| Literature DB >> 29398357 |
Naofumi Uesaka1, Manabu Abe2, Kohtarou Konno3, Maya Yamazaki2, Kazuto Sakoori4, Takaki Watanabe5, Tzu-Huei Kao5, Takayasu Mikuni4, Masahiko Watanabe3, Kenji Sakimura2, Masanobu Kano6.
Abstract
Elimination of redundant synapses formed early in development and strengthening of necessary connections are crucial for shaping functional neural circuits. Purkinje cells (PCs) in the neonatal cerebellum are innervated by multiple climbing fibers (CFs) with similar strengths. A single CF is strengthened whereas the other CFs are eliminated in each PC during postnatal development. The underlying mechanisms, particularly for the strengthening of single CFs, are poorly understood. Here we report that progranulin, a multi-functional growth factor implicated in the pathogenesis of frontotemporal dementia, strengthens developing CF synaptic inputs and counteracts their elimination from postnatal day 11 to 16. Progranulin derived from PCs acts retrogradely onto its putative receptor Sort1 on CFs. This effect is independent of semaphorin 3A, another retrograde signaling molecule that counteracts CF synapse elimination. We propose that progranulin-Sort1 signaling strengthens and maintains developing CF inputs, and may contribute to selection of single "winner" CFs that survive synapse elimination.Entities:
Keywords: Purkinje cell; Sort1; cerebellum; climbing fiber; frontotemporal dementia; mouse; postnatal development; progranulin; retrograde signal; synapse elimination
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Year: 2018 PMID: 29398357 DOI: 10.1016/j.neuron.2018.01.018
Source DB: PubMed Journal: Neuron ISSN: 0896-6273 Impact factor: 17.173