Awardee OrganizationUNIVERSITY OF MARYLAND BALTIMORE
Description
Abstract Text
The uterine endometrium undergoes extensive cellular differentiation and
development of new blood vessels, i.e. angiogenesis during each menstrual
cycle in preparation for implantation. Although estrogen and progesterone
have established role in neovascularization, the mechanisms underlying
this process have not been established. Specific growth-promoting
peptides, i.e. vascular endothelial growth/permeability factor (VEG/PF)
and basic fibroblast growth factor (bFGF), stimulate angiogenesis in other
systems. Therefore, the present combined basic-clinical research project
will utilize in vivo approaches in an established non-human primate model,
the baboon, and a microcarrier-based cocultivation system with human
endometrial cells to test the hypothesis that estrogen and/or progesterone
regulate angiogenesis with the endometrium by stimulating expression of
VEG/PR and bFGF and their receptors. In Study 1, angiogenesis,
microvascular permeability and expression and cellular localization of
VEG/PF and bFGF and their respective tyrosine kinase receptors will be
determined in baboons during the normal menstrual cycle and after
ovariectomy and the acute or chronic administration of estradiol and/or
progesterone. Study 2 will employ an adenovirus-mediated antisense
oligonucleotide transfer approach to disrupt the expression of VEG/PF and
bFGF in the uterus to test in vivo the hypothesis that these peptides have
essential roles upon angiogenesis within the endometrium and consequently
upon fertility of the baboon. Study 3 will use a microcarrier
cocultivation system to test the hypothesis that estrogen and/or
progesterone regulate angiogenesis in human endometrial cells by
simulating expression of VEG/PF and bFGF and their receptors. The
objective of this study is to transfer the knowledge gained on the
physiology and regulation of the angiogenesis system in vivo in the baboon
to the study of human endometrial cells in vitro. Completion of this
project will provide a fundamental basis for improving our understanding
of the etiology of, and establishing in future project years more
effective hormonal treatment modalities for, infertility in women.
Eunice Kennedy Shriver National Institute of Child Health and Human Development
CFDA Code
DUNS Number
188435911
UEI
Z9CRZKD42ZT1
Project Start Date
01-April-1999
Project End Date
31-March-2000
Budget Start Date
01-October-1998
Budget End Date
30-September-1999
Project Funding Information for 1999
Total Funding
$139,589
Direct Costs
Indirect Costs
Year
Funding IC
FY Total Cost by IC
1999
Eunice Kennedy Shriver National Institute of Child Health and Human Development
$139,589
Year
Funding IC
FY Total Cost by IC
Sub Projects
No Sub Projects information available for 5U54HD036207-02 0004
Publications
Publications are associated with projects, but cannot be identified with any particular year of the project or fiscal year of funding. This is due to the continuous and cumulative nature of knowledge generation across the life of a project and the sometimes long and variable publishing timeline. Similarly, for multi-component projects, publications are associated with the parent core project and not with individual sub-projects.
No Publications available for 5U54HD036207-02 0004
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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 5U54HD036207-02 0004
Clinical Studies
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