Medizinische Universität Graz - Research portal

Logo MUG Resarch Portal

Selected Publication:

SHR Neuro Cancer Cardio Lipid Metab Microb

Dorronsoro, A; Lang, V; Jakobsson, E; Ferrin, I; Salcedo, JM; Fernández-Rueda, J; Fechter, K; Rodriguez, MS; Trigueros, C.
Identification of the NF-κB inhibitor A20 as a key regulator for human adipogenesis.
Cell Death Dis. 2013; 4(1):e972-e972 Doi: 10.1038/cddis.2013.494 [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

Co-authors Med Uni Graz
Fechter Karoline
Altmetrics:

Dimensions Citations:

Plum Analytics:

Scite (citation analytics):

Abstract:
The zinc-finger protein A20 is a key player in the negative feedback regulation of the nuclear factor kappa-light-chain-enhancer of activated B-cell (NF-κB) pathway in response to multiple stimuli. Tumor necrosis factor alpha (TNFα), a cytokine with pleiotropic effects on cellular proliferation and differentiation, dramatically increases A20 expression in all tissues. As TNFα inhibits adipocyte differentiation, we have determined the contribution of A20 to the adipogenic capacity of human mesenchymal stromal cells (MSCs). Here we show that A20 is constitutively expressed in MSCs, which previously has been observed only in cells that are either tumor or immune cells (T/B lymphocytes). TNFα stimulation induced a rapid degradation of A20 protein mediated exclusively by the proteasome in MSCs and not by caspases. This degradation is concomitant to the induction of its own mRNA, which suggests that a tight regulation of NF-κB signaling in MSCs is fundamental. On one hand, we demonstrate that the knockdown of A20-mediated transcript dramatically decreases the adipogenic capacity of MSCs, which correlates with the phenotype observed in the presence of TNFα. On the other hand, A20 overexpression blocks NF-κB activation and drives to increased adipogenesis, even in the presence of TNFα treatment. In conclusion, our data demonstrate that the presence of A20 allows MSCs to differentiate into adipocytes by maintaining NF-κB signaling at a basal state.
Find related publications in this database (using NLM MeSH Indexing)
Adipocytes - cytology
Adipocytes - metabolism
Adipogenesis - genetics
Adipogenesis - physiology
Cell Differentiation - genetics
Cell Differentiation - physiology
Cells, Cultured -
DNA-Binding Proteins - genetics
DNA-Binding Proteins - metabolism
Gene Silencing - physiology
Humans -
Intracellular Signaling Peptides and Proteins - genetics
Intracellular Signaling Peptides and Proteins - metabolism
Mesenchymal Stromal Cells - cytology
Mesenchymal Stromal Cells - metabolism
NF-kappa B - antagonists & inhibitors
NF-kappa B - genetics
NF-kappa B - metabolism
Nuclear Proteins - genetics
Nuclear Proteins - metabolism
Reverse Transcriptase Polymerase Chain Reaction -
Tumor Necrosis Factor alpha-Induced Protein 3 -

Find related publications in this database (Keywords)
A20 inhibitor
mesenchymal stromal cell
adipogenesis
© Med Uni GrazImprint