Evidence map›Paper›PMID 22262862›Full record

ArticleThe Journal of biological chemistry2012

Externalized glycolytic enzymes are novel, conserved, and early biomarkers of apoptosis.

David S Ucker, Mohit Raja Jain, Goutham Pattabiraman, Karol Palasiewicz, Raymond B Birge, Hong Li

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

24 citing papers in PubMed, 49 citations in OpenAlex.

  1. Surface enolase is a virulence factor ofFrontiers in microbiology · 2026
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  2. Can the Quality of Semen Affect the Fertilisation Indices of Turkey Eggs?International journal of molecular sciences · 2025
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  9. When Place Matters: Shuttling of Enolase-1 Across Cellular Compartments.Frontiers in cell and developmental biology · 2019
    Review
  10. Article
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  18. From plasminogen to plasmin: role of plasminogen receptors in human cancer.International journal of molecular sciences · 2014
    Review
  19. 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

6 authors at 4 institutions in 1 country.

David S UckerDepartment of Microbiology and Immunology, University of Illinois College of Medicine, Chicago, Illinois 60612 and. Electronic address: duck@uic.edu.
Mohit Raja JainCenter for Advanced Proteomics Research, UMDNJ-New Jersey Medical School Cancer Center, Newark, New Jersey 07214; Department of Biochemistry and Molecular Biology, UMDNJ-New Jersey Medical School Cancer Center, Newark, New Jersey 07214.
Goutham PattabiramanDepartment of Microbiology and Immunology, University of Illinois College of Medicine, Chicago, Illinois 60612 and.
Karol PalasiewiczDepartment of Microbiology and Immunology, University of Illinois College of Medicine, Chicago, Illinois 60612 and.
Raymond B BirgeDepartment of Biochemistry and Molecular Biology, UMDNJ-New Jersey Medical School Cancer Center, Newark, New Jersey 07214.
Hong LiCenter for Advanced Proteomics Research, UMDNJ-New Jersey Medical School Cancer Center, Newark, New Jersey 07214; Department of Biochemistry and Molecular Biology, UMDNJ-New Jersey Medical School Cancer Center, Newark, New Jersey 07214. Electronic address: liho2@umdnj.edu.
Rutgers New Jersey Medical SchoolUniversity of Illinois Chicago · USRutgers, The State University of New Jersey · USUniversity of Illinois Urbana-Champaign · US

Funding

Rutgers Mass Spectrometry Core for Integrative Neuroscience ResearchP30NS046593 · NINDS · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI LOBEL, PETER · 2004 to 2018
$9.9M
Aging and Apoptotic Modulation of Immune ResponsivenessR01AG029633 · NIA · UNIVERSITY OF ILLINOIS AT CHICAGO · PI UCKER, DAVID S · 2008 to 2012
$1.6M
NIA NIH HHS AG029633NIA NIH HHS R01 AG029633NINDS NIH HHS NS046593NINDS NIH HHS P30 NS046593
6 · The paper itself

Abstract

The intriguing cell biology of apoptotic cell death results in the externalization of numerous autoantigens on the apoptotic cell surface, including protein determinants for specific recognition, linked to immune responses. Apoptotic cells are recognized by phagocytes and trigger an active immunosuppressive response ("innate apoptotic immunity" (IAI)) even in the absence of engulfment. IAI is responsible for the lack of inflammation associated normally with the clearance of apoptotic cells; its failure also has been linked to inflammatory and autoimmune pathology, including systemic lupus erythematosus and rheumatic diseases. Apoptotic recognition determinants underlying IAI have yet to be identified definitively; we argue that these molecules are surface-exposed (during apoptotic cell death), ubiquitously expressed, protease-sensitive, evolutionarily conserved, and resident normally in viable cells (SUPER). Using independent and unbiased quantitative proteomic approaches to characterize apoptotic cell surface proteins and identify candidate SUPER determinants, we made the surprising discovery that components of the glycolytic pathway are enriched on the apoptotic cell surface. Our data demonstrate that glycolytic enzyme externalization is a common and early aspect of cell death in different cell types triggered to die with distinct suicidal stimuli. Exposed glycolytic enzyme molecules meet the criteria for IAI-associated SUPER determinants. In addition, our characterization of the apoptosis-specific externalization of glycolytic enzyme molecules may provide insight into the significance of previously reported cases of plasminogen binding to α-enolase on mammalian cells, as well as mechanisms by which commensal bacteria and pathogens maintain immune privilege.

Indexed as

ApoptosisGlycolysisImmunity, InnateAnimalsBiomarkersHumansJurkat CellsLupus Erythematosus, SystemicMiceProteomicsU937 CellsBiomarkers

Identifiers

PMID22262862
PMCPMC3323007
OpenAlexW2157540279

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.