Evidence map›Paper›PMID 22784557›Full record

ReviewTrends in neurosciences2012

Chemokine CXCL12 in neurodegenerative diseases: an SOS signal for stem cell-based repair.

Meizhang Li, James S Hale, Jeremy N Rich, Richard M Ransohoff, Justin D Lathia

Abstract readReview
In one paragraph

Review in Trends in neurosciences, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

53 citing papers in PubMed, 101 citations in OpenAlex.

  1. Trial
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  3. Review
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  5. Article
  6. Review
  7. Review
  8. Article
  9. Proteomic analyses reveal plasma EFEMP1 and CXCL12 as biomarkers and determinants of neurodegeneration.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2024
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Review
  18. Article
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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

5 authors at 2 institutions in 1 country.

Meizhang LiDepartment of Cell Biology, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio, USA. Lim3@ccf.org
James S Hale
Jeremy N Rich
Richard M Ransohoff
Justin D Lathia
Cleveland Clinic Lerner College of Medicine · USCase Western Reserve University · US

Funding

Clinical and Translational Science Collaborative of ClevelandUL1TR000439 · NCATS · CASE WESTERN RESERVE UNIVERSITY · PI KONSTAN, MICHAEL W. · 2012 to 2016
$50.0M
CHEMOKINES IN CNS INFLAMMATIONR01NS032151 · NINDS · CLEVELAND CLINIC LERNER COM-CWRU · PI RANSOHOFF, RICHARD M. · 1994 to 2013
$3.7M
Targeting Brain Tumor Stem Cells Through Novel Therapeutic CombinationsR01CA154130 · NCI · CLEVELAND CLINIC LERNER COM-CWRU · PI RICH, JEREMY N · 2010 to 2014
$1.9M
Mentored Research: Chemokine Regulation on CNS Inflammation in MSK24NS051400 · NINDS · CLEVELAND CLINIC LERNER COM-CWRU · PI RANSOHOFF, RICHARD M. · 2006 to 2014
$1.4M
TGFbeta-PTEN Interactions in Glioma Biology & TherapyR01CA116659 · NCI · DUKE UNIVERSITY · PI RICH, JEREMY N · 2006 to 2010
$1.4M
Microenvironmental regulation of the cancer stem cell phenotype by integrin a6R00CA157948 · NCI · CLEVELAND CLINIC LERNER COM-CWRU · PI LATHIA, JUSTIN D. · 2012 to 2014
$725k
Modulating chemokine receptors at the blood-brain barrier under flowR21NS074820 · NINDS · CLEVELAND CLINIC LERNER COM-CWRU · PI RANSOHOFF, RICHARD M. · 2011 to 2012
$432k
Microenvironmental modulation as a result of glioma therapyK99CA157948 · NCI · CLEVELAND CLINIC LERNER COM-CWRU · PI LATHIA, JUSTIN D. · 2011 to 2011
$99k
NCATS NIH HHS UL1 TR000439NCI NIH HHS CA112958NCI NIH HHS CA116659NCI NIH HHS CA154130NCI NIH HHS K99 CA157948NCI NIH HHS K99/R00 CA157948NCI NIH HHS R00 CA157948NCI NIH HHS R01 CA116659NCI NIH HHS R01 CA154130NINDS NIH HHS K24 NS051400NINDS NIH HHS K24NS51400NINDS NIH HHS R01 NS032151NINDS NIH HHS R01NS32151NINDS NIH HHS R21 NS074820NINDS NIH HHS R21NS74820
6 · The paper itself

Abstract

The dynamic relation between stem cells and their niche governs self-renewal and progenitor cell deployment. The chemokine CXCL12 (C-X-C motif ligand 12) and its signaling receptor CXCR4 (C-X-C motif receptor 4) represent an important pathway that regulates homing and maintenance of stem cells in neural niches. Neural stem cells (NSCs) reside in specific niches where communication with blood vessels is regulated by CXCL12. In neurodegenerative diseases and brain tumors, reactive vasculature forms in response to diseased tissues to create new niches that secrete CXCL12, enhancing the recruitment of neural progenitor cells (NPCs) to lesion sites via long-range migration. These observations suggest that the CXCL12-CXCR4 axis maintains NSCs and serves as an emergent salvage signal for initiating endogenous stem cell-based tissue repair.

Indexed as

AnimalsChemokine CXCL12Disease Models, AnimalHumansModels, BiologicalNeural Stem CellsNeurodegenerative DiseasesNeurogenesisReceptors, CXCR4Signal TransductionChemokine CXCL12Receptors, CXCR4

Identifiers

PMID22784557
PMCPMC3461091
OpenAlexW2001372804

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.