Evidence map›Paper›PMID 17170130›Full record

ArticleBlood2007

The beta-tail domain (betaTD) regulates physiologic ligand binding to integrin CD11b/CD18.

Vineet Gupta, Annette Gylling, José Luis Alonso, Takashi Sugimori, Petre Ianakiev, Jiang-Ping Xiong, M Amin Arnaout

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
2.5field-weighted citation impact, top 12% 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

39 citing papers in PubMed, 55 citations in OpenAlex.

  1. Integrins as key regulators in tumor perineural invasion: mechanisms and clinical implications.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Review
  2. All-atom simulations reveal distinct pathways for αCellular and molecular life sciences : CMLS · 2026
    Article
  3. Review
  4. Article
  5. Review
  6. Integrin Alpha8 Beta1 (81): An In-Depth Review of an Overlooked RGD-Binding Receptor.Biocell : official journal of the Sociedades Latinoamericanas de Microscopia Electronica ... et. al · 2025
    Article
  7. Article
  8. Article
  9. Targeting integrin pathways: mechanisms and advances in therapy.Signal transduction and targeted therapy · 2023
    Review
  10. Article
  11. Review
  12. A humanized βCell reports · 2022
    Article
  13. β2 integrin activation and signal transduction in leukocyte recruitment.American journal of physiology. Cell physiology · 2021
    Review
  14. Article
  15. Article
  16. Review
  17. Review
  18. 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

7 authors at 2 institutions in 1 country.

Vineet GuptaNephrology Division, Leukocyte Biology and Inflammation Program, Massachusetts General Hospital, Harvard Medical School, 149 13th Street, Charlestown, MA 02129, USA.
Annette Gylling
José Luis Alonso
Takashi Sugimori
Petre Ianakiev
Jiang-Ping Xiong
M Amin Arnaout
Harvard University · USMassachusetts General Hospital · US

Funding

Structure and Function of beta2 IntegrinR01DK048549 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI ARNAOUT, M. AMIN · 1994 to 2016
$6.0M
Transcriptional regulation of beta2 integrinsP01DK050305 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI ARNAOUT, M. AMIN · 1995 to 2004
$5.8M
The Phagocyte MembraneR01DK074447 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI ARNAOUT, M. AMIN · 2005 to 2009
$2.1M
Beta2 Integrin Activation and SignalingK01DK068253 · NIDDK · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI GUPTA, VINEET · 2004 to 2010
$709k
NIDDK NIH HHS DK 068253NIDDK NIH HHS DK 48549NIDDK NIH HHS DK 50305NIDDK NIH HHS K01 DK068253NIDDK NIH HHS P01 DK050305NIDDK NIH HHS R01 DK048549NIDDK NIH HHS R01 DK074447
6 · The paper itself

Abstract

Crystallographic and electron microscopy studies revealed genuflexed (bent) integrins in both unliganded (inactive) and physiologic ligandbound (active) states, suggesting that local conformational changes are sufficient for activation. Herein we have explored the role of local changes in the contact region between the membrane-proximal beta-tail domain (betaTD) and the ligand-binding betaA domain of the bent conformation in regulating interaction of integrin CD11b/CD18 (alphaMbeta2) with its physiologic ligand iC3b. We replaced the betaTD CD loop residues D658GMD of the CD18 (beta2) subunit with the equivalent D672SSG of the beta3 subunit, with AGAA or with NGTD, expressed the respective heterodimeric receptors either transiently in epithelial HEK293T cells or stably in leukocytes (K562), and measured their ability to bind iC3b and to conformation-sensitive mAbs. In the presence of the physiologic divalent cations Ca(2+) plus Mg(2+) (at 1 mM each), the modified integrins showed increased (in HEK293) or constitutive (in K562) binding to iC3b compared with wild-type receptors. K562 expressing the betaTD-modified integrins bound in Ca(2+)Mg(2+) to the betaA-directed high-affinity reporter mAb 24 but not to mAb KIM127, a reporter of the genu-straightened state. These data identify a role for the membrane proximal betaTD as an allosteric modulator of integrin activation.

Indexed as

Models, MolecularAmino Acid SubstitutionAnimalsCalciumCD11b AntigenCD18 AntigensComplement C3bHumansK562 CellsLigandsMagnesiumMutagenesis, Site-DirectedProtein BindingProtein Structure, QuaternaryProtein Structure, SecondaryProtein Structure, TertiaryCalciumCD11b AntigenCD18 AntigensComplement C3bLigandsMagnesium

Identifiers

PMID17170130
PMCPMC1852245
OpenAlexW2100980133

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.