Evidence map›Paper›PMID 27585956›Full record

ReviewCellular and molecular life sciences : CMLS2017

Preparing the lethal hit: interplay between exo- and endocytic pathways in cytotoxic T lymphocytes.

Hsin-Fang Chang, Hawraa Bzeih, Praneeth Chitirala, Keerthana Ravichandran, Marwa Sleiman, Elmar Krause, Ulrike Hahn, Varsha Pattu, Jens Rettig

Abstract readReview
In one paragraph

Review in Cellular and molecular life sciences : CMLS, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
  2. Mechanoregulation of lymphocyte cytotoxicity.Nature reviews. Immunology · 2025
    Review
  3. Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Review
  10. Article
  11. Microclusters as T Cell Signaling Hubs: Structure, Kinetics, and Regulation.Frontiers in cell and developmental biology · 2020
    Review
  12. Endometrial Immune Dysfunction in Recurrent Pregnancy Loss.International journal of molecular sciences · 2019
    Review
  13. 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.

Hsin-Fang ChangCellular Neurophysiology, Center for Integrative Physiology and Molecular Medicine, Saarland University, 66421, Homburg, Germany.
Hawraa BzeihCellular Neurophysiology, Center for Integrative Physiology and Molecular Medicine, Saarland University, 66421, Homburg, Germany.
Praneeth ChitiralaCellular Neurophysiology, Center for Integrative Physiology and Molecular Medicine, Saarland University, 66421, Homburg, Germany.
Keerthana RavichandranCellular Neurophysiology, Center for Integrative Physiology and Molecular Medicine, Saarland University, 66421, Homburg, Germany.
Marwa SleimanCellular Neurophysiology, Center for Integrative Physiology and Molecular Medicine, Saarland University, 66421, Homburg, Germany.
Elmar KrauseCellular Neurophysiology, Center for Integrative Physiology and Molecular Medicine, Saarland University, 66421, Homburg, Germany.
Ulrike HahnCellular Neurophysiology, Center for Integrative Physiology and Molecular Medicine, Saarland University, 66421, Homburg, Germany.
Varsha PattuCellular Neurophysiology, Center for Integrative Physiology and Molecular Medicine, Saarland University, 66421, Homburg, Germany.
Jens RettigCellular Neurophysiology, Center for Integrative Physiology and Molecular Medicine, Saarland University, 66421, Homburg, Germany. jrettig@uks.eu.ORCID 0000-0001-6160-3954

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cytotoxic T lymphocytes patrol our body in search for infected cells which they kill through the release of cytotoxic substances contained in cytotoxic granules. The fusion of cytotoxic granules occurs at a specially formed contact site, the immunological synapse, and is tightly controlled to ensure specificity. In this review, we discuss the contribution of two intracellular compartments, endosomes and cytotoxic granules, to the formation, function and disassembly of the immunological synapse. We highlight a recently proposed sequential process of fusion events at the IS upon target cell recognition. First, recycling endosomes fuse with the plasma membrane to deliver cargo required for the docking of cytotoxic granules. Second, cytotoxic granules arrive and fuse upon docking in a SNARE-dependent manner. Following fusion, membrane components of the cytotoxic granule are retrieved through endocytosis to ensure the fast, efficient serial killing of target cells that is characteristic of cytotoxic T lymphocytes.

Indexed as

Cytotoxicity, ImmunologicEndocytosisExocytosisAnimalsCytoplasmic GranulesEndosomesHumansLysosomesMembrane FusionSNARE ProteinsT-Lymphocytes, CytotoxicSNARE ProteinsCorrelative light and electron microscopyEarly endosomesLate endosomesRecycling endosomesSNARE proteinsTotal internal reflection fluorescence microscopy

Identifiers

PMID27585956
PMCPMC5241346

What OpenQuestion holds

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LicenceCC BY
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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.