IL-6 is an inflammatory cytokine that is elevated in several autoimmune and inflammatory disorders, but also in a number of cancers. Inhibition of IL-6 by an anti-IL-6R antibody, tocilizumab, is tremendously therapeutic in this rheumatoid arthritis. This highlights the pathogenic role of IL-6 in this disease, and likely several other inflammatory disorders, and hence underscores the need to fully understand IL-6 function. IL-6 plays a critical role in determining the type of cytokines produced by effector CD4 T cells. Most of these functions of IL-6 have been assigned to a regulatory role on gene expression through the Stat3 transcription factor. However, recent studies have revealed that in addition to being localized in the cytosol and nucleus, Stat3 is also present in the mitochondria where it regulates the mitochondrial respiratory chain through association with Complex I. leaving a new area of research open to understand the mechanism, impact and development of novel therapies. We have recently identified a novel mechanism by which IL-6 regulates CD4 cell function using this alternative pathway. Using mouse models, we have shown that IL-6 sustains high mitochondrial membrane potential (MMP) late during in vitro activation of CD4 cells through Stat3, independently of its transcription activity. Mitochondrial hyperpolarization caused by IL-6 however is uncoupled from the production of ATP by oxidative phosphorylation. Instead, IL-6 uses the elevated MMP to promote mitochondrial Ca2+ accumulation in CD4 cells. Mitochondria are emerging as the primary subcellular Ca2+ stores that regulate cytosolic Ca2+ homeostasis and mediate the delivery of extracellular Ca2+ and Ca2+ form endoplasmic reticulum. We have shown that IL-6 uses mitochondrial Ca2+ to sustain elevated cytosolic Ca2+ levels in effector CD4 cells, and this contributes to a prolonged production of cytokines (IL-21 and IL-4) by these cells in vitro. To demonstrate the relevance of these novel findings, we now propose in this application to investigate the presence of this IL-6-mediated pathway in CD4 cells in vivo using mouse models, in human CD4 cells in vitro and in vivo, and its impact on in vivo cytokine production as well as in migration of CD4 cells since Ca2+ is an essential mediator for cell motility. Specifically we propose to investigate: 1) the regulation of MMP and mitochondrial Ca2+ through Stat3 by IL-6 in CD4 cells in vivo, and its impact on cytokine production; 2) whether IL-6 regulates migration of CD4 cells by enhancing mitochondrial Ca2+ homeostasis. 3) the effect of IL-6 on MMP and mitochondrial Ca2+ in human CD4 cells in vitro and in vivo, and the contribution of this pathway to cytokine production and/or migration. The studies can reveal a new mechanism for IL-6 in chronic diseases where CD4 cells play an important role, and they can lead to the development of new inhibitors targeting the mitochondrial Ca2+ pathway, as well as a redesign of inhibitors for Stat3 that also target mitochondrial Stat3.

Public Health Relevance

After decades of being first identified, Interleukin 6 (IL-6) is emerging as a key molecule that plays an active role in a number of diseases from autoimmune diseases to cancer and asthma. IL-6 can be targeted and a therapy (tocilizumab) to block IL-6 receptor (IL-6R) has been approved in the recent years for treatment of Rheumatoid Arthritis (RA) where it clearly has an effect in disease progression. Tocilizumab (a blocking anti-IL- 6R antibody) is currently been tested in other autoimmune disease. The mechanisms by which IL-6 contributes to the pathogenesis of these diseases remain unclear. We have recently identified a novel mechanism by which IL-6 can regulate the functions of cells: IL-6 as a regulator of mitochondria in homeostasis of intracellular calcium. The goal of this proposal is to investigate this mechanism in CD4 T cells and its impact in the immune response using both mouse models as well as human CD4 cells from healthy subjects and patients with rheumatoid arthritis. In this application, we focus on the role of IL-6 in mitochondria regulation in CD4 cells, but this new effect of IL-6 could be a broader mechanism by which this cytokine contributes to other diseases like cancer progression.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
High Priority, Short Term Project Award (R56)
Project #
1R56AI116255-01A1
Application #
9245931
Study Section
Hypersensitivity, Autoimmune, and Immune-mediated Diseases Study Section (HAI)
Program Officer
Peyman, John A
Project Start
2016-05-01
Project End
2017-04-30
Budget Start
2016-05-01
Budget End
2017-04-30
Support Year
1
Fiscal Year
2016
Total Cost
Indirect Cost
Name
University of Vermont & St Agric College
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
066811191
City
Burlington
State
VT
Country
United States
Zip Code