Anti-apoptotic effect of hyperglycemia can allow survival of potentially autoreactive T cells

作者：Ramakrishnan P; Kahn D A; Baltimore D^*

来源：Cell Death and Differentiation, 2011, 18(4): 690-699.

DOI：10.1038/cdd.2010.163

• NF-kappa B
• apoptosis
• diabetes
• T-cell development
• autoimmunity

Thymocyte development is a tightly controlled multi-step process involving selective elimination of self-reactive and nonfunctional T cells by apoptosis. This developmental process depends on signaling by Notch, IL-7 and active glucose metabolism. In this study, we explored the requirement of glucose for thymocyte survival and found that in addition to metabolic regulation, glucose leads to the expression of anti-apoptotic genes. Under hyperglycemic conditions, both mouse and human thymocytes demonstrate enhanced survival. We show that glucose-induced anti-apoptotic genes are dependent on NF-kappa B p65 because high glucose is unable to attenuate normal ongoing apoptosis of thymocytes isolated from p65 knockout mice. Furthermore, we demonstrate that in vivo hyperglycemia decreases apoptosis of thymocytes allowing for survival of potentially self-reactive thymocytes. These results imply that hyperglycemic conditions could contribute to the development of autoimmunity through dysregulated thymic selection. Cell Death and Differentiation (2011) 18, 690-699; doi:10.1038/cdd.2010.163; published online 17 December 2010

• 出版日期2011-4