Comparative effects of various nitric oxide donors on ferritin regulation, programmed cell death, and cell redox state in plant cells

Past studies investigating the regulatory functions of nitric oxide (NO) in plant cells have utilized various NO-donors that release NO in different redox forms, which has lead to problems in the interpretation of data. In the present study, the effects of different NO-donors releasing NO with eithe...

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Veröffentlicht in:Journal of plant physiology. - 1979. - 161(2004), 7 vom: 24. Juli, Seite 777-83
1. Verfasser: Murgia, Irene (VerfasserIn)
Weitere Verfasser: de Pinto, Maria Concetta, Delledonne, Massimo, Soave, Carlo, De Gara, Laura
Format: Aufsatz
Sprache:English
Veröffentlicht: 2004
Zugriff auf das übergeordnete Werk:Journal of plant physiology
Schlagworte:Comparative Study Journal Article Research Support, Non-U.S. Gov't NOC 18 Nitric Oxide Donors Nitroso Compounds Reactive Oxygen Species S-nitro-N-acetylpenicillamine Nitroprusside 169D1260KM mehr... Nitric Oxide 31C4KY9ESH S-Nitrosoglutathione 57564-91-7 Ferritins 9007-73-2 Penicillamine GNN1DV99GX
Beschreibung
Zusammenfassung:Past studies investigating the regulatory functions of nitric oxide (NO) in plant cells have utilized various NO-donors that release NO in different redox forms, which has lead to problems in the interpretation of data. In the present study, the effects of different NO-donors releasing NO with either NO+ (SNP) or NO' (SNAP, GSNO, NOC-18) character have been compared in plant cells. In particular, ferritin regulation, programmed cell death, cellular redox state, and ROS-scavenging enzymes in Arabidopsis thaliana and Nicotiana tabacum cells were examined. The results show that SNP behaves differently than the other NO-donors tested; indeed, SNP induces accumulation of ferritin transcripts in Arabidopsis, whereas SNAP inhibits its accumulation. Moreover, among the assortment of donors tested, only SNP caused programmed cell death and suppression of ROS-scavenging systems
Beschreibung:Date Completed 04.11.2004
Date Revised 13.12.2023
published: Print
Citation Status MEDLINE
ISSN:1618-1328