Damage to mtDNA in liver injury of patients with extrahepatic cholestasis: The protective effects of mitochondrial transcription factor A

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• 作者：Shang-Cheng Xu^a ; ¹ ; Yong-Biao Chen^b ; ¹ ; Heng Lin^b ; Hui-Feng Pi^a ; Ni-Xian Zhang^a ; Chang-Chun Zhao^b ; Ling Shuai^b ; Min Zhong^a ; Zheng-Ping Yu^a ; Zhou Zhou^a ; ^{xscsci2009@yahoo.cn} ; Ping Bie^b ; ^{biepingcyb@sina.com}
• 关键词：BDL ; bile duct ligation ; COX ; cytochrome c oxidase subunit ; GCDCA ; glycochenodeoxycholic acid ; MDA ; malondialdehyde ; mtDNA ; mitochondrial DNA ; ND ; NADH dehydrogenase subunit ; ROS ; reactive oxygen species ; TFAM ; mitochondrial transcription factor A ; ¦¤¦·m
• 刊名：Free Radical Biology and Medicine
• 出版年：2012
• 出版时间：1 May, 2012
• 年：2012
• 卷：52
• 期：9
• 页码：1543-1551
• 全文大小：1643 K

文摘

Oxidative stress and mitochondrial dysfunction are involved in the pathogenesis of chronic liver cholestasis. Mitochondrial DNA (mtDNA) is highly susceptible to oxidative stress and mtDNA damage leads to mitochondrial dysfunction. This study aimed to investigate the mtDNA alterations that occurred during liver injury in patients with extrahepatic cholestasis. Along with an increase in malondialdehyde (MDA) levels and a decrease in ATP levels, extrahepatic cholestatic patients presented a significant increase in mitochondrial 8-hydroxydeoxyguanosine (8-OHdG) levels and decreases in mtDNA copy number, mtDNA transcript levels, and mtDNA nucleoid structure. In L02 cells, glycochenodeoxycholic acid (GCDCA) induced similar damage to the mtDNA and mitochondria. In line with the mtDNA alterations, the mRNA and protein levels of mitochondrial transcription factor A (TFAM) were significantly decreased both in cholestatic patients and in GCDCA-treated L02 cells. Moreover, overexpression of TFAM could efficiently attenuate the mtDNA damage induced by GCDCA in L02 cells. However, without its C-tail, ¦¤C-TFAM appeared less effective against the hepatotoxicity of GCDCA than the wild-type TFAM. Overall, our study demonstrates that mtDNA damage is involved in liver damage in extrahepatic cholestatic patients. The mtDNA damage is attributable to the loss of TFAM. TFAM has mtDNA-protective effects against the hepatotoxicity of bile acid during cholestasis.