Please use this identifier to cite or link to this item: https://repositorio.unifesp.br/handle/11600/29627
Title: P2X(7)-induced apoptosis decreases by aging in mice myeloblasts
Authors: Paredes-Gamero, Edgar Julian
Dreyfuss, Juliana Luporini
Nader, Helena B.
Oshiro, Maria Etsuko Miyamoto [UNIFESP]
Ferreira, Alice Teixeira
Universidade Federal de São Paulo (UNIFESP)
Keywords: bone marrow
myeloblasts
apoptosis
aging
P2X(7) receptor
Issue Date: 1-Apr-2007
Publisher: Elsevier B.V.
Citation: Experimental Gerontology. Oxford: Pergamon-Elsevier B.V., v. 42, n. 4, p. 320-326, 2007.
Abstract: In the current study, the ability of ATP to promote apoptosis in myeloblasts at different ages was investigated. We have observed that high concentration of extracellular ATP (> 1 mM), which activates P2X(7) receptor, produced cell shrinkage an increase in the number of events in the sub-G(0)/G(1) region of the cellular cycle and annexin-V/propidium iodide label, which characterizes the apoptotic cell death. in addition, BzATP produced apoptosis, but not ADP and UTP. Gr-1(+) cells express the P2X(7) receptor and oxidized ATP, a specific P2X(7) inhibitor, blocked the ATP-dependent apoptosis. ATP-dependent apoptosis is decreased by aging in myeloblasts of 12 and 22-month-old mice. Furthermore, P2X(7) expression decrease was observed in older mice, explaining apoptosis decrease. This decrease in apoptosis by aging may be related to some diseases in the myelocyte lineage. (c) 2007 Published by Elsevier Inc.
URI: http://repositorio.unifesp.br/handle/11600/29627
ISSN: 0531-5565
Other Identifiers: http://dx.doi.org/10.1016/j.exger.2006.11.011
Appears in Collections:Em verificação - Geral

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