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1.
Leukemia ; 21(8): 1752-62, 2007 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-17554373

RESUMO

Parathyroid hormone-related protein (PTHrP) plays a primary role in the development of humoral hypercalcemia of malignancy (HHM) that occurs in the majority of patients with adult T-cell leukemia/lymphoma (ATLL) due to human T-cell lymphotropic virus type-1 (HTLV-1) infection. We previously showed that ATLL cells constitutively express high levels of PTHrP via activation of promoters P2 and P3, resulting in HHM. In this study, we characterized a nuclear factor-kappaB (NF-kappaB) binding site in the P2 promoter of human PTHrP. Using electrophoretic mobility shift assays, we detected a specific complex in Tax-expressing human T cells composed of p50/c-Rel, and two distinct complexes in ATLL cells consisting of p50/p50 homodimers and a second unidentified protein(s). Chromatin immunoprecipitation assays confirmed in vivo binding of p50 and c-Rel on the PTHrP P2 promoter. Using transient co-transfection with NF-kappaB expression plasmids and PTHrP P2 luciferase reporter-plasmid, we showed that NF-kappaB p50/p50 alone and p50/c-Rel or p50/Bcl-3 cooperatively upregulated the PTHrP P2 promoter. Furthermore, inhibition of NF-kappaB activity by Bay 11-7082 reduced PTHrP P2 promoter-initiated transcripts in HTLV-1-infected T cells. In summary, the data demonstrated that transcriptional regulation of PTHrP in ATLL cells can be controlled by NF-kappaB activation and also suggest a Tax-independent mechanism of activation of PTHrP in ATLL.


Assuntos
Regulação Neoplásica da Expressão Gênica , Leucemia-Linfoma de Células T do Adulto/genética , NF-kappa B/fisiologia , Proteína Relacionada ao Hormônio Paratireóideo/genética , Regiões Promotoras Genéticas , Adulto , Animais , Western Blotting , Linhagem Celular Tumoral , Cloranfenicol O-Acetiltransferase , Imunoprecipitação da Cromatina , Ensaio de Desvio de Mobilidade Eletroforética , Infecções por HTLV-I/metabolismo , Infecções por HTLV-I/virologia , Humanos , Leucemia-Linfoma de Células T do Adulto/metabolismo , Leucemia-Linfoma de Células T do Adulto/patologia , Camundongos , Camundongos Endogâmicos NOD , Camundongos SCID , Mutagênese Sítio-Dirigida , Proteína Relacionada ao Hormônio Paratireóideo/metabolismo , Plasmídeos , Reação em Cadeia da Polimerase , RNA Mensageiro/genética , RNA Mensageiro/metabolismo , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Ativação Transcricional , Transfecção
3.
Circ Res ; 40(1): 105-11, 1977 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-830433

RESUMO

Automaticity was induced in isolated guinea pig and cat papillary muscles by application of depolarizing constant current pulses. Increasing extracellular potassium from 1 to 15 mM caused a shift of pacemaker-like activity to less negative diastolic potentials and a decrease in maximum phase 4 slope. Membrane resistance, estimated from the relation of applied current to maximum diastolic potential, decreased when extracellular potassium was increased. Voltage clamps of cat papillary muscle demonstrated that action potentials activate a time-dependent outward current which has a reversal potential of -79.1 mV (+/- 0.99 SE, n = 20) at an extracellular potassium concentration of 5 mM. The reversal potential of this current varies with extracellular K+ with a slope of 50-60 mV per 10-fold concentration change. The current is activated by voltage clamps or action potential plateaus in the range of -30 to +30 mV. It has a time constant of deactivation which increases from approximately 100 to over 400 msec as clamp potential is increased from -90 to -60 mV. It is proposed that this current is equivalent to Ix1 demonstrated in other cardiac tissues and is responsible, in combination with inward currents, for automaticity in ventricular fibers.


Assuntos
Sistema de Condução Cardíaco/efeitos dos fármacos , Potássio/farmacologia , Função Ventricular , Potenciais de Ação/efeitos dos fármacos , Animais , Gatos , Estimulação Elétrica , Eletrocardiografia , Cobaias , Sistema de Condução Cardíaco/fisiologia , Técnicas In Vitro , Potenciais da Membrana/efeitos dos fármacos , Métodos , Contração Miocárdica/efeitos dos fármacos , Fatores de Tempo
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