Evidence map›Paper›PMID 22683734›Full record

ArticleShock (Augusta, Ga.)2012

Role of β1 integrin in tissue homing of neutrophils during sepsis.

Pranita P Sarangi, Young-Min Hyun, Yelena V Lerman, Anthony P Pietropaoli, Minsoo Kim

Open access · greenAbstract read
In one paragraph

Article in Shock (Augusta, Ga.), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
0.7field-weighted citation impact, top 34% 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

21 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Dysregulation of neutrophil in sepsis: recent insights and advances.Cell communication and signaling : CCS · 2025
    Review
  3. Article
  4. Article
  5. Article
  6. Frontline Science: The expression of integrin αJournal of leukocyte biology · 2021
    Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Cell adhesion protein fibulin-7 and its C-terminal fragment negatively regulate monocyte and macrophage migration and functions in vitro and in vivo.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2018
    Article
  15. Article
  16. Article
  17. Article
  18. Role of cellular events in the pathophysiology of sepsis.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2016
    Review
  19. Neutrophil migration under normal and sepsis conditions.Cardiovascular & hematological disorders drug targets · 2015
    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

5 authors at 1 institution in 1 country.

Pranita P SarangiDepartment of Microbiology and Immunology, David H. Smith Center for Vaccine Biology and Immunology, University of Rochester, NY 14642, USA. sarangipp@mail.nih.gov
Young-Min Hyun
Yelena V Lerman
Anthony P Pietropaoli
Minsoo Kim
University of Rochester · US

Funding

VASCULAR RELATIONS OF BLOOD CELLS AND PROTEINSP01HL018208 · NHLBI · UNIVERSITY OF ROCHESTER · PI WAUGH, RICHARD E · 1985 to 2014
$24.7M
LFA-1 in Lymphocyte MigrationR01HL087088 · NHLBI · UNIVERSITY OF ROCHESTER · PI KIM, MINSOO · 2007 to 2015
$3.8M
PHARMACOLOGY OF DRUG ABUSET32DA007232 · NIDA · UNIVERSITY OF ROCHESTER · PI BIDLACK, JEAN M · 1985 to 2011
$2.1M
Regulation of neutrophil migration by Activated Protein CR21HL094797 · NHLBI · UNIVERSITY OF ROCHESTER · PI KIM, MINSOO · 2009 to 2010
$422k
NHLBI NIH HHS HL018208NHLBI NIH HHS HL087088NHLBI NIH HHS HL094797NHLBI NIH HHS P01 HL018208NHLBI NIH HHS R01 HL087088NHLBI NIH HHS R21 HL094797NIDA NIH HHS DA007232NIDA NIH HHS T32 DA007232
6 · The paper itself

Abstract

Aberrant activation of neutrophils during sepsis results in the widespread release of proinflammatory mediators, leading to multiorgan system failure and death. However, aberrant activation of neutrophils during sepsis results in the widespread release of harmful inflammatory mediators causing host tissue injuries that can lead to multiorgan system failure and death. One of the pivotal components of neutrophil migration during inflammation is the expression of surface integrins. In this study, we show that administration of a cyclic analog of RGD peptide (Arg-Gly-Asp) significantly reduced the number of tissue-invading neutrophils and the degree of sepsis-induced lethality in mice as compared with control peptide. Second, β1 integrin (CD29) was highly upregulated on the neutrophils isolated from both septic patients and animals. Finally, conditional genetic ablation of β1 integrin from granulocytes also improved survival and bacterial clearance in septic animals Thus, our results indicate that expression of β1 integrin is important for modulating neutrophil trafficking during sepsis and that therapeutics designed against β1 integrins may be beneficial.

Indexed as

AnimalsAnti-Infective AgentsCD18 AntigensCell MovementHumansIntegrin beta1LigationLipopolysaccharidesMaleMiceMice, Inbred C57BLMice, KnockoutMultiple Organ FailureNeutrophil InfiltrationNeutrophilsOligopeptidesAnti-Infective Agentsarginyl-glycyl-aspartic acidCD18 AntigensIntegrin beta1LipopolysaccharidesOligopeptides

Identifiers

PMID22683734
PMCPMC3422399
OpenAlexW2035020770

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.