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α -synuclein, Lewy Bodies, Prions, and Parkinson’s Disease. Cody McCullough & Sara Homsi BCM 465 April 19 th , 2010. Parkinson’s Disease. 1817: James Parkinson Progressive neurodegenerative disorder 1.5 million Americans 85% are over age 65 60,000 new cases / year! 9.
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α-synuclein, Lewy Bodies, Prions, and Parkinson’s Disease Cody McCullough & Sara Homsi BCM 465 April 19th, 2010
Parkinson’s Disease • 1817: James Parkinson • Progressive neurodegenerative disorder • 1.5 million Americans • 85% are over age 65 • 60,000 new cases / year!9 Dr. James Parkinson
http://www.hipusa.com/webmd/images/health_and_medical_reference/brain_and_nervous_system/Parkinsons_Disease_Frequently_Asked_Questions.jpghttp://www.hipusa.com/webmd/images/health_and_medical_reference/brain_and_nervous_system/Parkinsons_Disease_Frequently_Asked_Questions.jpg
Tyrosine hydroxylase Dopamine Tyrosine http://en.wikipedia.org/wiki/File:L-tyrosine-skeletal.png http://encefalus.com/wp-content/uploads/2008/09/dopamine.jpg
http://www.oralchelationblog.com/wp-content/uploads/2008/08/parkinsonsdopamine.jpg
Lewy Bodies • Abnormal aggregates of proteins that develop inside nerve cells • α-synuclein aggregates + ubiquitin¹ http://en.wikipedia.org/wiki/File:Lewy_Koerperchen.JPG
What is α-synuclein? • Small protein: 14kDa • Encoded by SNCA gene • Highly conserved; expressed in brain¹,⁷ http://www.bio.purdue.edu/people/faculty/cramer/images/Alpha-Synuclein.jpg
α-synuclein transmission Neuron 1 Synapse α-synuclein Neuron 2
Lewy Body Formation Aggregation A30P E46K A53T Neuronal Cell Death ⁸, 9 Savitt, J.M., V.L. Dawson, and T.M. Dawson. 2006. Diagnosis and treatment of Parkinson’s disease: molecules to medicine. J. Clin. Invest. 116: 1744-1754.
α-synuclein as a Prion? • An infectious agent made up of protein (PrPC) • α-helical conformation • β-sheet conformation amyloid fibrils6 • Aggregation & transmission of the misfolded protein thought to be toxic 6
Previous Findings • α-synuclein and its aggregates can be exocytosed from neuronal cells³ • α-synuclein and its aggregates can be endocytosed by neurons in culture⁴,⁵
Desplats Paper • Demonstrates that nerve cells overexpressingα-synuclein can transmit the protein to healthy grafted neural stem cells in both in vitro and in vivo models² • Tests if α-synuclein pathology involves direct neuron-to-neuron transmission of α-synuclein aggregates via endocytosis • “There is much to suggest that α-synuclein behaves like a prion.” 6
References • Cookson, M.R. 2005. The biochemistry of Parkinson’s disease. Annu. Rev. Biochem. 74: 29-52. • Desplats, P., Lee, H-J., Bae, E-J., Patrick, C., Rockenstein, E., Crews, L., Spencer, B., Masliah, E., and S-J. 2009. Inclusion formation and neuronal cell death through neuron-to-neuron transmission of α-synuclein. PNAS 106: 13010-13015. • Lee, H-J., Patel, S., and S-J. Lee. 2005. Intravascular localization and exocytosis of α-synuclein and its aggregates. J Neurosci25: 6016-6024. • Lee, H-J., et al. 2008. Assembly-dependent endocytosis and clearance of extrancellularα-synuclein. Int J Biochem Cell Biol 40: 1835-1849. • Lee, H-J., Suk, J.E., Bae, E.J., and S-J. Lee. 2008. Clearance and deposition of extracellular α-synuclein aggregates in microglia. BiochemBiophys Res Commun372: 423-428. • Olanowa, C.W., and S.B. Prusiner. 2009. Is Parkinson’s disease a prion disorder? PNAS 106: 12571-12571. • Savitt, J.M., Dawson, V.L., and T.M. Dawson. 2006. Diagnosis and treatment of Parkinson’s disease: molecules to medicine. J. Clin. Invest. 116: 1744-1754. • Wood-Kaczmar, A., Gandhi, S., and N.W. Wood. 2006. Understanding the molecular causes of Parkinson’s disease. Trends Mol. Med. 12: 521-528. • Brown University, Deep Brain Stimulation: Parkinson's Disease