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Frizzled-1 receptor regulates adult hippocampal neurogenesis

Overview of attention for article published in Molecular Brain, March 2016
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  • Good Attention Score compared to outputs of the same age (68th percentile)
  • Good Attention Score compared to outputs of the same age and source (69th percentile)

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2 X users
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1 Wikipedia page

Citations

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59 Mendeley
Title
Frizzled-1 receptor regulates adult hippocampal neurogenesis
Published in
Molecular Brain, March 2016
DOI 10.1186/s13041-016-0209-3
Pubmed ID
Authors

Muriel D. Mardones, Gabriela A. Andaur, Manuel Varas-Godoy, Jenny F. Henriquez, Felipe Salech, María Isabel Behrens, Andrés Couve, Nibaldo C. Inestrosa, Lorena Varela-Nallar

Abstract

In the adult hippocampus new neurons are continuously generated from neural stem cells (NSCs) present at the subgranular zone of the dentate gyrus. This process is controlled by Wnt signaling, which plays a complex role in regulating multiple steps of neurogenesis including maintenance, proliferation and differentiation of progenitor cells and the development of newborn neurons. Differential effects of Wnt signaling during progression of neurogenesis could be mediated by cell-type specific expression of Wnt receptors. Here we studied the potential role of Frizzled-1 (FZD1) receptor in adult hippocampal neurogenesis. In the adult dentate gyrus, we determined that FZD1 is highly expressed in NSCs, neural progenitors and immature neurons. Accordingly, FZD1 is expressed in cultured adult hippocampal progenitors isolated from mouse brain. To evaluate the role of this receptor in vivo we targeted FZD1 in newborn cells using retroviral-mediated RNA interference. FZD1 knockdown resulted in a marked decrease in the differentiation of newborn cells into neurons and increased the generation of astrocytes, suggesting a regulatory role for the receptor in cell fate commitment. In addition, FZD1 knockdown induced an extended migration of adult-born neurons within the granule cell layer. However, no differences were observed in total dendritic length and dendritic arbor complexity between control and FZD1-deficient newborn neurons. Our results show that FZD1 regulates specific stages of adult hippocampal neurogenesis, being required for neuronal differentiation and positioning of newborn neurons into the granule cell layer, but not for morphological development of adult-born granule neurons.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 59 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 59 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 17 29%
Researcher 8 14%
Student > Master 6 10%
Student > Bachelor 5 8%
Professor 4 7%
Other 5 8%
Unknown 14 24%
Readers by discipline Count As %
Neuroscience 20 34%
Agricultural and Biological Sciences 10 17%
Biochemistry, Genetics and Molecular Biology 7 12%
Medicine and Dentistry 4 7%
Economics, Econometrics and Finance 1 2%
Other 3 5%
Unknown 14 24%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 4. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 08 March 2022.
All research outputs
#6,585,131
of 23,298,349 outputs
Outputs from Molecular Brain
#316
of 1,135 outputs
Outputs of similar age
#92,025
of 300,613 outputs
Outputs of similar age from Molecular Brain
#7
of 26 outputs
Altmetric has tracked 23,298,349 research outputs across all sources so far. This one has received more attention than most of these and is in the 70th percentile.
So far Altmetric has tracked 1,135 research outputs from this source. They typically receive a little more attention than average, with a mean Attention Score of 7.0. This one has gotten more attention than average, scoring higher than 71% of its peers.
Older research outputs will score higher simply because they've had more time to accumulate mentions. To account for age we can compare this Altmetric Attention Score to the 300,613 tracked outputs that were published within six weeks on either side of this one in any source. This one has gotten more attention than average, scoring higher than 68% of its contemporaries.
We're also able to compare this research output to 26 others from the same source and published within six weeks on either side of this one. This one has gotten more attention than average, scoring higher than 69% of its contemporaries.