Evidence map›Paper›PMID 21257828›Full record

ArticleStroke2011

Selectin-mediated recruitment of bone marrow stromal cells in the postischemic cerebral microvasculature.

Gokhan Yilmaz, Shantel Vital, Cigdem Erkuran Yilmaz, Karen Y Stokes, J Steven Alexander, D Neil Granger

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Stroke, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 2 pooled it
2.1field-weighted citation impact, top 13% 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

23 citing papers in PubMed, 2 syntheses or guidelines pooled it, 51 citations in OpenAlex.

  1. [Research progress of different types of stem cells in treatment of ischemic stroke].Zhongguo xiu fu chong jian wai ke za zhi = Zhongguo xiufu chongjian waike zazhi = Chinese journal of reparative and reconstructive surgery · 2021
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  12. Metallothionein I as a direct link between therapeutic hematopoietic stem/progenitor cells and cerebral protection in stroke.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2018
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  17. A possible new focus for stroke treatment - migrating stem cells.Expert opinion on biological therapy · 2015
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  19. Stem cell delivery of therapies for brain disorders.Clinical and translational medicine · 2014
    Review
  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

6 authors at 1 institution in 1 country.

Gokhan YilmazDepartment of Surgery, University of Medicine and Dentistry of New Jersey, Newark, NJ, USA.
Shantel Vital
Cigdem Erkuran Yilmaz
Karen Y Stokes
J Steven Alexander
D Neil Granger
University Hospital, Newark · US

Funding

TRANSCAPILLARY FLUID EXCHANGER01HL026441 · NHLBI · UNIVERSITY OF SOUTH ALABAMA · PI GRANGER, D. NEIL · 1985 to 2013
$4.0M
NHLBI NIH HHS HL26441NHLBI NIH HHS R01 HL026441
6 · The paper itself

Abstract

background and purposeThe therapeutic potential of bone marrow stromal cells (BMSCs) has been demonstrated in different models of stroke. Although it is well established that BMSCs selectively migrate to the site of brain injury, the mechanisms underlying this process are poorly understood. This study addresses the hypothesis that selectins mediate the recruitment of BMSCs into the postischemic cerebral microvasculature.

methodsFocal ischemic stroke was induced by middle cerebral artery occlusion and reperfusion. Cell recruitment was monitored using either fluorescent- or radiolabeled BMSCs detected by intravital microscopy or tissue radioactivity. Mice were treated with either a blocking antibody against P- or E-selectin or with the nonselective selectin antagonist, fucoidin. The role of CD44 in cell recruitment was evaluated using BMSCs from CD44 knockout mice.

resultsMiddle cerebral artery occlusion and reperfusion was associated with a significantly increased adhesion of BMSCs in cerebral venules compared with sham mice. Immunoneutralization of either E- or P-selectin blocked the middle cerebral artery occlusion and reperfusion-induced recruitment of adherent BMSCs. An attenuated recruitment response in the postischemic hemisphere was also noted after fucoidin treatment or administration of CD44-deficient BMSCs.

conclusionsCerebral vascular endothelium assume a proadhesive phenotype after ischemic stroke that favors the recruitment of BMSCs, which use both P- and E-selectin to home into the infarct site. CD44 may serve as the critical ligand for selectin-mediated BMSC recruitment.

Indexed as

AnimalsBone Marrow CellsBrain IschemiaCell AdhesionCell MovementCells, CulturedEndothelium, VascularE-SelectinHematopoietic Stem CellsHumansHyaluronan ReceptorsImmunophenotypingLigandsMaleMiceMice, Inbred C57BLCD44 protein, humanCd44 protein, mouseE-SelectinHyaluronan ReceptorsLigandsP-Selectin

Identifiers

PMID21257828
PMCPMC3042505
OpenAlexW1970505137

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.