Evidence map›Paper›PMID 22573886›Full record

ArticleMolecular biology of the cell2012

Electron tomography of late stages of FcRn-mediated antibody transcytosis in neonatal rat small intestine.

Mark S Ladinsky, Kathryn E Huey-Tubman, Pamela J Bjorkman

Abstract read
In one paragraph

Article in Molecular biology of the cell, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
3.5field-weighted citation impact, top 8% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 28 citations in OpenAlex.

  1. FcRn as a Transporter for Nasal Delivery of Biologics: A Systematic Review.International journal of molecular sciences · 2021
    Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. The proximal tubule and albuminuria: really!Journal of the American Society of Nephrology : JASN · 2014
    Review
  8. Article
  9. There's been a Flaw in Our Thinking.Frontiers in immunology · 2014
    Review
  10. Review
  11. The Role of FcRn in Antigen Presentation.Frontiers in immunology · 2014
    Review
  12. Using 2-photon microscopy to understand albuminuria.Transactions of the American Clinical and Climatological Association · 2014
    Review
  13. Article
  14. 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

3 authors at 1 institution in 1 country.

Mark S LadinskyDivision of Biology, California Institute of Technology, Pasadena, CA 91125, USA.
Kathryn E Huey-Tubman
Pamela J Bjorkman
California Institute of Technology · US

Funding

Analysis of the Neonatal Fc Receptor/IgG InteractionR37AI041239 · NIAID · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI BJORKMAN, PAMELA J · 2004 to 2013
$3.7M
Howard Hughes Medical InstituteNIAID NIH HHS 2 R37 AI041239-06A1NIAID NIH HHS R37 AI041239
6 · The paper itself

Abstract

The neonatal Fc receptor (FcRn) transports maternal immunoglobulin (IgG) across epithelia to confer passive immunity to mammalian young. In newborn rodents, FcRn transcytoses IgG from ingested milk across the intestinal epithelium for release into the bloodstream. We used electron tomography to examine FcRn transport of Nanogold-labeled Fc (Au-Fc) in neonatal rat jejunum, focusing on later aspects of transport by chasing Au-Fc before fixation. We observed pools of Au-Fc in dilated regions of the lateral intercellular space (LIS), likely representing exit sites where Au-Fc accumulates en route to the blood. Before weaning, the jejunum functions primarily in IgG transport and exhibits unusual properties: clathrin-rich regions near/at the basolateral LIS and multivesicular bodies (MVBs) expressing early endosomal markers. To address whether these features are related to IgG transport, we examined LIS and endocytic/transcytotic structures from neonatal and weaned animals. Weaned samples showed less LIS-associated clathrin. MVBs labeled with late endosomal/lysosomal markers were smaller than their neonatal counterparts but contained 10 times more internal compartments. These results are consistent with hypotheses that clathrin-rich basolateral regions in neonatal jejunum are involved in IgG exocytosis and that MVBs function in IgG transport while FcRn is expressed but switch to degradative functions after weaning, when the jejunum does not express FcRn or transport IgG.

Indexed as

TranscytosisAnimalsAnimals, NewbornClathrin-Coated VesiclesElectron Microscope TomographyHistocompatibility Antigens Class IIleumImmunoglobulin GIntestinal MucosaJejunumLysosomal-Associated Membrane Protein 1Lysosomal Membrane ProteinsMultivesicular BodiesProtein Transportrab5 GTP-Binding ProteinsRatsFc receptor, neonatalHistocompatibility Antigens Class IImmunoglobulin GLamp1 protein, ratLysosomal-Associated Membrane Protein 1Lysosomal Membrane Proteinsrab5 GTP-Binding ProteinsReceptors, Fc

Identifiers

PMID22573886
PMCPMC3386217
OpenAlexW2171227465

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.