Inhibition of cell cycle pathway by flavopiridol promotes survival of cerebellar granule cells after an excitotoxic treatment

Verdaguer, E; Jimenez, A; Canudas, AM; Jorda, EG; Sureda, FX; Pallas, M; Camins, A

Abstract

Kainic acid (KA)-induced neuronal damage and the protective effects of flavopiridol were studied in primary cultures of rat cerebellar granule cells (CGNs). When neurons were treated with 500 muM KA, the percentage of cells with condensed nuclei measured by nuclear counting increased by up to 55%. After flavopiridol treatment, an antitumoral drug that is a broad inhibitor of cyclin-dependent kinases, the percentage of condensed nuclei decreased by up to 26%. Furthermore, this KA-mediated cell death was only partially dependent on the activation of the initiator caspase-9 and the effector caspases-3 and -6. This argues for a minor role of caspases in the intracellular pathway leading to KA-induced programmed cell death in CGNs. We examined the possible implication of cell cycle proteins in KA-induced neurotoxicity. We found an increase in the expression of proliferating cell nuclear antigen and E2F-1, two proteins implicated in S-phase, by Western blot. KA increased bromodeoxyuridine incorporation in CGNs, a marker of cell proliferation, and flavopiridol attenuated this effect. These results indicated that flavopiridol decreased the expression of cell cycle markers in CGNs after KA treatment. Flavopiridol might thus be used as a preventive agent against neurodegenerative diseases associated with cell cycle activation.

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Título según WOS: ID WOS:000188467800027 Not found in local WOS DB
Título de la Revista: JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS
Volumen: 308
Número: 2
Editorial: AMER SOC PHARMACOLOGY EXPERIMENTAL THERAPEUTICS
Fecha de publicación: 2004
Página de inicio: 609
Página final: 616
DOI:

10.1124/jpet.103.057497

Notas: ISI