Evidence map›Paper›PMID 15804293›Full record

ArticleImmunology2005

Transforming growth factor-beta1 increases CXCR4 expression, stromal-derived factor-1alpha-stimulated signalling and human immunodeficiency virus-1 entry in human monocyte-derived macrophages.

Shuzhen Chen, Daniel L Tuttle, Joseph T Oshier, Harm J Knot, Wolfgang J Streit, Maureen M Goodenow, Jeffrey K Harrison

Open access · greenAbstract read
In one paragraph

Article in Immunology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
2.6field-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

34 citing papers in PubMed, 68 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Chemokine receptor Cxcr4 contributes to kidney fibrosis via multiple effectors.American journal of physiology. Renal physiology · 2015
    Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. CXCL12 induces hepatic stellate cell contraction through a calcium-independent pathway.American journal of physiology. Gastrointestinal and liver physiology · 2013
    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

7 authors at 1 institution in 1 country.

Shuzhen ChenDepartment of Pharmacology and Therapeutics, University of Florida, Gainesville, FL 32610-0267, USA.
Daniel L Tuttle
Joseph T Oshier
Harm J Knot
Wolfgang J Streit
Maureen M Goodenow
Jeffrey K Harrison
University of Florida · US

Funding

CHEMOKINE RECEPTOR EXPRESSION IN THE CNSR01NS034901 · NINDS · UNIVERSITY OF FLORIDA · PI HARRISON, JEFFREY K · 1997 to 2003
$986k
NINDS NIH HHS NS34901
6 · The paper itself

Abstract

Stromal-derived factor-1 (SDF-1/CXCL12) and its receptor CXCR4 play crucial roles in leukocyte migration and activation, as well as embryogenesis, angiogenesis, cancer and viral pathogenesis. CXCR4 is one of the major human immunodeficiency virus-1 (HIV-1) coreceptors on macrophages. In many tissues macrophages are one of the predominant cell types infected by HIV-1 and act as a reservoir for persistent infection and viral dissemination. In patients infected by HIV-1, blood and tissue levels of transforming growth factor-beta1 (TGF-beta1) are increased. The purpose of this study was to evaluate the effects of TGF-beta1 on CXCR4 expression and function in primary human monocyte-derived macrophages (MDMs) and rat microglia. TGF-beta1 up-regulated CXCR4 and enhanced SDF-1alpha-stimulated ERK1,2 phosphorylation in these cells. The increased CXCR4 expression in human MDMs resulted in increased susceptibility of the cells to entry by dual-tropic CXCR4-using HIV-1 (D-X4). In contrast, TGF-beta1 failed to increase CCR5 expression or infection by a CCR5-using virus in MDMs. Our data demonstrate that TGF-beta1 enhances macrophage responsiveness to SDF-1alpha stimulation and susceptibility to HIV-1 by selectively increasing expression of CXCR4. The results suggest that increased expression of CXCR4 on macrophages may contribute to the emergence of dual-tropic X4 viral variants at later stages of HIV-1 infection.

Indexed as

HIV-1AnimalsCells, CulturedChemokine CXCL12Chemokines, CXCExtracellular Signal-Regulated MAP KinasesFlow CytometryHIV InfectionsHumansMacrophagesMicrogliaMicroscopy, FluorescencePhosphorylationRatsReceptors, ChemokineReceptors, CXCR4Chemokine CXCL12Chemokines, CXCCXCL12 protein, humanCxcr4 protein, ratExtracellular Signal-Regulated MAP KinasesReceptors, ChemokineReceptors, CXCR4Transforming Growth Factor beta

Identifiers

PMID15804293
PMCPMC1782104
OpenAlexW1987183930

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.