Molecular mechanisms of steroid hormone secretion and trafficking
Project Number4R00HD073239-03
Former Number5K99HD073239-02
Contact PI/Project LeaderYAMANAKA, NAOKI
Awardee OrganizationUNIVERSITY OF CALIFORNIA RIVERSIDE
Description
Abstract Text
Project Summary/Abstract
Steroid hormones are a large family of molecules that play pivotal roles during childhood development. During
puberty in humans, elevated secretion of gonadal steroid hormones produces secondary sex characteristics
such as breast development and the appearance of facial hair. Because of such important roles of steroid
hormones in maturation processes, disruption of steroid hormone signaling during childhood can cause
developmental defects that last into adulthood. Understanding the machinery and regulatory mechanisms of
steroid hormone signaling in normal as well as pathological conditions, therefore, contributes greatly to the
promotion of healthy childhood development. The ultimate goal of this project is to elucidate as-yet-unknown
machinery and regulatory mechanisms of steroid hormone release and trafficking, by using the fruitfly Drosophila
as a model organism. In order to accomplish this purpose, the PI will test the hypothesis that the insect steroid
hormone ecdysone is secreted from the steroidogenic tissue in a vesicle-mediated manner, challenging the
conventional idea that all steroid hormones are secreted by free diffusion. During the first mentored phase of the
project, the PI will work closely with his mentor, Michael O'Connor, at the University of Minnesota to develop
some key in vitro methods necessary to elucidate his hypothesis. Those methods include the
immunohistochemical detection of ecdysone, in vitro transporter assay and in vitro steroidogenic tissue culture.
This initial step of the proposed project will help the PI master various biochemistry and cell biology techniques
required to conduct the next step of the project. During the mentored phase, the PI will also undergo extensive
training on teaching and scientific communication, which will be helpful in the next independent phase of his
career. In the subsequent independent investigator phase, the PI will work on the regulatory mechanisms of the
putative vesicle-mediated ecdysone release, by screening G protein-coupled receptors working in the
steroidogenic tissue. He will also screen for a putative ecdysone importer required for its uptake by peripheral
tissues. These approaches should tell us how well this novel machinery of steroid hormone secretion and
trafficking is conserved among different organisms. In the long run, the PI's work has the potential to shift the
paradigm of steroid hormone action and will impact a vast range of research on developmental and disease
processes.
Public Health Relevance Statement
Project Narrative
Steroid hormones regulate multiple physiological processes and are involved in many types of developmental
diseases and cancers. This project is designed to answer the question of how steroid hormone release and
uptake are regulated at the molecular level. The expected outcome of this project will shift the paradigm of
steroid hormone biology and thus will facilitate development of new strategies for disease treatment and human
health improvement.
Eunice Kennedy Shriver National Institute of Child Health and Human Development
CFDA Code
865
DUNS Number
627797426
UEI
MR5QC5FCAVH5
Project Start Date
01-April-2014
Project End Date
31-March-2017
Budget Start Date
01-April-2014
Budget End Date
31-March-2015
Project Funding Information for 2014
Total Funding
$248,473
Direct Costs
$163,469
Indirect Costs
$85,004
Year
Funding IC
FY Total Cost by IC
2014
Eunice Kennedy Shriver National Institute of Child Health and Human Development
$248,473
Year
Funding IC
FY Total Cost by IC
Sub Projects
No Sub Projects information available for 4R00HD073239-03
Publications
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Outcomes
The Project Outcomes shown here are displayed verbatim as submitted by the Principal Investigator (PI) for this award. Any opinions, findings, and conclusions or recommendations expressed are those of the PI and do not necessarily reflect the views of the National Institutes of Health. NIH has not endorsed the content below.
No Outcomes available for 4R00HD073239-03
Clinical Studies
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History
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