Evidence map›Paper›PMID 22529300›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2012

Stathmin regulates microtubule dynamics and microtubule organizing center polarization in activated T cells.

Erin L Filbert, Marie Le Borgne, Joseph Lin, John E Heuser, Andrey S Shaw

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

35 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. [Research progress in the role of STMN1 in tumor].Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2025
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Molecular Evolution and Characterization of Fish Stathmin Genes.Animals : an open access journal from MDPI · 2020
    Article
  16. Article
  17. Eosinophil cytolysis on Immunoglobulin G is associated with microtubule formation and suppression of rho-associated protein kinase signalling.Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology · 2020
    Article
  18. Article
  19. Review
  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

5 authors at 2 institutions in 1 country.

Erin L FilbertDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Marie Le Borgne
Joseph Lin
John E Heuser
Andrey S Shaw
Washington University in St. Louis · USHoward Hughes Medical Institute · US

Funding

TRAINING PROGRAM IN IMMUNOLOGY AND IMMUNOGENETICST32AI007163 · NIAID · WASHINGTON UNIVERSITY · PI Kenneth M Murphy, Kodi S Ravichandran · 1985 to 2026
$14.8M
Structure and Function of the Immunological SynapseR37AI057966 · NIAID · WASHINGTON UNIVERSITY · PI SHAW, ANDREY S. · 2004 to 2013
$3.2M
Howard Hughes Medical InstituteNIAID NIH HHS R37 AI057966NIAID NIH HHS R37-AI57966NIAID NIH HHS T32 AI007163NIAID NIH HHS T32-AI07163
6 · The paper itself

Abstract

Polarization of T cells involves reorientation of the microtubule organizing center (MTOC). Because activated ERK is localized at the immunological synapse, we investigated its role by showing that ERK activation is important for MTOC polarization. Suspecting that ERK phosphorylates a regulator of microtubules, we next focused on stathmin, a known ERK substrate. Our work indicates that during T cell activation, ERK is recruited to the synapse, allowing it to phosphorylate stathmin molecules near the immunological synapse. Supporting an important role of stathmin phosphorylation in T cell activation, we showed that T cell activation results in increased microtubule growth rate dependent on the presence of stathmin. The significance of this finding was demonstrated by results showing that CTLs from stathmin(-/-) mice displayed defective MTOC polarization and defective target cell cytolysis. These data implicate stathmin as a regulator of the microtubule network during T cell activation.

Indexed as

AnimalsCell EnlargementCell PolarityCells, CulturedHumansJurkat CellsLymphocyte ActivationMiceMice, Inbred C57BLMice, KnockoutMice, TransgenicMicrotubule-Organizing CenterPhosphorylationStathminT-Lymphocyte SubsetsStathminStmn1 protein, mouse

Identifiers

PMID22529300
PMCPMC3358357
OpenAlexW2142242016

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.