1. Mitochondrial bioenergetics linked to the manifestation of programmed cell death during somatic embryogenesis of Abies alba.
- Author
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Petrussa E, Bertolini A, Casolo V, Krajnáková J, Macrì F, and Vianello A
- Subjects
- Abies drug effects, Abies metabolism, Adenosine Triphosphate metabolism, Cell Respiration drug effects, Cytochromes c metabolism, DNA Fragmentation drug effects, Fatty Acids pharmacology, Glucose-6-Phosphate metabolism, Membrane Potential, Mitochondrial drug effects, Mitochondria drug effects, Mitochondria enzymology, Mitochondrial Proteins, NADP metabolism, Oxidoreductases metabolism, Oxygen metabolism, Plant Proteins, Potassium Channels metabolism, Abies cytology, Abies embryology, Apoptosis drug effects, Embryonic Development drug effects, Energy Metabolism drug effects, Mitochondria metabolism
- Abstract
The present work reports changes in bioenergetic parameters and mitochondrial activities during the manifestation of two events of programmed cell death (PCD), linked to Abies alba somatic embryogenesis. PCD, evidenced by in situ nuclear DNA fragmentation (TUNEL assay), DNA laddering and cytochrome c release, was decreased in maturing embryogenic tissue with respect to the proliferation stage. In addition, the major cellular energetic metabolites (ATP, NAD(P)H and glucose-6-phosphate) were highered during maturation. The main mitochondrial activities changed during two developmental stages. Mitochondria, isolated from maturing, with respect to proliferating cell masses, showed an increased activity of the alternative oxidase, external NADH dehydrogenase and fatty-acid mediated uncoupling. Conversely, a significant decrease of the mitochondrial K (ATP)(+) channel activity was observed. These results suggest a correlation between mitochondrial activities and the manifestation of PCD during the development of somatic embryos. In particular, it is suggested that the K (ATP)(+) channel activity could induce an entry of K(+) into the matrix, followed by swelling and a release of cytochrome c during proliferation, whereas the alternative pathways, acting as anti-apoptotic factors, may partially counteract PCD events occurring during maturation of somatic embryos.
- Published
- 2009
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