Journal
PROGRESS IN RETINAL AND EYE RESEARCH
Volume 29, Issue 6, Pages 610-621Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.preteyeres.2010.08.003
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Funding
- National Eye Research Centre
- Medical Research Council
- James Tudor Foundation
- Royal College of Pathologists
- Jean Shanks Foundation
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Tumour necrosis factor-alpha (TNF alpha) is a key mediator of inflammation and plays a crucial role during the early phase of a host's defence against bacterial, viral and parasitic infections. Persistent production of TNF alpha occurs in many autoimmune inflammatory diseases, including uveitis, and this is associated with significant tissue damage. Although uveitis represents a phenotypically heterogeneous group of intra-ocular inflammatory conditions, they have in common raised levels of TNF alpha in both serum and aqueous humour. Supporting a critical role for TNF activity during uveitis are reports that serum levels of TNF alpha correlate with disease status as well as the increasing evidence of therapeutic success of anti-TNF agents. TNF alpha is an archetypal pleiotropic cytokine and when acting systemically acute release may cause profound physiological decompensation. Yet, conversely, at tissue sites TNF alpha plays important roles governing homeostasis and during chronic inflammation regulating immune responses through control of, for example, macrophage-T cell functions. In a murine model of CD4(+) T cell mediated non-infectious uveitis, experimental autoimmune uveitis (EAU), activation of infiltrating macrophages mediates tissue damage. In EAU, whilst both T cells and macrophages generate TNF alpha, tissue damaging macrophage activation is dependent upon TNF receptor 1 (p55). TNF alpha protein production is controlled at the level of transcription, pre-mRNA processing, mRNA stability, translation and retention at the plasma membrane. The p38 MAP kinase and MAPKAP-2 pathway are involved in the post-transcriptional regulation of TNF alpha and are targeted by a functionally divergent group of cytokines including IL-10 and TGF beta 1. Common to many cytokines, TNF alpha mRNA 3' untranslated region (UTR) contains an AU-rich element (ARE), which drives repression by mRNA-binding proteins (RBPs). These include tristetraprolin (TTP), T cell antigen-1 (TIA-1), TIA-1-related protein (TIAR), human antigen R (HuR) and fragile-X-related protein 1 (FXR1). Disruption of several RBPs can dysregulate TNF alpha protein production and has, in some cases, been shown to exacerbate chronic inflammatory disease both in mice and in humans. Given that TNF alpha is central to clearance of infections, yet during chronic inflammation results in tissue damage, understanding the role that RBPs play in the control of TNF alpha may give rise to opportunities to not only develop targeted therapy for autoimmunity but also redress homeostasis without compromise and risking infection. The study of mRNA stability remains essential for the understanding of intracellular regulatory pathways and molecular mechanisms of pathology for infection, inflammation and degeneration. (C) 2010 Elsevier Ltd. All rights reserved.
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