The emerging role of the thioredoxin system in angiogenesis.

Arterioscler Thromb Vasc Biol

Department of Cardiology, Royal Prince Alfred Hospital, Missenden Rd, Camperdown, New South Wales, Australia.

Published: November 2010

AI Article Synopsis

  • Despite numerous studies, the mechanisms of angiogenesis are still not fully understood, with increasing evidence pointing to the significance of cellular redox homeostasis.
  • The thioredoxin (TRX) system is identified as a key antioxidant influencing endothelial cell function and plays roles in both traditional and new angiogenic signaling pathways, making it a potential target for therapy.
  • The TRX-interacting protein (TXNIP), which inhibits TRX activity and is linked to growth factor-induced angiogenesis, may be particularly relevant in diabetes due to its strong induction by glucose, suggesting its involvement in abnormal angiogenesis associated with the condition.

Article Abstract

Although there have been a multitude of studies, the mechanisms of angiogenesis remain incompletely understood. Increasing evidence suggests that cellular redox homeostasis is an important regulator of angiogenesis. The thioredoxin (TRX) system functions as an endogenous antioxidant that can exert influence over endothelial cell function via modulation of cellular redox status. It has become apparent that the cytosolic TRX1 isoform participates in both canonical and novel angiogenic signaling pathways and may represent an avenue for therapeutic exploitation. Recent studies have further identified a role for the mitochondrial isoform TRX2 in ischemia-induced angiogenesis. TRX-interacting protein (TXNIP) is the endogenous inhibitor of TRX redox activity that has been implicated in growth factor-mediated angiogenesis. As TXNIP is strongly induced by glucose, this molecule could be of consequence to disordered angiogenesis manifest in diabetes mellitus. This review will focus on data implicating the TRX system in endothelial cell homeostasis and angiogenesis.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3142174PMC
http://dx.doi.org/10.1161/ATVBAHA.110.209643DOI Listing

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