AUTHOR=Vendrell Joan J., R. Chacon Matilde
TITLE=TWEAK: A New Player in Obesity and Diabetes
JOURNAL=Frontiers in Immunology
VOLUME=Volume 4 - 2013
YEAR=2013
URL=https://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2013.00488
DOI=10.3389/fimmu.2013.00488
ISSN=1664-3224
ABSTRACT=
Obesity and type 2 diabetes (T2D) are associated with chronic low-grade inflammation. Mounting evidence suggests the involvement of an inflammatory switch in adipose tissue, both in mature adipocytes and immune-competent cells from the stromal vascular compartment, in the progression of obesity and insulin resistance. Several inflammatory cytokines secreted by obese adipose tissue, including TNFα and IL-6 have been described as hallmark molecules involved in this process, impairing insulin signalling in insulin-responsive organs. An increasing number of new molecules affecting the local and systemic inflammatory imbalance in obesity and T2D have been identified. In this complex condition, some molecules may exhibit opposing actions, depending on the cell type and on systemic or local influences.
TWEAK, a cytokine of the tumor necrosis (TNF) superfamily, is gaining attention as an important player in chronic inflammatory diseases. TWEAK can exist as a full-length membrane-associated (mTWEAK) form and as a soluble (sTWEAK) form and, by acting through its cognate receptor Fn14, can control many cellular activities including proliferation, migration, differentiation, apoptosis, angiogenesis and inflammation. Notably, sTWEAK has been proposed as a biomarker of cardiovascular diseases.
Here, we will review the recent findings relating to TWEAK and its receptor within the context of obesity and the associated disorder T2D.