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Title: Mitochondrial Dysfunction Represses HIF-1α Protein Synthesis through AMPK Activation in Human Hepatoma HepG2 Cells
Authors: Hsin-Chen Lee
Chia-Chi Hsu
Chun-Hui Wang
Ling-Chia Wu
Cheng-Yuan Hsia
Chin-Wen Chi
Pen-Hui Yin
Chun-Ju Chang
Ming-Ta Sung
Yau-Huei Wei
Shing-Hwa Lu
Contributors: 國立臺灣海洋大學:食品科學系
Keywords: Protein synthesis
Mitochondrial dysfunction
Hypoxia-inducible factor-1α
Adenosine monophosphate-activated protein kinase
Date: 2013-10
Issue Date: 2016-12-21T03:16:51Z
Publisher: Biochimica et Biophysica Acta (BBA) - General Subjects
Abstract: Abstract:

Hypoxia-inducible factor-1α (HIF-1α) is an important transcription factor that modulates cellular responses to hypoxia and also plays critical roles in cancer progression. Recently, somatic mutations and decreased copy number of mitochondrial DNA (mtDNA) were detected in hepatocellular carcinoma (HCC). These mutations were shown to have the potential to cause mitochondrial dysfunction. However, the effects and mechanisms of mitochondrial dysfunction on HIF-1α function are not fully understood. This study aims to explore the underlying mechanism by which mitochondrial dysfunction regulates HIF-1α expression.

Human hepatoma HepG2 cells were treated with various mitochondrial respiration inhibitors and an uncoupler, respectively, and the mRNA and protein expressions as well as transactivation activity of HIF-1α were determined. The role of AMP-activated protein kinase (AMPK) was further analyzed by compound C and AMPK knock-down.

Treatments of mitochondrial inhibitors and an uncoupler respectively reduced both the protein level and transactivation activity of HIF-1α in HepG2 cells under normoxia or hypoxia. The mitochondrial dysfunction-repressed HIF-1α protein synthesis was associated with decreased phosphorylations of p70S6K and 4E-BP-1. Moreover, mitochondrial dysfunction decreased intracellular ATP content and elevated the phosphorylation of AMPK. Treatments with compound C, an AMPK inhibitor, and knock-down of AMPK partially rescued the mitochondrial dysfunction-repressed HIF-1α expression.

Mitochondrial dysfunctions resulted in reduced HIF-1α protein synthesis through AMPK-dependent manner in HepG2 cells.

General significance
Our results provided a mechanism for communication from mitochondria to the nucleus through AMPK-HIF-1α. Mitochondrial function is important for HIF-1α expression in cancer progression.

AMPK, AMP-activated protein kinase; CAIX, carbonic anhydrase IX; CCCP, carbonyl cyanide m-chlorophenyl hydrazine; DMEM, Dulbecco's modified Eagle medium; HCC, hepatocellular carcinoma; HIF-1α, hypoxia-inducible factor-1α; LDHA, lactate dehydrogenase A; mtDNA, mitochondrial DNA; ROS, reactive oxygen species; RT-PCR, reverse transcription-polymerase chain reaction
Relation: 1830(10)
URI: http://ntour.ntou.edu.tw:8080/ir/handle/987654321/39558
Appears in Collections:[食品科學系] 期刊論文

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