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Mark R.Fielden
Graduate Student
Contact information
GenoSpectra, Inc.
6519 Dumbarton Circle
Fremont, CA 94555
Tel: 510.818.2674
Fax: 510.818.2650
e-mail: mfielden@genospectra.com
Education
B.Sc. Toxicology 1997, University of Guelph, Ontario,
Canada.
Ph.D Biochemisty and Environmental Toxicology. May 2002.
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Research Project
Reproductive and Genomic Effects of Male Endocrine Disruptors
Many studies suggest that gestational and lactational exposure
to endocrine disrupting chemicals can adversely affect reproductive
function at later stages of life.Studies on the male reproductive
system emphasize the importance of hormonal timing during gestation
and neonatal life for normal development of the reproductive
system. Variations in the timing of hormonal interference can
result in cryptorchidism, incomplete genitalia development,
and incomplete maturation of germ cells and the supporting Sertoli
and Leydig cells of the testes which may result in reduced sperm
production and/or testicular and germ cell cancers. Mechanistic
studies and epidemiological evidence of decreasing sperm quality
supports the hypothesis that human male fertility may be at
risk due to exposure to exogenous estrogenic chemicals during
development. To assess the effects of developmental exposure
to exogenous estrogenic chemicals, both natural and synthetic,
requires a comprehensive understanding of their effects at the
molecular, cellular and tissue level within the context of the
whole organism and its genome. To address these needs, we are
employing a comprehensive strategy in order to assess the effects
of male endocrine disruptors on development, spermatogenesis
and testicular gene expression.
Using the mouse as our model system, we are examining exposed
offspring at the tissue, cell and molecular level and at two
developmental stages; early and late adulthood. Tissue level
effects are assessed by examing testicular histology and development
of other hormone-dependent tissues. Cellular level effects are
assessed using a computer-assisting sperm analysis system and
an in vitro fertilization assay (IVF) to examine spermatogenesis.
In order to study the effects of male endocrine disruptors at
the molecular level, a testis-specific DNA microarray (dbTEST)
is being developed in our lab to measure testicular gene expression
profiles in affected male offspring. Integration of tissue,
cellular and molecular level effects should point to many new
hypotheses as to the mechanisms of action of a diverse set of
endocrine disruptors and may also reveal new insights into the
role of estrogens in male reproductive development and spermatogenesis.
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