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Page 55

Notes:

allied

academies

17

th

International Conference on

4

th

International Conference on

NEUROLOGY AND NEUROSCIENCE

&

MENTAL HEALTH AND PRIMARY CARE

October 16-18, 2017 | Toronto, Canada

J Neurol Neurorehabil Res 2017 | Volume 2 Issue 3

T

he conversion of the cellular prion protein (PrPC) to the

protease-resistant isoform is the key event in chronic

neurodegenerative diseases, including transmissible

spongiform encephalopathies (TSEs). Increased iron in

prion-related disease has been observed due to the prion

protein-ferritin complex. Additionally, the accumulation and

conversion of recombinant PrP (rPrP) is specifically derived

from Fe(III) but not Fe(II). Fe(III)-mediated PK-resistant

PrP (PrPres) conversion occurs within a complex cellular

environment rather than via direct contact between rPrP and

Fe(III). In this study, differentially expressed genes correlated

with prion degeneration by Fe(III) were identified using

Affymetrix microarrays. Following Fe(III) treatment, 97 genes

were differentially expressed, including 85 upregulated

genes and 12 downregulated genes (≥1.5-fold change in

expression). However, Fe(II) treatment produced moderate

alterations in gene expression without inducing dramatic

alterations in gene expression profiles. Moreover, functional

grouping of identified genes indicated that the differentially

regulated genes were highly associated with cell growth, cell

maintenance, and intra- and extracellular transport. These

findings showed that Fe(III) may influence the expression

of genes involved in PrP folding by redox mechanisms. The

identification of genes with altered expression patterns

in neural cells may provide insights into PrP conversion

mechanisms during the development and progression of

prion-related diseases.

Speaker Biography

Hee-Jong Woo Immunology VMD, Ph.D professor of faculty of veterinary medicine,

Seoul National University since 1992. Has completed his Ph.D of Immunology at the

University of Tokyo, Japan in 1987. His postdoctoral training was at the Division of

molecular diseases, Department of Pediatrics, School of medicine, University of

Pennsylvania, and was an instructor of Laboratory of cancer biology, Department of

surgery, School of Medicine at the Harvard University. He provides presentations on

topics related to the neurodegenerative diseases in brain. Expertise in all immunological

field and special interest in prion biology and the inflammation of brain.

e:

hjwoo@snu.ac.kr

Analysis of differentially expressed genes in iron-induced prion protein conversion

Hee-Jong Woo

Seoul National University, South Korea