 |
Contact Information
| Phone: | 218-726-7925 |
| Fax: | 218-726-8014 |
| Email: | ldrewes@d.umn.edu |
Address: 251 SMed
1035 Univeristy Dr.
Duluth, MN 55812 |
|
|
Professor and Head
Links
Academic Health Center Graduate Programs
Integrated Biosciences Graduate Program
Drewes Laboratory
Research
The brain depends upon a supply of blood-borne nutrients to maintain its physiological function. A hallmark characteristic of the brain vasculature is an endothelium with tight occluding junctions at positions of cell-cell contact. This absence of spac es between cells prevents bulk diffusion of plasma components into the surrounding tissue. The net result of this "blood-brain barrier" is that influx and efflux of metabolic substrates and nutrients (including glucose, amino acids, and nucleosi des) across the brain vasculature must occur via transport systems located in the luminal and abluminal plasma membranes of the endothelial cell.
For example, glucose is the primary substrate for brain metabolism and is transported into cells via specific membrane carriers. Under normal glycemic conditions, GLUT1 and GLUT3 are the known members of the glucose transporter family responsible for c arrying glucose from the blood and into the cells of the brain. This includes transport across both the luminal and abluminal sides of the endothelial cell and the plasma membranes of the neuronal and glial cells. Although recent studies have greatly expa nded our knowledge about glucose transporters in several tissues, much less is currently known about these integral membrane proteins in the brain or how they are regulated in response to pathophysiological conditions.
The long-term goals of my research are to characterize the molecular process by which nutrients are transported through the cells comprising the blood-brain barrier (endothelial cells) and the blood-CSF barrier (epithelial cells of the choroid plexus). These goals include an understanding of the molecular identity of the transporters, the membrane sites where transporters are located, the kinetic characteristics of substrate and inhibitor specificity, and, in the future, the mechanisms regulating trans porter activity and expression.
Research describing the molecular events of blood-brain transport may be valuable in understanding neurological dysfunctions associated with stroke, diabetes, neurodegenerative diseases and metabolic encephalopathies. Indeed, it could lead to treatment s for minimizing these dysfunctions or for designing therapeutic strategies.
Education
Ph.D. University of Minnesota, 1970
Laboratory Personnel
Mary Motari, Graduate Student
Mary Sneve, Assistant Scientist
Publications
Publications on PubMed
Books:
Drewes, L.R., and Betz, A.L. (eds.) (1993) Frontiers in Cerebral Vascular Biology: Transport and Its Regulation, Plenum Press, New York.
Chapters in Books, Editorials, and Reports:
Matson, C. and Drewes, L.R. (2003) “Detection of Endothelial Proteins by Western Blotting in Methods in Molecular Biology.” Volume X, in The Blood Brain Barrier: Biology and Research Protocols (S. Nag, ed.), p. 479-487.
Anderson, R., Drewes, L., Ntambi, J., Rapoport, S., Hibbeln, J., Yavin, E., Horrocks, L., Moore, S., Salem, N., Preuss, M., Spector, A., Lagarde, M., Kim, H.Y., and Horrobin, D. (2001) Brain uptake and utilization of fatty acids: Applications to peroxisomal biogenesis disorders (An International Workshop) - Roundtable discussion of Session 3: "The regulation and functions of DHA in neurons and neuronal membranes." J. Mol. Neurosci. 16(2-3):279-84. (Editorial)
Drewes, L.R., Gerhart, D.Z., Leino, R.L., and Enerson, B.E. (2001) Expression and Modulation of Blood-brain Monocarboxylate Transporters, in The Blood-brain Barrier (D. Koliber, ed.) Kluwer, Amsterdam. p. 9-17.
Articles in Journals:
Enerson, B.E., and Drewes, L.R. (2005) A molecular portrait of the blood-brain barrier. (under review)
Enerson, B.E., Sneve, M.G., and Drewes, L.R. (2005) Differential gene expression implicating calcium and GABA homeostasis in the anticonvulsant activity of the ketogenic diet. (under review)
Gerhart, D.Z., Froberg, M.K., Enerson, B.E., Duelli, R., and Drewes, L.R. (2005) Monocarboxylate transporter MCT1 is increased in brains of Alzheimer’s patients. (under review)
Smith, J.P., and Drewes, L.R. (2005) Modulation of MCT1 kinetic function by cAMP signaling pathway in rat brain endothelial cells. (in press)
Doolittle, N.D., Abrey, L.E., Bleyer, W.A., Brem, S., Davis, T.P., Dore-Duffy, P., Drewes, L.R., Hall, W.A., Hoffman, J.M., Korfel, A., Martuza, R., Muldoon, L.L., Peereboom, D., Peterson, D.R., Rabkin, S.D., Smith, Q., Stevens, G.H.J., and Neuwelt, E.A. (2005) New Frontiers in Translational Research in Neuro-oncology and the Blood-Brain Barrier: Report of the Tenth Annual Blood-Brain Barrier Disruption Consortium Meeting. Clin. Cancer Res. 11:421-428).
Enerson, B.E., and Drewes, L.R. (2003) Molecular features, regulation and function of monocarboxylate transporters: Implications for drug delivery. J. Pharmaceutical Sci. 92:1531-1544.
Régina, A., Morchoisne, S., Borson, N.D., McCall, A.L., Drewes, L.R., and Roux, F. (2001) Factors released by glucose-derived astrocytes enhance glucose transporter expression and activity in rat brain endothelial cells. Biochim. Biophys. Acta. 1540: 233-242.
Drewes, L.R. (2001) Molecular architecture of the brain microvasculature: Perspective on blood-brain transport. J. Mol. Neurosci. 16:7-12.
Froberg, M.K., Gerhart, D.Z., Enerson, B.E., Manivel, C., Guzman-Paz, M., Seacotte, N., and Drewes, L.R. (2001) Expression of monocarboxylate transporters MCT1 and MCT2 in normal and neoplastic human CNS tissues. Neuroreport. 12:761-765.
Leino, R.L., Gerhart, D.Z., Duelli, R., Enerson, B.E., and Drewes, L.R. (2001) Diet-induced ketosis increases monocarboxylate transporter (MCT1) levels in rat brain. Neurochem. Int. 38:519-527.
Duelli, R., Enerson, B.E., Gerhart, D.Z., and Drewes, L.R. (2001) Expression of large amino acid transporter LAT1 in rat brain endothelium. J. Cereb. Blood Flow Metab. 20:1557-1562.
Ishihara, H., Wang, H., Drewes, L.R., and Wollheim, C.B. (2000) Overexpression of monocarboxylate transporter and lactate dehydrogenase alters insulin secretory responses to pyruvate/lactate in -cells. J. Clinical Invest. 104:1621-1629.
Papers Read at Professional Meetings (Abstracts)
Matson, C., Basak, S, and Drewes, L.R. (2005) Prediction of blood: brain penetration of chemicals using computed molecular descriptors. Fourth Indo-U.S. Workshop on Mathematical Chemistry, Pune, Maharashtra, India.
Drewes, L.R. and Smith, J.P. (2004) Modulation of MCT1 kinetic function by the cAMP signaling pathway in rat brain endothelial cells. 7th Symposium Signal Transduction in the Blood-Brain Barriers, Potsdam, Germany.
Drewes, L.R. and Enerson, B.E. (2004) Brain vascular genomics following ischemia. Experimental Biology 2004, Washington, DC.
Drewes, L.R. and Enerson, B.E. (2004) Ischemia-induced modifications in the blood-brain barrier. New Frontiers in Translational Research in Neuro-oncology and the Blood-brain Barrier, Bend, OR.
Enerson, B.E., and Drewes, L.R. (2003) Transcript analysis of the blood-brain barrier. Third Indo-US Workshop on Mathematical Chemistry: With Applications to Drug discovery, Environmental Toxicology, Chemoinformatics and Bioinformatics, Duluth, MN.
Enerson, B.E., and Drewes, L.R. (2003) The rat blood-brain barrier transcriptome. 21st Internat'l Symposium on Cerebral Blood Flow and Metabolism, Calgary, Canada.
Drewes, L.R. (2003) Regulation of MCTs in Brain. Sixth International Meeting for Brain Energy Metabolism, Beijing, China.
Basak, N., and Drewes, L.R. (2003) A proteomic analysis of the blood-brain barrier. Third Indo-US Workshop on Mathematical Chemistry: With Applications to Drug discovery, Environmental Toxicology, Chemoinformatics and Bioinformatics, Duluth, MN.
Enerson, B.E., and Drewes, L.R. (2003) A serial analysis of gene expression view of the blood-brain barrier. Joint Meeting of the International Society for Neurochemistry, and Asian-Pacific Society for Neurochemistry, Hong Kong, China.
Basak, N., Peterson, D., and Drewes, L.R. (2003) A proteomic analysis of the blood-brain barrier. 5th Internat’l Conference on Cerebral Vascular Biology, Amarillo, TX.
Enerson, B.E., and Drewes, L.R. (2003) The molecular portrait of the cerebral microvasculature. 5th Internat’l Conference on Cerebral Vascular Biology, Amarillo, TX.
Henry, P.-G., Russeth, K.P., Tkac, I., Drewes, L.R., Andrews, M.T., and Gruetter, R. (2003) Neurochemical profile of the hibernating ground squirrel measured by 1H NMR spectroscopy. Joint Meeting of the International Society for Neurochemistry, and Asian-Pacific Society for Neurochemistry, Hong Kong, China.
Enerson, B.E., Sneve, M., Cormier, R.L. and Drewes, L.R. (2002) Differential gene expression in brains of rats fed a ketogenic diet. Experimental Biology 2002, New Orleans, LA.
Enerson, B.E., and Drewes, L.R. (2001) MCT1 induction by cobalt chloride in cultured brain endothelial cells. 4th Internat'l Conference Cerebral Vascular Biology Blood-brain Barrier, Cambridge, United Kingdom.
Gerhart, D.Z., Leino, R.L., and Drewes, L.R. (2001) Monocarboxylate transporter MCT1 is increased in cerebral cortical capillaries of rats injected with pentylenetetrazole. 4th Internat'l Conference Cerebral Vascular Biology Blood-brain Barrier, Cambridge, United Kingdom.
Enerson, B.E., Cormier, R.T., and Drewes, L.R. (2001) Generation of a transgenic mouse overexpressing MCT1 in the brain endothelium. 4th Internat'l Conference Cerebral Vascular Biology Blood-brain Barrier, Cambridge, United Kingdom.
Duelli, R., Canis, M., Maurer, M.H., Drewes, L.R. and Kuschinsky, W. (2001) Correlation between densities of monocarboxylate and glucose transporters in rat brain. 20th Internat'l Symposium on Cerebral Blood Flow and Metabolism, Taipei, Taiwan.
Duelli, R., Enerson, B.E., Gerhart, D.Z. and Drewes, L.R. (2001) Large amino acid transporter LAT1 is expressed at the blood-brain barrier. 20th Internat'l Symposium on Cerebral Blood Flow and Metabolism, Taipei, Taiwan.
Duelli, R., Enerson, B.E., Gerhart, D.Z. and Drewes, L.R. (2000) Large amino acid transporter LAT1 is expressed at the blood-brain barrier. Society for Neuroscience, Vol. 26, New Orleans, LA.