AIM: To investigate the multiple gene differential expression pattems in human ischemic liver and to produce the evidence about the hepatic ischemic safety time.METHODS: The responses of cells to hepatic ischemia and ...AIM: To investigate the multiple gene differential expression pattems in human ischemic liver and to produce the evidence about the hepatic ischemic safety time.METHODS: The responses of cells to hepatic ischemia and hypoxia at hepatic ischemia were analyzed by cDNA microarrary representing 4 000 different human genes containing 200 apoptotic correlative genes. RESULTS: There were lower or normal expression levels of apoptotic correlative genes during the periods of hepatic ischemia for 0-15 min, the maintenance homostatic genes were expressed significantly higher at the same time. But at the hepatic ischemia for 30 min, the expression levels of maintenance homeostatic genes were down-regulated, the expressions of many apoptotic correlative genes and nuclear transcription factors were activated and up-regulated.CONCLUSION: HIF-1, APAF-1, PCDC10, FBX5, DFF-40, DFFA XIAP, survivin may be regarded as the signal genes to judge the degree of hepatic ischemic-hypoxic injure, and the apoptotic liver cell injury due to ischemia in different time limits. The safe limit of human hepatic warm ischemic time appears to be generally less then 30 min.展开更多
基金Supported by the National Natural Science Foundation of China,No.30170928 and the Key Project of the Tenth-Five-year plan Foundation of PLA,No.01MA040
文摘AIM: To investigate the multiple gene differential expression pattems in human ischemic liver and to produce the evidence about the hepatic ischemic safety time.METHODS: The responses of cells to hepatic ischemia and hypoxia at hepatic ischemia were analyzed by cDNA microarrary representing 4 000 different human genes containing 200 apoptotic correlative genes. RESULTS: There were lower or normal expression levels of apoptotic correlative genes during the periods of hepatic ischemia for 0-15 min, the maintenance homostatic genes were expressed significantly higher at the same time. But at the hepatic ischemia for 30 min, the expression levels of maintenance homeostatic genes were down-regulated, the expressions of many apoptotic correlative genes and nuclear transcription factors were activated and up-regulated.CONCLUSION: HIF-1, APAF-1, PCDC10, FBX5, DFF-40, DFFA XIAP, survivin may be regarded as the signal genes to judge the degree of hepatic ischemic-hypoxic injure, and the apoptotic liver cell injury due to ischemia in different time limits. The safe limit of human hepatic warm ischemic time appears to be generally less then 30 min.
