Biography:Malú G. Tansey

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Short description: American Physiologist and Neuroscientist


Malú Tansey
NationalityAmerican
Alma materStanford University
University of Texas Southwestern
Washington University in St. Louis
Known forTNF in neuroinflammation and degenerative disease
Awards2013 GIN Faculty of the Year Award Emory University, 2000 O'Leary Prize Winner, 1991 Ida M. Green Award in Physiology
Scientific career
FieldsNeuroscience
InstitutionsUniversity of Florida

Malú G. Tansey is an American Physiologist and Neuroscientist as well as the Director of the Center for Translational Research in Neurodegenerative Disease at the University of Florida. Tansey holds the titles of Evelyn F. and William L. McKnight Brain Investigator and Norman Fixel Institute for Neurological Diseases Investigator. As the principal investigator of the Tansey Lab, Tansey guides a research program centered around investigating the role of neuroimmune interactions in the development and progression of neurodegenerative and neuropsychiatric disease. Tansey's work is primarily focused on exploring the cellular and molecular basis of peripheral and central inflammation in the pathology of age-related neurodegenerative diseases like Alzheimer's disease and amyotrophic lateral sclerosis.

Early life and education

In 1980, Tansey pursued her undergraduate education at Stanford University in Palo Alto, California.[1] She completed her bachelor's degree in Biological Sciences and then stayed at Stanford to complete her Master's in Biological Sciences as well.[2] After graduating in 1985, Tansey pursued her graduate studies in Physiology and Cell Cycle Regulation at the University of Texas Southwestern Medical Center.[3] Under the mentorship of James T. Stull, Tansey explored the role of myosin light chain kinase (MLCK) phosphorylation in the regulation of smooth muscle contraction.[4] Tansey found, early on in her PhD, that cellular mechanisms other than myosin light chain phosphorylation regulate contractile tension in smooth muscle cells.[5] She later found that calcium dependent phosphorylation of MLCK in smooth muscle lead to decreased calcium sensitivity of phosphorylated myosin light chains.[6] Tansey also proposed a model to understand the regulation of myosin light chain kinase phosphorylation by limited calmodulin availability.[6]

Following the completion of her graduate studies in 1992, Tansey moved to Washington University in St. Louis, Missouri, where she worked under the mentorship of Eugene M. Johnson in the Department of Molecular Pharmacology.[7] Tansey first explored the mechanisms of neuronal survival in cerebellar granule cells.[8] She and her team knew that depolarizing concentrations of potassium promoted survival, so they asked whether the downstream effects of potassium influx on survival were mediated by MAP kinase or PI-3-K.[8] They found that survival was dependent on depolarization induced PI-3-K activity.[8] Tansey then collaborated with Jeff Milbrandt's lab in the Department of Genetics at WashU to explore the GDNF family of ligands and the biology of their intracellular signalling.[7] The GDNF family of ligands (GFL) are neurotrophic factors found to be important in neuron survival, so Tansey and her colleagues probed the critical intracellular signalling component of the GFL receptor system, the receptor tyrosine kinase RET.[9] They found that in order for proper RET function and thus proper GFL signalling, RET needed to be interacting with a GPI-linked co-receptor associated with a lipid raft in order for proper functioning.[9] They further found that RET associates with members of the Src family kinases and that interaction and signalling through Src is instrumental in mediating the downstream effects of GFLs.[10]

Career and research

After completing her postdoctoral work, Tansey then moved to California to work in industry for a few years as the group leader of Chemical Genetics at Zencor Inc. in Monrovia.[7] Her work focused on developing tumor necrosis factor (TNF) inhibitors.[1] Tansey then returned to academia in 2002 and became an assistant professor of physiology at the University of Texas Southwestern.[1] At UT Southwestern, Tansey continued to study the role of the cytokine TNF in CNS signalling and disease.[7]

In 2008, Tansey was recruited to become an associate professor at Emory University in Atlanta, Georgia. Tansey became a tenured professor at Emory University, a member of the Center for Neurodegenerative Disease, and the Senior Director of Graduate Studies in Neuroscience.[11] As a Hispanic-American, Tansey worked to increase diversity and inclusion at Emory through her role as the Director of the Emory Initiative for Maximizing Student Development.[11]

In 2019, Tansey was recruited to the University of Florida to become the director of the Center for Translational Research in Neurodegenerative Disease.[12] Tansey also holds the titles of  Evelyn F, and William L McKnight Brain Investigator and Norman Fixel Institute for Neurological Diseases Investigator.[13] In addition to her leadership roles at UF, Tansey is also on the board of directors for the World Parkinson's Coalition.[7]

The Tansey Lab explores the interactions between the nervous and immune systems in the context of health and disease.[14] Tansey specifically focuses on the role of TNF in neuroinflammation and the context of Alzheimer's Disease and Parkinson's Disease.[14] Tansey also explores the roles of microglia and brain macrophages in neurological disease pathogenesis as well as how gene-environment interactions interface with chronic inflammatory states to predispose and perpetuate diseases of the central nervous system.[14]

Tumor necrosis factor signalling in disease

Tansey has been dedicated to exploring the role of TNF in disease and following the potential to inhibit its actions to ameliorate pathological inflammation in disease.[15] Since TNF had been implicated in pathology, Tansey explored a method to sequester TNF in vivo to act as an inhibitor of TNF function.[15] Tansey and her team developed a variant TNF protein that formed heterodimers with TNF in vivo rendering TNF unable to signal through TNF receptors.[15] They found that this appeared to abrogate TNF pathology in animal models.[15] Using this innovative TNF variant, Tansey and her team were able to probe the role of TNF in Alzheimer's Disease and Parkinson's Disease.[16] They found that when they blocked TNF signalling using the variant TNF technology, they were able to attenuate progressive pathology and even reduce microglial activation, which was associated with the loss of dopamine neurons in PD.[16] These findings suggested that targeting TNF might be a promising strategy to prevent the loss of dopamine neurons in PD and also prevent neuronal pathology on AD.[16]

Chronic inflammation and neurodegeneration

Tansey is a pioneer in the exploration of how chronic inflammation predisposes and perpetuates neurological disease. Contrary to previous reports, the immune system does exist in the central nervous system, and the major orchestrators of this immune response are the innate immune cells of the brain called microglia.[17] Short term activation of inflammation in the brain is present in disease, injury, or infection, and is useful in response to disease states, but if this inflammation is prolonged, it can lead to neuronal death.[17] Tansey has helped to educate the field on the concept of acute versus chronic brain inflammation, the purposes and roles of this inflammation, and its relation to chronic neurological diseases.[17] She emphasizes that microglia lie at a convergence point where stimuli can impact microglial activation and thus lead to aberrant brain inflammation and neuronal death in this way.[17] Tansey showed that the microglial GTPase RGS10 might play a protective role in a chronic inflammatory environment.[18] When RGS10 was knocked out in mice with chronic systemic inflammation, it led to overproduction of proinflammatory cytokines by microglia and death of dopaminergic neurons.[18] Since removal of RGS10 in dopaminergic neurons also made them more sensitive to the proinflammatory cytokines released by microglia, Tansey proposed RGS10 as a therapeutic target for PD.[18]

Tansey also explores the role of gene-environment interactions, or epigenetic mechanisms in neurodegenerative disease pathology and chronic inflammation.[19] She probed how diet effects immune infiltration into the brain since previous studies had showed that it might lead to compromised blood brain barrier function and increased immune cell infiltration into the CNS.[20] Conversely, her findings showed that high fat high fructose diets did not increase peripheral trafficking of immune cells into the CNS.[20] Tansey also explored the sex-specific effects of stress on neuro-immune reactivity and found that early life chronic stress led to increased neuro-immune reactivity but via different mechanisms in male versus female rats.[21]

Awards and honors

  • 2019 Keynote Address at the Alzheimer's Association International Conference-Satellite Symposium[22]
  • 2013 GIN Faculty of the Year Award Emory University[23]
  • 2000 O'Leary Prize Winner[24]
  • 1991 Ida M. Green Award in Physiology[25]

Select publications

References

  1. ↑ 1.0 1.1 1.2 "Malú Tansey". https://www.journals.elsevier.com/neurobiology-of-disease/editorial-board/malu-tansey. 
  2. ↑ "Tansey Lab Members" (in en). https://ctrnd.med.ufl.edu/faculty/dr-malu-tansey/tansey-lab-members/. 
  3. ↑ "Malú G. Tansey, Ph.D.". http://www.physiology.emory.edu/people-OLD/faculty/tansey-malu.html. 
  4. ↑ "Malu G. Tansey - Google Scholar Citations". https://scholar.google.com/citations?hl=en&user=zJhs5L0AAAAJ&view_op=list_works&sortby=pubdate. 
  5. ↑ Tansey, M.G.; Hori, M.; Karaki, H.; Kamm, K.E.; Stull, J.T. (17 September 1990). "Okadaic acid uncouples myosin light chain phosphorylation and tension in smooth muscle". FEBS Letters 270 (1–2): 219–221. doi:10.1016/0014-5793(90)81272-P. PMID 2171992. 
  6. ↑ 6.0 6.1 Tansey, M. G.; Word, R. A.; Hidaka, H.; Singer, H. A.; Schworer, C. M.; Kamm, K. E.; Stull, J. T. (25 June 1992). "Phosphorylation of myosin light chain kinase by the multifunctional calmodulin-dependent protein kinase II in smooth muscle cells.". Journal of Biological Chemistry 267 (18): 12511–12516. doi:10.1016/S0021-9258(18)42307-1. PMID 1319999. http://www.jbc.org/content/267/18/12511. 
  7. ↑ 7.0 7.1 7.2 7.3 7.4 "Board of Directors - World Parkinson Coalition". https://www.worldpdcoalition.org/page/Directors. 
  8. ↑ 8.0 8.1 8.2 Miller, Timothy M.; Tansey, Malú G.; Johnson, Eugene M.; Creedon, Douglas J. (11 April 1997). "Inhibition of Phosphatidylinositol 3-Kinase Activity Blocks Depolarization- and Insulin-like Growth Factor I-mediated Survival of Cerebellar Granule Cells". Journal of Biological Chemistry 272 (15): 9847–9853. doi:10.1074/jbc.272.15.9847. PMID 9092520. 
  9. ↑ 9.0 9.1 Tansey, Malú G.; Baloh, Robert H.; Milbrandt, Jeffrey; Johnson, Eugene M. (March 2000). "GFRα-Mediated Localization of RET to Lipid Rafts Is Required for Effective Downstream Signaling, Differentiation, and Neuronal Survival". Neuron 25 (3): 611–623. doi:10.1016/S0896-6273(00)81064-8. PMID 10774729. 
  10. ↑ Encinas, Mario; Tansey, Malú G.; Tsui-Pierchala, Brian A.; Comella, Joan X.; Milbrandt, Jeffrey; Johnson, Eugene M. (1 March 2001). "c-Src Is Required for Glial Cell Line-Derived Neurotrophic Factor (GDNF) Family Ligand-Mediated Neuronal Survival via a Phosphatidylinositol-3 Kinase (PI-3K)-Dependent Pathway". The Journal of Neuroscience 21 (5): 1464–1472. doi:10.1523/JNEUROSCI.21-05-01464.2001. PMID 11222636. 
  11. ↑ 11.0 11.1 "McKnight Brain Institute Neuromedicine Scholars". https://mbi.ufl.edu/files/2018/07/MBI-NS_8-8-18_F.pdf. 
  12. ↑ "Renowned neuroscientists to join UF Health, propel discovery of treatments for neurological diseases". March 18, 2019. https://mbi.ufl.edu/2019/03/18/renowned-neuroscientists-to-join-uf-health-propel-discovery-of-treatments-for-neurological-diseases/. 
  13. ↑ "Dr. Tansey Named the Principal Investigator of a new Parkinson's Foundation Research Center of Excellence Award". July 30, 2019. https://ctrnd.med.ufl.edu/2019/07/30/dr-tansey-named-the-principal-investigator-of-a-new-parkinsons-foundation-research-center-of-excellence-award/. 
  14. ↑ 14.0 14.1 14.2 "Tansey Lab Research" (in en). https://ctrnd.med.ufl.edu/faculty/dr-malu-tansey/tansey-lab-research/. 
  15. ↑ 15.0 15.1 15.2 15.3 Steed, Paul M.; Tansey, Malú G.; Zalevsky, Jonathan; Zhukovsky, Eugene A.; Desjarlais, John R.; Szymkowski, David E.; Abbott, Christina; Carmichael, David et al. (26 September 2003). "Inactivation of TNF Signaling by Rationally Designed Dominant-Negative TNF Variants". Science 301 (5641): 1895–1898. doi:10.1126/science.1081297. PMID 14512626. Bibcode: 2003Sci...301.1895S. 
  16. ↑ 16.0 16.1 16.2 Tansey, Malu G; McCoy, Melissa K; Frank-Cannon, Tamy; McAlpine, Fiona E; Botterman, Barry R; Tansey, Keith E (6 March 2006). "The role of TNF in in vitro and in vivo models of neurodegeneration". The FASEB Journal 20 (4): A505. doi:10.1096/fasebj.20.4.A505-b. 
  17. ↑ 17.0 17.1 17.2 17.3 Frank-Cannon, Tamy C; Alto, Laura T; McAlpine, Fiona E; Tansey, Malú G (2009). "Does neuroinflammation fan the flame in neurodegenerative diseases?". Molecular Neurodegeneration 4 (1): 47. doi:10.1186/1750-1326-4-47. PMID 19917131. 
  18. ↑ 18.0 18.1 18.2 Lee, Jae Kyung; McCoy, Melissa K; Harms, Ashley S; Ruhn, Kelly A; Gold, Stephen J; Tansey, Malu G (1 March 2008). "Regulator of G-protein signaling (RGS10) regulates microglial response to chronic inflammatory stimuli and impacts dopaminergic neuron survival.". The FASEB Journal 22 (1_supplement): 1072.5. doi:10.1096/fasebj.22.1_supplement.1072.5. 
  19. ↑ Tansey, Malú G.; McCoy, Melissa K.; Frank-Cannon, Tamy C. (November 2007). "Neuroinflammatory mechanisms in Parkinson's disease: Potential environmental triggers, pathways, and targets for early therapeutic intervention". Experimental Neurology 208 (1): 1–25. doi:10.1016/j.expneurol.2007.07.004. PMID 17720159. 
  20. ↑ 20.0 20.1 Sniffen, Lindsey J.; Eidson, Lori N.; Herrick, Mary K.; MacPherson, Kathryn P.; de Sousa Rodrigues, Maria E.; Tansey, Malu G. (1 April 2018). "Effect of High Fat High Fructose Diet on Peripheral Immune Cell Trafficking into the Brain in CCR2 Mouse Model". The FASEB Journal 32 (1_supplement): 740.10. doi:10.1096/fasebj.2018.32.1_supplement.740.10. 
  21. ↑ Bekhbat, M.; Mukhara, D.; Dozmorov, M. J.; Stansfield, J. C.; Benusa, S. D.; Rowson, S. A.; Kelly, S. D.; Tharp, G. K. et al. (1 February 2019). "Abstract # 3111 Chronic adolescent stress differentially sensitizes neuro-immune reactivity in male and female rats". Brain, Behavior, and Immunity 76: e20. doi:10.1016/j.bbi.2018.11.235. 
  22. ↑ "Women who inspire researchers making their mark". https://alz.org/blog/alz/february-2020/women-who-inspire-researchers-making-their-mark-i?fbclid=IwAR31BSVnAEegVZyQr_Bwongm0-9gNa8CBLwR_Rr5j__QeLM51Um6n0VUEI0. 
  23. ↑ "2012-2013 Honors and Awards| GDBBS | Emory University". http://biomed.emory.edu/PROGRAM_SITES/NS/students/honors-and-awards/2012-2013-honors-and-awards.html. 
  24. ↑ "O'Leary Prize recipients | Office of Neuroscience Research | Washington University in St. Louis". https://neuroscienceresearch.wustl.edu/education-events/competitions/oleary-prize/oleary-prize-recipients/. 
  25. ↑ "Previous Ida M. Green Award Recipients" (in en-US). https://www.utsouthwestern.edu/education/graduate-school/about-us/green-award-recipients.html. 




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