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[Abstract Title]. - Society for Neuroscience

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Authors: F. MARQUES 1 , A. L. FALCÃO 1 , J. C. SOUSA 1 , G. COPPOLA 3 , D. GESCHWIND 3 ,<br />

N. SOUSA 1 , M. CORREIA-NEVES 1 , *J. A. PALHA 2 ;<br />

1 Life and Hlth. Sci. Res. Inst. (ICVS), Sch. of Hlth. Sci., 2 Hlth. Sci. Sch., Univ. of Minho, Braga,<br />

Portugal; 3 Dept. of Neurology, David Geffen Sch. of Med., UCLA, Los Angeles, CA<br />

<strong>Abstract</strong>: Iron is essential <strong>for</strong> normal mammalian cellular homeostasis but, in excess, promotes<br />

free radical <strong>for</strong>mation and its accumulation has been associated with some neurodegenerative<br />

disorders. Iron is also required <strong>for</strong> microbial growth and in case of infection the host activates<br />

several mechanisms to prevent iron availability <strong>for</strong> bacteria. We have recently shown that the<br />

choroid plexus can contribute to the brain innate immune response by synthesizing and secreting<br />

lipocalin 2 into the cerebrospinal fluid (CSF). Here, we show the involvement of other genes in<br />

regulating iron homeostasis in the brain. We now show that hepcidin (HAMP) mRNA levels are<br />

up-regulated in the choroid plexus after intraperitoneal administration of lipopolysaccharide.<br />

HAMP is known to be a liver-derived hormone that regulates iron availability by decreasing<br />

ferroportin (FPN)-mediated iron export from the enterocyte into the bloodstream. Other genes<br />

also involved in the regulation of iron metabolism are up-regulated by the peripheral<br />

inflammatory stimulus. We propose that upon an acute peripheral inflammatory stimulus HAMP<br />

decreases FPN-mediated iron delivery into the CSF, there<strong>for</strong>e decreasing iron availability <strong>for</strong><br />

bacterial growth and dissemination within the brain.<br />

Disclosures: F. Marques, None; J.A. Palha , None; A.L. Falcão, None; J.C. Sousa, None; M.<br />

Correia-Neves, None; N. Sousa, None; D. Geschwind, None; G. Coppola, None.<br />

Poster<br />

287. Blood Brain Barrier and CSF<br />

Time: Sunday, November 16, 2008, 1:00 pm - 5:00 pm<br />

Program#/Poster#: 287.13/RR7<br />

Topic: E.01.d. Development<br />

Support: The Roy J. Carver Charitable Trust<br />

<strong>Title</strong>: Localization of gamma-protocadherin proteins to the apical surface of choroid plexus and<br />

ependymal epithelial cells suggests novel functions distinct from cell-cell adhesion<br />

Authors: *J. A. WEINER, L. F. HELSPER;<br />

Dept Biolog Sci., Univ. Iowa, Iowa City, IA<br />

<strong>Abstract</strong>: Protocadherins (Pcdhs) comprise a large family of putative adhesion molecules related<br />

to the well-studied, homophilic classical cadherins. Genes encoding ~60 Pcdh molecules are

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