RESUMO
Vascular endothelial cells synthesize and secrete perlecan, a large heparan sulfate proteoglycan that increases the anticoagulant activity of vascular endothelium by inducing antithrombin III and intensifying fibroblast growth factor (FGF)-2 activity to promote migration and proliferation in the repair process of damaged endothelium during the progression of atherosclerosis. However, the exact regulatory mechanisms of endothelial perlecan expression remain unclear. Since organic-inorganic hybrid molecules are being developed rapidly as tools to analyze biological systems, we searched for a molecular probe to analyze these mechanisms using a library of organoantimony compounds and found that the Sb-phenyl-N-methyl-5,6,7,12-tetrahydrodibenz[c,f][1,5]azastibocine (PMTAS) molecule promotes the expression of perlecan core protein gene without exhibiting cytotoxicity in vascular endothelial cells. In the present study, we characterized proteoglycans synthesized by cultured bovine aortic endothelial cells using biochemical techniques. The results indicated that PMTAS selectively induced perlecan core protein synthesis, without affecting the formation of its heparan sulfate chain, in vascular endothelial cells. The results also implied that this process is independent of the endothelial cell density, whereas in vascular smooth muscle cells, it occurred only at high cell density. Thus, PMTAS would be a useful tool for further studies on the mechanisms underlying perlecan core protein synthesis in vascular cells, which is critical in the progression of vascular lesions, such as those during atherosclerosis.
Assuntos
Antimônio , Células Endoteliais , Proteoglicanas de Heparan Sulfato , Compostos Organometálicos , Animais , Bovinos , Antimônio/farmacologia , Aterosclerose/metabolismo , Células Cultivadas , Células Endoteliais/efeitos dos fármacos , Células Endoteliais/metabolismo , Proteínas da Matriz Extracelular/metabolismo , Proteoglicanas de Heparan Sulfato/metabolismo , Heparitina Sulfato/metabolismo , Compostos Organometálicos/farmacologiaRESUMO
Adult T-cell leukemia is one of the life-threatening diseases that occur in individuals infected with human T-cell leukemia virus type 1 (HTLV-1). Clinical trials of hematopoietic stem cell transplantation therapy are being performed in addition to chemotherapy; however, neither is satisfactory. As a pretreatment for transplantation, anticancer drugs or whole-body irradiation is used to decrease the number of HTLV-1-infected cells, but there are numerous side effects. Therefore, in the present study, using a mouse model of HTLV-1 infection, the long-term survival and number of infected cells in the reservoir organ were investigated in order to determine the effect of γ-irradiation on HTLV-1-infected mice in vivo. There was no improvement in the survival period following γ-irradiation in the γ-irradiated group after HTLV-1 infection when compared with the HTLV-1-infected group. It was also found that the incidence of splenomegaly was ≥80% in the HTLV-1-infected and γ-irradiated group, which was significantly higher than that in the HTLV-1-infected mice. The tissue morphology in the spleen became non-uniform because of γ-rays. Importantly, the number of infected cells in the spleen was increased 4.1-fold in the HTLV-1-infected and γ-irradiated mice compared with that in the HTLV-1-infected mice. Careful consideration might be necessary when using whole-body irradiation in patients with HTLV-1 infection.
Assuntos
Infecções por HTLV-I/radioterapia , Vírus Linfotrópico T Tipo 1 Humano/fisiologia , Irradiação Corporal Total , Animais , Feminino , Linfoma/patologia , Camundongos Endogâmicos C57BL , Baço/patologia , Esplenomegalia/patologia , Timo/patologia , Carga ViralRESUMO
Extracts of bitter melon, soybean, dokudami and welsh onion by 40% methanol increased the accumulation of rhodamine-123 by Caco-2 cells, suggesting that these extracts inhibited P-glycoprotein (P-gp). The extract of bitter melon was separated in a tC18 cartridge column and the eluate from 80% acetonitrile most markedly increased the [(3)H]-daunomycin accumulation by Caco-2 cells. The inhibitory compounds in the bitter melon fraction were isolated by HPLC with Pegasil C4 and Pegasil ODS columns. The HPLC fraction having the highest activity was analyzed by (1)H-NMR and FAB-MS, and the active compound was identified as 1-monopalmitin. The inhibitory activities of 1-monopalmitin and its related compounds suggested that the inhibition of P-gp activity was not dependent on the degree of unsaturation of fatty acid in the monoglyceride, but on the chain length. It was also suggested that the monoglyceride structure played an important role in the inhibition of P-gp activity. Monoglycerides could therefore alter the pharmacokinetics of drugs by inhibiting the P-gp-mediated efflux.
Assuntos
Subfamília B de Transportador de Cassetes de Ligação de ATP/metabolismo , Momordica charantia , Extratos Vegetais/farmacologia , Subfamília B de Transportador de Cassetes de Ligação de ATP/antagonistas & inibidores , Adenocarcinoma/metabolismo , Adenocarcinoma/patologia , Aminoácidos/farmacocinética , Transporte Biológico/efeitos dos fármacos , Células CACO-2 , Cromatografia Líquida de Alta Pressão/métodos , Neoplasias do Colo/metabolismo , Neoplasias do Colo/patologia , Daunorrubicina/farmacocinética , Relação Dose-Resposta a Droga , Frutas , Glicerídeos/farmacologia , Temperatura Alta , Humanos , L-Lactato Desidrogenase/metabolismo , Espectrometria de Massas/métodos , Metanol/química , Extratos Vegetais/isolamento & purificação , Extratos Vegetais/metabolismo , Pronase/metabolismo , Rodamina 123/farmacocinética , VerdurasRESUMO
P-glycoprotein (P-gp) is a 170 kDa membrane protein that belongs to the ATP-binding cassette (ABC) transporter superfamily. In normal tissues, P-gp functions as an ATP-dependent efflux pump that excretes highly hydrophobic xenobiotic compounds, playing an important role in protecting the cells/tissues from xenobiotics. In the present study, chemical substances that could directly modulate the intestinal P-gp activity were searched in vegetables and fruits. By using human intestinal epithelial Caco-2 cells as a model of the small intestinal cells, we observed that a bitter melon fraction extracted from 40% methanol showed the greatest increase of the rhodamine-123 accumulation by Caco-2 cells. Inhibitory compounds in the bitter melon fraction were then isolated by HPLC using Pegasil C4 and Pegasil ODS columns. The HPLC fraction having the highest activity was analyzed by (1)H-NMR and FAB-MS, and the active compound was identified as 1-monopalmitin. It is interesting that certain types of monoglyceride might be involved in the drug bioavailability by specifically inhibiting the efflux mediated by P-gp.
Assuntos
Membro 1 da Subfamília B de Cassetes de Ligação de ATP/antagonistas & inibidores , Cucurbitaceae , Glicerídeos/farmacologia , Extratos Vegetais/farmacologia , Membro 1 da Subfamília B de Cassetes de Ligação de ATP/efeitos dos fármacos , Linhagem Celular Tumoral , Cromatografia Líquida de Alta Pressão , Neoplasias do Colo , Daunorrubicina/farmacocinética , Humanos , Ácido Palmítico/farmacologia , Fitoterapia , Extratos Vegetais/isolamento & purificaçãoRESUMO
The present study investigated age differences in the effects of a self-choice elaboration and an experimenter-provided elaboration on incidental memory. Adults, sixth grade, and second grade subjects chose which of two sentence frames the target fit better in a self-choice elaboration condition. They then judged whether each target made sense in its sentence frame in the experimenter-provided elaboration, then did free recall tests. Only adults recalled better the targets with an image sentence with self-choice elaboration, rather than experimenter-provided elaboration. However, self-choice elaboration was far superior for the recall of targets with nonimage sentences only for second graders. Thus, the effects of self-choice elaboration were determined both by age and by type of sentence frame.
Assuntos
Comportamento de Escolha , Memória , Adulto , Feminino , Humanos , Masculino , Rememoração MentalRESUMO
Netherton syndrome (NS) is a rare autosomal recessive disorder which is caused by mutations in the SPINK5 gene encoding the serine-protease inhibitor LEKTI. Characteristic symptoms of NS include erythroderma with diffuse desquamation, hair abnormalities and atopic manifestations. Here, we report two Japanese patients with NS, one of whom had a novel mutation in the SPINK5 gene which leads to p.C367Lfs*3. The upregulation of interleukin-33 (IL-33) was evident in basal and thickened lower spinous layers of the epidermis in those cases. This suggests that IL-33 may be involved in the pathophysiology of NS as well as in atopic dermatitis.
Assuntos
Epiderme/metabolismo , Interleucinas/metabolismo , Síndrome de Netherton/metabolismo , Epiderme/patologia , Feminino , Humanos , Recém-Nascido , Recém-Nascido Prematuro , Interleucina-33 , Síndrome de Netherton/genética , Síndrome de Netherton/patologia , Proteínas Secretadas Inibidoras de Proteinases/genética , Inibidor de Serinopeptidase do Tipo Kazal 5 , Regulação para CimaRESUMO
Adult T-cell leukemia/lymphoma (ATL) is characterized by monoclonal proliferation of tumor cells that harbor integrated human T-cell leukemia virus type-1 (HTLV-1). These malignant cells accumulate in various organs including the liver, spleen and skin in addition to blood and lymph nodes. Although there have been several reports of animal models of HTLV-1 infection in which proviral distribution has been examined, clonal expansion of the experimentally infected host cells has not been extensively analyzed. Here we provide experimental evidence that clonal proliferation of the infected host cells occurs in the spleen for more than one year. During a 15 month period of persistent infection, two out of ten mice developed spontaneous tumors. Although the tumors were not ATL-like, cells exhibiting mono- or oligoclonal proliferation and having the same site of HTLV-1 integration were identified in tumor tissues as well as in the spleen. Quantitative analysis of the cells belonging to each cell clone suggested that these proliferating cell clones were associated with the tumors and that spontaneous tumor tissues might provide a suitable microenvironment for proliferation and accumulation of infected cell clones at the late stage of infection.
Assuntos
Proliferação de Células , Transformação Celular Viral , Infecções por HTLV-I/virologia , Vírus Linfotrópico T Tipo 1 Humano/patogenicidade , Neoplasias/virologia , Baço/virologia , Infecções Tumorais por Vírus/virologia , Animais , Animais Recém-Nascidos , Linhagem Celular , Células Clonais , Infecções por HTLV-I/patologia , Histiocitoma/patologia , Histiocitoma/virologia , Humanos , Leucemia Mieloide/patologia , Leucemia Mieloide/virologia , Lipossarcoma/patologia , Lipossarcoma/virologia , Camundongos , Camundongos Endogâmicos C3H , Neoplasias/patologia , Neoplasias de Tecidos Moles/patologia , Neoplasias de Tecidos Moles/virologia , Baço/patologia , Neoplasias Esplênicas/patologia , Neoplasias Esplênicas/virologia , Fatores de Tempo , Infecções Tumorais por Vírus/patologia , Carga Viral , Integração ViralRESUMO
BACKGROUND: Atopic dermatitis is the most frequently seen childhood allergic disease in outpatient clinics. Improvement, exacerbation, and response to treatment are typically assessed subjectively and occasionally inaccurately. METHODS: The authors developed two forms for scoring of dermal manifestations and used them to assess 56 children. The correlation between two pediatricians' scores and correspondence to established categories (mild, moderate, and severe) were determined. RESULT: The two physicians' scores for the children correlated well for both forms of scoring. Correspondence of scores as 'mild' and 'moderate' categories were significant (few children participating were 'severe'). CONCLUSION: Use of well-constructed scoring forms should improve clinical assessment of patient course and treatment response.