Evidence map›Paper›PMID 27842058›Full record

ArticleNature cell biology2016

Developmentally programmed germ cell remodelling by endodermal cell cannibalism.

Yusuff Abdu, Chelsea Maniscalco, John M Heddleston, Teng-Leong Chew, Jeremy Nance

Abstract read
In one paragraph

Article in Nature cell biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
3.6field-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

52 citing papers in PubMed, 85 citations in OpenAlex.

  1. Review
  2. Danger at the border: Rac turns nibblers into murderers.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  3. Hyperactive Rac converts sublethal to lethal trogocytosis in vivo.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  4. Article
  5. Article
  6. Hyperactive Rac converts sublethal nibbling to lethal phagocytosisbioRxiv : the preprint server for biology · 2025
    Article
  7. Article
  8. Cross-species protection suggestsInfection and immunity · 2025
    Article
  9. Mitochondrial curation for the next generation.Current opinion in genetics & development · 2025
    Review
  10. Review
  11. Article
  12. Article
  13. Review
  14. Extracellular vesicles.Genetics · 2024
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. OSGN-1 is a conserved flavin-containing monooxygenase required to stabilize the intercellular bridge in late cytokinesis.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 3 institutions in 1 country.

Yusuff AbduHelen L. and Martin S. Kimmel Center for Biology and Medicine at the Skirball Institute of Biomolecular Medicine, NYU School of Medicine, New York, New York 10016, USA.
Chelsea ManiscalcoHelen L. and Martin S. Kimmel Center for Biology and Medicine at the Skirball Institute of Biomolecular Medicine, NYU School of Medicine, New York, New York 10016, USA.
John M HeddlestonAdvanced Imaging Center, Janelia Research Campus, Howard Hughes Medical Institute, Ashburn, Virginia 20147, USA.
Teng-Leong ChewAdvanced Imaging Center, Janelia Research Campus, Howard Hughes Medical Institute, Ashburn, Virginia 20147, USA.
Jeremy NanceHelen L. and Martin S. Kimmel Center for Biology and Medicine at the Skirball Institute of Biomolecular Medicine, NYU School of Medicine, New York, New York 10016, USA.
New York University · USHoward Hughes Medical Institute · USImaging Center · US

Funding

Vaccine FacilityP30CA016087 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ADRIANA HEGUY · 1985 to 2026
$83.1M
The Role of Cell Interactions in Shaping DevelopmentR35GM118081 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI Jeremy Nance · 2016 to 2026
$6.4M
Endodermal regulation of primordial germ cellsR21HD084809 · NICHD · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI NANCE, JEREMY · 2015 to 2016
$464k
NCI NIH HHS P30 CA016087NICHD NIH HHS R21 HD084809NIGMS NIH HHS R35 GM118081
6 · The paper itself

Abstract

Primordial germ cells (PGCs) in many species associate intimately with endodermal cells, but the significance of such interactions is largely unexplored. Here, we show that Caenorhabditis elegans PGCs form lobes that are removed and digested by endodermal cells, dramatically altering PGC size and mitochondrial content. We demonstrate that endodermal cells do not scavenge lobes PGCs shed, but rather, actively remove lobes from the cell body. CED-10 (Rac)-induced actin, DYN-1 (dynamin) and LST-4 (SNX9) transiently surround lobe necks and are required within endodermal cells for lobe scission, suggesting that scission occurs through a mechanism resembling vesicle endocytosis. These findings reveal an unexpected role for endoderm in altering the contents of embryonic PGCs, and define a form of developmentally programmed cell remodelling involving intercellular cannibalism. Active roles for engulfing cells have been proposed in several neuronal remodelling events, suggesting that intercellular cannibalism may be a more widespread method used to shape cells than previously thought.

Indexed as

Cellular ReprogrammingCytophagocytosisAnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsDynaminsEndodermGerm CellsMitochondriaCaenorhabditis elegans ProteinsDynamins

Identifiers

PMID27842058
PMCPMC5129868
OpenAlexW2556688419

What OpenQuestion holds

Textmetadata
LicenceTDM
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.