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The role of microglia and their CX3CR1 signaling in adult neurogenesis in the olfactory bulb.


ABSTRACT: Microglia play important roles in perinatal neuro- and synapto-genesis. To test the role of microglia in these processes during adulthood, we examined the effects of microglia depletion, via treatment of mice with the CSF-1 receptor antagonist PLX5622, and abrogated neuronal-microglial communication in CX3C receptor-1 deficient (Cx3cr1-/-) mice. Microglia depletion significantly lowered spine density in young (developing) but not mature adult-born-granule-cells (abGCs) in the olfactory bulb. Two-photon time-lapse imaging indicated that microglia depletion reduced spine formation and elimination. Functionally, odor-evoked responses of mitral cells, which are normally inhibited by abGCs, were increased in microglia-depleted mice. In Cx3cr1-/- mice, abGCs exhibited reduced spine density, dynamics and size, concomitantly with reduced contacts between Cx3cr1-deficient microglia and abGCs' dendritic shafts, along with increased proportion of microglia-contacted spines. Thus, during adult neurogenesis, microglia regulate the elimination (pruning), formation, and maintenance of synapses on newborn neurons, contributing to the functional integrity of the olfactory bulb circuitry.

SUBMITTER: Reshef R 

PROVIDER: S-EPMC5734876 | biostudies-literature | 2017 Dec

REPOSITORIES: biostudies-literature

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The role of microglia and their CX3CR1 signaling in adult neurogenesis in the olfactory bulb.

Reshef Ronen R   Kudryavitskaya Elena E   Shani-Narkiss Haran H   Isaacson Batya B   Rimmerman Neta N   Mizrahi Adi A   Yirmiya Raz R  

eLife 20171218


Microglia play important roles in perinatal neuro- and synapto-genesis. To test the role of microglia in these processes during adulthood, we examined the effects of microglia depletion, via treatment of mice with the CSF-1 receptor antagonist PLX5622, and abrogated neuronal-microglial communication in CX3C receptor-1 deficient (<i>Cx3cr1<sup>-/-</sup></i>) mice. Microglia depletion significantly lowered spine density in young (developing) but not mature adult-born-granule-cells (abGCs) in the o  ...[more]

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