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Selective regulation of axonal growth from developing hippocampal neurons by tumor necrosis factor superfamily member APRIL()

APRIL (A Proliferation-Inducing Ligand, TNFSF13) is a member of the tumor necrosis factor superfamily that regulates lymphocyte survival and activation and has been implicated in tumorigenesis and autoimmune diseases. Here we report the expression and first known activity of APRIL in the nervous sys...

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Autores principales: Osório, Catarina, Chacón, Pedro J., White, Matthew, Kisiswa, Lilian, Wyatt, Sean, Rodríguez-Tébar, Alfredo, Davies, Alun M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academic Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4008386/
https://www.ncbi.nlm.nih.gov/pubmed/24444792
http://dx.doi.org/10.1016/j.mcn.2014.01.002
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author Osório, Catarina
Chacón, Pedro J.
White, Matthew
Kisiswa, Lilian
Wyatt, Sean
Rodríguez-Tébar, Alfredo
Davies, Alun M.
author_facet Osório, Catarina
Chacón, Pedro J.
White, Matthew
Kisiswa, Lilian
Wyatt, Sean
Rodríguez-Tébar, Alfredo
Davies, Alun M.
author_sort Osório, Catarina
collection PubMed
description APRIL (A Proliferation-Inducing Ligand, TNFSF13) is a member of the tumor necrosis factor superfamily that regulates lymphocyte survival and activation and has been implicated in tumorigenesis and autoimmune diseases. Here we report the expression and first known activity of APRIL in the nervous system. APRIL and one of its receptors, BCMA (B-Cell Maturation Antigen, TNFRSF17), are expressed by hippocampal pyramidal cells of fetal and postnatal mice. In culture, these neurons secreted APRIL, and function-blocking antibodies to either APRIL or BCMA reduced axonal elongation. Recombinant APRIL enhanced axonal elongation, but did not influence dendrite elongation. The effect of APRIL on axon elongation was inhibited by anti-BCMA and the expression of a signaling-defective BCMA mutant in these neurons, suggesting that the axon growth-promoting effect of APRIL is mediated by BCMA. APRIL promoted phosphorylation and activation of ERK1, ERK2 and Akt and serine phosphorylation and inactivation of GSK-3β in cultured hippocampal pyramidal cells. Inhibition of MEK1/MEK2 (activators of ERK1/ERK2), PI3-kinase (activator of Akt) or Akt inhibited the axon growth-promoting action of APRIL, as did pharmacological activation of GSK-3β and the expression of a constitutively active form of GSK-3β. These findings suggest that APRIL promotes axon elongation by a mechanism that depends both on ERK signaling and PI3-kinase/Akt/GSK-3β signaling.
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spelling pubmed-40083862014-05-02 Selective regulation of axonal growth from developing hippocampal neurons by tumor necrosis factor superfamily member APRIL() Osório, Catarina Chacón, Pedro J. White, Matthew Kisiswa, Lilian Wyatt, Sean Rodríguez-Tébar, Alfredo Davies, Alun M. Mol Cell Neurosci Article APRIL (A Proliferation-Inducing Ligand, TNFSF13) is a member of the tumor necrosis factor superfamily that regulates lymphocyte survival and activation and has been implicated in tumorigenesis and autoimmune diseases. Here we report the expression and first known activity of APRIL in the nervous system. APRIL and one of its receptors, BCMA (B-Cell Maturation Antigen, TNFRSF17), are expressed by hippocampal pyramidal cells of fetal and postnatal mice. In culture, these neurons secreted APRIL, and function-blocking antibodies to either APRIL or BCMA reduced axonal elongation. Recombinant APRIL enhanced axonal elongation, but did not influence dendrite elongation. The effect of APRIL on axon elongation was inhibited by anti-BCMA and the expression of a signaling-defective BCMA mutant in these neurons, suggesting that the axon growth-promoting effect of APRIL is mediated by BCMA. APRIL promoted phosphorylation and activation of ERK1, ERK2 and Akt and serine phosphorylation and inactivation of GSK-3β in cultured hippocampal pyramidal cells. Inhibition of MEK1/MEK2 (activators of ERK1/ERK2), PI3-kinase (activator of Akt) or Akt inhibited the axon growth-promoting action of APRIL, as did pharmacological activation of GSK-3β and the expression of a constitutively active form of GSK-3β. These findings suggest that APRIL promotes axon elongation by a mechanism that depends both on ERK signaling and PI3-kinase/Akt/GSK-3β signaling. Academic Press 2014-03 /pmc/articles/PMC4008386/ /pubmed/24444792 http://dx.doi.org/10.1016/j.mcn.2014.01.002 Text en © 2014 The Authors http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/).
spellingShingle Article
Osório, Catarina
Chacón, Pedro J.
White, Matthew
Kisiswa, Lilian
Wyatt, Sean
Rodríguez-Tébar, Alfredo
Davies, Alun M.
Selective regulation of axonal growth from developing hippocampal neurons by tumor necrosis factor superfamily member APRIL()
title Selective regulation of axonal growth from developing hippocampal neurons by tumor necrosis factor superfamily member APRIL()
title_full Selective regulation of axonal growth from developing hippocampal neurons by tumor necrosis factor superfamily member APRIL()
title_fullStr Selective regulation of axonal growth from developing hippocampal neurons by tumor necrosis factor superfamily member APRIL()
title_full_unstemmed Selective regulation of axonal growth from developing hippocampal neurons by tumor necrosis factor superfamily member APRIL()
title_short Selective regulation of axonal growth from developing hippocampal neurons by tumor necrosis factor superfamily member APRIL()
title_sort selective regulation of axonal growth from developing hippocampal neurons by tumor necrosis factor superfamily member april()
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4008386/
https://www.ncbi.nlm.nih.gov/pubmed/24444792
http://dx.doi.org/10.1016/j.mcn.2014.01.002
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