Role of Interleukin-6 in Vascular Health and Disease

Paulina Villar-Fincheira, Fernanda Sanhueza-Olivares, Ignacio Norambuena-Soto, Nicole Cancino-Arenas, Felipe Hernandez-Vargas, Rodrigo Troncoso, Luigi Gabrielli, Mario Chiong

Research output: Contribution to journalReview articlepeer-review

72 Citations (Scopus)

Abstract

IL-6 is usually described as a pleiotropic cytokine produced in response to tissue injury or infection. As a pro-inflammatory cytokine, IL-6 activates innate and adaptative immune responses. IL-6 is released in the innate immune response by leukocytes as well as stromal cells upon pattern recognition receptor activation. IL-6 then recruits immune cells and triggers B and T cell response. Dysregulated IL-6 activity is associated with pathologies involving chronic inflammation and autoimmunity, including atherosclerosis. However, IL-6 is also produced and released under beneficial conditions, such as exercise, where IL-6 is associated with the anti-inflammatory and metabolic effects coupled with physical adaptation to intense training. Exercise-associated IL-6 acts on adipose tissue to induce lipogenesis and on arteries to induce adaptative vascular remodeling. These divergent actions could be explained by complex signaling networks. Classical IL-6 signaling involves a membrane-bound IL-6 receptor and glycoprotein 130 (gp130), while trans-signaling relies on a soluble version of IL-6R (sIL-6R) and membrane-bound gp130. Trans-signaling, but not the classical pathway, is regulated by soluble gp130. In this review, we discuss the similarities and differences in IL-6 cytokine and myokine signaling to explain the differential and opposite effects of this protein during inflammation and exercise, with a special focus on the vascular system.

Original languageEnglish
Article number641734
JournalFrontiers in Molecular Biosciences
Volume8
DOIs
Publication statusPublished - Mar 16 2021

Bibliographical note

Publisher Copyright:
© Copyright © 2021 Villar-Fincheira, Sanhueza-Olivares, Norambuena-Soto, Cancino-Arenas, Hernandez-Vargas, Troncoso, Gabrielli and Chiong.

Funding

This work was supported by FONDECYT 1180157 (MC, RT) FONDECYT 1170963 (LG, MC) and FONDAP 15130011 (LG, MC).

FundersFunder number
Fondo Nacional de Desarrollo Científico y Tecnológico1170963, 1180157
Fondo de Financiamiento de Centros de Investigación en Áreas Prioritarias15130011

    ASJC Scopus Subject Areas

    • Biochemistry
    • Molecular Biology
    • Biochemistry, Genetics and Molecular Biology (miscellaneous)

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