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Dadun > Depósito Académico > CIMA (Centro de Investigación Médica Aplicada) > Área de Oncología > Microambiente tumoral > DA - CIMA - Oncología - Microambiente tumoral - Artículos de revista >

Nitric oxide activates granule-associated DNase in human monocytes
Authors: Pio, R. (Rubén)
Lopez-Zabalza, M. (María J.)
Rouzaut, A. (Ana)
Santiago, E. (Esteban)
Lopez-Moratalla, N. (Natalia)
Keywords: Nitric oxide
DNase activity
Human monocytes
Cytotoxic monocytes
Issue Date: 1998
Publisher: Elsevier
Publisher version: http://www.sciencedirect.com/science/article/pii/S1089860398901756
ISSN: 1089-8611
Citation: Pio R, Lopez-Zabalza MJ, Rouzaut A, Santiago E, Lopez-Moratalla N. Nitric oxide activates granule-associated DNase in human monocytes. Nitric Oxide 1998;2(3):165-173.
Abstract
Activated and differentiated human monocytes with a CD14+CD16+ phenotype were found to contain a DNase activity associated with secretion granules. Activated cells were obtained from patients with autoimmune diseases. Activation and differentiation of monocytes were also achieved after incubation of PBMC from healthy subjects with protein A (SpA) or immunopotentiating peptides. DNase activity corresponded to a 66-kDa protein, similar to that described in granules from T lymphocytes, active preferentially on double-strand DNA. DNA fragmentation activity increased when NO donors were present; the activity was higher in the presence of Ca2+, and at low pH values. The Ca2+-dependent activity was inhibited by Zn2+. NO-dependent activity was additive with that of Ca2+-dependent and it was not inhibited by Zn2+. Dithiothreitol did not modify the effect of NO on DNase activity. Incubation of PBMC in the presence of NMLA, an inhibitor of NO synthases, decreased this DNase activity. Data reported clearly suggest a regulatory role of NO in granule-associated DNase activity
Permanent link: http://hdl.handle.net/10171/20313
Appears in Collections:DA - CIMA - Oncología - Biomarcadores - Artículos de Revista
DA - Ciencias - Bioquímica y Biología molecular - Artículos de Revista
DA - CIMA - Oncología - Microambiente tumoral - Artículos de revista

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