Cited by 96Neurogenesis and neuroplasticity mechanismsOlfactory and Sensory Function StudiesNerve injury and regeneration

Olfactory ensheathing cells are the main phagocytic cells that remove axon debris during early development of the olfactory system

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Nazareth, Lynnmaria, Lineburg, Katie E., Chuah, Meng Inn, Tello Velasquez, Johana, Chehrehasa, Fatemeh, St John, James A., Ekberg, Jenny A.K.·2015·Journal of Comparative Neurology

Abstract

During development of the primary olfactory system, axon targeting is inaccurate and axons inappropriately project within the target layer or overproject into the deeper layers of the olfactory bulb. As a consequence there is considerable apoptosis of primary olfactory neurons during embryonic and postnatal development and axons of the degraded neurons need to be removed. Olfactory ensheathing cells (OECs) are the glia of the primary olfactory nerve and are known to phagocytose axon debris in the adult and postnatal animal. However, it is unclear when phagocytosis by OECs first commences. We investigated the onset of phagocytosis by OECs in the developing mouse olfactory system by utilizing two transgenic reporter lines: OMP‐ZsGreen mice which express bright green fluorescent protein in primary olfactory neurons, and S100β‐DsRed mice which express red fluorescent protein in OECs. In crosses of these mice, the fate of the degraded axon debris is easily visualized. We found evidence of axon degradation at embryonic day (E)13.5. Phagocytosis of the primary olfactory axon debris by OECs was first detected at E14.5. Phagocytosis of axon debris continued into the postnatal animal during the period when there was extensive mistargeting of olfactory axons. Macrophages were often present in close proximity to OECs but they contributed only a minor role to clearing the axon debris, even after widespread degeneration of olfactory neurons by unilateral bulbectomy and methimazole treatment. These results demonstrate that from early in embryonic development OECs are the primary phagocytic cells of the primary olfactory nerve. J. Comp. Neurol. 523:479–494, 2015. © 2014 Wiley Periodicals, Inc.

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  • Most microbes are likely eliminated by phagocytic glia, olfactory ensheathing cells (OECs) and trigeminal Schwann cells (TgSCs), should they penetrate the epithelium and reach the nerves.

    “Most microbes are, however, likely eliminated by phagocytic glia, olfactory ensheathing cells (OECs) and trigeminal Schwann cells (TgSCs), should they penetrate the epithelium and reach the nerves29–31.”

    From Chlamydia pneumoniae can infect the central nervous system via the olfactory and trigeminal nerves and contributes to Alzheimer’s disease risk (2022) · cites this paper as [29]

    The section ‘OECs are the main phagocytic cell during early development’ (page not provided) reports that OECs can phagocytose bacteria in vitro. ‘Morphology changes after widespread degeneration’ says OECs could phagocytose invading bacteria, but also describes how bacteria can evade them and migrate toward the brain. The paper does not establish that most microbes reaching the nerves are eliminated, or that trigeminal Schwann cells eliminate them. (LLM, conf=0.88)

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  1. Panni P, Ferguson IA, Beacham I, Mackay-Sim A, Ekberg JA, St John JA (2013) Phagocytosis of bacteria by olfactory ensheathing cells and Schwann cells. Neuroscience letters 539:65-70.

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Authors
Nazareth, L., Lineburg, K. E., Chuah, M. I., Tello Velasquez, J., Chehrehasa, F., St John, J. A., & Ekberg, J. A. K.
Affiliations
  • School of Biomedical Sciences, Queensland University of Technology Brisbane 4000 Queensland Australia
  • QIMR Berghofer Medical Research Institute (AU)
  • University of Tasmania (AU)
  • Eskitis Institute for Drug Discovery, Griffith University Nathan 4111 Queensland Australia
  • Griffith University (AU)
Corresponding author
Ekberg, Jenny A.K.
Venue
Journal of Comparative Neurology
Publisher
Wiley
Published
2014-11-03
Volume
523
Issue
3
Pages
479-494
ISSN
  • 0021-9967 (ISSN-L)
  • 1096-9861
OpenAlex
W1519910945
Cited by
96
References
0
Citations by year
2026: 3 · 2025: 8 · 2024: 13 · 2023: 2 · 2022: 12 · 2021: 9 · 2020: 16 · 2019: 9 · 2018: 8 · 2017: 5 · 2016: 7 · 2015: 4
FWCI
1.71
Type
journal article
Language
en
Open access
Locations
  • The Journal of Comparative Neurology (publishedVersion)
  • PubMed (publishedVersion)
  • eCite Digital Repository (University of Tasmania) (submittedVersion)
  • Figshare (submittedVersion, cc-by)
  • Griffith Research Online (submittedVersion)
  • Faculty of Health; Institute of Health and Biomedical Innovation
Funders
Australian Research Council (DP0986294)
Topics
  • Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
  • Life Sciences › Neuroscience › Sensory Systems › Olfactory and Sensory Function Studies
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Nerve injury and regeneration
Keywords
olfactory ensheathing cells, olfactory bulb development, macrophages, embryonic development, postnatal development, axonal degeneration, S100β
MeSH terms
Animals, Animals, Newborn, Calcium-Binding Proteins, Cells, Cultured, Drug Combinations, Estradiol, Luminescent Proteins, Mice, Transgenic, Microfilament Proteins, Neuroglia, Norethindrone, Olfactory Bulb, Olfactory Mucosa, Olfactory Pathways, Phagocytes, Testosterone, Ultrasonography, Receptor, Macrophage Colony-Stimulating Factor, Receptors, Nerve Growth Factor, Gene Expression Regulation, Developmental, GAP-43 Protein, Mice, Olfactory Marker Protein, Lysosomal-Associated Membrane Protein 1, S100 Calcium Binding Protein beta Subunit

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