Evidence map›Paper›PMID 27534551›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2016

Dynein Separately Partners with NDE1 and Dynactin To Orchestrate T Cell Focused Secretion.

Shubhankar Nath, Laura Christian, Sarah Youngsun Tan, Sanghee Ki, Lauren I R Ehrlich, Martin Poenie

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.7field-weighted citation impact, top 11% 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

25 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
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  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Connexin-Mediated Signaling at the Immunological Synapse.International journal of molecular sciences · 2020
    Review
  13. Inducible Polarized Secretion of Exosomes in T and B Lymphocytes.International journal of molecular sciences · 2020
    Review
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. Article
  20. 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

6 authors at 1 institution in 1 country.

Shubhankar NathDepartment of Molecular Biosciences, University of Texas at Austin, Austin, TX 78712; and.ORCID 0000-0001-5778-7615
Laura ChristianDepartment of Molecular Cell and Developmental Biology, University of Texas at Austin, Austin, TX 78712.ORCID 0000-0003-3141-1710
Sarah Youngsun TanDepartment of Molecular Cell and Developmental Biology, University of Texas at Austin, Austin, TX 78712.ORCID 0000-0002-3428-4676
Sanghee KiDepartment of Molecular Biosciences, University of Texas at Austin, Austin, TX 78712; and.
Lauren I R EhrlichDepartment of Molecular Biosciences, University of Texas at Austin, Austin, TX 78712; and.ORCID 0000-0002-1697-1755
Martin PoenieDepartment of Molecular Biosciences, University of Texas at Austin, Austin, TX 78712; and poenie@austin.utexas.edu.ORCID 0000-0003-2524-4039
The University of Texas at Austin · US

Funding

The contribution of GPCRs to thymocyte medullary entry and central toleranceR01AI104870 · NIAID · UNIVERSITY OF TEXAS AT AUSTIN · PI Lauren Ilyse Richie EHRLICH · 2014 to 2026
$7.6M
NIAID NIH HHS R01 AI104870
6 · The paper itself

Abstract

Helper and cytotoxic T cells accomplish focused secretion through the movement of vesicles toward the microtubule organizing center (MTOC) and translocation of the MTOC to the target contact site. In this study, using Jurkat cells and OT-I TCR transgenic primary murine CTLs, we show that the dynein-binding proteins nuclear distribution E homolog 1 (NDE1) and dynactin (as represented by p150(Glued)) form mutually exclusive complexes with dynein, exhibit nonoverlapping distributions in target-stimulated cells, and mediate different transport events. When Jurkat cells expressing a dominant negative form of NDE1 (NDE1-enhanced GFP fusion) were activated by Staphylococcus enterotoxin E-coated Raji cells, NDE1 and dynein failed to accumulate at the immunological synapse (IS) and MTOC translocation was inhibited. Knockdown of NDE1 in Jurkat cells or primary mouse CTLs also inhibited MTOC translocation and CTL-mediated killing. In contrast to NDE1, knockdown of p150(Glued), which depleted the alternative dynein/dynactin complex, resulted in impaired accumulation of CTLA4 and granzyme B-containing intracellular vesicles at the IS, whereas MTOC translocation was not affected. Depletion of p150(Glued) in CTLs also inhibited CTL-mediated lysis. We conclude that the NDE1/Lissencephaly 1 and dynactin complexes separately mediate two key components of T cell-focused secretion, namely translocation of the MTOC and lytic granules to the IS, respectively.

Indexed as

1-Alkyl-2-acetylglycerophosphocholine EsteraseCalcium SignalingCytotoxicity, ImmunologicDynactin ComplexDyneinsHumansJurkat CellsMicrotubule-Associated ProteinsMicrotubule-Organizing CenterSecretory VesiclesSynapsesT-LymphocytesT-Lymphocytes, Cytotoxic1-Alkyl-2-acetylglycerophosphocholine EsteraseDynactin ComplexDyneinsMicrotubule-Associated ProteinsNde1 protein, humanPAFAH1B1 protein, human

Identifiers

PMID27534551
PMCPMC5010990
OpenAlexW2510692193

What OpenQuestion holds

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Registered trials

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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.