Evidence map›Paper›PMID 30451835›Full record

ArticleNature communications2018

Engulfing cells promote neuronal regeneration and remove neuronal debris through distinct biochemical functions of CED-1.

Hui Chiu, Yan Zou, Nobuko Suzuki, Yi-Wen Hsieh, Chiou-Fen Chuang, Yi-Chun Wu, Chieh Chang

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
3.4field-weighted citation impact, top 6% 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

18 citing papers in PubMed, 43 citations in OpenAlex.

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  11. Two intrinsic timing mechanisms set start and end times for dendritic arborization of a nociceptive neuron.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  12. Review
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  14. JNK Pathway in CNS Pathologies.International journal of molecular sciences · 2021
    Review
  15. Article
  16. Article
  17. Article
  18. The nucleoside diphosphate kinase NDK-1/NME1 promotes phagocytosis in concert with DYN-1/Dynamin.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    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

7 authors at 2 institutions in 3 countries.

Hui ChiuDepartment of Biological Sciences, University of Illinois at Chicago, Chicago, Illinois, 60607, USA.
Yan ZouDepartment of Biological Sciences, University of Illinois at Chicago, Chicago, Illinois, 60607, USA.
Nobuko SuzukiDepartment of Biological Sciences, University of Illinois at Chicago, Chicago, Illinois, 60607, USA.
Yi-Wen HsiehDepartment of Biological Sciences, University of Illinois at Chicago, Chicago, Illinois, 60607, USA.
Chiou-Fen ChuangDepartment of Biological Sciences, University of Illinois at Chicago, Chicago, Illinois, 60607, USA.
Yi-Chun WuInstitute of Molecular and Cellular Biology, National Taiwan University, Taipei, 10617, Taiwan.
Chieh ChangDepartment of Biological Sciences, University of Illinois at Chicago, Chicago, Illinois, 60607, USA. chieh.chang1@gmail.com.
University of Illinois Chicago · USNational Taiwan University · TW

Funding

Specification of Stochastic Left-Right Asymmetric Neuronal Fates in C. elegansR01GM098026 · NIGMS · UNIVERSITY OF ILLINOIS AT CHICAGO · PI CHUANG, CHIOU-FEN · 2012 to 2016
$1.5M
Understanding timing mechanisms for age-related decline in neuronal regenerationR01GM111320 · NIGMS · UNIVERSITY OF ILLINOIS AT CHICAGO · PI CHANG, CHIEH · 2014 to 2019
$1.4M
NIGMS NIH HHS R01 GM098026NIGMS NIH HHS R01 GM111320
6 · The paper itself

Abstract

Two important biological events happen coincidently soon after nerve injury in the peripheral nervous system in C. elegans: removal of axon debris and initiation of axon regeneration. But, it is not known how these two events are co-regulated. Mutants of ced-1, a homolog of Draper and MEGF10, display defects in both events. One model is that those events could be related. But our data suggest that they are actually separable. CED-1 functions in the muscle-type engulfing cells in both events and is enriched in muscle protrusions in close contact with axon debris and regenerating axons. Its two functions occur through distinct biochemical mechanisms; extracellular domain-mediated adhesion for regeneration and extracellular domain binding-induced intracellular domain signaling for debris removal. These studies identify CED-1 in engulfing cells as a receptor in debris removal but as an adhesion molecule in neuronal regeneration, and have important implications for understanding neural circuit repair after injury.

Indexed as

Amino Acid SequenceAnimalsAnimals, Genetically ModifiedBinding SitesCaenorhabditis elegansCaenorhabditis elegans ProteinsCell AdhesionCell DeathDrosophila melanogasterDrosophila ProteinsGene Expression Regulation, DevelopmentalMembrane ProteinsMuscle CellsNerve RegenerationNeuronsPeripheral Nerve InjuriesCaenorhabditis elegans Proteinsced-1 protein, C elegansDrosophila Proteinsdrpr protein, DrosophilaMEGF10, humanMembrane Proteins

Identifiers

PMID30451835
PMCPMC6242819
OpenAlexW2901021725

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.