Grant: Discovery Grants Program - Individual
Laurentian University of Sudbury
$25,000.00
Regulation of the phenylethanolamine N-methyltransferase gene by hypoxia
EF 2015-16
Résumé
Oxygen is a critical component of normal cellular function and homeostasis in mammalian cells. Mammals are capable of eliciting a stress-response to reduced oxygen to facilitate either removal or adaptation to hypoxia. The mammalian stress-response is mediated via activation of the hypothalamic-pituitary-adrenal (HPA) axis and the sympatho-adrenal (SA) axis, resulting in the release of the stress hormones, cortisosterone/cortisol and adrenaline. Adrenaline is synthesized and released by the adrenal glands and is the neurotransmitter/neurohormone responsible for the mamallian ""fight or flight response"". Although adrenaline synthesis may be regulated via the HPA and SA axis in response to hypoxic stress, recent studies have shown that adrenal chromaffin cells are oxygen sensitive and may therefore regulate homeostatic mechanism, including catecholamine biosynthesis, independent of hormonal and neural activation. This is critically important during fetal development prior to sympathetic innervation of chromaffin cells. The goal of this proposal is to determine the impact hypoxia on the synthesis and regulation of the stress hormone, adrenaline, via its biosynthetic enzyme phenylethanolamine N-methyltransferase (PNMT). This proposal will utilize a cell to systems biology approach to examine the role of hypoxia in the regulation of the PNMT gene. Utilizing advanced in vitro cellular and molecular techniques, the mechanism involved in the regulation of the PNMT gene in response to hypoxia will be delineated. In addition, the role of oxygen in modulating the stress axis activation of adrenaline synthesis will also be examined. Furthermore, in-vivo studies of acute and chronic hypoxia will also be utilized to examine the whether the molecular regulatory mechanisms identified in-vitro are involved in the whole organism's response to hypoxic stress. The results from this grant will provide new insight into the fundamental cellular processes involved in response to hypoxia. In addition, it will also provide insight into the role of stress the hormone, adrenaline, in the mammalian stress response to and in the adaptation to hypoxia.
Programme
Discovery Grants Program - Individual
Bénéficiaire
Emplacement
Ontario, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
NSERC's Awards Data
Tel que publié
Application id
312776-2012
Name nom
Tai, TzeChun
Department département
Medicine, Faculty of (East Campus)
Organization id
26
Institution établissement
Laurentian University of Sudbury
Province en
Ontario
Province fr
Ontario
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2015
Competition year année de concours
2012
Award amount
25000
Program id
RGPIN
Program name en
Discovery Grants Program - Individual
Program name fr
Programme de subventions à la découverte - individuelles
Group en
Discovery grants programs
Group fr
Programmes de subventions à la découverte
Committee code
1502
Committee name en
Biological Systems and Functions
Committee name fr
Systèmes et fonctions biologiques
Area of application code
1200
Area of application group en
Advancement of knowledge
Area of application group fr
Avancement des connaissances
Area of application en
Advancement of knowledge
Area of application fr
Avancement des connaissances
Research subject code
5503
Research subject group en
Animal biology
Research subject group fr
Biologie animale
Research subject en
Endocrinology
Research subject fr
Endocrinologie
Partie
4
Nb partie
5
Application title
Regulation of the phenylethanolamine N-methyltransferase gene by hypoxia
Keyword
NSERC
Application summary
Oxygen is a critical component of normal cellular function and homeostasis in mammalian cells. Mammals are capable of eliciting a stress-response to reduced oxygen to facilitate either removal or adaptation to hypoxia. The mammalian stress-response is mediated via activation of the hypothalamic-pituitary-adrenal (HPA) axis and the sympatho-adrenal (SA) axis, resulting in the release of the stress hormones, cortisosterone/cortisol and adrenaline. Adrenaline is synthesized and released by the adrenal glands and is the neurotransmitter/neurohormone responsible for the mamallian ""fight or flight response"". Although adrenaline synthesis may be regulated via the HPA and SA axis in response to hypoxic stress, recent studies have shown that adrenal chromaffin cells are oxygen sensitive and may therefore regulate homeostatic mechanism, including catecholamine biosynthesis, independent of hormonal and neural activation. This is critically important during fetal development prior to sympathetic innervation of chromaffin cells. The goal of this proposal is to determine the impact hypoxia on the synthesis and regulation of the stress hormone, adrenaline, via its biosynthetic enzyme phenylethanolamine N-methyltransferase (PNMT). This proposal will utilize a cell to systems biology approach to examine the role of hypoxia in the regulation of the PNMT gene. Utilizing advanced in vitro cellular and molecular techniques, the mechanism involved in the regulation of the PNMT gene in response to hypoxia will be delineated. In addition, the role of oxygen in modulating the stress axis activation of adrenaline synthesis will also be examined. Furthermore, in-vivo studies of acute and chronic hypoxia will also be utilized to examine the whether the molecular regulatory mechanisms identified in-vitro are involved in the whole organism's response to hypoxic stress. The results from this grant will provide new insight into the fundamental cellular processes involved in response to hypoxia. In addition, it will also provide insight into the role of stress the hormone, adrenaline, in the mammalian stress response to and in the adaptation to hypoxia.