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Systematic substrate identification indicates a central role for the metalloprotease ADAM10 in axon targeting and synapse function

Metzincin metalloproteases have major roles in intercellular communication by modulating the function of membrane proteins. One of the proteases is the a-disintegrin-and-metalloprotease 10 (ADAM10) which acts as alpha-secretase of the Alzheimer's disease amyloid precursor protein. ADAM10 is als...

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Autores principales: Kuhn, Peer-Hendrik, Colombo, Alessio Vittorio, Schusser, Benjamin, Dreymueller, Daniela, Wetzel, Sebastian, Schepers, Ute, Herber, Julia, Ludwig, Andreas, Kremmer, Elisabeth, Montag, Dirk, Müller, Ulrike, Schweizer, Michaela, Saftig, Paul, Bräse, Stefan, Lichtenthaler, Stefan F
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4786429/
https://www.ncbi.nlm.nih.gov/pubmed/26802628
http://dx.doi.org/10.7554/eLife.12748
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author Kuhn, Peer-Hendrik
Colombo, Alessio Vittorio
Schusser, Benjamin
Dreymueller, Daniela
Wetzel, Sebastian
Schepers, Ute
Herber, Julia
Ludwig, Andreas
Kremmer, Elisabeth
Montag, Dirk
Müller, Ulrike
Schweizer, Michaela
Saftig, Paul
Bräse, Stefan
Lichtenthaler, Stefan F
author_facet Kuhn, Peer-Hendrik
Colombo, Alessio Vittorio
Schusser, Benjamin
Dreymueller, Daniela
Wetzel, Sebastian
Schepers, Ute
Herber, Julia
Ludwig, Andreas
Kremmer, Elisabeth
Montag, Dirk
Müller, Ulrike
Schweizer, Michaela
Saftig, Paul
Bräse, Stefan
Lichtenthaler, Stefan F
author_sort Kuhn, Peer-Hendrik
collection PubMed
description Metzincin metalloproteases have major roles in intercellular communication by modulating the function of membrane proteins. One of the proteases is the a-disintegrin-and-metalloprotease 10 (ADAM10) which acts as alpha-secretase of the Alzheimer's disease amyloid precursor protein. ADAM10 is also required for neuronal network functions in murine brain, but neuronal ADAM10 substrates are only partly known. With a proteomic analysis of Adam10-deficient neurons we identified 91, mostly novel ADAM10 substrate candidates, making ADAM10 a major protease for membrane proteins in the nervous system. Several novel substrates, including the neuronal cell adhesion protein NrCAM, are involved in brain development. Indeed, we detected mistargeted axons in the olfactory bulb of conditional ADAM10-/- mice, which correlate with reduced cleavage of NrCAM, NCAM and other ADAM10 substrates. In summary, the novel ADAM10 substrates provide a molecular basis for neuronal network dysfunctions in conditional ADAM10-/- mice and demonstrate a fundamental function of ADAM10 in the brain. DOI: http://dx.doi.org/10.7554/eLife.12748.001
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spelling pubmed-47864292016-03-17 Systematic substrate identification indicates a central role for the metalloprotease ADAM10 in axon targeting and synapse function Kuhn, Peer-Hendrik Colombo, Alessio Vittorio Schusser, Benjamin Dreymueller, Daniela Wetzel, Sebastian Schepers, Ute Herber, Julia Ludwig, Andreas Kremmer, Elisabeth Montag, Dirk Müller, Ulrike Schweizer, Michaela Saftig, Paul Bräse, Stefan Lichtenthaler, Stefan F eLife Cell Biology Metzincin metalloproteases have major roles in intercellular communication by modulating the function of membrane proteins. One of the proteases is the a-disintegrin-and-metalloprotease 10 (ADAM10) which acts as alpha-secretase of the Alzheimer's disease amyloid precursor protein. ADAM10 is also required for neuronal network functions in murine brain, but neuronal ADAM10 substrates are only partly known. With a proteomic analysis of Adam10-deficient neurons we identified 91, mostly novel ADAM10 substrate candidates, making ADAM10 a major protease for membrane proteins in the nervous system. Several novel substrates, including the neuronal cell adhesion protein NrCAM, are involved in brain development. Indeed, we detected mistargeted axons in the olfactory bulb of conditional ADAM10-/- mice, which correlate with reduced cleavage of NrCAM, NCAM and other ADAM10 substrates. In summary, the novel ADAM10 substrates provide a molecular basis for neuronal network dysfunctions in conditional ADAM10-/- mice and demonstrate a fundamental function of ADAM10 in the brain. DOI: http://dx.doi.org/10.7554/eLife.12748.001 eLife Sciences Publications, Ltd 2016-01-23 /pmc/articles/PMC4786429/ /pubmed/26802628 http://dx.doi.org/10.7554/eLife.12748 Text en © 2016, Kuhn et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Cell Biology
Kuhn, Peer-Hendrik
Colombo, Alessio Vittorio
Schusser, Benjamin
Dreymueller, Daniela
Wetzel, Sebastian
Schepers, Ute
Herber, Julia
Ludwig, Andreas
Kremmer, Elisabeth
Montag, Dirk
Müller, Ulrike
Schweizer, Michaela
Saftig, Paul
Bräse, Stefan
Lichtenthaler, Stefan F
Systematic substrate identification indicates a central role for the metalloprotease ADAM10 in axon targeting and synapse function
title Systematic substrate identification indicates a central role for the metalloprotease ADAM10 in axon targeting and synapse function
title_full Systematic substrate identification indicates a central role for the metalloprotease ADAM10 in axon targeting and synapse function
title_fullStr Systematic substrate identification indicates a central role for the metalloprotease ADAM10 in axon targeting and synapse function
title_full_unstemmed Systematic substrate identification indicates a central role for the metalloprotease ADAM10 in axon targeting and synapse function
title_short Systematic substrate identification indicates a central role for the metalloprotease ADAM10 in axon targeting and synapse function
title_sort systematic substrate identification indicates a central role for the metalloprotease adam10 in axon targeting and synapse function
topic Cell Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4786429/
https://www.ncbi.nlm.nih.gov/pubmed/26802628
http://dx.doi.org/10.7554/eLife.12748
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