Prothymosin alpha and cell death mode switch, a novel target for the prevention of cerebral ischemia-induced damage

作者：Ueda Hiroshi^*

来源：Pharmacology & Therapeutics, 2009, 123(3): 323-333.

DOI：10.1016/j.pharmthera.2009.05.007

• Necrosis
• Apoptosis
• Glucose transporter
• Glia
• Protein kinase C
• Brain-derived neurotrophic factor

Following stroke or traumatic damage, neuronal death via both necrosis and apoptosis causes loss of functions including memory, sensory perception and motor skills. Since necrosis has the nature to expand, while apoptosis stops the cell death cascade in the brain, necrosis is considered to be a promising target for rapid treatment for stroke. Pure neuronal necrosis occurs when cortical neurons are cultured under serum-free and low-density conditions. Prothymosin alpha (PrdT alpha) isolated from conditioned medium after serum-free culture was found to prevent necrosis by recovering the energy crisis due to endocytosed glucose transporters. At a later time point under the same starvation conditions, ProT alpha causes apoptosis, which in turn seems to inhibit the rapidly occurring necrosis by cleaving poly (ADP-ribose) polymerase, a major machinery involved in ATP consumption. Indeed, ProT alpha administered via systemic routes markedly inhibits the histological and functional damage induced by cerebral and retinal ischemia. Although ProT alpha also causes a cell death mode switch from necrosis to apoptosis in vivo, the induced apoptosis was found to be completely inhibited by endogenously occurring brain-derived neurotrophic factor or erythropoietin. Since forced downregulation of ProT alpha deteriorates the ischemic damage, it is evident that ProT alpha plays in vivo neuroprotective roles after ischemic events. Analyses in terms of the therapeutic time window and potency suggest that ProT alpha could be the prototypic compound to develop the medicine useful for treatment of stroke in clinics.

• 出版日期2009-9