2009 Apr.
Article in English | MEDLINE | ID: mdl-19097065

ABSTRACT

We have been investigating the effects of natural polyamines and polyamine analogues on the survival and apoptosis of chondrocytes, which are cells critical for cartilage integrity. Treatment of human C-28/I2 chondrocytes with N(1),N(11)-diethylnorspermine (DENSPM), a polyamine analogue with clinical relevance as an experimental anticancer agent, rapidly induced spermidine/spermine N(1)-acetyltransferase (SSAT) and spermine oxidase (SMO), key enzymes of polyamine catabolism and down-regulated ornithine decarboxylase, the first enzyme of polyamine biosynthesis, thus depleting all main polyamines within 24 h. The treatment with DENSPM did not provoke cell death and caspase activation when given alone for 24 h, but caused a caspase-3 and -9 dependent apoptosis in chondrocytes further exposed to cycloheximide (CHX). In other cellular models, enhanced polyamine catabolism or polyamine depletion has been implicated as mechanisms involved in DENSPM-related apoptosis. However, the simultaneous addition of DENSPM and CHX rapidly increased caspase activity in C-28/I2 cells in the absence of SSAT and SMO induction or significant reduction of polyamine levels. Moreover, caspase activation induced by DENSPM plus CHX was not prevented by a N(1)-acetylpolyamine oxidase (PAO)/SMO inhibitor, and depletion of all polyamines obtained by specific inhibitors of polyamine biosynthesis did not reproduce DENSPM effects in the presence of CHX. DENSPM/CHX-induced apoptosis was associated with changes in the amount or activation of signalling kinases, Akt and MAPKs, and increased uptake of DENSPM. In conclusion, the results suggest that DENSPM can favour apoptosis in chondrocytes independently of its effects on polyamine metabolism and levels.


Subject(s)
Antineoplastic Agents/pharmacology , Apoptosis/drug effects , Chondrocytes/drug effects , Chondrocytes/metabolism , Polyamines/metabolism , Spermine/analogs & derivatives , Caspase 3/metabolism , Caspase 9/metabolism , Cell Line , Chondrocytes/cytology , Cycloheximide/pharmacology , Enzyme Activation , Humans , Mitogen-Activated Protein Kinases/genetics , Mitogen-Activated Protein Kinases/metabolism , Protein Synthesis Inhibitors/pharmacology , Signal Transduction/physiology , Spermine/pharmacology
5.
J Cell Biochem ; 103(4): 1046-52, 2008 Mar 01.
Article in English | MEDLINE | ID: mdl-18240140

ABSTRACT

The efficiency of in vitro mesenchymal stem cell (MSC) differentiation into the myocardial lineage is generally poor. In order to improve cardiac commitment, bone marrow GFP+MSCs obtained from transgenic rats were cultured with adult wild type rat cardiomyocytes for 5 days in the presence of difluoromethylornithine (DFMO), an inhibitor of polyamine synthesis and cell proliferation. The percentage of GFP+MSCs showing cardiac myofibril proteins (cMLC2, cTnI) was about threefold higher after DFMO addition (3%) relative to the untreated control (1%). Another set of experiments was performed with cardiomyocytes incubated for 1 day in the absence of glucose and serum and under hypoxic conditions (pO2 < 1%), in order to simulate severe ischemia. The percentage of cardiac committed GFP+MSCs was about 5% when cultured with the hypoxic/starved cardiomyocytes and further increased to 7% after DFMO addition. The contemporary presence of putrescine in DFMO-treated cells markedly blunted differentiation, while the cytostatic mitomycin C was not able to induce cardiac commitment. The involvement of histone acetylation in DFMO-induced differentiation was evidenced by the strong attenuation of cardiac commitment exerted by anacardic acid, an inhibitor of histone acetylase. Moreover, the percentage of acetylated histone H3 significantly increased in bone marrow MSCs obtained from wild type rats and treated with DFMO. These results suggest that polyamine depletion can represent a useful strategy to improve MSC differentiation into the cardiac lineage, especially in the presence of cardiomyocytes damaged by an ischemic environment.


Subject(s)
Bone Marrow Cells/cytology , Eflornithine/pharmacology , Mesenchymal Stem Cells/cytology , Myocytes, Cardiac/cytology , Acetylation , Anacardic Acids/pharmacology , Animals , Animals, Genetically Modified , Bone Marrow Cells/physiology , Cardiac Myosins/metabolism , Cell Culture Techniques , Cell Differentiation , Cell Hypoxia , Cell Lineage , Cell Proliferation , Cells, Cultured , Coculture Techniques , Histones/metabolism , Mesenchymal Stem Cells/physiology , Mitomycin/pharmacology , Myocytes, Cardiac/physiology , Myosin Light Chains/metabolism , Polyamines/pharmacology , Rats
6.
J Cell Physiol ; 216(1): 153-61, 2008 Jul.
Article in English | MEDLINE | ID: mdl-18231987

ABSTRACT

Chondrocyte survival is closely linked to cartilage integrity, and forms of chondrocyte apoptotic death can contribute to cartilage degeneration in articular diseases. Since growing evidence also implicates polyamines in the control of cell death, we have been investigating the role of polyamine metabolism in chondrocyte survival and apoptosis. Treatment of human C-28/I2 chondrocytes with N(1),N(11)-diethylnorspermine (DENSPM), a polyamine analogue with clinical relevance as an experimental anticancer agent, inhibited polyamine biosynthesis and induced polyamine catabolism, thus rapidly depleting all main polyamines. DENSPM did not increase significantly caspase activity, but provoked a late cell death associated to DNA fragmentation. A short treatment with DENSPM did not reduce cell viability when given alone, but enhanced caspase-3 and -9 activation in chondrocytes exposed to tumor necrosis factor-alpha (TNF) and cycloheximide (CHX). A longer treatment with DENSPM however reduced caspase response to TNF plus CHX. Depletion of all polyamines obtained by specific inhibitors of polyamine biosynthesis did not cause cell death and contrasted apoptosis by decreasing caspase activities. In conclusion, following DENSPM treatment, C-28/I2 chondrocytes are initially sensitized to caspase 9-dependent apoptosis in the presence of TNF and CHX and may eventually undergo a late and mainly caspase-independent cell death in the absence of other stimuli. Moreover, these results indicate that a reduction of polyamine levels not only leads to inhibition of cell proliferation, but also of caspase-mediated pathways of chondrocyte apoptosis.


Subject(s)
Antineoplastic Agents/pharmacology , Apoptosis/drug effects , Cell Survival/drug effects , Chondrocytes/drug effects , Chondrocytes/physiology , Spermine/analogs & derivatives , Acetyltransferases/metabolism , Amidines/metabolism , Apoptosis/physiology , Caspases/metabolism , Cell Line , Chondrocytes/cytology , Cycloheximide/metabolism , DNA Fragmentation , Eflornithine/metabolism , Enzyme Activation , Enzyme Inhibitors/metabolism , Humans , Indans/metabolism , Ornithine Decarboxylase/metabolism , Polyamines/metabolism , Protein Synthesis Inhibitors/metabolism , Spermine/pharmacology , Tumor Necrosis Factor-alpha/metabolism
7.
Exp Gerontol ; 41(8): 800-4, 2006 Aug.
Article in English | MEDLINE | ID: mdl-16806781

ABSTRACT

The survival of mesenchymal stem cells (MSCs) to tumor necrosis factor alpha (TNFalpha) stimulation was evaluated after a long-term antioxidant treatment, or caloric restriction, in aged rats. MSCs were isolated from bone marrow of 30-month-old rats which orally received N-acetylcysteine in the last 18 months. The necrotic cell death-induced in vitro by TNFalpha, determined by trypan blue exclusion, was markedly attenuated in MSCs obtained from treated vs. control aged rats (percent mean+/-SEM: 10.9+/-2.17 vs. 17.8+/-0.53; p<0.05). Also, the proliferation rate of MSCs from control, but not N-acetylcysteine-treated, aged rats evaluated up to 2 weeks was significantly higher than that of MSCs from younger (4-month-old) rats. No significant effect was observed relative to the parameters investigated when the aged rats were previously subjected to a hypocaloric diet for 18 months. In conclusion, a prolonged supplementation with N-acetylcysteine in rats can increase resistance to necrotic death of MSCs and may also counteract an excessive rate of MSC proliferation.


Subject(s)
Acetylcysteine/pharmacology , Aging/pathology , Caloric Restriction , Mesenchymal Stem Cells/drug effects , Tumor Necrosis Factor-alpha/pharmacology , Animals , Antioxidants/pharmacology , Apoptosis/drug effects , Cell Death/drug effects , Cell Proliferation/drug effects , Drug Administration Schedule , Male , Mesenchymal Stem Cells/pathology , Rats , Rats, Wistar
8.
J Cell Physiol ; 206(1): 138-46, 2006 Jan.
Article in English | MEDLINE | ID: mdl-15965903

ABSTRACT

Chondrocyte apoptosis can be an important contributor to cartilage degeneration, thereby making it a potential therapeutic target in articular diseases. To search for new approaches to limit chondrocytic cell death, we investigated the requirement of polyamines for apoptosis favored by tumor necrosis factor-alpha (TNF), using specific polyamine biosynthesis inhibitors in human chondrocytes. The combined treatment of C-28/I2 chondrocytes with TNF and cycloheximide (CHX) resulted in a prompt effector caspase activation and internucleosomal DNA fragmentation. Pre-treatment of chondrocytes with alpha-difluoromethylornithine (DFMO), an ornithine decarboxylase (ODC) inhibitor, markedly reduced putrescine and spermidine content as well as the caspase-3 activation and DNA fragmentation induced by TNF and CHX. DFMO treatment also inhibited the increase in effector caspase activity provoked by TNF plus MG132, a proteasome inhibitor. DFMO decreased caspase-8 activity and procaspase-8 content, an apical caspase essential for TNF-induced apoptosis. Although DFMO increased the amount of active, phosphorylated Akt, inhibitors of the Akt pathway failed to restore the TNF-induced increase in caspase activity blunted by DFMO. DFMO also reduced the increase in caspase activity induced by staurosporine, but in this case Akt inhibition prevented the DFMO effect. Pre-treatment with CGP 48664, an S-adenosylmethionine decarboxylase (SAMDC) inhibitor markedly reduced spermidine and spermine levels, and provoked effects similar to those caused by DFMO. Finally DFMO was effective even in primary osteoarthritis (OA) chondrocyte cultures. These results suggest that the intracellular depletion of polyamines in chondrocytes can inhibit both the death receptor pathway by reducing the level of procaspase-8, and the apoptotic mitochondrial pathway by activating Akt.


Subject(s)
Apoptosis/physiology , Chondrocytes/drug effects , Chondrocytes/physiology , Polyamines/metabolism , Signal Transduction/physiology , Tumor Necrosis Factor-alpha/pharmacology , Caspase 8 , Caspase Inhibitors , Caspases/genetics , Caspases/metabolism , Cell Line , Chondrocytes/cytology , Cycloheximide/pharmacology , DNA Fragmentation , Eflornithine/pharmacology , Enzyme Activation , Enzyme Inhibitors/pharmacology , Humans , Protein Synthesis Inhibitors/pharmacology , Proto-Oncogene Proteins c-akt/metabolism
9.
Stem Cells ; 23(7): 983-91, 2005 Aug.
Article in English | MEDLINE | ID: mdl-15941855

ABSTRACT

Polyamines are powerful modulators of both growth and survival in mammalian cells. In this study, we investigated the possibility of attenuating the process of apoptosis in bone marrow stromal cells (BMSCs), which comprise mesenchymal stem cells, by reducing the intracellular levels of polyamines. BMSCs were isolated from rat femurs and expanded for 12 days. At this time, BMSCs were CD34neg, CD45neg, and mostly CD90pos. BMSCs were grown for an additional 2 days in the presence of 1 mM alpha-difluoromethylornithine (DFMO), an inhibitor of ornithine decarboxylase, which reduced the content of both putrescine and spermidine by nearly 90%. DFMO treatment progressively slowed down BMSC proliferation, as determined by the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazoliumbromide (MTT) assay, without arresting their growth completely. The effect of polyamine depletion on caspase-3 activity was evaluated in BMSCs after treatment with 500 U/ml tumor necrosis factor-alpha (TNFalpha) and 5 microM MG132, an inhibitor of proteasome. Caspase-3 activity increased linearly over a period of 24-hour stimulation (p<.01), but this augmentation was blunted by 50% after DFMO administration (p<.05). The effect of DFMO on TNFalpha/MG132-induced upregulation of caspase-3 activity was reversed by the addition of 100 microM putrescine, confirming that polyamines were really involved in the apoptotic process. Also, the number of apoptotic BMSCs after TNFalpha/MG132 treatment, as determined by terminal transferase-mediated dUTP nick end-labeling (TUNEL) assay, were threefold reduced after polyamine depletion (p<.05). On the contrary, DFMO did not affect the MG132-mediated increase in p53 abundance, nor its translocation to the nucleus. Thus, polyamine depletion can be considered a useful tool for counteracting programmed cell death in BMSCs without involving the p53 proapoptotic protein.


Subject(s)
Apoptosis , Bone Marrow Cells/cytology , Leupeptins/pharmacology , Polyamines/metabolism , Stromal Cells/cytology , Tumor Necrosis Factor-alpha/metabolism , Animals , Antigens, CD34/biosynthesis , Blotting, Western , Caspase 3 , Caspases/metabolism , Cell Adhesion , Cell Cycle , Cell Nucleus/metabolism , Cell Proliferation , Cell Separation , Coloring Agents/pharmacology , Eflornithine/pharmacology , Femur/metabolism , Flow Cytometry , In Situ Nick-End Labeling , Leukocyte Common Antigens/biosynthesis , Microscopy, Fluorescence , Ornithine Decarboxylase/metabolism , Osteocytes/metabolism , Proteasome Inhibitors , Putrescine/metabolism , Rats , Rats, Wistar , Spermidine/metabolism , Tetrazolium Salts/pharmacology , Thiazoles/pharmacology , Time Factors , Tumor Suppressor Protein p53/metabolism
10.
Coll Antropol ; 27(2): 573-9, 2003 Dec.
Article in English | MEDLINE | ID: mdl-14746145

ABSTRACT

The objective of this paper is to present the growth patterns of school children in Osijek--the city which was exposed to severe attacks during the aggression on Croatia. The mean height and weight of Osijek schoolchildren aged 7 to 18 and the menarcheal age in girls in academic year 1995/96 were compared to the analogous data collected in 1980/81. The secular changes in height were heterogeneous. In older age groups from 12 in girls and 13 in boys, the mean height in 1995/96 increased markedly, whereas from 9 to 11 or 12, changes were undulating. In the youngest groups--at the age of 7 in both genders, and at 8 in boys, negative changes were observed. Markedly smaller height in this cohort was still pronounced in 1999/2000 when these children reached the age of 11. However, one year later (2000/01), at the age of 12, boys and girls caught up with their peers in the previous generations. These children during the war were approximately at the age of 2.5 to 4, a period when growth patterns are highly sensitive to adverse environmental influences. It might be possible that the emotional stress caused by a change of environment and separation from home, contributed to the deceleration of growth rate, i.e. the smaller height in a large part of childhood.


Subject(s)
Body Height , Growth , Warfare , Adolescent , Body Mass Index , Child , Croatia , Female , Humans , Male
11.
FEBS Lett ; 527(1-3): 223-28, 2002 Sep 11.
Article in English | MEDLINE | ID: mdl-12220664

ABSTRACT

Activation of the extracellular signal-regulated kinases (ERKs) 1 and 2 is correlated to cell survival, but in some cases ERKs can act in signal transduction pathways leading to apoptosis. Treatment of mouse fibroblasts with 20 microM etoposide elicited a sustained phosphorylation of ERK 1/2, that increased until 24 h from the treatment in parallel with caspase activity. The inhibitor of ERK activation PD98059 abolished caspase activation, but caspase inhibition did not reduce ERK 1/2 phosphorylation, suggesting that ERK activation is placed upstream of caspases. Both ERK and caspase activation were blocked in cells depleted of polyamines by the ornithine decarboxylase inhibitor alpha-difluoromethylornithine (DFMO). In etoposide-treated cells, DFMO also abolished phosphorylation of c-Jun NH(2)-terminal kinases triggered by the drug. Polyamine replenishment with exogenous putrescine restored the ability of the cells to undergo caspase activation and ERK 1/2 phosphorylation in response to etoposide. Ornithine decarboxylase activity decreased after etoposide, indicating that DFMO exerts its effect by depleting cellular polyamines before induction of apoptosis. These results reveal a role for polyamines in the transduction of the death signal triggered by etoposide.


Subject(s)
Caspases/metabolism , Etoposide/pharmacology , Fibroblasts/metabolism , Mitogen-Activated Protein Kinases/metabolism , Polyamines/metabolism , Animals , Apoptosis/drug effects , Apoptosis/physiology , Caspase Inhibitors , Caspases/drug effects , Coumarins/pharmacology , Eflornithine/pharmacology , Enzyme Activation/drug effects , Enzyme Inhibitors/pharmacology , Fibroblasts/drug effects , Fibroblasts/pathology , Mice , Mitogen-Activated Protein Kinase 1/drug effects , Mitogen-Activated Protein Kinase 1/metabolism , Mitogen-Activated Protein Kinase 3 , Mitogen-Activated Protein Kinases/drug effects , Oligopeptides/pharmacology , Ornithine Decarboxylase Inhibitors , Phosphorylation , Putrescine/pharmacology , Signal Transduction
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