Evidence map›Paper›PMID 29641231›Full record

ArticleAmerican journal of physiology. Regulatory, integrative and comparative physiology2018

A role for the CXCR4-CXCL12 axis in the little skate, Leucoraja erinacea.

Taylor A Hersh, Alexandria L Dimond, Brittany A Ruth, Noah V Lupica, Jacob C Bruce, John M Kelley, Benjamin L King, Bram V Lutton

Open access · bronzeAbstract read
In one paragraph

Article in American journal of physiology. Regulatory, integrative and comparative physiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.3field-weighted citation impact, top 45% 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

5 citing papers in PubMed, 10 citations in OpenAlex.

  1. mBio · 2025
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  5. Editors' Picks for 2018 demonstrate the diversity of research in regulatory, integrative, and comparative physiology.American journal of physiology. Regulatory, integrative and comparative physiology · 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

8 authors at 4 institutions in 1 country.

Taylor A HershMount Desert Island Biological Laboratory , Bar Harbor, Maine.ORCID 0000-0002-7891-596X
Alexandria L DimondMount Desert Island Biological Laboratory , Bar Harbor, Maine.
Brittany A RuthMount Desert Island Biological Laboratory , Bar Harbor, Maine.
Noah V LupicaMount Desert Island Biological Laboratory , Bar Harbor, Maine.
Jacob C BruceMount Desert Island Biological Laboratory , Bar Harbor, Maine.
John M KelleySchool of Arts and Sciences, Endicott College , Beverly, Massachusetts.
Benjamin L KingDepartment of Molecular and Biomedical Sciences, University of Maine , Orono, Maine.
Bram V LuttonMount Desert Island Biological Laboratory , Bar Harbor, Maine.
Endicott College · USMount Desert Island Biological Laboratory · USBeth Israel Deaconess Medical Center · USUniversity of Maine · US

Funding

The Maine Biomedical Research Network (INBRE)P20GM103423 · NIGMS · MOUNT DESERT ISLAND BIOLOGICAL LAB · PI Dustin Lynn Updike · 2012 to 2026
$60.0M
Understanding the role of thyroid hormone signaling during axolotl limb regenerationP20GM104318 · NIGMS · MOUNT DESERT ISLAND BIOLOGICAL LAB · PI DRUMMOND, IAIN A. · 2013 to 2023
$23.0M
MDIBL STEER: Pathways of Chemical Action in Human DiseaseR25ES016254 · NIEHS · MOUNT DESERT ISLAND BIOLOGICAL LAB · PI STANTON, BRUCE A. · 2008 to 2012
$223k
NIEHS NIH HHS R25 ES016254NIGMS NIH HHS P20 GM103423NIGMS NIH HHS P20 GM104318
6 · The paper itself

Abstract

The interaction between C-X-C chemokine receptor type 4 (CXCR4) and its cognate ligand C-X-C motif chemokine ligand 12 (CXCL12) plays a critical role in regulating hematopoietic stem cell activation and subsequent cellular mobilization. Extensive studies of these genes have been conducted in mammals, but much less is known about the expression and function of CXCR4 and CXCL12 in non-mammalian vertebrates. In the present study, we identify simultaneous expression of CXCR4 and CXCL12 orthologs in the epigonal organ (the primary hematopoietic tissue) of the little skate, Leucoraja erinacea. Genetic and phylogenetic analyses were functionally supported by significant mobilization of leukocytes following administration of Plerixafor, a CXCR4 antagonist and clinically important drug. Our results provide evidence that, as in humans, Plerixafor disrupts CXCR4/CXCL12 binding in the little skate, facilitating release of leukocytes into the bloodstream. Our study illustrates the value of the little skate as a model organism, particularly in studies of hematopoiesis and potentially for preclinical research on hematological and vascular disorders.

Indexed as

LeukopoiesisAnimalsBenzylaminesChemokine CXCL12CyclamsFish ProteinsGene Expression RegulationHematopoietic Stem CellsHeterocyclic CompoundsLeukocytesPhylogenyReceptors, CXCR4Signal TransductionSkates, FishTranscriptomeBenzylaminesChemokine CXCL12CyclamsFish ProteinsHeterocyclic CompoundsplerixaforReceptors, CXCR4C-X-C chemokine ligand 12C-X-C chemokine receptor type 4elasmobranchmobilizationPlerixafor/AMD3100

Identifiers

PMID29641231
PMCPMC6139610
OpenAlexW2797256711

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.