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1.
Allergy ; 73(11): 2205-2213, 2018 11.
Artículo en Inglés | MEDLINE | ID: mdl-29672867

RESUMEN

BACKGROUND: The skin of atopic dermatitis (AD) patients presents a significant dysbalance of the microbiome with a high colonization by Staphylococcus aureus (S. aureus), which positively correlates with the severity of the disease. OBJECTIVE: Understanding the role of epidermal dendritic cells (DC) as link between the innate and the adaptive immune systems in AD. METHODS: Comparative phenotypic and functional analysis of TLR2 on Langerhans cells (LC) and inflammatory dendritic epidermal cells (IDEC) in organotypic models as well as freshly isolated cells from healthy and AD skin. RESULTS: In situ analysis of freshly isolated LC and IDEC from AD skin revealed decreased TLR2 expression compared to LC from healthy skin. In contrast to IDEC, LC from AD skin failed to display any evidence for in situ activation. Exposure to TLR2 ligand Pam3Cys resulted in maturation and increased migratory activity of LC from normal skin. LC and IDEC from AD were unresponsive to TLR2 ligand in that they failed to mature and displayed a high spontaneous migratory activity. Keratinocytes from both healthy and AD skin expressed similar levels of TLR2. The production of IL-6 and IL-10 was impaired by Pam3Cys in supernatants from AD skin. IL-18 was significantly higher in supernatants from AD skin and not influenced by TLR2 ligation, when compared to healthy skin. CONCLUSION: Our results suggest that TLR2-mediated sensing of S. aureus-derived signals is strongly impaired in LC from AD skin. This phenomenon may partly contribute to the immune deviation in AD and the lack of S. aureus clearance.


Asunto(s)
Dermatitis Atópica/inmunología , Dermatitis Atópica/metabolismo , Tolerancia Inmunológica , Células de Langerhans/inmunología , Células de Langerhans/metabolismo , Receptor Toll-Like 2/metabolismo , Inmunidad Adaptativa , Biomarcadores , Movimiento Celular/inmunología , Citocinas/metabolismo , Dermatitis Atópica/patología , Femenino , Expresión Génica , Humanos , Inmunidad Innata , Inmunoglobulina E/sangre , Inmunoglobulina E/inmunología , Inmunofenotipificación , Queratinocitos/metabolismo , Masculino , Unión Proteica , Índice de Severidad de la Enfermedad , Staphylococcus aureus/inmunología , Receptor Toll-Like 2/genética
2.
Br J Dermatol ; 177(5): 1442-1446, 2017 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-28346662

RESUMEN

Autoantibodies to melanoma differentiation-associated protein 5 (MDA5) are associated with a subset of patients with dermatomyositis (DM) who have rapidly progressive interstitial lung disease (RP-ILD) with poor prognosis. Intensive immunosuppressive therapy is initiated before irreversible lung damage can occur; however, there are few lines of evidence for the treatment of RP-ILD. Here, we report three cases of anti-MDA5 antibody-associated DM with RP-ILD in which the patients were treated with combined-modality therapy, including high-dose prednisolone, tacrolimus, intravenous cyclophosphamide and intravenous immunoglobulin (IVIG). In all three cases, serum ferritin levels, which are known to represent the disease activity of RP-ILD, were decreased after IVIG administration. IVIG might contribute to the control of the disease activity of anti-MDA5 antibody-positive DM. Moreover, palmar violaceous macules/papules around the interphalangeal joints, which was observed in all three cases in the incipient stage, might be a useful sign in suggesting a diagnosis of anti-MDA5 antibody-associated DM.


Asunto(s)
Dermatomiositis/prevención & control , Dermatosis de la Mano/prevención & control , Inmunoglobulinas Intravenosas/uso terapéutico , Helicasa Inducida por Interferón IFIH1/inmunología , Enfermedades Pulmonares Intersticiales/prevención & control , Anciano , Antiinflamatorios/administración & dosificación , Autoanticuerpos/sangre , Terapia Combinada , Ciclofosfamida/administración & dosificación , Femenino , Humanos , Inmunosupresores/administración & dosificación , Masculino , Persona de Mediana Edad , Prednisolona/administración & dosificación , Tacrolimus/administración & dosificación , Resultado del Tratamiento
3.
Pharmacopsychiatry ; 50(2): 74-78, 2017 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-27656915

RESUMEN

Introduction: Although adjunctive aripiprazole improves hyperprolactinemia, sufficient evidence for its effects on sexual dysfunction has not been obtained. We assessed the usefulness of adjunctive aripiprazole for schizophrenia with sexual dysfunction. Methods: 22 Japanese schizophrenia patients with antipsychotic-induced hyperprolactinemia and sexual dysfunction were enrolled, and 19 of them completed the study. Aripiprazole was administrated in a flexible titration schedule to participants according to the judgment of each doctor, and patients were followed for 24 weeks. Serum prolactin, Clinical Global Impression Scales-Severity (CGI-S), and Nagoya Sexual Function Questionnaire (NSFQ) were measured at baseline and at 4, 8, 12, and 24 weeks. Results: Prolactin at week 4 and later was significantly lower than that at baseline. Compared to baseline, we observed a significant improvement in total sexual dysfunction as measured by NSFQ at week 8 and later. In males, erectile dysfunction was significantly reduced at week 24. In females, menstrual irregularity and galactorrhea were significantly reduced at week 24. CGI-S did not significantly change. Discussion: Although the small sample size is a limitation in this study, adjunctive aripiprazole may be useful treatment for sexual dysfunction including hyperprolactinemia in schizophrenia.


Asunto(s)
Aripiprazol/uso terapéutico , Esquizofrenia/complicaciones , Disfunciones Sexuales Fisiológicas/complicaciones , Disfunciones Sexuales Fisiológicas/tratamiento farmacológico , Adulto , Antipsicóticos/efectos adversos , Antipsicóticos/uso terapéutico , Quimioterapia Combinada , Femenino , Humanos , Hiperprolactinemia/sangre , Hiperprolactinemia/inducido químicamente , Hiperprolactinemia/complicaciones , Hiperprolactinemia/tratamiento farmacológico , Masculino , Prolactina/sangre , Esquizofrenia/sangre , Esquizofrenia/tratamiento farmacológico , Disfunciones Sexuales Fisiológicas/inducido químicamente
4.
Clin Exp Dermatol ; 42(5): 527-531, 2017 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-28543395

RESUMEN

A 26-year-old woman presented with recurrent attacks of widespread urticaria and systemic symptoms. The patient was a nurse, and the attacks occurred only in her workplace, without an apparent trigger. A patch test to cefotiam (CTM) induced an immediate skin reaction. ELISA detected the patient's serum IgE antibody binding to CTM conjugated with human serum albumin (CTM-HSA), and her basophils released histamine in response to CTM-HSA in a histamine release assay (HRA). Both reactions in ELISA and HRA were inhibited by pretreatment of the patient's serum or basophils with cefotiam. No crossreactivity in skin tests or in vitro assays was observed against other antibiotics, even those containing a beta-lactam ring and/or side chains similar to CTM. Certain antibiotics including CTM may cause extremely sensitive and specific contact urticaria syndrome, which is mediated by IgE and evoked even without apparent skin contact with the culprit drug and in the absence of any history of an allergic reaction against other antibiotics with similar structures.


Asunto(s)
Cefotiam/inmunología , Inmunoglobulina E/inmunología , Enfermedades Profesionales/inducido químicamente , Urticaria/inducido químicamente , Adulto , Cefotiam/efectos adversos , Femenino , Humanos , Personal de Enfermería en Hospital , Enfermedades Profesionales/inmunología , Urticaria/inmunología
6.
J Wound Care ; 26(5): 267-270, 2017 May 02.
Artículo en Inglés | MEDLINE | ID: mdl-28475443

RESUMEN

OBJECTIVE: The number of patients with foot gangrene caused by critical ischaemia and severe infection is increasing significantly in developed countries. The measurement of perilesional skin blood flow by skin perfusion pressure (SPP) is useful to select the appropriate treatment of gangrenous lesions, in that it is not affected by calcifications of blood vessels. However, the prognosis of a foot ulcer may also be affected by the level of blood sugar and infections. This study aimed to validate the use of SPP in cases of foot gangrene and ulcers in patients with and without diabetes mellitus (DM) and infection. METHOD: Clinical symptoms, ankle-brachial pressure index (ABPI) and SPP were assessed to evaluate the condition of each foot ulcer. Every foot ulcer was treated as independent, even if a participant had multiple ulcers. All ulcers for which we measured SPP were subject to the analysis. All ulcers were purely ischaemic in nature and were exclusively located on the foot or toes. RESULTS: Data were collected from 117 foot ulcers on 91 toes and feet from 65 patients. Almost all SPP values in healed cases were > 27 mmHg. There were three patients whose ulcers failed to heal by conservative treatments were complicated with severe infection. However, no effect of DM on the relationship between SPP values and prognosis was observed. Logistic regression analysis of all ulcers except for the 5 cases complicated with infection revealed that those with 30 mmHg or lower SPP values are likely to heal by conservative treatment with 23% or lower probability, whereas any ulcer with more than 50 mmHg SPP value and without severe infection may heal without the need for further operations with 80% or higher probability. CONCLUSION: The combination of SPP and careful evaluation of infection may be a good parameter to decide the appropriate treatment for ischaemic skin ulcers, regardless of the complication of DM.


Asunto(s)
Diabetes Mellitus , Pie Diabético/fisiopatología , Enfermedades Vasculares Periféricas/fisiopatología , Piel/irrigación sanguínea , Cicatrización de Heridas , Adulto , Anciano , Anciano de 80 o más Años , Angioplastia , Índice Tobillo Braquial , Pie Diabético/etiología , Pie Diabético/cirugía , Femenino , Pie/patología , Úlcera del Pie/fisiopatología , Úlcera del Pie/cirugía , Gangrena , Humanos , Modelos Logísticos , Masculino , Persona de Mediana Edad , Enfermedades Vasculares Periféricas/cirugía , Presión , Pronóstico , Flujo Sanguíneo Regional , Estudios Retrospectivos , Adulto Joven
8.
Artículo en Inglés | MEDLINE | ID: mdl-22697007

RESUMEN

BACKGROUND: Immunoglobulin (Ig) E plays an important role in the pathogenesis of allergic diseases such as atopic dermatitis and allergic asthma.We previously reported that a sulfate polysaccharide, fucoidan, suppressed IgE production by murine B cells in vitro. However, the mechanism by which fucoidan suppresses IgE production remains unclear. OBJECTIVE: We incorporated sulfate groups into cellulose and studied their biological characteristics in vitro to explore the possibility of converting biologically neutral polysaccharides to active reagents with antiallergic functions. MATERIAL AND METHODS: Cellulose was chemically processed using N,N-dimethylformamide (DMF) and DMF-sulfurtrioxide and recovered as cellulose sulfate with a molecular weight of around 10 kDa. We then studied the effect of cellulose sulfate on IgE production from B cells, IgE class-switching, and populations of IgE-secreting B cells prepared from murine spleen. We also investigated the effects of sulfated cellulose on the production of interleukin (IL) 4 and interferon (IFN) gamma and the expression of T-bet mRNA by splenic T cells. The cytotoxicity of cellulose sulfate was also examined. RESULTS: Cellulose sulfate suppressed IgE production in B cells stimulated with IL-4 and anti-CD40 antibody by inhibiting IgE class-switch recombination and decreasing the number of IgE-secreting B cells in vitro. Moreover, both cellulose sulfate and fucoidan suppressed IL-4 production and enhanced IFN-gamma production by murine T cells stimulated with anti-CD3 and anti-CD28 antibodies, despite the decrease in T-bet mRNA expression. CONCLUSIONS: Cellulose gains an antiallergic effect on B cells and T cells with the addition of sulfate groups.


Asunto(s)
Linfocitos B/efectos de los fármacos , Celulosa/análogos & derivados , Inmunoglobulina E/biosíntesis , Animales , Antialérgicos/inmunología , Antialérgicos/farmacología , Anticuerpos/inmunología , Linfocitos B/inmunología , Antígenos CD40/inmunología , Células Cultivadas , Celulosa/inmunología , Celulosa/farmacología , Dimetilformamida , Formamidas/química , Inmunoglobulina E/inmunología , Interferón gamma/inmunología , Interleucina-4/inmunología , Masculino , Ratones , Ratones Endogámicos BALB C , Peso Molecular , Polisacáridos/inmunología , Polisacáridos/farmacología , Bazo/efectos de los fármacos , Bazo/inmunología , Proteínas de Dominio T Box/inmunología , Linfocitos T/efectos de los fármacos , Linfocitos T/inmunología
9.
Clin Exp Dermatol ; 37(1): 20-3, 2012 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-21790735

RESUMEN

C1 inhibitor (C1-INH) deficiency [hereditary or acquired angio-oedema (HAE or AAE)] is characterized by recurring episodes of subcutaneous or submucosal oedema. Many different mutations in the C1-INH gene have been identified as a cause of HAE. We investigated the molecular basis of the disease in a Japanese woman with sporadic HAE. Direct sequencing of genomic DNA revealed no point mutation in the C1-INH gene. Quantitative real-time PCR showed that the copy number of the C1-INH gene in the patient was half that of a healthy control. Furthermore, we identified a 650-kbp deletion on the chromosome, which included the C1-INH gene. We evaluated the correlation between the patient's attacks and her coagulation activity. The levels of D-dimer were high during the angio-oedema attacks, and often exceeded the normal range even during remission, thus the level of D-dimer reflected the activity of HAE in this patient.


Asunto(s)
Angioedemas Hereditarios/genética , Proteína Inhibidora del Complemento C1/genética , Eliminación de Secuencia , Adulto , Angioedemas Hereditarios/sangre , Pueblo Asiatico , Exones/genética , Femenino , Productos de Degradación de Fibrina-Fibrinógeno/análisis , Predisposición Genética a la Enfermedad , Humanos , Reacción en Cadena en Tiempo Real de la Polimerasa
10.
Phys Rev Lett ; 106(1): 015501, 2011 Jan 07.
Artículo en Inglés | MEDLINE | ID: mdl-21231752

RESUMEN

We present optical conductivity studies of the type-I clathrate Ba8Ga16Sn30, using a terahertz time-domain spectrometer (0.3-3.0 THz). The lowest-lying spectral peak at 0.72 THz due to the Ba(2) ion's off-center vibration in the oversized cage shows a drastic and anomalous temperature dependence. Below about 100 K, the single broad peak splits into two subpeaks, and with further lowering of the temperature, the spectral shape of this so-called rattling phonon shows non-Boltzmann broadening to the point that the linewidth becomes comparable to the peak frequency. Whereas the initial splitting can be understood by assuming a multiwell anharmonic potential, the strong linewidth broadening toward low temperature cannot, since the Boltzmann factor generally sharpens the low-temperature spectra. The observed behavior suggests strong interaction between the local anharmonic phonons and other excitations.

11.
Biochemistry (Mosc) ; 76(8): 912-4, 2011 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-22022964

RESUMEN

Pre-mRNA of serotonin 2C receptor (HTR2C, 5-hydroxytryptamine (serotonin) receptor 2C) undergoes A-to-I type RNA editing, which is a post-transcriptional event leading to the change of genomically encoded information. RNA editing generates various HTR2C isoforms, each of which has distinctive receptor activity. Postmortem, animal, and pharmacological studies have suggested that the altered RNA editing of HTR2C is involved in the pathophysiology of mental disorders, although results remain inconsistent. Here we review the techniques used for estimation of RNA editing of HTR2C. Among the techniques reported so far, a high-throughput sequencing-based method would be the most powerful method of choice for the large-scale experiments. Several different methods that were previously developed, such as pyrosequencing and capillary electrophoresis, should be suitable for validation as well as for rapid screening or exploratory purposes.


Asunto(s)
Electroforesis Capilar/métodos , Técnicas Genéticas , Secuenciación de Nucleótidos de Alto Rendimiento/métodos , Edición de ARN , Receptor de Serotonina 5-HT2C/genética , Animales , Secuencia de Bases , Humanos , Datos de Secuencia Molecular , Receptor de Serotonina 5-HT2C/metabolismo
12.
Allergy ; 65(5): 649-56, 2010 May.
Artículo en Inglés | MEDLINE | ID: mdl-19845571

RESUMEN

BACKGROUND: The evaluation of disease severity and activity of chronic urticaria (CU) is essential for the adequate treatment of patients. However, there is no reliable biomarker for such evaluations. Recently, markers of blood coagulation and fibrinolysis have been revealed to be elevated in severe cases of CU. In this article, we studied the coagulation/fibrinolysis and inflammation markers and their relationship to disease activity in patients with CU. METHODS: Plasma fibrin degradation products (FDP), d-dimer and serum C-reactive protein (CRP) were measured with the assessment of disease severity and skin reaction to autologous serum in 82 patients with CU and 37 patients with acute urticaria, idiopathic angioedema (AE) or inducible types of urticaria (IU). RESULTS: The levels of FDP in patients with CU were significantly higher than those in patients with IU, but no other differences in FDP, d-dimer and CRP were observed among patients with different types of urticaria. These markers of patients with CU were well correlated with each other and significantly associated with disease severity of CU, but not with skin reactions to autologous serum. In 37 patients with CU, levels of all these parameters reduced as their disease condition improved, while they increased when the disease became aggravated. Regarding FDP, this relationship was observed even if FDP concentrations were within normal range throughout the study. CONCLUSIONS: The measurement of plasma FDP, d-dimer and serum CRP may be useful for the assessment of disease activity of CU.


Asunto(s)
Biomarcadores/sangre , Proteína C-Reactiva/análisis , Productos de Degradación de Fibrina-Fibrinógeno/análisis , Inflamación/sangre , Urticaria/sangre , Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Biomarcadores/análisis , Coagulación Sanguínea/fisiología , Niño , Preescolar , Enfermedad Crónica , Femenino , Fibrinólisis/fisiología , Humanos , Inflamación/inmunología , Masculino , Persona de Mediana Edad , Pruebas Cutáneas , Urticaria/inmunología , Adulto Joven
13.
Mol Psychiatry ; 13(4): 429-41, 2008 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-17471289

RESUMEN

To search DNA methylation difference between monozygotic twins discordant for bipolar disorder, we applied a comprehensive genome scan method, methylation-sensitive representational difference analysis (MS-RDA) to lymphoblastoid cells derived from the twins. MS-RDA isolated 10 DNA fragments derived from 5' region of known genes/ESTs. Among these 10 regions, four regions showed DNA methylation differences between bipolar twin and control co-twin confirmed by bisulfite sequencing. We performed a case-control study of DNA methylation status of these four regions by pyrosequencing. Two regions, upstream regions of spermine synthase (SMS) and peptidylprolyl isomerase E-like (PPIEL) (CN265253), showed aberrant DNA methylation status in bipolar disorder. SMS, a gene on X chromosome, showed significantly higher DNA methylation level in female patients with bipolar disorder compared with control females. However, there was no difference of mRNA expression. In PPIEL, DNA methylation level was significantly lower in patients with bipolar II disorder than in controls. The expression level of PPIEL was significantly higher in bipolar II disorder than in controls. We found strong inverse correlation between gene expression and DNA methylation levels of PPIEL. These results suggest that altered DNA methylation statuses of PPIEL might have some significance in pathophysiology of bipolar disorder..


Asunto(s)
Trastorno Bipolar/genética , Ciclofilinas/genética , Metilación de ADN , Enfermedades en Gemelos , Compensación de Dosificación (Genética) , Espermina Sintasa/genética , Adulto , Análisis de Varianza , Trastorno Bipolar/patología , Células Cultivadas , Femenino , Genoma , Humanos , Linfocitos , Masculino , Persona de Mediana Edad , Datos de Secuencia Molecular , Análisis de Secuencia de ADN/métodos , Gemelos Monocigóticos
14.
Science ; 276(5317): 1378-82, 1997 May 30.
Artículo en Inglés | MEDLINE | ID: mdl-9190677

RESUMEN

Spectroscopic and photometric evidence indicates that Type Ia supernovae (SNe Ia) are the thermonuclear explosions of accreting white dwarfs. However, the progenitor binary systems and hydrodynamical models for SNe Ia are still controversial. The relatively uniform light curves and spectral evolution of SNe Ia have led to their use as a standard candle for determining cosmological parameters, such as the Hubble constant, the density parameter, and the cosmological constant. Recent progress includes the calibration of the absolute maximum brightness of SNe Ia with the Hubble Space Telescope, the reduction of the dispersion in the Hubble diagram through the use of the relation between the light curve shape and the maximum brightness of SNe Ia, and the discovery of many SNe Ia with high red shifts.


Asunto(s)
Astronomía , Fenómenos Astronómicos , Carbono/química , Elementos Químicos , Evolución Planetaria , Medio Ambiente Extraterrestre , Luz , Física Nuclear
15.
Neuroradiology ; 51(11): 755-9, 2009 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-19578842

RESUMEN

INTRODUCTION: The transvenous approach via the superior ophthalmic vein (SOV) is an available approach for carotid cavernous fistula (CCF), especially in the event that there is no other suitable approach route to the fistula. Surgical exposure of the peripheral roots of the SOV is commonly used; however, often, the SOV is often not accessible because of anatomical problems and/or complications. In this paper, we present and discuss our original direct-puncture approach to the extraconal portion of the SOV. METHODS: An attempt on three patients with traumatic CCF failed with the transarterial approach and the conventional venous approach via the inferior petrosal sinus; therefore, the patients were treated with the direct-puncture approach to the extraconal portion of the SOV using two-dimensional digital subtraction angiography with local anesthesia. RESULTS: All cases that had tortuous and partially stenotic division of the SOV were treated successfully with this approach and without complications. CONCLUSION: This approach will become an alternate approach, especially when the peripheral roots of the SOV are focally narrowed and tortuous, making it impossible to insert a catheter.


Asunto(s)
Fístula del Seno Cavernoso de la Carótida/cirugía , Procedimientos Neuroquirúrgicos/métodos , Venas/cirugía , Adulto , Angiografía de Substracción Digital/métodos , Encéfalo/irrigación sanguínea , Encéfalo/patología , Encéfalo/cirugía , Arterias Carótidas/patología , Arterias Carótidas/cirugía , Fístula del Seno Cavernoso de la Carótida/patología , Angiografía Cerebral , Estudios de Seguimiento , Humanos , Angiografía por Resonancia Magnética , Masculino , Resultado del Tratamiento , Venas/patología
16.
Clin Nephrol ; 71(6): 608-16, 2009 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-19473628

RESUMEN

BACKGROUND: An imbalance of Th1 and Th2 cytokines has been reported in MCNS. Interleukin-13 (IL-13: Th2 cytokine) has been implicated in the pathogenesis of MCNS, but Th1/Th2 regulators such as T-bet (Th1-specific transcription factor) and GATA-3 (Th2-specific transcription factor) have not been examined. METHODS: We isolated PBMC from 25 patients with MCNS during nephrosis and remission phases, from 17 nephrotic patients with membranous nephropathy (MN), and from 25 healthy subjects. We measured mRNA expression levels of T-bet, GATA-3, Stat5A (regulator of Th2 priming), IFN-gamma (Th1 cytokine), IL-2 (Th1 cytokine and activator of Stat5), IL-4 (Th2 cytokine), and IL-13 in PBMC, using real-time RT-PCR. RESULTS: GATA-3, Stat5A, and IL-13 mRNA expression levels were higher in the nephrotic MCNS group compared to the others. IL-2 mRNA expression levels were higher in nephrotic patients with MCNS and MN than in MCNS patients in remission and healthy controls. There were no differences in mRNA expression levels of T-bet, IFN-gamma, and IL-4 between MCNS and MN patients and healthy controls. CONCLUSIONS: This study is the first to reveal increased mRNA expression levels of GATA-3 and Stat5A in PBMC from MCNS patients in nephrosis. This study also supports recent findings suggesting the role of IL-13 in the development of MCNS. A predominant Th2 type of T cell activation may be involved in the pathogenesis of MCNS.


Asunto(s)
Factor de Transcripción GATA3/genética , Expresión Génica , Glomerulonefritis Membranosa/genética , Leucocitos Mononucleares/metabolismo , Nefrosis Lipoidea/genética , Adolescente , Adulto , Anciano , Estudios de Casos y Controles , Femenino , Factor de Transcripción GATA3/metabolismo , Humanos , Interferón gamma/genética , Interleucina-13/genética , Interleucina-2/genética , Interleucina-4/genética , Masculino , Persona de Mediana Edad , ARN Mensajero/genética , Factor de Transcripción STAT5/genética , Proteínas de Dominio T Box/genética , Regulación hacia Arriba , Adulto Joven
17.
Appl Microbiol Biotechnol ; 83(4): 697-704, 2009 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-19277641

RESUMEN

An increase in compactin (ML-236B) production was achieved by introducing a whole compactin biosynthetic gene cluster or the regulatory gene mlcR into compactin high-producing Penicillium citrinum. In the previous report, we introduced mlcR encoding the positive regulator of compactin biosynthetic genes into compactin high-producing strain no. 41520, and most of the transformants produced higher amounts of compactin. Here, we characterize one of the resulting high producers (strain TIR-35, which produced 50% more compactin) and reveal that TIR-35 contained five copies of mlcR and that early, enhanced expression of mlcR caused compactin overproduction. Similarly, the introduction of mlcR into strain T48.19, which was created previously from strain no. 41520 by introducing a partial compactin biosynthetic gene cluster, enhanced compactin production further. Our results indicated that genetic engineering is an effective tool to improve compactin production, even in compactin high producers.


Asunto(s)
Vías Biosintéticas/genética , Ingeniería Genética , Lovastatina/análogos & derivados , Penicillium/genética , Penicillium/metabolismo , Proteínas Fúngicas/genética , Dosificación de Gen , Lovastatina/biosíntesis , Familia de Multigenes , Transactivadores/genética
18.
Clin Exp Immunol ; 152(3): 482-7, 2008 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-18373699

RESUMEN

Recent studies in animal models for systemic lupus erythematosus (SLE) have shown that Toll-like receptors (TLR-7 and TLR-9) and interferon (IFN)-alpha are involved in the pathogenesis of murine lupus. Recent studies using flow cytometry have also shown increased expression of TLR-9 in peripheral blood mononuclear cells (PBMCs) from SLE patients. In this study, we performed quantitative real-time reverse transcription-polymerase chain reaction analyses of PBMCs from 21 SLE patients and 21 healthy subjects, to estimate TLR2, TLR3, TLR4, TLR5, TLR7, TLR8, TLR9, IFN-alpha and LY6E (a type I IFN-inducible gene) mRNA expression levels. Expression levels of TLR2, TLR7, TLR9, IFN-alpha and LY6E mRNAs in SLE patients were significantly higher than those in healthy controls. Expression levels of TLR7 and TLR9 mRNAs correlated with that of IFN-alpha mRNA in SLE patients. These results suggest that up-regulated expression of TLR7 and TLR9 mRNAs together with increased expression of IFN-alpha mRNA in PBMCs may also contribute to the pathogenesis of human lupus.


Asunto(s)
Leucocitos Mononucleares/inmunología , Lupus Eritematoso Sistémico/inmunología , Receptores Toll-Like/biosíntesis , Regulación hacia Arriba/inmunología , Adolescente , Adulto , Anciano , Antígenos de Superficie/biosíntesis , Antígenos de Superficie/genética , Femenino , Proteínas Ligadas a GPI , Humanos , Interferón-alfa/biosíntesis , Interferón-alfa/genética , Masculino , Proteínas de la Membrana/biosíntesis , Proteínas de la Membrana/genética , Persona de Mediana Edad , ARN Mensajero/genética , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa/métodos , Receptores Toll-Like/genética
19.
Artículo en Inglés | MEDLINE | ID: mdl-28714277

RESUMEN

BACKGROUND: Short-chain fatty acids (SCFA) are microbial fermentation products absorbed by the colon. We recently reported that activation of the SCFA receptor termed free fatty acid receptor 3 (FFA3), expressed on cholinergic nerves, suppresses nicotinic acetylcholine receptor (nAChR)-mediated transepithelial anion secretion. This study aimed to clarify how activation of neurally expressed FFA3 affects colonic motor function. METHODS: FFA3-expressing myenteric neurons were identified by immunostaining; contractions of isolated circular muscle strips obtained from rat proximal colon were measured by isometric transducers. The effect of FFA3 agonists on defecation in vivo was examined in an exogenous serotonin-induced defecation model. KEY RESULTS: FFA3 immunoreactivity was located in nitrergic and cholinergic neurons in the myenteric plexus. In isolated circular muscle strips without mucosa and submucosa, the addition of nicotine (10 µM) or serotonin transiently relaxed the muscle through nitrergic neurons, whereas high concentrations of nicotine (100 µM) induced large-amplitude contractions that were mediated by cholinergic neurons. Pretreatment with FFA3 agonists inhibited nicotine- or serotonin-induced motility changes but had no effect on bethanechol-induced direct muscle contractions. The Gi/o inhibitor pertussis toxin reversed the inhibitory effect of an FFA3 agonist AR420626 on nicotine-evoked contractions, suggesting that FFA3 activation suppresses nAChR-mediated neural activity in myenteric neurons, consistent with an FFA3-mediated antisecretory effect. In conscious rats, exogenous serotonin increased the volume of fecal output, compared with the vehicle- or AR420626-treated groups. Pretreatment with AR420626 significantly suppressed serotonin-induced fecal output. CONCLUSION AND INFERENCES: FFA3 is a promising target for the treatment of neurogenic diarrheal disorders by suppressing nAChR-mediated neural pathways.


Asunto(s)
Colon/fisiología , Motilidad Gastrointestinal , Neuronas/fisiología , Receptores Acoplados a Proteínas G/fisiología , Animales , Neuronas Colinérgicas/metabolismo , Colon/metabolismo , Defecación , Masculino , Contracción Muscular , Plexo Mientérico/fisiología , Neuronas/metabolismo , Nicotina/administración & dosificación , Agonistas Nicotínicos/administración & dosificación , Neuronas Nitrérgicas/metabolismo , Ratas Sprague-Dawley , Receptores Acoplados a Proteínas G/agonistas , Receptores Acoplados a Proteínas G/metabolismo , Serotonina/administración & dosificación , Antagonistas de la Serotonina/administración & dosificación
20.
Transplant Proc ; 50(8): 2539-2544, 2018 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-30316394

RESUMEN

OBJECTIVES: We aimed to evaluate the feasibility and efficacy of surgical prostatectomy in renal transplant recipients (RTRs). METHODS: Between January 2008 and February 2017, we identified 13 RTRs who were diagnosed with localized prostate cancer and underwent radical prostatectomy. We reviewed all available clinicopathologic data for these 13 patients. RESULTS: The median patient age was 61 years and median serum prostate-specific antigen (PSA) was 8.79 ng/mL. The mean period between transplantation and diagnosis of prostate cancer was 136 months. The sources for the kidney transplants included 10 living and 3 deceased donors. Biopsies indicated that the Gleason scores were 7 in 10 patients and 8 to 10 in 3 patients. Meanwhile, the D'Amico risk classification indicated an intermediate risk in 9 patients and a high risk in 4 patients. Eight patients were at stage cT1 and 5 were at stage cT2. The surgical procedure was retropubic radical prostatectomy in one recipient, laparoscopic radical prostatectomy in 3 recipients, and robot-assisted radical prostatectomy in 9 RTRs. Intraoperative complications were not noted in any patient, although one patient demonstrated postoperative complications (Clavien grade ≥ 3). An indwelling urinary catheter was required in 3 patients for over 3 weeks due to delayed wound healing. Biochemical recurrence evaluated by PSA monitoring occurred in four patients. Postoperative graft function was stable in all but one patient who required resumption of dialysis before prostatectomy; however, all patients are alive at the time of publication with 12 patients showing well-functioning renal allografts. CONCLUSION: Prostatectomy may be a feasible and effective technique as an initial treatment for RTRs with localized prostate cancer.


Asunto(s)
Trasplante de Riñón , Prostatectomía/métodos , Neoplasias de la Próstata/complicaciones , Neoplasias de la Próstata/cirugía , Receptores de Trasplantes , Anciano , Humanos , Masculino , Persona de Mediana Edad , Antígeno Prostático Específico/sangre , Neoplasias de la Próstata/patología , Estudios Retrospectivos
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