Publication | Open Access
Regulation of Lymphocyte Function by PPAR<i>γ</i>: Relevance to Thyroid Eye Disease‐Related Inflammation
34
Citations
142
References
2008
Year
Disease ProgressionImmune RegulationImmunologyInsulin SignalingImmune DysregulationThyroid Eye DiseaseInflammationMetabolic SyndromeSignaling PathwayImmunopathologyMetabolic SignalingCell SignalingMolecular SignalingMolecular PhysiologyAutoimmune DiseaseOphthalmologyChronic InflammationAutoimmunityImmune FunctionLymphocyte FunctionCell BiologySignal TransductionPpar γMetabolic RegulationThyroid HormoneMedicine
Thyroid eye disease (TED) is an autoimmune condition in which intense inflammation leads to orbital tissue remodeling, including the accumulation of extracellular macromolecules and fat. Disease progression depends upon interactions between lymphocytes and orbital fibroblasts. These cells engage in a cycle of reciprocal activation which produces the tissue characteristics of TED. Peroxisome proliferator‐activated receptor‐ γ (PPAR γ ) may play divergent roles in this process, both attenuating and promoting disease progression. PPAR γ has anti‐inflammatory activity, suggesting that it could interrupt intercellular communication. However, PPAR γ activation is also critical to adipogenesis, making it a potential culprit in the pathological fat accumulation associated with TED. This review explores the role of PPAR γ in TED, as it pertains to crosstalk between lymphocytes and fibroblasts and the development of therapeutics targeting cell‐cell interactions mediated through this signaling pathway.
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