Evidence map›Paper›PMID 23111152›Full record

ArticleNeural development2012

Midkine-A functions upstream of Id2a to regulate cell cycle kinetics in the developing vertebrate retina.

Jing Luo, Rosa A Uribe, Sarah Hayton, Anda-Alexandra Calinescu, Jeffrey M Gross, Peter F Hitchcock

Open access · goldAbstract read
In one paragraph

Article in Neural development, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

28 citing papers in PubMed, 44 citations in OpenAlex.

  1. Review
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  5. Brain sciences · 2022
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  10. Midkine-a Is Required for Cell Cycle Progression of Müller Glia during Neuronal Regeneration in the Vertebrate Retina.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2020
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  13. Dual regulation ofThe Journal of cell biology · 2019
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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

6 authors at 2 institutions in 1 country.

Jing LuoDepartment of Ophthalmology and Visual Sciences, University of Michigan, W, K, Kellogg Eye Center, 1000 Wall Street, Ann Arbor, MI 48105-0714, USA.
Rosa A Uribe
Sarah Hayton
Anda-Alexandra Calinescu
Jeffrey M Gross
Peter F Hitchcock
University of Michigan–Ann Arbor · USThe University of Texas at Austin · US

Funding

ZEBRAFISH INTERNATIONAL RESOURCE CENTERP40RR012546 · NCRR · UNIVERSITY OF OREGON · PI WESTERFIELD, MONTE · 1998 to 2011
$21.9M
VIVARIUM MODULEP30EY007003 · NEI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI James D Weiland · 1987 to 2026
$17.6M
RETINAL DEVELOPMENT--DENDRITIC GROWTH SYNAPSER01EY007060 · NEI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI HITCHCOCK, PETER F · 1987 to 2021
$7.0M
Genetic Regulation of Eye Development in ZebrafishR01EY018005 · NEI · UNIVERSITY OF TEXAS AT AUSTIN · PI GROSS, JEFFREY · 2008 to 2017
$3.3M
The In Vivo Function of Id2 in Retinal Proliferation and DifferentiationF31EY019239 · NEI · UNIVERSITY OF TEXAS AT AUSTIN · PI URIBE, ROSA A · 2008 to 2011
$138k
NCRR NIH HHS P40 RR012546.NEI NIH HHS F31 EY19239NEI NIH HHS P30 EY07003NEI NIH HHS R01 EY007060NEI NIH HHS R01 EY018005NEI NIH HHS R01 EY07060NEI NIH HHS R01 EY18005
6 · The paper itself

Abstract

backgroundMidkine is a small heparin binding growth factor expressed in numerous tissues during development. The unique midkine gene in mammals has two paralogs in zebrafish: midkine-a (mdka) and midkine-b (mdkb). In the zebrafish retina, during both larval development and adult photoreceptor regeneration, mdka is expressed in retinal stem and progenitor cells and functions as a molecular component of the retina's stem cell niche. In this study, loss-of-function and conditional overexpression were used to investigate the function of Mdka in the retina of the embryonic zebrafish.

resultsThe results show that during early retinal development Mdka functions to regulate cell cycle kinetics. Following targeted knockdown of Mdka synthesis, retinal progenitors cycle more slowly, and this results in microphthalmia, a diminished rate of cell cycle exit and a temporal delay of cell cycle exit and neuronal differentiation. In contrast, Mdka overexpression results in acceleration of the cell cycle and retinal overgrowth. Mdka gain-of-function, however, does not temporally advance cell cycle exit. Experiments to identify a potential Mdka signaling pathway show that Mdka functions upstream of the HLH regulatory protein, Id2a. Gene expression analysis shows Mdka regulates id2a expression, and co-injection of Mdka morpholinos and id2a mRNA rescues the Mdka loss-of-function phenotype.

conclusionsThese data show that in zebrafish, Mdka resides in a shared Id2a pathway to regulate cell cycle kinetics in retinal progenitors. This is the first study to demonstrate the function of Midkine during retinal development and adds Midkine to the list of growth factors that transcriptionally regulate Id proteins.

Indexed as

AnimalsAnimals, Genetically ModifiedBromodeoxyuridineCell CycleCell DeathCell DifferentiationCytokinesDNA-Binding ProteinsEmbryo, NonmammalianFlow CytometryGene Expression Regulation, DevelopmentalHistonesInhibitor of Differentiation Protein 2KineticsLarvaMidkineBromodeoxyuridineCytokinesDNA-Binding ProteinsHistonesId2a protein, zebrafishInhibitor of Differentiation Protein 2MidkineMorpholinosRNA, MessengerZebrafish Proteins

Identifiers

PMID23111152
PMCPMC3531272
OpenAlexW2145376923

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.