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Biomedical subjects

P Bethke

Publications and source records attributed to P Bethke.

3 recordsLinked to original sources

Programmed cell death in cereal aleurone.

Progress in understanding programmed cell death (PCD) in the cereal aleurone is described. Cereal aleurone cells are specialized endosperm cells that function to synthesize and secrete hydrolytic enzymes that break down reserves in the starchy endosperm. Unlike the cells of the starchy endosperm, aleurone cells are viable in mature grain but undergo PCD when germination is triggered or when isolated aleurone layers or protoplasts are incubated in gibberellic acid (GA). Abscisic acid (ABA) slows down the process of aleurone cell death and isolated aleurone protoplasts can be kept alive in media containing ABA for up to 6 months. Cell death in barley aleurone occurs only after cells become highly vacuolated and is manifested in an abrupt loss of plasma membrane integrity. Aleurone cell death does not follow the apoptotic pathway found in many animal cells. The hallmarks of apoptosis, including internucleosomal DNA cleavage, plasma membrane and nuclear blebbing and formation of apoptotic bodies, are not observed in dying aleurone cells. PCD in barley aleurone cells is accompanied by the accumulation of a spectrum of nuclease and protease activities and the loss of organelles as a result of cellular autolysis.

Apoptosis↗

Assessment of ferrocytochrome C oxidation by hydrogen peroxide.

The reduction of ferricytochrome C is commonly employed for the quantitation of O2-.H2O2 arising from the dismutation of O2- is capable of oxidizing ferrocytochrome C. In order to assess whether this may interfere with O2- quantitation, the amount of H2O2 required for the oxidation of ferrocytochrome C was determined. While H2O2 concentrations below 10(-5) M were ineffective, one half of the reduced cytochrome was oxidized by 5 x 10(-5) M H2O2 within 15 min. H2O2 in the concentration range at which ferrocytochrome C is oxidized is generated upon interaction of hypoxanthine with xanthine oxidase and upon stimulation of human polymorphonuclear neutrophilic granulocytes by phorbol myristate acetate or the phagocytosis of opsonized zymosan. It is suggested that O2- quantitation by cytochrome C reduction is routinely performed in the presence of catalase.

Catalase↗