 |
Pamela J. Skinner, Ph.D.
Assistant Professor
Veterinary and Biomedical Sciences Department
University of Minnesota, 1998, Ph.D.
skinn002@umn.edu
612-624-2644 office
612-624-2644 lab
|
Research Interests:
Neurodegenerative disease and HIV pathogenesis Research
in our laboratory focuses on two distinct projects. The goal
of the first project is to gain insights into prion and Alzheimer
disease pathogenesis. The goal of the second project is to
gain insights into human immunodeficiency virus (HIV) and
simian immunodeficiency virus (SIV) pathogenesis. Prion and
Alzheimer diseases are fatal neurodegenerative diseases with
no known cure. Increased understanding of the molecular events
that lead to neurodegeneration in each of these diseases is
needed for early diagnosis and the development of new drug
therapies. Current efforts in our lab involve the use of cDNA
microarrays to identify alterations in gene expression that
occur during prion-induced pathogenesis and Alzheimer's disease
pathogenesis. The ultimate goal of the prion/Alzheimer research
project is to increase our understanding of the molecular
events that occur during these disease processes, identify
markers for early diagnosis, and identify new targets for
drug therapy. The HIV/SIV project is motivated by the fact
that over 35 million people worldwide are infected with HIV.
A pressing biomedical priority is the development of an effective
HIV vaccine. Several lines of evidence have indicated that
the development of an effective HIV vaccine will require the
induction of a strong virus specific cytotoxic T lymphocyte
(CTL) response. Using MHC-class I tetramers, I developed a
method to stain antigen specific CTLs in tissue
sections. This technique is referred to as in situ tetramer
staining (IST). We are using IST to evaluate SIV and HIV specific
T cells in tissues after infection, and plan to use IST to
evaluate the effects of
vaccination on the development of anti-viral T cells in tissues.
Selected Recent Publications:
- Skinner PJ, Abbassi H, Chesebro B, Race RE, Reilly C, Haase AT. 2006. Gene expression alterations in brains of mice infected with three strains of scrapie. BMC Genomics. 7:114.
- Skinner PJ, Vierra-Green CA, Emamian E, Zoghbi HY, Orr
HT. 2002 Amino acids in a region of ataxin-1 outside of
the polyglutamine tract influence the course of disease
in SCA1 transgenic mice. Neuromolecular
Medicine. 1(1):33-42.
- Mothé, BR, Horton, H, Carter, DK, Liebl,
ME, Skinner, PJ, Allen, TM, Vogel, TU, Franchini,
G, Rehrauer, W, Wilson, N, Altman, JD, Haase, AT,
Picker, LJ, Sette, AD, Watkins, DI. 2002. Dominance
of CD8 Responses Specific for Epitopes Bound by a Single
MHC Class I Molecule During Both the Acute and Chronic Phases
of Viral Infection. Journal of Virology. 76(2): 875-84
- Skinner, PJ, Vierra-Green, CA, Clark, HB, Zoghbi,
HY, and Orr, HT. 2001. Altered trafficking of membrane
proteins in Purkinje cells of SCA1 transgenic mice. American
Journal of Pathology. 159, 905-13.
- Skinner, PJ, Allen, TM, Mothe, BR, Watkins, DI,
and Haase, AT. 2001. In situ tetramer staining of SIV
specific T cells. Pharma-Transfer.
- Fernandez-Funez, P, ML Nino-Rosales, B de Gouyon,
WC She, JM Luchak, P Martinez, E Turiegano, J Benito,
M Capovilla, P J Skinner, A McCall, I Canal, HT
Orr, HY Zoghbi, and J Botas. 2000. Identification
of genes that modify ataxin-1-induced
neurodegeneration. Nature.
408:101-6.
- Kaytor, MD, Duvick, LA, Skinner, PJ, Koob, MD,
Ranum, LPW, and Orr, HT. 1999. Nuclear localization
of the spinocerebellar ataxia type 7 protein, ataxin-7.
Human
Molecular Genetics 8(9): 1657-1664.
Last modified on: October 24, 2006 |