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1.
Eur Rev Med Pharmacol Sci ; 26(7): 2330-2342, 2022 04.
Article in English | MEDLINE | ID: mdl-35442487

ABSTRACT

OBJECTIVE: In this study, we used autologous bone marrow aspirate concentrate (BMAC) transplantation to treat children with cerebral palsy (CP) to improve their motor and cognitive functions. PATIENTS AND METHODS: Forty-two patients with CP received BMAC. The transplantation of stem cells via the intrathecal route includes three BMAC applications. The patients' examination was before the injection of stem cells, with follow-ups on 1, 3, 6, and 12 months after the injections. The assessments included the gross motor function classification scale, the Ashworth scale, and the Learning accomplishment profile-diagnostic scale. RESULTS: This study included 42 patients with CP who received three BMAC intrathecal administrations. A personalized home rehabilitation program was designed and included for each patient in the study. After the treatment, we observed a reduction of spasticity in 58% of patients and significant cognitive improvement in 35% of patients. CONCLUSIONS: The outcome of this study indicates that stem cell therapy and personalized training can improve the development of children with CP. The crucial goal of this therapeutic intervention is to substitute injured tissue with new tissues by activating the regenerative capacity of stem cells.


Subject(s)
Cerebral Palsy , Bone Marrow , Bone Marrow Transplantation , Cerebral Palsy/surgery , Child , Humans , Muscle Spasticity , Transplantation, Autologous
2.
Eur Rev Med Pharmacol Sci ; 24(15): 8075-8080, 2020 08.
Article in English | MEDLINE | ID: mdl-32767334

ABSTRACT

OBJECTIVE: Autism Spectrum Disorder is a complex brain disorder and has multiple causes that occur in diverse combinations. There is a need to classify children with ASD at a very young age so that they can access evidence-based intervention that can significantly improve their outcomes. CASE REPORT: In this report we present a case of autism, which underwent intrathecal autologous bone marrow mononuclear cells transplantation along with neurorehabilitation. The primary goal of the treatment is to improve the quality of life of the patient. After the procedure, the child started to speak, therefore, the third communication subscale was scored within the GARS-2 assessment instrument. With these three subscales, a score of 91 has been achieved, representing an autism index of 27%, a significant improvement over the previous score. CONCLUSIONS: Our study demonstrated evidences to support the safety and effectiveness of BMAC transplantation in the management of autism.


Subject(s)
Autistic Disorder/therapy , Bone Marrow Transplantation , Autistic Disorder/diagnosis , Child, Preschool , Humans , Quality of Life , Transplantation, Autologous
3.
Br J Cancer ; 109(1): 76-82, 2013 Jul 09.
Article in English | MEDLINE | ID: mdl-23807161

ABSTRACT

BACKGROUND: Several lines of evidence suggest a dichotomy between immune active and quiescent cancers, with the former associated with a good prognostic phenotype and better responsiveness to immunotherapy. Central to such dichotomy is the master regulator of the acute inflammatory process interferon regulatory factor (IRF)-1. However, it remains unknown whether the responsiveness of IRF-1 to cytokines is able to differentiate cancer immune phenotypes. METHODS: IRF-1 activation was measured in 15 melanoma cell lines at basal level and after treatment with IFN-γ, TNF-α and a combination of both. Microarray analysis was used to compare transcriptional patterns between cell lines characterised by high or low IRF-1 activation. RESULTS: We observed a strong positive correlation between IRF-1 activation at basal level and after IFN-γ and TNF-α treatment. Microarray demonstrated that three cell lines with low and three with high IRF-1 inducible translocation scores differed in the expression of 597 transcripts. Functional interpretation analysis showed mTOR and Wnt/ß-cathenin as the top downregulated pathways in the cell lines with low inducible IRF-1 activation, suggesting that a low IRF-1 inducibility recapitulates a cancer phenotype already described in literature characterised by poor prognosis. CONCLUSION: Our findings support the central role of IRF-1 in influencing different tumour phenotypes.


Subject(s)
Interferon Regulatory Factor-1/metabolism , Interferon-gamma/pharmacology , Melanoma/immunology , Cell Line, Tumor , Enzyme Activation , Humans , Immunotherapy , Interferon-gamma/metabolism , Melanoma/therapy , NF-kappa B/metabolism , TOR Serine-Threonine Kinases/metabolism , Transcription, Genetic , Tumor Necrosis Factor-alpha/pharmacology , Wnt Proteins/metabolism , beta Catenin/metabolism
4.
J Blood Disord Transfus ; 4(5)2013 Sep 20.
Article in English | MEDLINE | ID: mdl-25309814

ABSTRACT

BACKGROUND: Endothelial progenitor cells (EPC) are markers of endothelial injury and may serve as a surrogate marker for vascular repair in interventional clinical trials. Objectives of this study were to modify a method of isolation of peripheral blood mononuclear cells (PBMC) and enumeration of EPC and mature endothelial cells (EC) from peripheral blood and to evaluate influence of cryopreservation on viability of PBMC and on numbers of EPC and EC. PATIENTS/METHODS: EPC and EC were analyzed in healthy volunteers in freshly isolated PBMC collected in CPT (cell preparation tubes) and in PBMC cryopreserved with: 1) Gibco Recovery™ Cell Culture Freezing Medium, 2) custom freezing medium. Viability of PBMC was tested using DAPI. EPC were gated for CD45- CD34+CD133+/-VEGFR2+/- and EC were gated for CD45-CD146+CD34+/-VEGFR2+/-. RESULTS: Cryopreservation for 7 days at -80°C decreased viable PBMC from 94 ± 0.5% (fresh) to 84 ± 4% (the custom medium) and to 69 ± 8% (Gibco medium), while cryopreservation at -65°C decreased viability to 60 ± 6% (p<0.001, the custom medium) and 49 ± 5% (p<0.001, Gibco medium). In fresh samples early EPC (CD45- CD34+CD133+VEGFR2+) were enumerated as 0.2 ± 0.06%, late EPC(CD45-CD146+CD34+VEGFR2+) as 0.6 ± 0.1% and mature EC (CD45-CD146+CD34-VEGFR2+) as 0.8 ± 0.3%of live PBMC. Cryopreservation with Gibco and the custom freezing medium at -80°C for 7 days decreased numbers EPC and EC, however, this decrease was not statistically significant. CONCLUSIONS: Our data indicate that cryopreservation at -80°C for 7 days decreases, although not significantly, viability of PBMC and numbers of subsets of EC and EPC. This method may provide an optimized approach to isolation and short-term cryopreservation of subsets of EPC and of mature EC suitable for multicenter trials.

5.
Phys Rev E Stat Nonlin Soft Matter Phys ; 84(5 Pt 2): 055401, 2011 Nov.
Article in English | MEDLINE | ID: mdl-22181466

ABSTRACT

In this paper investigations of the voltage required to break down water vapor are reported for the region around the Paschen minimum and to the left of it. In spite of numerous applications of discharges in biomedicine, and recent studies of discharges in water and vapor bubbles and discharges with liquid water electrodes, studies of the basic parameters of breakdown are lacking. Paschen curves have been measured by recording voltages and currents in the low-current Townsend regime and extrapolating them to zero current. The minimum electrical breakdown voltage for water vapor was found to be 480 V at a pressure times electrode distance (pd) value of around 0.6 Torr cm (~0.8 Pa m). The present measurements are also interpreted using (and add additional insight into) the developing understanding of relevant atomic and particularly surface processes associated with electrical breakdown.


Subject(s)
Biomedical Engineering/methods , Biophysics/methods , Steam , Water/chemistry , Electricity , Electrodes , Equipment Design , Gases , Ions , Pressure
6.
J Fish Biol ; 79(5): 1094-110, 2011 Nov.
Article in English | MEDLINE | ID: mdl-22026595

ABSTRACT

One mtDNA gene (cytochrome b), one nuclear DNA fragment, five microsatellites and a suite of morphological characters were evaluated in samples of Rutilus spp. from Skadar, Ohrid and Prespa Lakes. Both genetic and phenotypic data supported two sympatric taxa in Lake Skadar, whereby Prespa and Ohrid Lakes revealed only a single taxon each. One of the taxa from Lake Skadar was similar to samples from Lake Prespa, whereas the second taxon was the most divergent in the data set. The estimated time to the most recent common ancestor of these two sympatric taxa in Lake Skadar was between 125 000 and 500 000 years. The data did not support existing taxonomic schemes for Rutilus in these lakes. This study poses the following working hypothesis: (1) Rutilus prespensis lives both in Lake Prespa and Lake Skadar and therefore is not endemic to Lake Prespa, (2) Rutilus ohridanus lives in Lake Ohrid only and therefore could be considered an endemic if its species status is retained and (3) a third recently described taxon (Rutilus albus) sympatric to R. prespensis lives in Lake Skadar.


Subject(s)
Cyprinidae/anatomy & histology , Cyprinidae/genetics , Genetic Variation , Lakes , Phenotype , Animals , Classification , Cytochromes b/genetics , Genotype , Microsatellite Repeats/genetics , Molecular Sequence Data , Phylogeny
7.
Neurology ; 75(23): 2059-62, 2010 Dec 07.
Article in English | MEDLINE | ID: mdl-21135380

ABSTRACT

OBJECTIVES: Circulating endothelial progenitor cells (EPC) are markers of vascular injury and their numbers decrease in acute stroke. However, the relation of EPC levels to stroke severity has not been quantified. MRI measurements of lesion volume provide an objective method for stroke severity assessment and outcome prediction. This cross-sectional study aims to determine whether EPC are correlated with lesion volume at baseline, lesion growth, and final lesion volume. METHODS: Seventeen patients (median age 63 years, NIH Stroke Scale score 7) were selected from 175 patients with imaging-confirmed acute ischemic stroke. EPC were quantified by flow cytometry using CD34, CD133, and VEGFR2 surface markers. Brain MRI was performed at baseline and at days 1 and 5 after the stroke onset. Stroke lesion volumes were quantified. RESULTS: Larger lesion volumes measured on diffusion-weighted images (DWI) at baseline were associated with low EPC levels, while smaller lesion volumes and less lesion growth were linked with high levels of EPC subsets (CD34+CD133+, CD133+VEGFR2+, and CD34+ CD133+VEGFR2+). Similar results were observed with DWI lesion volumes and EPC (CD34+CD133+) on day 1. Lesion growth volume, represented as a difference between final lesion volume and baseline DWI, was larger in patients with lower day 1 EPC (CD133+VEGFR2+). After adjustments for age and admission glucose (model 1), mean arterial pressure and white blood cells (model 2), INR and hematocrit (model 3), the CD34+CD133+ subset remained predictive of baseline and day 1 lesion volumes, while CD133+VEGFR2+ predicted baseline lesion volume and growth of lesion volume. CONCLUSIONS: Higher EPC levels were indicative of smaller volumes of acute lesion, final lesion, and lesion growth, and may serve as markers of acute phase stroke severity. However, a larger prospective study is needed to confirm our findings.


Subject(s)
Brain/pathology , Endothelial Cells/pathology , Stem Cells/pathology , Stroke/pathology , Aged , Antigens, CD/metabolism , Diffusion Magnetic Resonance Imaging/methods , Female , Humans , Male , Middle Aged , Pilot Projects , Prospective Studies , Retrospective Studies , Statistics, Nonparametric , Time Factors
8.
J BUON ; 15(1): 136-40, 2010.
Article in English | MEDLINE | ID: mdl-20414941

ABSTRACT

PURPOSE: To find out the trends of distribution in different histological types of lung cancer in both genders in a period of 20 years. METHODS: The most frequent histological types of lung cancer in tissue specimens obtained by bronchoscopy or percutaneous needle biopsy were analysed in terms of age and gender. The studied population included 6289 patients (16.6% females and 83.1% males). Statistical significance was established by x(2) test at the level p<0.05. RESULTS: Squamous cell carcinoma (SCC) prevailed in the total number of patients in all investigated years (58.0%), and separately in male (60.4%) and female (45.7%) patients. This histological type was predominant in all age groups in both genders (41.6% in males and 38.1% in females). CONCLUSION: SCC has the highest incidence in Serbia. Continuous campaign against smoking and helping its cessation, improving working and socioeconomic conditions is a strategy for decreasing all histological types of lung cancer patients.


Subject(s)
Adenocarcinoma/epidemiology , Adenocarcinoma/pathology , Carcinoma, Squamous Cell/epidemiology , Carcinoma, Squamous Cell/pathology , Lung Neoplasms/epidemiology , Lung Neoplasms/pathology , Small Cell Lung Carcinoma/epidemiology , Small Cell Lung Carcinoma/pathology , Age Distribution , Aged , Biopsy, Needle , Bronchoscopy , Chi-Square Distribution , Female , Humans , Incidence , Male , Middle Aged , Retrospective Studies , Risk Factors , Serbia/epidemiology , Sex Distribution , Time Factors
9.
Mikrobiologiia ; 79(6): 812-8, 2010.
Article in English | MEDLINE | ID: mdl-21446633

ABSTRACT

The aim of the research is to explore the overall in vitro antioxidant activity, total phenol content, reduction power and antimicrobial activity of the methanol extracts of the lichens Cetraria pinastri, Cladonia digitata, Cladonia fimbriata, Fulgensia fulgens, Ochrolechia parella and Parmelia crinita. The methanol extract of the Cetraria pinastri showed a strong antioxidant activity, whereas the extracts of the species Fulgenesi fulgens, Cladonia fimbriata and Parmelia crinita showed the moderate one and the extract of the species Ochrolechia parella and Cladonia digitata the weak one. The methanol extract of the lichen Cetraria pinastri had the biggest total phenol content (32.9 mg/g of the dry extract). A certain correlation was established between the antioxidant activity and the total phenol content for the researched lichen extracts. The work also explores the antimicrobial activity of the methanol extracts of the mentioned species of lichens against six bacterial and eleven fungi species by the disc-diffusion method and by establishing the minimum inhibitory concentration (MIC). The methanol extracts of the lichens Cetraria pinastri and Parmelia crinita showed the strongest both antibacterial and antifungal activity against most of the tested microorganisms. These researches suggest that the lichens Cetraria prunastri can be used as new sources of the natural antioxidants and the substances with antimicrobial features.


Subject(s)
Anti-Bacterial Agents/pharmacology , Antifungal Agents/pharmacology , Antioxidants/pharmacology , Lichens/chemistry , Plant Extracts/pharmacology , Bacteria/drug effects , Fungi/drug effects , Ketoconazole/pharmacology , Methanol/chemistry , Microbial Sensitivity Tests , Phenols/analysis , Plant Extracts/chemistry , Streptomycin/pharmacology , Structure-Activity Relationship
10.
Neoplasma ; 57(1): 1-7, 2010.
Article in English | MEDLINE | ID: mdl-19895165

ABSTRACT

UNLABELLED: Patients with advanced non-small cell lung cancer (NSCLC) usually undergo toxic treatment (chemotherapy and/or radiotherapy). They can experience devastating effects of illness and therapies on their psychological and emotional well-being. On the other hand, untreated psychological distress is associated with reduced quality of life and inadequate palliation of physical symptoms.
In order to estimate frequency of anxiety and depressive symptoms and influence of demographic, socioeconomic and clinical factors on psychological well-being, we performed this cross-sectional study in group of 100 patients with advanced stage of disease. Symptoms of anxiety and depression were assessed using the Hamilton Anxiety Rating Scale (HARS) and Hamilton Depression Rating scale (HDRS). Health-related quality of life data are obtained by EORTC QLC C30 and SF 36.
Patients with poor performance status (PS) experienced significantly more anxiety and depressive symptoms (p=0.001) and worse emotional (p=0.001) and mental functioning (p=0.001). Treated patients had significantly better mental (p=0.011) and emotional (p=0.001) functioning in compared to newly diagnosed ones. Somewhat unusual, unemployed participants reported significantly less anxiety (p=0.029) and depressive (p=0.002) symptoms, better mental (p=0.030) and emotional functioning (p=0.007). Additionally, nausea and vomiting adversely affected mental health and emotional functioning and correlated significantly positively with HARS and HDRS scores.
Our findings suggest significant impact of some disease-related factors (PS, active treatment) and treatment-related factors (chemotherapy -induced nausea and vomiting) on psychological well-being of patients with advanced NSCLC. This should be taking an account when appropriate interventions are planned. KEYWORDS: lung cancer, anxiety, depression, quality of life, chemotherapy, chemotherapy-induced nausea and vomiting.


Subject(s)
Carcinoma, Non-Small-Cell Lung/psychology , Lung Neoplasms/drug therapy , Age Factors , Aged , Antineoplastic Agents/adverse effects , Anxiety/etiology , Carcinoma, Non-Small-Cell Lung/drug therapy , Cross-Sectional Studies , Depression/etiology , Female , Humans , Lung Neoplasms/psychology , Male , Middle Aged , Quality of Life , Serbia , Sex Factors
11.
Eur J Cancer Care (Engl) ; 19(5): 594-602, 2010 Sep.
Article in English | MEDLINE | ID: mdl-20030692

ABSTRACT

The objective of this study was to assess health-related quality of life (HRQoL) in patients with advanced non-small cell lung cancer (NSCLC). In Serbia, there is the lack of available data on HRQoL in lung cancer patients. The special attention in our study has been paid on relationships between socio-economic factors and HRQoL. This cross-sectional study was undertaken in group of 100 NSCLC patients with advanced stage diseases. HRQoL was measured using three standard instruments: 36-item Short Form Health Survey, EORTC QLQ-C30 and its Lung Cancer module (EORTC QLQ-LC13). Unexpected, highly educated patients reported significantly worse social functioning (P=0.044), and higher degree of financial difficulties (P=0.047), in comparison with less-educated. Also unusual, unemployed patients had significantly better HRQoL in all domains and significantly lower symptom distress. Significantly better overall HRQoL (P=0.043), social (P=0.024), emotional (P=0.001) and mental functioning (P=0.011) were observed in patients treated with chemotherapy in comparison with newly diagnosed ones. In addition, the most prominent side effects of chemotherapy were nausea and vomiting, and all QoL domains correlated significantly with them. Patients who undergo active treatment improve their HRQoL but chemotherapy-induced emesis adversely affects many HRQoL domains. Additionally, HRQoL is highly dependent on patient's socio-economic characteristic.


Subject(s)
Antineoplastic Agents/adverse effects , Carcinoma, Non-Small-Cell Lung/drug therapy , Lung Neoplasms/drug therapy , Quality of Life , Carcinoma, Non-Small-Cell Lung/economics , Cross-Sectional Studies , Female , Health Status , Humans , Lung Neoplasms/economics , Male , Middle Aged , Nausea/chemically induced , Serbia , Socioeconomic Factors , Surveys and Questionnaires , Vomiting/chemically induced
12.
Stress ; 11(5): 370-80, 2008 Sep.
Article in English | MEDLINE | ID: mdl-18800309

ABSTRACT

The ability of immobilization stress (IMO) to decrease Leydig cell steroidogenesis and serum androgen concentration has been previously observed, but the possible mechanism(s) involved in the adaptation to prolonged or repeated stress have not been identified. In this study, we investigated whether the Leydig cells obtained from adult rats subjected to acute (15 min, 30 min or 2 h) and repeated (2 or 10 days, 2 h daily) IMO show adaptive mechanism(s) in response to stress-impaired steroidogenesis. The results showed that basal and human chorionic gonadotropin-stimulated cAMP production by Leydig cells isolated from rats exposed to both acute and repeated IMO was significantly reduced. Despite the reduced cAMP production, immunoblot analysis revealed increased immunoreactivity for both protein kinase A (PKA) and steroidogenic acute regulatory (StAR) protein in Leydig cells obtained from rats repeatedly exposed to IMO. Also, the phosphorylation and production of mature StAR protein was evident during exposure of rats to repeated IMO treatment. Treatment with cholesterol, the steroid substrate transported into mitochondria by StAR, significantly increased androgen and progesterone production by Leydig cells isolated from rats exposed to repeated IMO. In contrast, when other steroid substrates (22(R)-OH-cholesterol, pregnenolone, progesterone, Delta4-androstenedione) were present in the culture media, Leydig cell steroidogenesis was still reduced by IMO. Thus, PKA-mediated phosphorylation of StAR protein is an important mechanism in the adaptive response of Leydig cells to repeated IMO.


Subject(s)
Cyclic AMP-Dependent Protein Kinases/biosynthesis , Leydig Cells/metabolism , Phosphoproteins/biosynthesis , Restraint, Physical/physiology , Adaptation, Physiological/physiology , Animals , Luteinizing Hormone/blood , Male , Rats , Rats, Wistar , Testosterone/blood
13.
Neuroscience ; 153(4): 1126-34, 2008 Jun 02.
Article in English | MEDLINE | ID: mdl-18440154

ABSTRACT

Posttraumatic stress disorder (PTSD) is one of the most common psychiatric disorders. Despite the extensive study of the neurobiological correlates of this disorder, the underlying mechanisms of PTSD are still poorly understood. Recently, a study demonstrated that dexamethasone (Dex), a synthetic glucocorticoid, can up-regulate p11, known as S100A10-protein which is down-regulated in patients with depression, (Yao et al., 1999; Huang et al., 2003) a common comorbid disorder in PTSD. These observations led to our hypothesis that traumatic stress may alter expression of p11 mediated through a glucocorticoid receptor. Here, we demonstrate that inescapable tail shock increased both prefrontal cortical p11 mRNA levels and plasma corticosterone levels in rats. We also found that Dex up-regulated p11 expression in SH-SY5Y cells through glucocorticoid response elements (GREs) within the p11 promoter. This response was attenuated by either RU486, a glucocorticoid receptor (GR) antagonist or mutating two of three glucocorticoid response elements (GRE2 and GRE3) in the p11 promoter. Finally, we showed that p11 mRNA levels were increased in postmortem prefrontal cortical tissue (area 46) of patients with PTSD. The data obtained from our work in a rat model of inescapable tail shock, a p11-transfected cell line and postmortem brain tissue from PTSD patients outline a possible mechanism by which p11 is regulated by glucocorticoids elevated by traumatic stress.


Subject(s)
Annexin A2/metabolism , Dexamethasone/pharmacology , Glucocorticoids/pharmacology , Nuclear Proteins/metabolism , Promoter Regions, Genetic/drug effects , Prosencephalon/metabolism , S100 Proteins/metabolism , Stress, Psychological/pathology , Up-Regulation/drug effects , Animals , Animals, Newborn , Annexin A2/genetics , Cells, Cultured , Chromatin Immunoprecipitation/methods , Disease Models, Animal , Dose-Response Relationship, Drug , Drug Interactions , Electroshock/adverse effects , Hormone Antagonists/pharmacology , Humans , Male , Mifepristone/pharmacology , Nuclear Proteins/genetics , Prosencephalon/cytology , Prosencephalon/drug effects , Rats , Rats, Sprague-Dawley , S100 Proteins/genetics , Stress, Psychological/etiology , Time Factors , Up-Regulation/physiology
14.
Phys Rev E Stat Nonlin Soft Matter Phys ; 74(2 Pt 2): 026406, 2006 Aug.
Article in English | MEDLINE | ID: mdl-17025549

ABSTRACT

In this paper we present measurements of the secondary electron emission yield (gamma) of a carbonaceous dust particle material, which was grown in argon diluted acetylene plasmas. One aim was to reach a better understanding of charging and discharging processes of dust particles in complex plasmas due to secondary electron emission and consequently to try to explain the anomalous behavior of electron density observed in afterglows of pulsed rf plasmas. We compared the results of a simple model and of a Monte Carlo simulation to the previously measured time dependence of the electron density in complex plasma afterglow. It was found that the value of the intrinsic secondary electron yield from the carbonaceous dust material is too low to explain the increase of electron density in the afterglow. It is, however, possible that the electrons charging the particles are weakly attached so that they may be released with high efficiency by ion bombardment due to field induced emission or by other mechanisms.

15.
Neuroscience ; 131(2): 275-82, 2005.
Article in English | MEDLINE | ID: mdl-15708472

ABSTRACT

17Beta-estradiol (E2) is a major neuroregulator, exerting both genomic and non-genomic actions. E2 regulation of Slack (sequence like a calcium-activated potassium channel) potassium channels has not been identified in the CNS. We demonstrate E2-induced activation of Slack channels, which display a unitary conductance of about 60 pS, are inhibited by intracellular calcium, and are abundantly expressed in the nervous system. In lipid bilayers derived from rat cortical neuronal membranes, E2 increases Slack open probability and appears to decrease channel inactivation. Additionally, E2 binds to the Slack channel and activates outward currents in human embryonic kidney-293 cells that express Slack channels but not classical estrogen receptors (i.e. ERalpha or ERbeta). Neither E2-induced activation nor the binding intensity of E2 to the Slack channel is blocked by tamoxifen, an ER antagonist/agonist. Thus, E2 activates a potassium channel, Slack, through a non-traditional membrane binding site, adding to known non-genomic mechanisms by which E2 exerts pharmacological and toxicological effects in the CNS.


Subject(s)
Estradiol/metabolism , Nerve Tissue Proteins/metabolism , Potassium Channels/metabolism , Animals , Cell Line , Dose-Response Relationship, Drug , Humans , Nerve Tissue Proteins/genetics , Neurons/metabolism , Potassium Channels/genetics , Potassium Channels, Sodium-Activated , Protein Binding/physiology
16.
Exp Neurol ; 190(2): 276-88, 2004 Dec.
Article in English | MEDLINE | ID: mdl-15530869

ABSTRACT

The mammalian central nervous system (CNS) has little capacity for self-repair after injury, and neurons are not capable of proliferating. Therefore, neural tissue engineering that combines neural stem and progenitor cells and biologically derived polymer scaffolds may revolutionize the medical approach to the treatment of damaged CNS tissues. Neural stem and progenitor cells isolated from embryonic rat cortical or subcortical neuroepithelium were dispersed within type I collagen, and the cell-collagen constructs were cultured in serum-free medium containing basic fibroblast growth factor. The collagen-entrapped stem and progenitors actively expanded and efficiently generated neurons, which developed neuronal polarity, neurotransmitters, ion channels/receptors, and excitability. Ca2+ imaging showed that differentiation from BrdU+/TuJ1- to BrdU-/TuJ1+ cells was accompanied by a shift in expression of functional receptors for neurotransmitters from cholinergic and purinergic to predominantly GABAergic and glutamatergic. Spontaneous postsynaptic currents were recorded by patch-clamping from precursor cell-derived neurons and these currents were partially blocked by 10-microM bicuculline, and completely blocked by additional 10 microM of the kainate receptor antagonist CNQX, indicating an appearance of both GABAergic and glutamatergic synaptic activities. Staining with endocytotic marker FM1-43 demonstrated active synaptic vesicle recycling occurring among collagen-entrapped neurons. These results show that neural stem and progenitor cells cultured in 3D collagen gels recapitulate CNS stem cell development; this is the first demonstration of CNS stem and progenitor cell-derived functional synapse and neuronal network formation in a 3D matrix. The proliferative capacity and neuronal differentiating potential of neural progenitors in 3D collagen gels suggest their potential use in attempts to promote neuronal regeneration in vivo.


Subject(s)
Cell Differentiation/physiology , Collagen Type I , Gels , Neurons/cytology , Stem Cells/cytology , Tissue Engineering/methods , Animals , Astrocytes/cytology , Brain/cytology , Brain/metabolism , Cell Proliferation , Cells, Cultured , Embryo, Mammalian , Immunohistochemistry , Microscopy, Confocal , Neurons/metabolism , Oligodendroglia/cytology , Patch-Clamp Techniques , Rats , Stem Cells/metabolism
17.
Neurology ; 63(8): 1446-51, 2004 Oct 26.
Article in English | MEDLINE | ID: mdl-15505163

ABSTRACT

OBJECTIVE: To determine if the CD4+CD28- T-cell subset is expanded in patients with recurrent stroke or death after acute ischemic stroke. This subset of the peripheral blood T-cell lymphocyte population has a strong pro-inflammatory and tissue-damaging potential. METHODS: Consecutive patients within the first 48 hours of ischemic stroke were prospectively studied. Peripheral blood CD4+CD28- cells were quantified by flow cytometry. The study endpoint was recurrent stroke or death from any cause during 1 year of follow-up. RESULTS: One hundred six patients (mean age 75.0 +/- 13.5 years; 50 women) were studied. The median CD4+CD28- cell count was 4.5% (range 0.2 to 72.2%). Twenty-seven endpoints (10 recurrent strokes and 17 deaths) occurred during follow-up. Stroke recurrence/death rates were significantly associated with increasing CD4+CD28- counts, rising from 14.2% in patients with CD4+CD28- levels of <1.0 to 48.1% for those with CD4+CD28- counts of >8.0% (p = 0.003, Cochran linear test of trend). Higher CD4+CD28- counts were also present in patients with a history of prior stroke (p = 0.03). After adjustment for age, admission NIH Stroke Scale score, prior stroke, and atrial fibrillation, CD4+CD28- counts of >8.0% were associated with a cumulative hazard ratio of 5.81 (95% CI: 1.58 to 21.32) for stroke recurrence or death. CONCLUSIONS: Rising counts of circulating CD4+CD28- cells are associated with an increasing risk of stroke recurrence and death, in addition to an observed association with prior stroke. Expansion of this T-cell subset presumably represents a biomarker and possibly a contributory pathogenic mechanism of recurrent stroke and death after ischemic stroke.


Subject(s)
Brain Ischemia/immunology , CD28 Antigens/immunology , CD4-Positive T-Lymphocytes/immunology , Lymphocytes/immunology , Stroke/immunology , T-Lymphocyte Subsets/immunology , Acute Disease , Aged , Aged, 80 and over , Atrial Fibrillation/complications , Biomarkers/blood , Brain Ischemia/blood , Brain Ischemia/mortality , CD4 Lymphocyte Count , Encephalitis/immunology , Encephalitis/physiopathology , Female , Humans , Lymphocyte Activation/immunology , Male , Middle Aged , Mortality , Predictive Value of Tests , Prospective Studies , Recurrence , Risk Factors , Stroke/blood , Stroke/mortality , Up-Regulation/immunology
18.
J BUON ; 9(4): 423-6, 2004.
Article in English | MEDLINE | ID: mdl-17415849

ABSTRACT

PURPOSE: The morphology of the epithelioid malignant mesothelioma (MM) of the pleura is similar to lung adenocarcinoma involving pleura. The aim of this study was to evaluate the value of immunohistochemistry in the accurate diagnosis of MM, especially of the epithelioid type with needle biopsy of the pleura. MATERIALS AND METHODS: The diagnosis of MM was established with pleural needle biopsy and tumor immunophenotyping in 30 patients. A broad spectrum of monoclonal antibodies was applied: HBME-1, E-cadherin, calretinin, cytokeratin 5/6, vimentin, thyroid transcription factor (TTF-1) and surfactant apoprotein A (SP-A). RESULTS: We diagnosed 24 epithelioid, 2 biphasic and 4 sarcomatoid MM. HMBE-1 was the most sensitive tumor marker of the epithelioid type, being positive in 100% of the cases. Calretinin, E-cadherin and cytokeratin 5/6 were positive in 70%, 73%, and 50% of all tumors, respectively. TTF-1 and SP-A were negative in all MM. Vimentin was positive in spindle cells of all sarcomatoid and biphasic MM (20%). CONCLUSION: The accurate diagnosis of MM is mandatory for appropriate treatment decision (surgical or nonsurgical). Our results demonstrate that HMBE-1 is a most useful diagnostic antibody for epithelioid MM, and TTF-1 for lung adenocarcinoma (its thyroid origin excluded) involving pleura.

19.
Neuroscience ; 118(1): 37-47, 2003.
Article in English | MEDLINE | ID: mdl-12676135

ABSTRACT

We have expanded neuroepithelial cells dissociated from the embryonic rat telencephalon in serum-free defined medium containing basic fibroblast growth factor (bFGF) in order to generate a model neuroepithelium to study the interaction of ethanol with both growth factor- and transmitter-stimulated proliferation. Ethanol blocked proliferation stimulated by bFGF and by carbachol, an agonist at muscarinic acetylcholine receptors, in a dose-dependent manner. In addition, ethanol attenuated autonomous expansion of neuroepithelial cells occurring following withdrawal of bFGF. The latter effect was associated with an increase in the number of apoptotic cells identified by terminal deoxynucleotidyltransferase-mediated dUTP nick end labeling labeling. We studied the effects of ethanol on carbachol-stimulated signaling pathways critical to its proliferative effects. Ethanol significantly reduced carbachol-stimulated Ca(2+) signaling, as well as Erk1/Erk2, Akt and cyclic AMP-response element-binding phosphorylations in a dose-dependent manner. Comparison of the potency of ethanol in attenuating carbachol-stimulated proliferation and signal transduction showed that mitogen-activated protein kinase phosphorylation was less sensitive to ethanol than the other parameters. The results indicate that ethanol's suppression of proliferation induced by carbachol in this model neuroepithelium likely involves multiple signaling pathways. These effects in vitro may help to explain the devastating effects of prenatal ethanol exposure in vivo, which contribute to the fetal alcohol syndrome.


Subject(s)
Alcohol-Induced Disorders, Nervous System/metabolism , Brain/drug effects , Cell Division/drug effects , Ethanol/toxicity , Fetal Alcohol Spectrum Disorders/metabolism , Neurons/drug effects , Protein Serine-Threonine Kinases , Stem Cells/drug effects , Acetylcholine/antagonists & inhibitors , Acetylcholine/metabolism , Alcohol-Induced Disorders, Nervous System/physiopathology , Animals , Brain/embryology , Brain/physiopathology , Calcium Signaling/drug effects , Calcium Signaling/physiology , Carbachol/antagonists & inhibitors , Cell Division/physiology , Cells, Cultured , Cyclic AMP Response Element-Binding Protein/drug effects , Cyclic AMP Response Element-Binding Protein/metabolism , Female , Fetal Alcohol Spectrum Disorders/physiopathology , Fetus , Fibroblast Growth Factor 2/antagonists & inhibitors , Fibroblast Growth Factor 2/deficiency , MAP Kinase Signaling System/drug effects , MAP Kinase Signaling System/physiology , Muscarinic Antagonists/toxicity , Neurons/metabolism , Pregnancy , Proto-Oncogene Proteins/drug effects , Proto-Oncogene Proteins/metabolism , Proto-Oncogene Proteins c-akt , Rats , Rats, Sprague-Dawley , Receptors, Muscarinic/drug effects , Receptors, Muscarinic/metabolism , Stem Cells/metabolism
20.
Selección (Madr.) ; 11(5): 351-354, dic. 2002.
Article in Es | IBECS | ID: ibc-18449

ABSTRACT

El tratamiento de lesiones músculoesqueléticas mediante ondas de choque extracorpóreas, ha suscitado el interés de la comunidad científica europea en los últimos veinte años. A nivel mundial ha despertado enorme interés desde que la F.D.A. (Federal Drug Administration) norteamericana aprobara su uso para el tratamiento conservador de la fascitis plantar en octubre de 2000. En la actualidad las ondas de choque extracorpóreas se presentan como una alternativa más en el arsenal de los métodos conservadores del tratamiento de las afecciones del aparato locomotor. Este artículo de revisión resume el estado actual de la evidencia científica de la indicación del uso de las ondas de choque extracorpóreas en patología músculoesquelética (AU)


Subject(s)
Humans , Musculoskeletal Diseases/therapy , Lithotripsy
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