RESUMO
Mesenchymal stem cells (MSCs) have been used to repair connective tissue defects in several animal models. Compared to "natural healing" controls (no added cells), MSC-collagen gel constructs in rabbit tendon defects significantly improve repair biomechanics. However, ectopic bone forms in 28% of MSC-treated rabbit tendons. To understand the source of bone formation, three studies were performed. In the first study, the hypothesis was tested that MSCs delivered during surgery contribute to bone formation in the in vivo repair site. Adjacent histological sections in the MSC-treated repair tissue were examined for pre-labeled MSCs and for cells showing positive alkaline phosphatase (ALP) activity. Both cells were observed in serial sections in regions of ectopic bone. Contralateral "natural healing" tendons lacked both markers. In the other two studies, the effects of osteogenic supplements and construct geometry (monolayer vs. 3-D) on ALP activity were studied to test three hypotheses: that rabbit MSCs increase ALP activity over time in monolayer culture conditions; that adding osteogenic inducing supplements to the culture medium increases cellular protein in monolayer culture; and that rabbit MSCs increase ALP activity both in monolayer and in 3-D constructs, with and without media supplements. Culture in monolayer under similar conditions to in vivo (as in the first study) did not increase ALP at 2 or 4 weeks. Medium designed to increase osteogenic activity significantly increased cell numbers (cellular protein increased by 260%) but did not affect ALP activity either in monolayer or 3-D constructs (p>0.12). However, MSCs in 3-D constructs exhibited higher ALP activity than cells in monolayer, both in the presence (p<0.045) and absence of supplement (p<0.005). These results suggest that in vitro conditions may critically influence cell differentiation and protein expression. Mechanisms responsible for these effects are currently under investigation.
Assuntos
Fosfatase Alcalina/metabolismo , Transplante de Células-Tronco Mesenquimais , Células-Tronco Mesenquimais/citologia , Osteogênese , Tendões/cirurgia , Animais , Diferenciação Celular , Feminino , Células-Tronco Mesenquimais/enzimologia , CoelhosAssuntos
Jogo de Azar , Trabalho Sexual , Fatores Socioeconômicos , Viagem , California/etnologia , Jogo de Azar/psicologia , História do Século XX , Renda/história , México/etnologia , Sistemas Políticos/história , Trabalho Sexual/etnologia , Trabalho Sexual/história , Trabalho Sexual/legislação & jurisprudência , Trabalho Sexual/psicologia , Viagem/economia , Viagem/história , Viagem/legislação & jurisprudência , Viagem/psicologia , Saúde da Mulher/economia , Saúde da Mulher/etnologia , Saúde da Mulher/história , Saúde da Mulher/legislação & jurisprudência , Mulheres Trabalhadoras/educação , Mulheres Trabalhadoras/história , Mulheres Trabalhadoras/legislação & jurisprudência , Mulheres Trabalhadoras/psicologiaRESUMO
Botulinum toxin is a valuable technology for the treatment of regional movement disease. High-dose applications ( > 100 LD50 units per injection cycle) have been associated with sensitization that renders further therapeutic injections ineffective. The true incidence of sensitization is probably underestimated by the mouse bioassay. Other immunotypes of botulinum toxin have been effective in producing some therapeutic benefit; however, duration of action (botulinum toxin type F) and lower potencies may make these less attractive alternatives than botulinum type A. Increased specific activity botulinum toxin may be a method to reduce antigen exposure and mitigate against immunoresistance associated with dystonia therapy. Limiting the dose to < or = 100 LD50 units per injection cycle may limit this complication in the interim.
Assuntos
Toxinas Botulínicas/imunologia , Toxinas Botulínicas/uso terapêutico , Transtornos dos Movimentos/tratamento farmacológico , Humanos , Transtornos dos Movimentos/imunologiaRESUMO
Crystalline botulinum toxin type A was licensed in December 1989 by the Food and Drug Administration for treatment of certain spasmodic muscle disorders following 10 or more years of experimental treatment on human volunteers. Botulinum toxin exerts its action on a muscle indirectly by blocking the release of the neurotransmitter acetylcholine at the nerve ending, resulting in reduced muscle activity or paralysis. The injection of only nanogram quantities (1 ng = 30 mouse 50% lethal doses [U]) of the toxin into a spastic muscle is required to bring about the desired muscle control. The type A toxin produced in anaerobic culture and purified in crystalline form has a specific toxicity in mice of 3 x 10(7) U/mg. The crystalline toxin is a high-molecular-weight protein of 900,000 Mr and is composed of two molecules of neurotoxin (ca. 150,000 Mr) noncovalently bound to nontoxic proteins that play an important role in the stability of the toxic unit and its effective toxicity. Because the toxin is administered by injection directly into neuromuscular tissue, the methods of culturing and purification are vital. Its chemical, physical, and biological properties as applied to its use in medicine are described. Dilution and drying of the toxin for dispensing causes some detoxification, and the mouse assay is the only means of evaluation for human treatment. Other microbial neurotoxins may have uses in medicine; these include serotypes of botulinum toxins and tetanus toxin. Certain neurotoxins produced by dinoflagellates, including saxitoxin and tetrodotoxin, cause muscle paralysis through their effect on the action potential at the voltage-gated sodium channel. Saxitoxin used with anaesthetics lengthens the effect of the anaesthetic and may enhance the effectiveness of other medical drugs. Combining toxins with drugs could increase their effectiveness in treatment of human disease.
Assuntos
Toxinas Bacterianas/farmacologia , Doenças Musculares/tratamento farmacológico , Neurotoxinas/uso terapêutico , Toxinas Botulínicas/farmacologia , Humanos , Saxitoxina/farmacologia , Tetrodotoxina/farmacologia , Fatores de Virulência de Bordetella/farmacologiaRESUMO
The amino acid sequence of staphylococcal enterotoxin A is presented. Staphylococcal enterotoxin A is a single-chain polypeptide which consists of 233 amino acid residues with a molecular weight of 27,078 and has the amino acid composition Cys2, Asp17, Asn19, Thr16, Ser13, Glu15, Gln12, Pro4, Gly15, Ala7, Val13, Met2, Ile10, Leu23, Tyr18, Phe8, His6, Lys24, Arg7, Trp2, with serine as both amino- and carboxyl-terminal amino acids. Automated sequence analysis of intact enterotoxin A, as well as characterization of the peptides obtained from cyanogen bromide treatment and trypsin and chymotrypsin digestion, led to the elucidation of the complete primary structure of this protein. Less structural homology is observed among staphylococcal enterotoxins A, B (Huang, I-Y., and Bergdoll, M. S. (1970) J. Biol. Chem. 245, 3518-3525), and C1 (Schmidt, J. J., and Spero, L. (1983) J. Biol. Chem. 258, 6300-6306) than that seen between enterotoxins B and C1.
Assuntos
Enterotoxinas , Sequência de Aminoácidos , Quimotripsina/metabolismo , Brometo de Cianogênio/metabolismo , Enterotoxinas/metabolismo , Peso Molecular , Fragmentos de Peptídeos/metabolismo , Staphylococcus aureus , Tripsina/metabolismoAssuntos
Saxitoxina , Animais , Humanos , Toxinas Marinhas , Camundongos , Saúde Pública , Saxitoxina/toxicidade , Frutos do Mar , Relação Estrutura-AtividadeRESUMO
Samples of Saxidomus nuttali and Mytilus californianus collected during the 1981 dinoflagellate bloom at Bodega Bay, California, were analyzed for the presence of paralytic toxins. Neck tissue of S. nuttali contained saxitoxin (STX) and neoSTX (95% of the total toxicity), whereas the bodies contained neoSTX and a mixture of the gonyautoxins. In a sample of M. californianus the presence of neoSTX and the gonyautoxins was demonstrated, whereas a second sample, collected at a different site, contained almost exclusively neoSTX.
Assuntos
Bivalves/metabolismo , Dinoflagellida/metabolismo , Toxinas Marinhas/análise , Moluscos/metabolismo , Paralisia/induzido quimicamente , Animais , California , Cromatografia em Camada Fina , Masculino , Toxinas Marinhas/toxicidade , Camundongos , Camundongos Endogâmicos ICR , Saxitoxina/análogos & derivados , Saxitoxina/análiseRESUMO
Extracellular proteins produced by Bacillus cereus B-4ac were separated by chromatography on Amberlite CG-400, QAE-Sephadex, Sephadex G-75, and hydroxylapatite. A fraction, containing three detectable antigens, obtained from chromatography on hydroxylapatite caused fluid accumulation in ligated rabbit ileal loops, was dermonecrotic to rabbit skin, was cytotoxic to cultured cells, and was lethal to mice after intravenous injection. Two other fractions obtained from chromatography on hydroxylapatite showed essentially no toxic activity when tested individually. Each nontoxic fraction contained two of the three proteins present in the toxic material. When the two nontoxic fractions were combined, activity in all of the biological assays was observed. Antiserum against either of the nontoxic fractions neutralized the dermonecrotic response of the combined material. These results suggest that all of these biological activities probably are due to a single entity and that more than one component probably comprise the toxic entity.
Assuntos
Antígenos de Bactérias/isolamento & purificação , Bacillus cereus/análise , Enterotoxinas/isolamento & purificação , Animais , Anticorpos Antibacterianos , Reações Antígeno-Anticorpo , Antígenos de Bactérias/administração & dosagem , Antígenos de Bactérias/imunologia , Bacillus cereus/imunologia , Diarreia/etiologia , Diarreia/microbiologia , Enterotoxinas/administração & dosagem , Enterotoxinas/imunologia , Feminino , Concentração de Íons de Hidrogênio , Macaca mulatta , Masculino , Peso Molecular , Testes de Neutralização , CoelhosRESUMO
A report focused on the causes of paralytic shellfish poisoning and the precautions that should be taken to prevent outbreaks of this disease. Chapters offer a description of the marine organisms concerned and the methods for the detection and toxicological analysis of the biotoxins involved. The book concludes with an outline of the principles required in surveillance programmes