Cited by 185Neuroscience and Neuropharmacology ResearchAxon Guidance and Neuronal SignalingGenetics and Neurodevelopmental Disorders

AnkyrinG is required to maintain axo-dendritic polarity in vivo

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Sobotzik, Jürgen-Markus, Sie, Jana Maria, Politi, Chrisoula, Del Turco, Domenico, Bennett, Vann, Deller, Thomas, Schultz, Christian·2009·Proceedings of the National Academy of Sciences

Abstract

Neurons are highly polarized cells that extend a single axon and several dendrites. Studies with cultured neurons indicate that the proximal portion of the axon, denoted as the axon initial segment (AIS), maintains neuronal polarity in vitro. The membrane-adaptor protein ankyrinG (ankG) is an essential component of the AIS. To determine the relevance of ankG for neuronal polarity in vivo, we studied mice with a cerebellum-specific ankG deficiency. Strikingly, ankG-depleted axons develop protrusions closely resembling dendritic spines. Such axonal spines are enriched with postsynaptic proteins, including ProSAP1/Shank2 and ionotropic and metabotropic glutamate receptors. In addition, immunofluorescence indicated that axonal spines are contacted by presynaptic glutamatergic boutons. For further analysis, double mutants were obtained by crossbreeding ankG(-/-) mice with L7/Purkinje cell-specific promoter 2 (PCP2) mice expressing enhanced green fluorescent protein (EGFP) in Purkinje cells (PCs). This approach allowed precise confocal microscopic mapping of EGFP-positive spiny axons and their subsequent identification at the electron microscopic level. Ultrastructurally, axonal spines contained a typical postsynaptic density and established asymmetric excitatory synapses with presynaptic boutons containing synaptic vesicles. In the shaft of spiny axons, typical ultrastructural features of the AIS, including the membrane-associated dense undercoating and cytoplasmic bundles of micr…

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Crossref · 10.1073/pnas.0909267106

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  • Loss of the ankyrinG-based AIS has been shown to disrupt the maintenance of neuronal polarity and to allow the axon to acquire molecular features of dendrites, such as axonal MAP2 and postsynaptic proteins.

    “Loss of the ankyrinG-based AIS has been shown to disrupt the maintenance of neuronal polarity and to allow the axon to acquire molecular features of dendrites, such as axonal MAP2 (30) and postsynaptic proteins (31).”

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Authors
Sobotzik, J.-M., Sie, J. M., Politi, C., Del Turco, D., Bennett, V., Deller, T., & Schultz, C.
Affiliations
  • Goethe University Frankfurt (DE)
  • Institute of Clinical Neuroanatomy, Neuroscience Center, Goethe-University, D-60590 Frankfurt/Main, Germany; and
  • Howard Hughes Medical Institute (US)
Venue
Proceedings of the National Academy of Sciences
Published
2009-10-13
Volume
106
Issue
41
Pages
17564-17569
ISSN
  • 0027-8424 (ISSN-L)
  • 1091-6490
OpenAlex
W2125760448
Cited by
185
References
2
Citations by year
2026: 4 · 2025: 7 · 2024: 11 · 2023: 6 · 2022: 11 · 2021: 6 · 2020: 13 · 2019: 8 · 2018: 10 · 2017: 15 · 2016: 13 · 2015: 13 · 2014: 16 · 2013: 16 · 2012: 12
FWCI
4.99
Type
journal article
Language
en
Open access
Locations
  • Proceedings of the National Academy of Sciences (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • Deutsche Forschungsgemeinschaft
  • Universität Ulm
Topics
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Axon Guidance and Neuronal Signaling
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetics and Neurodevelopmental Disorders
Keywords
ankyrin-G, axon initial segment, Purkinje cells, cerebellum, neuronal polarity, postsynaptic density, glutamatergic synapses, dendritic spines, axon ultrastructure, organotypic slice cultures
MeSH terms
Animals, Axons, Dendrites, Neurons, Promoter Regions, Genetic, Purkinje Cells, Synapses, Cell Polarity, Ankyrins, Genes, Reporter, Mice, Knockout, Mice, Synaptic Potentials

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