Evidence map›Paper›PMID 15719365›Full record

ArticleEuropean journal of immunology2005

T cell homeostasis requires G protein-coupled receptor-mediated access to trophic signals that promote growth and inhibit chemotaxis.

Ryan M Cinalli, Catherine E Herman, Brian O Lew, Heather L Wieman, Craig B Thompson, Jeffrey C Rathmell

Open access · greenAbstract read
In one paragraph

Article in European journal of immunology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.3field-weighted citation impact, top 44% 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

11 citing papers in PubMed, 18 citations in OpenAlex.

  1. Multimodal analysis definesbioRxiv : the preprint server for biology · 2025
    Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. The metabolic life and times of a T-cell.Immunological reviews · 2010
    Review
  9. Article
  10. Review
  11. 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 3 institutions in 2 countries.

Ryan M CinalliAbramson Family Cancer Research Institute, Departments of Cancer Biology and Medicine, University of Pennsylvania, Philadelphia, USA.
Catherine E Herman
Brian O Lew
Heather L Wieman
Craig B Thompson
Jeffrey C Rathmell
Cancer Research Institute · USDuke University · USDuke University Hospital · US

Funding

Control of lymphocyte trophic state by extrinsic signalsK01CA091905 · NCI · UNIVERSITY OF PENNSYLVANIA · PI RATHMELL, JEFFREY C · 2001 to 2005
$730k
NCI NIH HHS K01 CA091905
6 · The paper itself

Abstract

Signals that regulate T cell homeostasis are not fully understood. G protein-coupled receptors (GPCR), such as the chemokine receptors, may affect homeostasis by direct signaling or by guiding T cell migration to distinct location-restricted signals. Here, we show that blockade of Galphai-associated GPCR signaling by treatment with pertussis toxin led to T cell atrophy and shortened life-span in T cell-replete hosts and prevented T cell homeostatic growth and proliferation in T cell-deficient hosts. In vitro, however, neither GPCR inhibition nor chemokine stimulation affected T cell atrophy, survival, or proliferation. These findings suggest that GPCR signals are not trophic stimuli, but instead may be required for migration to distinct trophic signals, such as IL-7 or self-peptide/MHC. Surprisingly, while chemokines did not affect atrophy, atrophic T cells displayed increased chemokine-induced chemotaxis that was prevented by IL-7 and submitogenic anti-CD3 antibody treatment. This increase in migration was associated with increased levels of GTP-bound Rac and the ability to remodel actin. These data suggest a novel mechanism of T cell homeostasis wherein GPCR may promote T cell migration to distinct location-restricted homeostatic trophic cues for T cell survival and growth. Homeostatic trophic signals, in turn, may suppress chemokine sensitivity and cytoskeletal remodeling, to inhibit further migration.

Indexed as

ActinsAdoptive TransferAnimalsAtrophyBlotting, WesternCell ProliferationCell SurvivalChemotaxisCytoskeletonFlow CytometryGrowth SubstancesHomeostasisInterleukin-7Lymphoid TissueMicePertussis ToxinActinsGrowth SubstancesInterleukin-7Pertussis ToxinReceptors, Antigen, T-CellReceptors, CytokineReceptors, G-Protein-Coupled

Identifiers

PMID15719365
PMCPMC2628485
OpenAlexW1503941601

What OpenQuestion holds

Textmetadata
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.