Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5508685 | Biochimica et Biophysica Acta (BBA) - Molecular Cell Research | 2016 | 33 Pages |
Abstract
Our present data show that both, class I PI3K inhibitor and Akt inhibitor did not alter axon specification in hippocampal neurons, but greatly reduced axon length. However, in the same experiments LY294002 effectively impeded axonal polarization, as previously reported. Our biochemical data show that both, class I PI3K and Akt inhibitors, effectively block downstream elements from Akt to S6K1 activity. Both inhibitors are stable in culture medium along the time period analysed, maintaining the inhibition better than LY294002. Besides, we found evidence that LY294002 directly inhibits mTORC1. However, further analysis using an mTORC1 inhibitor showed no change in neuron polarity. Same result was obtained using a general class III PI3K inhibitor. Interestingly, we found that either, wild-type PTEN, or a phosphatase-dead form of PTEN, disrupted axonal polarization, strongly suggesting that the role of PTEN in axonal polarity can be independent of PIP3.
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Authors
Héctor Diez, Ma José Benitez, Silvia Fernandez, Ignacio Torres-Aleman, Juan José Garrido, Francisco Wandosell,