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[Abstract Title]. - Society for Neuroscience

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common dementia among older people and is the 4th cause of death in developed countries.<br />

Many studies are focused on Tau protein which is the principal component of neurofibrillary<br />

tangles (NFT). Tau localization is changed during the pathology development. However it had<br />

not been reported the analysis of Tau membrane localization and its importance in the<br />

pathological Tau precipitation. The purpose of this job was to develop a cellular model to<br />

analyze the possible role of the miss-localization of truncated Tau in AD neurodegeneration. We<br />

used 2 gene constructs: 1) soluble truncated Tau (151-391 aa) and 2) a chimerical <strong>for</strong>m with a<br />

membrane anchored signal (IFNγR1-151-391). Through retroviral system and transfection<br />

analysis, we expressed the constructions in neuronal culture. We noticed the presence of β-sheet<br />

structures when we induce differentiation from neural stem cells to neuronal culture in the<br />

transduced cell that expressed the Tau anchored to membrane. These data suggests the<br />

participation of neuronal membrane as nucleation center to abnormal aggregation of Tau and<br />

sustain the importance of truncation as a post-translation modification to the development of AD.<br />

Disclosures: M.A. De Anda-Hernandez, None; K.I. Lira-De Leon, None; P. Figueroa-<br />

Corona, None; M.A. Meraz-Rios, None; V. Campos-Peña, None.<br />

Poster<br />

245. Tau and Alzheimer's disease<br />

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

Program#/Poster#: 245.21/P3<br />

Topic: C.01.j. Cognitive function<br />

Support: NIH grant AG 05146<br />

Intramural Research Program of the NIA, NIH.<br />

Burroughs Wellcome Fund <strong>for</strong> Translational Research<br />

<strong>Title</strong>: No quantitative differences in 1-42β-amyloid and hyperphosphorylated-tau tangles loads<br />

in the brains of subjects with asymptomatic AD and mild cognitive impairment (MCI). The<br />

BLSA study<br />

Authors: *D. IACONO 1 , R. O' BRIEN 2 , S. M. RESNIK 3 , A. ZONDERMAN 3 , O.<br />

PLETNIKOVA 1 , G. RUDOW 1 , B. CRAIN 1 , J. C. TRONCOSO 1 ;<br />

1 Dept Pathol, Div. Neuropathol, 2 Dept of Neurol., Johns Hopkins Univ., Baltimore, MD;<br />

3 Personality and Cognition Lab., Natl. Inst. of Aging, Baltimore, MD

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