The role of adenylyl cyclase signaling pathways in developmental dendritogenesis in vivo

The period of early brain development involves an exceptional amount of neuronal morphological growth and refinement to form functional brain circuits. Although it is known that neural activity influences dendrite morphogenesis, the molecular pathways which convert a neural activity input to changes...

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Main Author: Duncan, Blair
Language:English
Published: University of British Columbia 2012
Online Access:http://hdl.handle.net/2429/41996
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spelling ndltd-LACETR-oai-collectionscanada.gc.ca-BVAU.-419962013-06-05T04:20:14ZThe role of adenylyl cyclase signaling pathways in developmental dendritogenesis in vivoDuncan, BlairThe period of early brain development involves an exceptional amount of neuronal morphological growth and refinement to form functional brain circuits. Although it is known that neural activity influences dendrite morphogenesis, the molecular pathways which convert a neural activity input to changes in morphology are not well understood. Here I show that activation of the adenylyl cyclase pathway promotes growth of developing brain neurons in vivo, in a neuron maturation-dependent manner. Rapid time-lapse two-photon imaging of single neuron growth within the developing vertebrate brain and pharmacological manipulations reveal a synergistic role for PKA and Epac in growth downstream of β-adrenergic receptors and adenylyl cyclase. Inhibition of the protease calpain increases axonal and dendritic filopodial density, but only in axons is this effect downstream of PKA. Furthermore, experiments indicate that PKA localization by AKAPs may be important in its regulation of dendritogenesis. Together, the results presented here outline multiple steps of a signaling pathway important in dynamic dendritogenesis and axogenesis in vivo.University of British Columbia2012-04-16T17:16:57Z2012-04-16T17:16:57Z20122012-04-162012-05Electronic Thesis or Dissertationhttp://hdl.handle.net/2429/41996eng
collection NDLTD
language English
sources NDLTD
description The period of early brain development involves an exceptional amount of neuronal morphological growth and refinement to form functional brain circuits. Although it is known that neural activity influences dendrite morphogenesis, the molecular pathways which convert a neural activity input to changes in morphology are not well understood. Here I show that activation of the adenylyl cyclase pathway promotes growth of developing brain neurons in vivo, in a neuron maturation-dependent manner. Rapid time-lapse two-photon imaging of single neuron growth within the developing vertebrate brain and pharmacological manipulations reveal a synergistic role for PKA and Epac in growth downstream of β-adrenergic receptors and adenylyl cyclase. Inhibition of the protease calpain increases axonal and dendritic filopodial density, but only in axons is this effect downstream of PKA. Furthermore, experiments indicate that PKA localization by AKAPs may be important in its regulation of dendritogenesis. Together, the results presented here outline multiple steps of a signaling pathway important in dynamic dendritogenesis and axogenesis in vivo.
author Duncan, Blair
spellingShingle Duncan, Blair
The role of adenylyl cyclase signaling pathways in developmental dendritogenesis in vivo
author_facet Duncan, Blair
author_sort Duncan, Blair
title The role of adenylyl cyclase signaling pathways in developmental dendritogenesis in vivo
title_short The role of adenylyl cyclase signaling pathways in developmental dendritogenesis in vivo
title_full The role of adenylyl cyclase signaling pathways in developmental dendritogenesis in vivo
title_fullStr The role of adenylyl cyclase signaling pathways in developmental dendritogenesis in vivo
title_full_unstemmed The role of adenylyl cyclase signaling pathways in developmental dendritogenesis in vivo
title_sort role of adenylyl cyclase signaling pathways in developmental dendritogenesis in vivo
publisher University of British Columbia
publishDate 2012
url http://hdl.handle.net/2429/41996
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