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UNDERGRADUATE RESEARCH
Kris White
Drosophila pericardial cells express
biotransformation and detoxification enzymes
The developing Drosophila heart is initially composed of cells that differentiate
into two cell types: cardioblasts that give rise to the dorsal heart
tube and pericardial cells that flank the heart. A number of recent
studies have identified key genetic switches that differentiate cardial
cells from pericardial cells during development. In addition, the morphology
of the pupal and adult heart and pericardial cells has now been studied,
but the function of the pericardial cells remains poorly defined. Various
functions that have been ascribed to these cells but most often they
are said to play a role in hemolymph filtration and detoxification.
This function has been assumed based on morphological data, not demonstrated
by physiological tests. Studies in moths have linked pericardial cells
to the sequestration of juvenile hormone esterase and the production
of biliverdin reductase and peroxidase. Drosophila pericardial cells have previously been shown to have
endogenous b-galactosidase activity and to express an ecdysteriod UDP-glucosyl/UDP
glucuronosyl transferase. Kris is using a combination of subtractive
hybridization, standard Northern analysis and in situ hybridization to determine what enzymes pericardial
cells express at high levels. A number of enzymes involved in the biotransformation
of waste and/or toxic materials, including endogenous peroxidase, and
Ugt37c1 are being examined specifically. Other enzymes under study include:
cytochromeP-450 monoxygenages and reductases, biliverdin reductase,
phenol-O-methyltransferase, N-acetyltransferase and g-glutamethyltransferase.

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