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Profiles and Dynamics of the Transcriptome of Microglial Cells Reveal their Inflammatory Status

Keren Zohar, View ORCID ProfileElyad Lezmi, Fanny Reichert, Tsiona Eliyahu, View ORCID ProfileShlomo Rotshenker, View ORCID ProfileMarta Weinstock, View ORCID ProfileMichal Linial
doi: https://doi.org/10.1101/2021.12.20.473548
Keren Zohar
1Department of Biological Chemistry, School of Pharmacy, The Hebrew University of Jerusalem, Jerusalem, Israel
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Elyad Lezmi
2Department of Genetics, Faculty of Life Sciences, School of Pharmacy, The Hebrew University of Jerusalem, Jerusalem, Israel
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  • ORCID record for Elyad Lezmi
Fanny Reichert
3Department of Medical Neurobiology, IMRIC, Faculty of Medicine, School of Pharmacy, The Hebrew University of Jerusalem, Jerusalem, Israel
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Tsiona Eliyahu
1Department of Biological Chemistry, School of Pharmacy, The Hebrew University of Jerusalem, Jerusalem, Israel
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Shlomo Rotshenker
3Department of Medical Neurobiology, IMRIC, Faculty of Medicine, School of Pharmacy, The Hebrew University of Jerusalem, Jerusalem, Israel
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  • ORCID record for Shlomo Rotshenker
Marta Weinstock
4Institute of Drug Research, School of Pharmacy, The Hebrew University of Jerusalem, Jerusalem, Israel
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  • ORCID record for Marta Weinstock
Michal Linial
1Department of Biological Chemistry, School of Pharmacy, The Hebrew University of Jerusalem, Jerusalem, Israel
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  • ORCID record for Michal Linial
  • For correspondence: michall@cc.huji.ac.il
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Abstract

The primary role of microglia in the maintenance of brain homeostasis is to respond to disturbances in the microenvironment. In this study, we cultured murine neonatal microglia and activated them with lipopolysaccharide (LPS) and benzoyl ATP (bzATP) to characterize changes in the transcriptome in response to various in vivo stimuli caused by pathogens, injury, or toxins. Activation by bzATP, an agonist of purinergic receptors, induces a transient wave of transcriptional changes. However, a long-lasting transcriptional profile affecting thousands of genes occurs only following a combination of bzATP and LPS. This profile is dominated by a coordinated induction of cytokines (e.g., IL1-α and IL1-β), chemokines, and their direct regulators. Many of these inflammatory-related genes are up-regulated by several orders of magnitude. We identified the TNF-α and NF-κB pathways as the principal hubs for signaling of interleukin and chemokine induction in this cell system. We propose that primary microglia under controlled activation paradigms can be used for testing reagents that could attenuate their activated state. Such a microglial system could serve as a model for changes occurring in the aging brain and neurodegenerative diseases.

Highlight points

  • * Primary murine microglia cultures release cytokines following activation with bzATP and LPS

  • * The wave of changes in gene expression by bzATP is transient.

  • * bzATP+LPS causes a transcription program dominated by the induction of interleukins and chemokines.

Competing Interest Statement

The authors have declared no competing interest.

  • Abbreviations

    AD
    Alzheimer’s disease
    ATP
    Adenosine tri-phosphate
    BSA
    Bovine serum albumin
    CNS
    Central nervous system
    DE
    Differentially expressed
    DMEM
    Dulbecco’s modified Eagle medium
    FC
    Fold change
    FDR
    False discovery rate
    GO
    Gene ontology
    Hrs
    Hours
    IL
    Interleukin
    IFNγ
    Interferon gamma
    LPS
    Lipopolysaccharide
    NT
    Not treated
    PCA
    Principal component analysis
    PD
    Parkinson’s disease
    RNA-seq
    RNA sequencing analysis
    SD
    Standard deviation
    TMM
    Trimmed mean of means
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    Posted December 21, 2021.
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    Profiles and Dynamics of the Transcriptome of Microglial Cells Reveal their Inflammatory Status
    Keren Zohar, Elyad Lezmi, Fanny Reichert, Tsiona Eliyahu, Shlomo Rotshenker, Marta Weinstock, Michal Linial
    bioRxiv 2021.12.20.473548; doi: https://doi.org/10.1101/2021.12.20.473548
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    Profiles and Dynamics of the Transcriptome of Microglial Cells Reveal their Inflammatory Status
    Keren Zohar, Elyad Lezmi, Fanny Reichert, Tsiona Eliyahu, Shlomo Rotshenker, Marta Weinstock, Michal Linial
    bioRxiv 2021.12.20.473548; doi: https://doi.org/10.1101/2021.12.20.473548

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