Evidence map›Paper›PMID 25497737›Full record

ArticleCytokine2015

Structural and agonist properties of XCL2, the other member of the C-chemokine subfamily.

Jamie C Fox, Takashi Nakayama, Robert C Tyler, Tara L Sander, Osamu Yoshie, Brian F Volkman

Open access · greenAbstract read
In one paragraph

Article in Cytokine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

48 citing papers in PubMed, 73 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. The multifaceted role of XCL1 in health and disease.Protein science : a publication of the Protein Society · 2025
    Review
  5. Article
  6. Article
  7. Article
  8. Molecular basis for chemokine recognition and activation of XCR1.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
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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 2 institutions in 2 countries.

Jamie C FoxDepartment of Biochemistry, Medical College of Wisconsin, 8701 Watertown Plank Road, Milwaukee, WI 53226, USA.
Takashi NakayamaDivision of Chemotherapy, Kinki University, Faculty of Pharmacy, Higashi-osaka 577-8502, Japan.
Robert C TylerDepartment of Biochemistry, Medical College of Wisconsin, 8701 Watertown Plank Road, Milwaukee, WI 53226, USA.
Tara L SanderDepartment of Pediatric Pathology, Medical College of Wisconsin, Milwaukee, WI 53226, USA.
Osamu YoshieKinki University, Faculty of Medicine, Osaka-Sayama, Osaka 589-851, Japan.
Brian F VolkmanDepartment of Biochemistry, Medical College of Wisconsin, 8701 Watertown Plank Road, Milwaukee, WI 53226, USA. Electronic address: bvolkman@mcw.edu.
Medical College of Wisconsin · USKindai University · JP

Funding

Structural Basis for Chemokine FunctionR01AI058072 · NIAID · MEDICAL COLLEGE OF WISCONSIN · PI VOLKMAN, BRIAN F · 2004 to 2019
$4.1M
Structural Basis for Chemokine FunctionR37AI058072 · NIAID · MEDICAL COLLEGE OF WISCONSIN · PI Brian F Volkman · 2020 to 2026
$2.8M
Conformational duality in the human chemokine Ltn/XCL1R01AI063325 · NIAID · MEDICAL COLLEGE OF WISCONSIN · PI VOLKMAN, BRIAN F · 2005 to 2009
$1.4M
500 MHz NMR Spectrometer at the Medical College of WisconsinS10RR024665 · NCRR · MEDICAL COLLEGE OF WISCONSIN · PI VOLKMAN, BRIAN F · 2009 to 2009
$500k
Structural and energetic origins of metamorphic protein foldingR56AI103225 · NIAID · MEDICAL COLLEGE OF WISCONSIN · PI VOLKMAN, BRIAN F · 2013 to 2013
$353k
Conformational duality in the human chemokine Ltn/XCL1R56AI063325 · NIAID · MEDICAL COLLEGE OF WISCONSIN · PI VOLKMAN, BRIAN F · 2011 to 2011
$352k
NCRR NIH HHS S10 RR024665NIAID NIH HHS AI013325NIAID NIH HHS AI058072NIAID NIH HHS R01 AI058072NIAID NIH HHS R01 AI063325NIAID NIH HHS R37 AI058072NIAID NIH HHS R56 AI063325NIAID NIH HHS R56 AI103225
6 · The paper itself

Abstract

Known for its unusual metamorphic native state structure, XCL1 has been the focus of most efforts to elucidate the structural, functional, and physiological properties of chemokines in the C subfamily. By comparison, its closely related paralog XCL2 remains virtually uncharacterized. Based on the importance of the chemokine N-terminus in receptor activation, it was hypothesized that two amino acid differences in XCL2 would alter its agonist activity relative to XCL1 for their shared receptor XCR1. This present study reveals several properties of XCL2 that were unexamined until now. Structurally, XCL1 and XCL2 are very similar, exchanging between the monomeric chemokine fold and an unrelated dimeric state under physiological NaCl and temperature conditions. Ca(2+) flux, chemotaxis, and heparin binding assays showed that the monomer form of XCL2 is responsible for G protein-coupled receptor activation while the dimeric form is important for GAG binding. Despite their high structural similarity, XCL2 displays a slightly higher affinity for heparin than XCL1. Because their in vitro functional profiles are virtually identical, distinct physiological roles for XCL1 and XCL2 are probably encoded at the level of expression.

Indexed as

Amino Acid SequenceAnimalsCalciumChemokines, CChemotaxisComputational BiologyHeparinHumansHydrogen-Ion ConcentrationKineticsLymphokinesMagnetic Resonance SpectroscopyMolecular Sequence DataProtein BindingProtein DenaturationProtein MultimerizationCalciumChemokines, CHeparinLymphokineslymphotactinSialoglycoproteinsSodium ChlorideUreaXCL1 protein, humanXCL2 protein, humanCa(2+) fluxChemotaxisLymphotactinXCL1XCL2

Identifiers

PMID25497737
PMCPMC4297508
OpenAlexW1993728343

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.