Depletion of the Central Metabolite NAD Leads to Oncosis-mediated Cell Death

作者：Del Nagro Christopher; Xiao Yang; Rangell Linda; Reichelt Mike; O'Brien Thomas^*

来源：Journal of Biological Chemistry, 2014, 289(51): 35182-35192.

DOI：10.1074/jbc.M114.580159

• Apoptosis
• ATP
• Cell Death
• Cell Metabolism
• Nicotinamide Adenine Dinucleotide (NAD)
• GNE-617
• NAMPT
• Oncosis

Depletion of the central metabolite NAD in cells results in broad metabolic defects leading to cell death and is a proposed novel therapeutic strategy in oncology. There is, however, a limited understanding of the underlying mechanisms that connect disruption of this central metabolite with cell death. Here we utilize GNE-617, a small molecule inhibitor of NAMPT, a rate-limiting enzyme required for NAD generation, to probe the pathways leading to cell death following NAD depletion. In all cell lines examined, NAD was rapidly depleted (average t(1/2) of 8.1 h) following NAMPT inhibition. Concurrent with NAD depletion, there was a decrease in both cell proliferation and motility, which we attribute to reduced activity of NAD-dependent deacetylases because cells fail to deacetylate -tubulin-K40 and histone H3-K9. Following depletion of NAD by >95%, cells lose the ability to regenerate ATP. Cell lines with a slower rate of ATP depletion (average t(1/2) of 45 h) activate caspase-3 and show evidence of apoptosis and autophagy, whereas cell lines with rapid depletion ATP (average t(1/2) of 32 h) do not activate caspase-3 or show signs of apoptosis or autophagy. However, the predominant form of cell death in all lines is oncosis, which is driven by the loss of plasma membrane homeostasis once ATP levels are depleted by >20-fold. Thus, our work illustrates the sequence of events that occurs in cells following depletion of a key metabolite and reveals that cell death caused by a loss of NAD is primarily driven by the inability of cells to regenerate ATP.

• 出版日期2014-12-19