Evidence map›Paper›PMID 17384151›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2007

Elucidation of intracellular recycling pathways leading to exocytosis of the Fc receptor, FcRn, by using multifocal plane microscopy.

Prashant Prabhat, Zhuo Gan, Jerry Chao, Sripad Ram, Carlos Vaccaro, Steven Gibbons, Raimund J Ober, E Sally Ward

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 91 papers.

0numbers the graph read from it
0cells of the map it votes in
91citing papers in PubMed
–field-weighted citation impact
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

91 citing papers in PubMed.

  1. Trial
  2. Review
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Targeting the Neonatal Fc Receptor in Autoimmune Diseases: Pipeline and Progress.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2025
    Review
  11. Review
  12. Article
  13. Article
  14. The therapeutic age of the neonatal Fc receptor.Nature reviews. Immunology · 2023
    Review
  15. Review
  16. Article
  17. Review
  18. Neonatal Fc Receptor-Targeted Therapies in Neurology.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2022
    Review
  19. Article
  20. Article

31 more citing papers are in PubMed but not listed here.

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

8 authors.

Prashant PrabhatDepartment of Immunology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
Zhuo Gan
Jerry Chao
Sripad Ram
Carlos Vaccaro
Steven Gibbons
Raimund J Ober
E Sally Ward

Funding

STRUCTURE/FUNCTION STUDIES OF HUMAN FCRNR01AI039167 · NIAID · UT SOUTHWESTERN MEDICAL CENTER · PI WARD, ELIZABETH SALLY · 1995 to 2008
$2.8M
Quantitative Aspects of Single Molecule DetectionR01GM071048 · NIGMS · UNIVERSITY OF TEXAS DALLAS · PI OBER, RAIMUND J · 2005 to 2008
$1.0M
NIAID NIH HHS R01 AI039167NIGMS NIH HHS R01 GM071048
6 · The paper itself

Abstract

The intracellular events on the recycling pathway that lead from sorting endosomes to exocytosis at the plasma membrane are central to cellular function. However, despite intensive study, these processes are poorly characterized in spatial and dynamic terms. The primary reason for this is that, to date, it has not been possible to visualize rapidly moving intracellular compartments in three dimensions in cells. Here, we use a recently developed imaging setup in which multiple planes can be simultaneously imaged within the cell in conjunction with visualization of the plasma membrane plane by using total internal reflection fluorescence microscopy. This has allowed us to track and characterize intracellular events on the recycling pathway that lead to exocytosis of the MHC Class I-related receptor, FcRn. We observe both direct delivery of tubular and vesicular transport containers (TCs) from sorting endosomes to exocytic sites at the plasma membrane, and indirect pathways in which TCs that are not in proximity to sorting endosomes undergo exocytosis. TCs can also interact with different sorting endosomes before exocytosis. Our data provide insight into the intracellular events that precede exocytic fusion.

Indexed as

beta 2-MicroglobulinCell Culture TechniquesCell LineEndosomesEndothelial CellsExocytosisGreen Fluorescent ProteinsHistocompatibility Antigens Class IHumansMicroscopy, FluorescencePlasmidsReceptors, FcTransfectionbeta 2-MicroglobulinFc receptor, neonatalGreen Fluorescent ProteinsHistocompatibility Antigens Class IReceptors, Fc

Identifiers

PMID17384151
PMCPMC1851587

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.