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Exendin-4 Promotes Actin Cytoskeleton Rearrangement and Protects Cells from Nogo-A-Δ20 Mediated Spreading Inhibition and Growth Cone Collapse by Down-regulating RhoA Expression and Activation Via the PI3K Pathway

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Date 2018 Nov 6
PMID 30396070
Citations 4
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Abstract

Exendin-4 is a protein of the GLP-1 family currently used to treat diabetes. Recently, a greater number of biological properties have been associated with the GLP-1 family. Our data shows that exendin-4 treatment significantly increases the cytoskeleton rearrangement, which leads to an increasingly differentiated phenotype and reduced cell migration. We also found that exendin-4 could prevent SH-SY5Y and PC12 cells from Nogo-A-Δ20 mediated spreading inhibition and neurite collapse. Western blot analysis indicated that exendin-4 treatment both reduced the expression and activation of RhoA via the PI3K signaling pathway. These data suggest that exendin-4 may protect nerve regeneration by preventing the inhibition of Nogo-A via down-regulating RhoA expression and activation.

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