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Actions of Rab27B‐GTPase on mammalian central excitatory synaptic transmission

Members of the Rab3 gene family are considered central to membrane trafficking of synaptic vesicles at mammalian central excitatory synapses. Recent evidence, however, indicates that the Rab27B‐GTPase, which is highly homologous to the Rab3 family, is also enriched on SV membranes and co‐localize wi...

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Autores principales: Arias‐Hervert, Erwin R., Xu, Nicole, Njus, Meredith, Murphy, Geoff G., Hou, Yanan, Williams, John A., Lentz, Stephen I., Ernst, Stephen A., Stuenkel, Edward L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7195558/
https://www.ncbi.nlm.nih.gov/pubmed/32358861
http://dx.doi.org/10.14814/phy2.14428
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author Arias‐Hervert, Erwin R.
Xu, Nicole
Njus, Meredith
Murphy, Geoff G.
Hou, Yanan
Williams, John A.
Lentz, Stephen I.
Ernst, Stephen A.
Stuenkel, Edward L.
author_facet Arias‐Hervert, Erwin R.
Xu, Nicole
Njus, Meredith
Murphy, Geoff G.
Hou, Yanan
Williams, John A.
Lentz, Stephen I.
Ernst, Stephen A.
Stuenkel, Edward L.
author_sort Arias‐Hervert, Erwin R.
collection PubMed
description Members of the Rab3 gene family are considered central to membrane trafficking of synaptic vesicles at mammalian central excitatory synapses. Recent evidence, however, indicates that the Rab27B‐GTPase, which is highly homologous to the Rab3 family, is also enriched on SV membranes and co‐localize with Rab3A and Synaptotagmin at presynaptic terminals. While functional roles of Rab3A have been well‐established, little functional information exists on the role of Rab27B in synaptic transmission. Here we report on functional effects of Rab27B at SC‐CA1 and DG‐MF hippocampal synapses. The data establish distinct functional actions of Rab27B and demonstrate functions of Rab27B that differ between SC‐CA1 and DG‐MF synapses. Rab27B knockout reduced frequency facilitation compared to wild‐type (WT) controls at the DG/MF‐CA3 synaptic region, while increasing facilitation at the SC‐CA1 synaptic region. Remarkably, Rab27B KO resulted in a complete elimination of LTP at the MF‐CA3 synapse with no effect at the SC‐CA1 synapse. These actions are similar to those previously reported for Rab3A KO. Specificity of action on LTP to Rab27B was confirmed as LTP was rescued in response to lentiviral infection and expression of human Rab27B, but not to GFP, in the DG in the Rab27B KO mice. Notably, the effect of Rab27B KO on MF‐CA3 LTP occurred in spite of continued expression of Rab3A in the Rab27B KO. Overall, the results provide a novel perspective in suggesting that Rab27B and Rab3A act synergistically, perhaps via sequential effector recruitment or signaling for presynaptic LTP expression in this hippocampal synaptic region.
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spelling pubmed-71955582020-05-04 Actions of Rab27B‐GTPase on mammalian central excitatory synaptic transmission Arias‐Hervert, Erwin R. Xu, Nicole Njus, Meredith Murphy, Geoff G. Hou, Yanan Williams, John A. Lentz, Stephen I. Ernst, Stephen A. Stuenkel, Edward L. Physiol Rep Original Research Members of the Rab3 gene family are considered central to membrane trafficking of synaptic vesicles at mammalian central excitatory synapses. Recent evidence, however, indicates that the Rab27B‐GTPase, which is highly homologous to the Rab3 family, is also enriched on SV membranes and co‐localize with Rab3A and Synaptotagmin at presynaptic terminals. While functional roles of Rab3A have been well‐established, little functional information exists on the role of Rab27B in synaptic transmission. Here we report on functional effects of Rab27B at SC‐CA1 and DG‐MF hippocampal synapses. The data establish distinct functional actions of Rab27B and demonstrate functions of Rab27B that differ between SC‐CA1 and DG‐MF synapses. Rab27B knockout reduced frequency facilitation compared to wild‐type (WT) controls at the DG/MF‐CA3 synaptic region, while increasing facilitation at the SC‐CA1 synaptic region. Remarkably, Rab27B KO resulted in a complete elimination of LTP at the MF‐CA3 synapse with no effect at the SC‐CA1 synapse. These actions are similar to those previously reported for Rab3A KO. Specificity of action on LTP to Rab27B was confirmed as LTP was rescued in response to lentiviral infection and expression of human Rab27B, but not to GFP, in the DG in the Rab27B KO mice. Notably, the effect of Rab27B KO on MF‐CA3 LTP occurred in spite of continued expression of Rab3A in the Rab27B KO. Overall, the results provide a novel perspective in suggesting that Rab27B and Rab3A act synergistically, perhaps via sequential effector recruitment or signaling for presynaptic LTP expression in this hippocampal synaptic region. John Wiley and Sons Inc. 2020-05-01 /pmc/articles/PMC7195558/ /pubmed/32358861 http://dx.doi.org/10.14814/phy2.14428 Text en © 2020 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of The Physiological Society and the American Physiological Society. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Arias‐Hervert, Erwin R.
Xu, Nicole
Njus, Meredith
Murphy, Geoff G.
Hou, Yanan
Williams, John A.
Lentz, Stephen I.
Ernst, Stephen A.
Stuenkel, Edward L.
Actions of Rab27B‐GTPase on mammalian central excitatory synaptic transmission
title Actions of Rab27B‐GTPase on mammalian central excitatory synaptic transmission
title_full Actions of Rab27B‐GTPase on mammalian central excitatory synaptic transmission
title_fullStr Actions of Rab27B‐GTPase on mammalian central excitatory synaptic transmission
title_full_unstemmed Actions of Rab27B‐GTPase on mammalian central excitatory synaptic transmission
title_short Actions of Rab27B‐GTPase on mammalian central excitatory synaptic transmission
title_sort actions of rab27b‐gtpase on mammalian central excitatory synaptic transmission
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7195558/
https://www.ncbi.nlm.nih.gov/pubmed/32358861
http://dx.doi.org/10.14814/phy2.14428
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