NIH Training Grant in Basic Aging Research
Abstract
As the U.S. population ages, it
is increasingly important that we understand the molecular and cellular
basis of aging. Aging is the major risk factor for a broad spectrum
of pathologies including cardiovascular dysfunction, cancer, osteoporosis,
osteoarthritis, type II diabetes and neurodegenerative disorders such
as Parkinson's and Alzheimer's disease. It is generally accepted that
at least some age-related molecular changes are causal factors in the
onset of these diseases. It is also clear that individuals differ, both
qualitatively and quantitatively, in how they age. Rational approaches
to preventing and intervening in age-related processes depend on a thorough
understanding of the molecular, cellular and physiologic basis of human
aging, as well as the genetic and environmental factors that contribute
to inter-individual differences.
This proposed training program brings
together cell and molecular biologists and physiologists from the Lawrence
Berkeley National Laboratory (LBNL) and the University of California
Berkeley (UCB) who share contiguous and overlapping facilities in Berkeley,
CA. The program offers outstanding research training in the genetic
and environmental factors that influence aging rates, and in the molecular
cellular and physiological causes and consequences of aging in mammals.
The proposed trainers are experienced investigators with diverse but
complementary research interests and experimental approaches. the training
program will be enhanced by the strong biomedical research community
that exists in the Berkeley/San Francisco Bay area, and the growing
commitment to aging research at LBNL.
The proposed training program is
for individuals holding a Ph.D. or M.D. degree, and interest in career
in aging research. In addition to the research projects described herein,
the trainees will attend regular seminars and research meetings that
will provide them with a broad education in aging and related topics
and critical feedback on their research projects. The research facilities
available to trainees include the Center for Functional Imaging with
its ability to produce short-lived isotopes for use in PET and MRI scans,
a barrier and transgenic mouse facility, a high throughput DNA sequencing
facility, the Resource for Molecular Cytogenetics with its emphasis
on positional cloning and functional genomics, and extensive cell culture
and molecular biology facilities.
FACULTY
| Judith Campisi |
Lawrence Berkeley National Laboratory
|
Program Director |
| Bruce Ames |
UC Berkeley |
Preceptor |
| Thomas Budinger |
Lawrence Berkeley National Laboratory,
UC San Francisco |
Preceptor |
| William Jagust |
Lawrence Berkeley National Laboratory,
UC Davis |
Preceptor |
| Arnold Kahn |
UC San Francisco |
Executive Committee Member |
| Yoshinori Kohwi |
Lawrence Berkeley National Laboratory |
Preceptor |
| Ronald Krauss |
Lawrence Berkeley National Laboratory |
Preceptor |
| Stuart Linn |
UC Berkeley |
Preceptor |
Research Specialties in Relation
to Aging
| Research Area |
Preceptors |
Projects in Preceptor's Laboratory |
| Cellular Senescence |
Campisi |
Senescence-specific
gene expression; cell cycle regulation; cell senescence in vivo. |
|
Ames |
Role of exidative
damage and mitochondrial function in cell senescence. |
|
Linn |
Mechanisms of DNA
replication |
| Genetic Factors |
Campisi |
Senescence and
longevity in genes; Werner's syndrome, telomere biology |
|
Krauss |
Lipoprotein genes;
genetic loci for cardiovascular disease and aging |
| Oxidative Damage |
Ames |
Role of oxidative
damage in cancer and aging; tissue differences in generation and
repair of oxidative damage; mutagenesis |
|
Krauss |
Oxidation of lipoproteins;
oxidation-induced changes in gene expression |
|
Linn |
Repair of oxidatively
damaged DNA |
| Neurodegeneration |
Budinger |
Metabolism and
blood flow imaging in normal, diseased, and aging brain. |
|
Jagust |
Brain imaging during
cognitive and functional decline due to aging, Alzhheimer's and
Parkinson's disease; brain imaging for gene therapy. |
|
Kohwi |
Molecular biology
of triplet repeat binding protein; brain physiology and triplet
repeat binding protein function |
| Cancer |
Ames |
Oxidative DNA damage
and carcinogen-induced cell proliferation in cancer |
|
Budinger |
Development of
imaging probes for primary tumors and metastases |
|
Campisi |
Oncogenes and
tumor suppressor genes in immortalization; role of cell senescence
in tumorigenesis |
|
Kohwi |
Role of DNA structure
in carcinogen-DNA interactions |
|
Linn |
Mechanisms of DNA
damage and repair. |