[PDF][PDF] TXNIP maintains the hematopoietic cell pool by switching the function of p53 under oxidative stress

H Jung, MJ Kim, DO Kim, WS Kim, SJ Yoon, YJ Park… - Cell metabolism, 2013 - cell.com
H Jung, MJ Kim, DO Kim, WS Kim, SJ Yoon, YJ Park, SR Yoon, TD Kim, HW Suh, S Yun…
Cell metabolism, 2013cell.com
Reactive oxygen species (ROS) are critical determinants of the fate of hematopoietic stem
cells (HSCs) and hematopoiesis. Thioredoxin-interacting protein (TXNIP), which is induced
by oxidative stress, is a known regulator of intracellular ROS. Txnip−/− old mice exhibited
elevated ROS levels in hematopoietic cells and showed a reduction in hematopoietic cell
population. Loss of TXNIP led to a dramatic reduction of mouse survival under oxidative
stress. TXNIP directly regulated p53 protein by interfering with p53-mouse double minute 2 …
Summary
Reactive oxygen species (ROS) are critical determinants of the fate of hematopoietic stem cells (HSCs) and hematopoiesis. Thioredoxin-interacting protein (TXNIP), which is induced by oxidative stress, is a known regulator of intracellular ROS. Txnip−/− old mice exhibited elevated ROS levels in hematopoietic cells and showed a reduction in hematopoietic cell population. Loss of TXNIP led to a dramatic reduction of mouse survival under oxidative stress. TXNIP directly regulated p53 protein by interfering with p53- mouse double minute 2 (MDM2) interactions and increasing p53 transcriptional activity. Txnip−/− mice showed downregulation of the antioxidant genes induced by p53. Introduction of TXNIP or p53 into Txnip−/− bone marrow cells rescued the HSC frequency and greatly increased survival in mice following oxidative stress. Overall, these data indicate that TXNIP is a regulator of p53 and plays a pivotal role in the maintenance of the hematopoietic cells by regulating intracellular ROS during oxidative stress.
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