Evidence map›Paper›PMID 27122175›Full record

ArticleDevelopment (Cambridge, England)2016

Fat3 and Ena/VASP proteins influence the emergence of asymmetric cell morphology in the developing retina.

Alexandra Krol, Steven J Henle, Lisa V Goodrich

Open access · greenAbstract read
In one paragraph

Article in Development (Cambridge, England), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.0field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

29 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Nervous system-wide analysis of allScience advances · 2025
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  7. Review
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  14. Frontiers in neuroscience · 2022
    Article
  15. Observational
  16. Article
  17. Ancestral roles of atypical cadherins in planar cell polarity.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  18. Article
  19. Dendrite morphogenesis from birth to adulthood.Current opinion in neurobiology · 2018
    Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

Alexandra KrolDepartment of Neurobiology, Harvard Medical School, Boston, MA 02115, USA.
Steven J HenleDepartment of Neurobiology, Harvard Medical School, Boston, MA 02115, USA.
Lisa V GoodrichDepartment of Neurobiology, Harvard Medical School, Boston, MA 02115, USA Lisa_Goodrich@hms.harvard.edu.ORCID 0000-0002-3331-8600
Harvard University · US

Funding

FUNDAMENTAL NEUROBIOLOGYT32NS007484 · NINDS · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI REGEHR, WADE G · 2000 to 2014
$5.9M
Super-Resolution ImagingP30NS072030 · NINDS · HARVARD MEDICAL SCHOOL · PI REGEHR, WADE G · 2011 to 2020
$5.8M
Mouse Neurodevelopmental Behavior CoreU54HD090255 · NICHD · BOSTON CHILDREN'S HOSPITAL · PI POMEROY, SCOTT LOREN · 2016 to 2020
$5.2M
Molecular control of neuronal shape and connectivity in the developing retinaR01EY024884 · NEI · HARVARD MEDICAL SCHOOL · PI GOODRICH, LISA · 2016 to 2019
$1.7M
The role of Fat3 in amacrine cell dendrite development.R21EY022725 · NEI · HARVARD MEDICAL SCHOOL · PI GOODRICH, LISA · 2012 to 2013
$447k
Role of Fat3 at the intersection of neuronal morphology and synapse localizationF32EY024184 · NEI · MEDICAL COLLEGE OF WISCONSIN · PI HENLE, STEVEN J · 2014 to 2015
$106k
NEI NIH HHS F32 EY024184NEI NIH HHS R01 EY024884NEI NIH HHS R21 EY022725NICHD NIH HHS U54 HD090255NINDS NIH HHS P30 NS072030NINDS NIH HHS T32 NS007484
6 · The paper itself

Abstract

Neurons exhibit asymmetric morphologies throughout development - from migration to the elaboration of axons and dendrites - that are correctly oriented for the flow of information. For instance, retinal amacrine cells migrate towards the inner plexiform layer (IPL) and then retract their trailing processes, thereby acquiring a unipolar morphology with a single dendritic arbor restricted to the IPL. Here, we provide evidence that the Fat-like cadherin Fat3 acts during multiple stages of amacrine cell development in mice to orient overall changes in cell shape towards the IPL. Using a time-lapse imaging assay, we found that developing amacrine cells are less directed towards the IPL in the absence of Fat3, during both migration and retraction. Consistent with its predicted role as a cell-surface receptor, Fat3 functions cell-autonomously and is able to influence the cytoskeleton directly through its intracellular domain, which can bind and localize Ena/VASP family actin regulators. Indeed, a change in Ena/VASP protein distribution is sufficient to recapitulate the Fat3 mutant amacrine cell phenotype. Thus, Fat-like proteins might control the polarized development of tissues by sculpting the cytoskeleton of individual cells.

Indexed as

Cell ShapeActinsAmacrine CellsAmino Acid SequenceAnimalsBinding SitesCadherinsCell MovementCell PolarityConserved SequenceDNA-Binding ProteinsMice, Inbred C57BLModels, BiologicalMutationNeuritesRetinaActinsCadherinsDNA-Binding ProteinsENA-VASP proteinsFat3 protein, mouseAmacrine cellEna/VASPFat3Planar polarityRetinal development

Identifiers

PMID27122175
PMCPMC4920175
OpenAlexW2342700770

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.