Go to The Journal of Clinical Investigation
  • About
  • Editors
  • Consulting Editors
  • For authors
  • Publication ethics
  • Publication alerts by email
  • Transfers
  • Advertising
  • Job board
  • Contact
  • Physician-Scientist Development
  • Current issue
  • Past issues
  • By specialty
    • COVID-19
    • Cardiology
    • Immunology
    • Metabolism
    • Nephrology
    • Oncology
    • Pulmonology
    • All ...
  • Videos
  • Collections
    • In-Press Preview
    • Resource and Technical Advances
    • Clinical Research and Public Health
    • Research Letters
    • Editorials
    • Perspectives
    • Physician-Scientist Development
    • Reviews
    • Top read articles

  • Current issue
  • Past issues
  • Specialties
  • In-Press Preview
  • Resource and Technical Advances
  • Clinical Research and Public Health
  • Research Letters
  • Editorials
  • Perspectives
  • Physician-Scientist Development
  • Reviews
  • Top read articles
  • About
  • Editors
  • Consulting Editors
  • For authors
  • Publication ethics
  • Publication alerts by email
  • Transfers
  • Advertising
  • Job board
  • Contact
Inflammatory arthritis disrupts gut resolution mechanisms, promoting barrier breakdown by Porphyromonas gingivalis
Magdalena B. Flak, … , Jesmond Dalli, Costantino Pitzalis
Magdalena B. Flak, … , Jesmond Dalli, Costantino Pitzalis
Published October 24, 2022
Citation Information: JCI Insight. 2022;7(20):e165600. https://doi.org/10.1172/jci.insight.165600.
View: Text | PDF | Amended Article
Corrigendum

Inflammatory arthritis disrupts gut resolution mechanisms, promoting barrier breakdown by Porphyromonas gingivalis

  • Text
  • PDF
Abstract

Authors

Magdalena B. Flak, Romain A. Colas, Estefanía Muñoz-Atienza, Michael A. Curtis, Jesmond Dalli, Costantino Pitzalis

×

Figure 2

Arthritis dysregulates intestinal lipid mediator profiles.

Options: View larger image (or click on image) Download as PowerPoint
Arthritis dysregulates intestinal lipid mediator profiles.
Arthritis was...
Arthritis was initiated by injection of K/BxN serum (50 μL per mouse, i.p.; days 0 and 2). On day 8, ilea were harvested from arthritic and naive mice and lipid mediators identified and quantified using lipid mediator profiling (see Methods for details). (A) MS/MS spectrum employed for the identification of RvD5n-3 DPA. Labeled ions are those matching assigned ion fragments for RvD5n-3 DPA. Inset, portion of the molecule that corresponds to each of the diagnostic ions; M, molecular mass. (B) Orthogonal partial least squares discriminant analysis (oPLS-DA) of intestinal lipid mediator profiles. Cumulative tissue concentrations for SPMs (i.e., arachidonic-, eicosapentaenoic acid–, n-3 docosapentaenoic– [DPA–], and docosahexaenoic acid–derived [DHA-derived] proresolving mediators) (C), RvDn-3 DPA (i.e., RvD1n-3 DPA, RvD2n-3 DPA, and RvD5n-3 DPA) (D), and RvD5n-3 DPA (E). Results for A are representative of n = 24 mice; for B are representative of n = 8 mice per group; for C–E are mean ± SEM for n = 8 mice per group from 2 independent experiments; *P ≤ 0.05 versus naive using Mann-Whitney U test. Results are expressed as pg/10 mg tissue.

Copyright © 2025 American Society for Clinical Investigation
ISSN 2379-3708

Sign up for email alerts