Evidence map›Paper›PMID 23420480›Full record

ArticleCellular and molecular life sciences : CMLS2013

RIAM (Rap1-interacting adaptor molecule) regulates complement-dependent phagocytosis.

Iria Medraño-Fernandez, Raquel Reyes, Isabel Olazabal, Elena Rodriguez, Francisco Sanchez-Madrid, Vassiliki A Boussiotis, Pedro A Reche, Carlos Cabañas, Esther M Lafuente

Abstract read
In one paragraph

Article in Cellular and molecular life sciences : CMLS, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.0field-weighted citation impact, top 15% 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

18 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Expression of the phagocytic receptors αFrontiers in immunology · 2022
    Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Frontiers in immunology · 2020
    Review
  12. Review
  13. Review
  14. Review
  15. KNOWLEDGE-ASSISTED APPROACH TO IDENTIFY PATHWAYS WITH DIFFERENTIAL DEPENDENCIES.Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing · 2016
    Article
  16. Review
  17. Article
  18. 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

9 authors at 4 institutions in 2 countries.

Iria Medraño-FernandezDepartamento de Microbiología I, Inmunología, Facultad de Medicina, Universidad Complutense de Madrid, 28040 Madrid, Spain.
Raquel Reyes
Isabel Olazabal
Elena Rodriguez
Francisco Sanchez-Madrid
Vassiliki A Boussiotis
Pedro A Reche
Carlos Cabañas
Esther M Lafuente
Universidad Complutense de Madrid · ESHospital Universitario de La Princesa · ESBeth Israel Deaconess Medical Center · USCentro de Biología Molecular Severo Ochoa · ES

Funding

Prevention of acute GvHD by inhibition of cdk2R21HL107997 · NHLBI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI BOUSSIOTIS, VASSILIKI A · 2011 to 2012
$482k
The role of Rap1 and its novel associated molecules in T cell responsesR56AI043552 · NIAID · BETH ISRAEL DEACONESS MEDICAL CENTER · PI BOUSSIOTIS, VASSILIKI A · 2011 to 2011
$392k
NHLBI NIH HHS HL107997-01NHLBI NIH HHS R21 HL107997NIAID NIH HHS R56 AI043552NIAID NIH HHS R56AI43552
6 · The paper itself

Abstract

Phagocytosis mediated by the complement receptor CR3 (also known as integrin αMß2 or Mac-1) is regulated by the recruitment of talin to the cytoplasmic tail of the ß2 integrin subunit. Talin recruitment to this integrin is dependent on Rap1 activation. However, the mechanism by which Rap1 regulates this event and CR3-dependent phagocytosis remains largely unknown. In the present work, we examined the role of the Rap1 effector RIAM, a talin-binding protein, in the regulation of complement-mediated phagocytosis. Using the human myeloid cell lines HL-60 and THP-1, we determined that knockdown of RIAM impaired αMß2 integrin affinity changes induced by stimuli fMLP and LPS. Phagocytosis of complement-opsonized RBC particles, but not of IgG-opsonized RBC particles, was impaired in RIAM knockdown cells. Rap1 activation via EPAC induced by 8-pCPT-2'-O-Me-cAMP resulted in an increase of complement-mediated phagocytosis that was abrogated by knockdown of RIAM in HL-60 and THP-1 cell lines and in macrophages derived from primary monocytes. Furthermore, recruitment of talin to ß2 integrin during complement-mediated phagocytosis was reduced in RIAM knockdown cells. These results indicate that RIAM is a critical component of the phagocytosis machinery downstream of Rap1 and mediates its function by recruiting talin to the phagocytic complement receptors.

Indexed as

Adaptor Proteins, Signal TransducingCD18 AntigensCells, CulturedComplement System ProteinsGene Knockdown TechniquesHL-60 CellsHumansMacrophage-1 AntigenMacrophagesMembrane ProteinsModels, BiologicalNeutrophilsPhagocytosisrap1 GTP-Binding ProteinsTalinAdaptor Proteins, Signal TransducingAPBB1IP protein, humanCD18 AntigensComplement System ProteinsMacrophage-1 AntigenMembrane Proteinsrap1 GTP-Binding ProteinsTalin

Identifiers

PMID23420480
PMCPMC5474120
OpenAlexW2036882237

What OpenQuestion holds

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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.