Liu Qinlong, Krishnasamy Yasodha, Rehman Hasibur, Lemasters John J, Schnellmann Rick G, Zhong Zhi
Department of Drug Discovery & Biomedical Sciences, Medical University of South Carolina, Charleston, South Carolina, United States of America; The Second Affiliated Hospital of Dalian Medical University, Dalian, Liaoning Province, China.
Department of Drug Discovery & Biomedical Sciences, Medical University of South Carolina, Charleston, South Carolina, United States of America.
PLoS One. 2015 Oct 19;10(10):e0140906. doi: 10.1371/journal.pone.0140906. eCollection 2015.
Suppressed mitochondrial biogenesis (MB) contributes to acute kidney injury (AKI) after many insults. AKI occurs frequently after liver transplantation (LT) and increases mortality. This study investigated whether disrupted mitochondrial homeostasis plays a role in AKI after LT.
Livers were explanted from Lewis rats and implanted after 18 h cold storage. Kidney and blood were collected 18 h after LT.
In the kidney, oxidative phosphorylation (OXPHOS) proteins ATP synthase-β and NADH dehydrogenase-3 decreased 44% and 81%, respectively, with marked reduction in associated mRNAs. Renal PGC-1α, the major regulator of MB, decreased 57% with lower mRNA and increased acetylation, indicating inhibited synthesis and suppressed activation. Mitochondrial transcription factor-A, which controls mtDNA replication and transcription, protein and mRNA decreased 66% and 68%, respectively, which was associated with 64% decreases in mtDNA. Mitochondrial fission proteins Drp-1 and Fis-1 and mitochondrial fusion protein mitofusin-1 all decreased markedly. In contrast, PTEN-induced putative kinase 1 and microtubule-associated protein 1A/1B-light chain 3 increased markedly after LT, indicating enhanced mitophagy. Concurrently, 18- and 13-fold increases in neutrophil gelatinase-associated lipocalin and cleaved caspase-3 occurred in renal tissue. Both serum creatinine and blood urea nitrogen increased >2 fold. Mild to moderate histological changes were observed in the kidney, including loss of brush border, vacuolization of tubular cells in the cortex, cast formation and necrosis in some proximal tubular cells. Finally, myeloperoxidase and ED-1 also increased, indicating inflammation.
Suppression of MB, inhibition of mitochondrial fission/fusion and enhancement of mitophagy occur in the kidneys of recipients of liver grafts after long cold storage, which may contribute to the occurrence of AKI and increased mortality after LT.
多种损伤后线粒体生物合成(MB)受抑制会导致急性肾损伤(AKI)。肝移植(LT)后AKI频繁发生且会增加死亡率。本研究调查了线粒体稳态破坏是否在LT后AKI中起作用。
从Lewis大鼠获取肝脏,经18小时冷保存后植入。LT后18小时收集肾脏和血液。
在肾脏中,氧化磷酸化(OXPHOS)蛋白ATP合酶-β和NADH脱氢酶-3分别下降44%和81%,相关mRNA显著减少。肾脏中MB的主要调节因子PGC-1α下降57%,mRNA水平降低且乙酰化增加,表明合成受抑制且激活受抑制。控制线粒体DNA复制和转录的线粒体转录因子A,其蛋白和mRNA分别下降66%和68%,这与线粒体DNA下降64%相关。线粒体分裂蛋白Drp-1和Fis-1以及线粒体融合蛋白线粒体融合蛋白-1均显著下降。相反,PTEN诱导的假定激酶1和微管相关蛋白1A/1B轻链3在LT后显著增加,表明线粒体自噬增强。同时,肾组织中中性粒细胞明胶酶相关脂质运载蛋白和裂解的半胱天冬酶-3分别增加18倍和13倍。血清肌酐和血尿素氮均增加超过2倍。在肾脏中观察到轻度至中度组织学变化,包括刷状缘丧失、皮质肾小管细胞空泡化、管型形成以及一些近端肾小管细胞坏死。最后,髓过氧化物酶和ED-1也增加,表明存在炎症。
长时间冷保存后肝移植受者的肾脏中发生MB抑制、线粒体分裂/融合受抑制以及线粒体自噬增强,这可能导致AKI的发生以及LT后死亡率增加。