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Danxia Liu, Ph.D.
Professor of Neurology
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Education:
Undergraduate education in
Biology and Physics, 1963
Graduate education in
Biophysics and Biochemistry, MS (1966)
Graduate education in
Biochemistry, Ph.D. (1982)
Beijing (Peking)
University, Beijing, China
Postdoctoral Researcher
in Neurochemistry in Department of Neurology, Stout Neuroscience
Mass Spectrometry Laboratory, University of Tennessee at Memphis,
College of Medicine, 1986-1987. Sponsor: Dr. D. M. Desiderio.
Area of Research:
To identify substances
that contribute to secondary cell death and to explore the molecular
mechanisms of neuron degeneration and death caused by these
substances in order to develop therapeutic strategies to prevent
such death following central nervous system injury and neurological
disorders. The currently research project is to investigate the
roles and pathways by which reactive species cause cell death,
particularly apoptosis, after spinal cord injury and to explore the
therapeutic potential of a metalloporphyrin - a superoxide dismutase
mimetic and a broad spectrum scavenger of reactive species - in
spinal cord injury and other neurological disorders.
To identify the proteins
most susceptible to oxidative damage and the proteins important in
apoptotic cell death pathways following central nervous system
injury and neurological disorders by utilizing proteomic
technology. This will offer accurate targets for therapeutic
intervention.
Research Support: The
research projects have been
continuously supported by the PI's grants from NIH (NINDS, RO1s) and
other agencies.
Teaching
Responsibility: Lectures in graduate and medical school courses and
directs a course "Proteomics in Neuroscience”
in the graduate school.
Service:
Grant Reviewer
for the NIH (study section: Special Emphasis Panel for RFA in
2000), Paralyzed Veterans of America, Spinal Cord Research
Foundation, Department of Veterans Affairs, Western Research &
Development Center
Journal Reviewer For Annuals of Neurology, the
Journal of Neuroscience, Journal of Neurochemistry, Neuroscience,
Experimental Neurology, Brain Research, Neuroscience Letters, Free
Radical Biology and Medicine, Neurochemistry International,
Anesthesiology, Anesthesia & Analgesia
Selected Publications in Peer-Reviewed Journals:
1. Liu, D., Bao, F., Wen, J., and
Liu, J. Mutation of Superoxide Dismutase Elevates Reactive Species:
Comparison of Nitration and Oxidation of Proteins in Different Brain
Regions of Transgenic Mice with Amyotrophic Lateral Sclerosis.
Neuroscience, 146: 255-264, 2007
2. Ling, X., and
Liu, D. The temporal and spatial profile of cell loss after
spinal cord injury: Reduction by a metalloporphyrin. J. Neurosci.
Res. 85: 2175-2185, 2007.
3. Hachmeister, J. E.,
Valluru, L., Bao, F., and Liu, D. Mn (III) Tetrakis
(4-Benzoic Acid) Porphyrin Administered into the Intrathecal Space
Reduces Oxidative Damage and Neuron Death after Spinal Cord Injury:
A Comparison with Methylprednisolone. J. Neurotrauma, 23: 1766-1778,
2006.
4.
Liu, D., Bao,
F., Prough, D. S., and Dewitt, D. S. Peroxynitrite generated at the
level produced by spinal cord injury induces peroxidation of
membrane phospholipids in normal rat cord: Reduction by a
metalloporphyrin. J. Neurotrauma, 22: 1123-1133, 2005.
5. Bao, F., and
Liu, D.,
Hydroxyl radicals generated in the rat spinal cord at the level
produced by impact injury induce cell death by necrosis and
apoptosis: Protection by a metalloporphyrin. Neuroscience, 126:
285-295, 2004.
6.
Liu, D.,
Liu, J., sun, D., and Wen, J. The time course of hydroxyl radical
formation following spinal cord injury: the possible role of the
iron-catalyzed Haber-Weiss reaction. J. Neurotrauma, 21: 805-816,
2004.
7. Bao, F., and
Liu, D.,
Peroxynitrite generated in the rat spinal cord induces apoptotic
cell death and activates caspase-3. Neuroscience, 116: 59-70, 2003.
8. Bao, F., Dewitt, d. S.,
Prough, D. S., and Liu, D., Peroxynitrite generated in
the rat spinal cord induces oxidation and nitration of proteins:
Reduction by Mn (III) tetrakis (4-benxoic acid) porphyrin. J.
Neurosci. Res., 71: 220-227, 2003.
9.
Liu, D.,
Liu, J., Sun, D., Alcock, N. W., and Wen, J. Spinal injury increases
iron: Catalytic production of hydroxyl radicals. Free Rad. Biol.
Med., 34: 64-71, 2003.
10. Bao, F., and
Liu, D.,
Peroxynitrite generated in the rat spinal cord induces neuron death
and neurological deficits. Neuroscience, 115: 839-849, 2002.
11.
Liu, D.,
Li, L., and Augustus, L. Prostaglandin release by impact injury
mediates hydroxyl radical and malondialdehyde production and cell
death: A site of the neuroprotective action of methylprednisolone.
J. Neurochem. 77: 1036-1047, 2001.
12. Leski, M. L., Bao, F., Wu,
L., Qian, H., Sun, D., and Liu, D., Protein and DNA
oxidation in spinal injury: Neurofilaments - an oxidation target.
Free Rad. Biol. Med., 30: 613-624, 2001.
13.
Liu, D.,
Ling, X., Wen, J., and Liu, J. The role of reactive nitrogen
species in secondary spinal cord injury: Formation of nitric oxide,
peroxynitrite, and nitrated protein. J. Neurochem. 75: 2144-2154,
2000.
14.
Liu, D.,
Wen, J., Liu, J., and Li, L. The roles of free radicals in
amyotrophic lateral sclerosis: Reactive oxygen species and elevated
oxidation of protein, DNA and membrane phospholipids. FASEB
Journal, 13: 2318-2328, 1999. (Accepted
without revision)
15.
Liu, D.,
Liu, J., and Wen, J. Elevation of hydrogen peroxide after spinal
cord injury detected by using the Fenton reaction. Free Rad. Biol.
Med. 27: 478-482, 1999.
16. Liu, D.,
Xu, G., Pan, E., and McAdoo, D.J. Neurotoxicity of glutamate at the
concentration released upon spinal cord injury. Neuroscience. 93:
1383-1389, 1999.
17.
Liu, D.,
Sybert, T. E., Qian, H., and Liu, J. Superoxide production after
spinal injury detected by microperfusion of cytochrome c. Free Rad.
Biol. Med. 25: 298-304, 1998.
18. Qian, H., and
Liu,
D., The time course of malondialdehyde production following
impact injury to rat spinal cord as measured by microdialysis and
high pressure liquid chromatography. Neurochem. Res. 22:
1231-1236, 1997.
19. Liu, D.,
Yang, J., Li, L., and McAdoo, D.J. Paraquat - a superoxide generator
- kills neurons in rat spinal cord. Free Rad. Biol. Med. 18:
861-867, 1995.
20. Liu, D.,
and Li, L. Prostaglandin F2α rises in extracellular fluid
in response to hydroxyl radical generated in vivo in rat
spinal cord. Free Rad. Biol. Med. 18: 571-576, 1995.
21. Liu, D.,
Yang, R., Yan, X., and McAdoo, D.J. Hydroxyl radical generated in
vivo kills neurons in spinal cord: electrophysiological,
histological, and neurochemical results. J. Neurochem. 62: 37-44,
1994. (Accepted without revision)