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[Abstract Title]. - Society for Neuroscience

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Authors: *Y. RAMIRO 1 , J. MORÁN 2 ;<br />

1 INSTITUTO DE FISIOLOGIA CELULA, MEXICO, D.F., Mexico; 2 INSTITUTO DE<br />

FISIOLOGIA CELULAR, Mexico, d.f., Mexico<br />

<strong>Abstract</strong>: Apoptotic cell death is an intricate process involving a wide range of signaling<br />

pathways, including the Jun N-terminal Kinases (JNK), a member of mitogen-activated protein<br />

kinases (MAPKs). It has been reported that JNK pathway is activated under stress in many type<br />

of cells. When cerebellar granule neurons (CGN) are cultured in a medium with high potassium<br />

(K25) during 6-8 days in vitro and then transferred to a medium with low potassium (K5) or<br />

staurosporine (Sts), most of the cells die after 24-48 hrs by apoptosis. We reported that apoptosis<br />

induced by K5 and Sts induces an early increase of ROS levels, followed by the activation of the<br />

apoptotic machinery. In the present study we found that the inhibition of JNK activation with<br />

SP600125 prevented caspase 3 activation, nuclear condensation and cell death induced by K5. In<br />

contrast, JNK inhibition did not affect cell death induced by Sts. On the other hand, antioxidants<br />

increased ASK1 phosphorylation and decreased JNK1/2 and c-Jun activation induced by K5.<br />

These results suggest that apoptosis induced by K5 is JNK-dependent and mediated by ROS, but<br />

apoptosis induced by Sts is not dependent of JNK, suggesting that other signaling pathway is<br />

responsible of cell death induced by Sts.<br />

Disclosures: Y. Ramiro, None; J. Morán, None.<br />

Poster<br />

232. Developmental Cell Death: Biological Effects<br />

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

Program#/Poster#: 232.14/B54<br />

Topic: A.06.a. Developmental cell death: Biological effects<br />

Support: NIH P20 RR-16460<br />

<strong>Title</strong>: Rat cortical subplate comparisons across development and aging<br />

Authors: *T. J. TEAGUE-ROSS 1 , S. M. LANTZ 1 , C. M. DAVIS 1 , A. L. JAMES 1 , G. N.<br />

BRATTON 2 , B. CLANCY 1 ;<br />

1 Biol., 2 Mathematics, Univ. Central Arkansas, Conway, AR<br />

<strong>Abstract</strong>: Subplate neurons participate extensively in the development of the mammalian cortex<br />

and although many undergo apoptosis, a subset remains in adult brains. In conventional models<br />

of development, the persisting subplate cells are considered simply a remnant population.<br />

However, these neurons remain active across aging in advantageous positions in and above the

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