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FEBS Lett. 2010 Apr 16;584(8):1615-22. doi: 10.1016/j.febslet.2010.03.025. Epub 2010 Mar 18.

Decreased GLT-1 and increased SOD1 and HO-1 expression in astrocytes contribute to lumbar spinal cord vulnerability of SOD1-G93A transgenic mice.

Author information

1
Department of Neurology, The Second Hospital of Hebei Medical University, Hebei, China.

Abstract

The SOD1-G93A transgenic mouse is a widely used ALS model, but the death of lower motor neurons is the hallmark. Here, we show that the SOD1-G93A transgene and HO-1 are preferentially over-expressed in the lumbar spinal cord, particularly in the activated astrocytes of the transgenic mice. We also show down-regulation of GLT-1 in spite of the proliferating astrocytes. However, GLT-1, SOD1-G93A transgene and HO-1 expression were not obviously changed in the motor cortex. Our data link spinal cord vulnerability to relatively decreased expression of GLT-1, and high expression of the transgene and HO-1 in astrocytes in SOD1-G93A transgenic mice.

PMID:
20303959
DOI:
10.1016/j.febslet.2010.03.025
[Indexed for MEDLINE]
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