Evidence map›Paper›PMID 20685998›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2010

LIM-homeobox gene Lhx5 is required for normal development of Cajal-Retzius cells.

Amaya Miquelajáuregui, Alfredo Varela-Echavarría, M Laura Ceci, Fernando García-Moreno, Itzel Ricaño, Kimmi Hoang, Daniela Frade-Pérez, Carlos Portera-Cailliau, Elisa Tamariz, Juan A De Carlos and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

32 citing papers in PubMed, 56 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. The Role of ISL1 and LHX5 LIM Homeobox Genes in Bladder Tumourigenesis.The Malaysian journal of medical sciences : MJMS · 2020
    Article
  14. Article
  15. Article
  16. Overexpression of NEUROG2 and NEUROG1 in human embryonic stem cells produces a network of excitatory and inhibitory neurons.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    Article
  17. Article
  18. Article
  19. Lateral Thalamic Eminence: A Novel Origin for mGluR1/Lot Cells.Cerebral cortex (New York, N.Y. : 1991) · 2017
    Article
  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

12 authors at 8 institutions in 3 countries.

Amaya MiquelajáureguiInstituto de Neurobiología, Universidad Nacional Autónoma de México, Querétaro, Querétaro 76230, Mexico.
Alfredo Varela-Echavarría
M Laura Ceci
Fernando García-Moreno
Itzel Ricaño
Kimmi Hoang
Daniela Frade-Pérez
Carlos Portera-Cailliau
Elisa Tamariz
Juan A De Carlos
Heiner Westphal
Yangu Zhao
Universidad Nacional Autónoma de México · MXInstituto Cajal · ESNational Institutes of Health · USAutonomous University of Queretaro · MXConsejo Superior de Investigaciones Científicas · ESEunice Kennedy Shriver National Institute of Child Health and Human Development · USInstituto Nacional de Rehabilitación · MXUniversity of California, Los Angeles · US

Funding

Mammalian Developmental Genetics and Stem CellsZIAHD000071 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI WESTPHAL, HEINER · 2009 to 2012
$8.5M
Intramural NIH HHS Z99 HD999999Wellcome Trust 071174Wellcome Trust GR071174AIA
6 · The paper itself

Abstract

Cajal-Retzius (C-R) cells play important roles in the lamination of the mammalian cortex via reelin secretion. The genetic mechanisms underlying the development of these neurons have just begun to be unraveled. Here, we show that two closely related LIM-homeobox genes Lhx1 and Lhx5 are expressed in reelin+ cells in various regions in the mouse telencephalon at or adjacent to sites where the C-R cells are generated, including the cortical hem, the mantle region of the septal/retrobulbar area, and the ventral pallium. Whereas Lhx5 is expressed in all of these reelin-expressing domains, Lhx1 is preferentially expressed in the septal area and in a continuous domain spanning from lateral olfactory region to caudomedial territories. Genetic ablation of Lhx5 results in decreased reelin+ and p73+ cells in the neocortical anlage, in the cortical hem, and in the septal, olfactory, and caudomedial telencephalic regions. The overall reduction in number of C-R cells in Lhx5 mutants is accompanied by formation of ectopic reelin+ cell clusters at the caudal telencephalon. Based on differential expression of molecular markers and by fluorescent cell tracing in cultured embryos, we located the origin of reelin+ ectopic cell clusters at the caudomedial telencephalic region. We also confirmed the existence of a normal migration stream of reelin+ cells from the caudomedial area to telencephalic olfactory territories in wild-type embryos. These results reveal a complex role for Lhx5 in regulating the development and normal distribution of C-R cells in the developing forebrain.

Indexed as

AnimalsCell Adhesion Molecules, NeuronalCell MovementCerebral CortexEmbryo Culture TechniquesExtracellular Matrix ProteinsHomeodomain ProteinsImmunohistochemistryIn Situ HybridizationLIM-Homeodomain ProteinsMiceMice, KnockoutNerve Tissue ProteinsNeuronsReelin ProteinReverse Transcriptase Polymerase Chain ReactionCell Adhesion Molecules, NeuronalExtracellular Matrix ProteinsHomeodomain ProteinsLhx1 protein, mouseLhx5 protein, mouseLIM-Homeodomain ProteinsNerve Tissue ProteinsReelin ProteinReln protein, mouseSerine EndopeptidasesTranscription Factors

Identifiers

PMID20685998
PMCPMC2927820
OpenAlexW2082600067

What OpenQuestion holds

Textmetadata
LicenceTDM
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.