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Effects of CCCP on the expression of GABARAPL2 in C6 glioma cells

Yoshimitsu Kiriyama

Tokushima Bunri University, Kagawa School of Pharmaceutical Sciences, Japan

Airi Ozaki

Tokushima Bunri University, Kagawa School of Pharmaceutical Sciences, Japan

Katsuhito Kino

Tokushima Bunri University, Kagawa School of Pharmaceutical Sciences, Japan

Hiromi Nochi

Tokushima Bunri University, Kagawa School of Pharmaceutical Sciences, Japan

E-mail : nochi@kph.bunri-u.ac.jp

DOI: 0.15761/IMM.1000133

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Abstract

Astrocytes play an important role in the central nervous system. Ischemia, hypoxia, and traumatic injury cause mitochondrial damage in neurons and astrocytes. Damaged mitochondria are isolated and removed by macroautophagy (hereafter referred to as autophagy), which degrades cellular components with autophagosomes. Autophagy that removes mitochondria is called mitophagy. Phosphatidylethanolamine (PE)-conjugated microtubule-associated protein 1 light chain 3B (LC3B) (LC3B-II) plays a crucial role in the formation of autophagosomes, and the conversion of unconjugated-LC3B (LC3B-I) to LC3B-II is the index of the induction of autophagy. Gamma-aminobutyric acid receptor-associated protein-like 2 (GABARAPL2) is the paralog of LC3B, and its function is not clear. In this study, we demonstrated that both the expression of total GABARAPL2 and the conversion of unconjugated-GABARAPL2 (GABARAPL2-I) to PE-conjugated GABARAPL2 (GABARAPL2-II) were upregulated by carbonyl cyanide 3-chlorophenylhydrazine (CCCP), which induces mitochondrial dysfunction and fragmentation. In contrast, CCCP upregulated the conversion of LC3B-I to LC3B-II, but it did not affect the expression of total LC3B. Thus, GABARAPL2 might function in the process of mitophagy during the formation of autophagosomes, and the expressions of GABARAPL2 and LC3B were regulated differently. The mechanism underlying the role of GABARAPL2 in mitophagy requires further investigations.

Key words

autophagy, mitophagy, LC3, GABARAPL2, GATE-16, GABARAP

Introduction

Astrocytes function to form the blood–brain barrier, provide nutrients to neurons, retain the extracellular ion balance, surround synapses, and process information with neurons [1-4]. Ischemia, hypoxia and traumatic injury cause oxidative stress which results in mitochondrial damage [5-7]. This mitochondrial damage leads to the dysfunction and death of astrocytes [8,9]. Therefore, the isolation and removal of damaged mitochondria are necessary to maintain the function of astrocytes.

Macroautophagy (hereafter referred to as autophagy) is the bulk degradation process of cellular cytosolic components, such as defective proteins and damaged organelles [10]. The processes in autophagy include the stages of initiation, elongation and closure, and maturation [11-14]. In the process of autophagy, cellular cytosolic components are isolated by the autophagosome. The autophagosome is formed during the stage of elongation and closure, and the important proteins that form autophagosomes are the members of the microtubule-associated protein 1 light chain 3 (LC3) subfamily and gamma-aminobutyric-acid-type-A receptor-associated protein (GABARAP) subfamily. In rats, the LC3 subfamily includes LC3A and LC3B, and the GABARAP subfamily includes GABARAP, GABARAP-like 1 (GABARAPL1), and GABARAP-like 2 (GABARAPL2, which is also known as GATE-16) [15-19]. Among the LC3 subfamily and the GABARAP subfamily, LC3B is most commonly used for studying autophagy. LC3B is catalyzed by ATG4 and is then conjugated to phosphatidylethanolamine (PE) by the ATG12–ATG5–ATG16 complex. LC3B-PE (LC3B-II) plays a crucial role in the formation of the autophagosome, and the conversion of unconjugated-LC3B (LC3B-I) to LC3B-II is the index of the induction of autophagy [18]. Although the physiological functions of the members of the LC3 subfamily, except for LC3B, and the GABARAP subfamily are not clear, the members of the LC3 subfamily and GABARAP subfamily are linked to PE, and they play a role in the formation of autophagosomes [16,20]. The degradation of cellular contents by autophagy occurs through both nonselective and selective pathways. The degradation of damaged mitochondria is considered as the selective autophagy (mitophagy) [21]. Nix, which is an outer mitochondrial membrane protein, binds LC3A, GABARAP, GABARAPL1, and GABARAPL2 but only weakly binds LC3B. Nix and GABARAPL1 are engaged in mitophagy by carbonyl cyanide 3-chlorophenylhydrazone (CCCP) [22]. However, the functions of GABARAPL2 in damaged mitochondria remain unclear.

In this study, rat C6 glioma cells, which are often used as a model for astrocytes, were used to observe the expression of the mRNA of all of the members of the LC3 subfamily and GABARAP subfamily. In addition, we examined the effects of CCCP, which causes mitochondrial damage, on the expression of GABARAPL2 in C6 glioma cells.

Materials and methods

Materials

 CCCP and an anti-actin antibody were from Sigma (St. Louis, MO, USA). Anti-LC3B antibody and anti-GABARAPL2 (GATE-16) antibody was from MBL (Nagoya, Japan). Horseradish peroxidase-linked secondary antibodies were from Zymed Laboratories (South San Francisco, CA, USA). Mitotracker Red CMXRos Mitochondria Probe was purchased from Lonza Walkersville, Inc (Walkersville, MD, USA).

Cell culture

 Rat C6 glioma cells were obtained from JCRB cell bank (Osaka, Japan) and were maintained in DMEM supplemented with 10% FBS, 100 units/ml penicillin, and 100 mg/ml streptomycin.

Reverse transcription - PCR

 Total RNA isolated from cells was purified using RNeasy Mini Kits (Qiagen, Valencia, CA, USA). Reverse transcriptase reactions were performed on 1 μg of RNA using a PrimeScript II 1st strand cDNA Synthesis Kit (Takara Bio, Otsu, Japan) in a 20 ml volume at 42°C for 60 min. PCR was performed for 45cycles using EmeraldAmp MAX PCR Master Mix (Takara Bio, Otsu, Japan) with the following primers: LC3A, 5′- ATGCCCTCCGACCGGCCTTTC-3′ and 5′- TCAGAAGCCGAAGGTTTCT-3′; LC3B, 5′- ATGCCGTCCGAGAAGACCTTC-3′ and 5′- TTACACAGCCAGTGCTGTCC-3′; Gabarap, 5′- ATGAAGTTCGTGTACAAAGA-3′ and 5′-TCACAGACCGTAGACGCTTTC-3′; GabarapL1, 5′-ATGAAGTTCCAGTATAAAGA-3′ and 5′-TCATTTCCCGTAGACACTTTC-3′; GabarapL2, 5′- ATGAAGTGGATGTTTAAGGA-3′ and 5′-TCAGAAGCCAAAAGTGTTC-3′.

All primer sets were selected to span intron(s) to obtain mRNA-specific PCR products and to amplify between 300 bp and 400 bp.

Western blot analysis

C6 glioma cells treated with vehicle or CCCP were harvested and lysed in modified RIPA buffer (50 mM Tris-HCl, pH 7.4, 1% NP-40, 0.25% sodium deoxycholate, 150 mM NaCl, 1 mM EDTA, 2 mM diisopropylfluorophosphate, 10 mg/mL of leupeptin, 10 mg/mL of aprotinin, and 10 mg/mL of pepstatin) on ice for 20 min. Cell lysates were sonicated and centrifuged at 12,000 × g at 4°C for 10 min. Proteins in the supernatants were electrophoresed in sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and transferred to Immobilon P membranes (Millipore, Billerica, MA). The membranes were blocked with 1% skim milk in 0.1% Tween 20/PBS (PBS-T) and incubated with primary antibodies (dilutions based on manufacturer’s recommendations). The membranes were washed three times in PBS-T and incubated for 1h with a horseradish peroxidase-conjugated secondary antibody. Immunoreactive proteins were detected with ImmunoStar LD (Wako Pure Chemical Industries, Osaka, Japan).

Mitochondria staining

Rat C6 glioma cells were cultured on 35-mm glass-bottomed dishes (Iwaki, Shizuoka, Japan). The cells were treated with CCCP for 4h. Mitotracker Red CMXRos Mitochondria Probe (final concentrations of 50 nM) was added at 30 minutes before the end of incubation. Images were acquired using a Leica DMI 6000 B microscope with AF6000 software (Leica, Wetzlar, Germany).

Statistical analysis

 Results of multiple observations are presented as means ± SEM. One-way analysis of variance (ANOVA) followed by the Dunnett’s test was used for multiple comparisons. P<0.05 was considered significant.

Results

    The levels of mRNA expression of the members of the LC3 subfamily and GABARAP subfamily in C6 glioma cells were assessed by RT-PCR (Figure 1). The mRNAs of all of the members of the LC3 subfamily and GABARAP subfamily were expressed in C6 glioma cells. The mRNA of LC3B was expressed most abundantly, and the mRNAs of LC3A, GABARAP, and GABARAPL2 were moderately expressed. The mRNA of GABARAPL1 was slightly expressed. We examined the effects of CCCP on the expression of GABARAPL2-II and total GABARAPL2. GABARAPL2-II, which is the PE-conjugated form of GABARAPL2, can bind autophagosomes. Thus, the levels of GABARAPL2-II are considered to reflect the activity of GABARAPL2. GABARAPL2-I, which is the unconjugated form, migrates slower than GABARAPL2-II on SDS-PAGE [16]. GABARAPL2-II expression levels were increased seven times compared to that of the control in response to 20 µM of CCCP, and the increase in GABARAPL2-II expression reached a maximum (12 times that of the control) in response to 100 µM of CCCP. Total GABARAPL2 expression levels increased to twice that of the control in response to 100 µM of CCCP, and total GABARAPL2 expression in response to 120 µM of CCCP remained at this level (Figure 2A). In addition, we investigated the effects of 120 µM of CCCP on the expression of GABARAPL2-II and total GABARAPL2 at various time points up to 6 h. GABARAPL2-II was increased to 13 times that of the control in response to 120 µM of CCCP at 1 h, after which the expression level of GABARAPL2-II remained at this level. Total GABARAPL2 was increased about twice that of control in response to 120 µM of CCCP at 1h, after which the GABARAPL2 expression remained at this level.

The effects of 120 µM of CCCP on the expression of LC3 were examined at various time points up to 6 h (Figure 3A) because the conversion of LC3 from LC3-I to LC3-II reflects the induction of autophagy and is a key step in the forming of autophagosomes. Similar to the results of GABARAPL2, LC3B-II expression was increased about ten times that of the control in response to 120 µM of CCCP at 1h, after which it remained at this level. However, total LC3B expression levels were not affected by 120 µM of CCCP (Figure 3A). The fragmentation of mitochondria precedes mitophagy [23]. We confirmed that the reticular mitochondrial network was fragmented by 120 µM of CCCP (Figure 3B). These results indicated that mitochondrial dysfunction correlated with the expression and activity of GABARAPL2.

Figure 1. The expression of mRNAs for the members of LC3 subfamily and GABARAP subfamily in C6 glioma cells. Total RNA was isolated from C6 glioma cells and LC3A, LC3B, GABARAP, GABARAPL1, and GABARAPL2 mRNA expression were detected by RT-PCR for 45 cycles. All primer sets spanned more than one intron of the target gene and were designed to amplify between 300 bp and 400 bp.

Figure 2. GABARAPL2 expression by CCCP in C6 glioma cells. (A) C6 glioma cells were treated with the indicated concentrations of CCCP for 4h. (B) C6 glioma cells were treated with 120 µM of CCCP for the indicated times. Cell lysates were subjected to a western blot analysis with an anti-GABARAPL2 antibody. The expression levels of GABARAPL2 were compared with those of actin, which was used as an internal control. The results are the ratios of the treated to control levels (means ± SEM, n = 3). p values <0.05 were considered statistically significant.

Figure 3. LC3B expression and the change in mitochondrial morphology in response to CCCP. (A) C6 glioma cells were treated with 120 µM of CCCP for the indicated times. Cell lysates were subjected to a western blot analysis with an anti-LC3B antibody. The expression levels of LC3B were compared with those of actin, which was used as an internal control. Results are the ratios of treated to control levels (means ± SEM, n = 3). p values <0.05 were considered statistically significant. (B) C6 glioma cells were treated with vehicle or 120 µM of CCCP for 4h, and the morphology of mitochondria was visualized with mitotracker. Corresponding DIC images are shown. Scale bars, 10 µm.

Discussion

The segregation and exclusion of damaged mitochondria are crucial to maintain the function of astrocytes. Damaged mitochondria are sequestered and eliminated by mitophagy, which is accompanied by the formation of autophagosomes. LC3B, which is a member of the LC3 subfamily and GABARAP subfamily, is a well-characterized protein that is involved in the formation of autophagosomes. However, the functions of the other members of the LC3 subfamily and GABARAP subfamily have not been completely elucidated. Although the physiological functions of GABARAPL2 in mitophagy are not well understood, it has been shown that GABARAPL2 is linked to phospholipids in the same manner as LC3 phospholipidation and may play a role in autophagy [16]. Moreover, GABARAPL2 binds to an ubiquitin-binding protein, p62 [24], and to a mitochondrion-localized protein, Nix [22]. Both p62 and Nix are involved in mitophagy that is induced by CCCP. In CCCP-induced mitophagy, voltage-dependent anion channels (VDACs), which are on the surface of mitochondria, are ubiquitinated by PINK1 and Parkin, and p62 then binds ubiquitinated-VDACs. LC3B carries p62 with ubiquitinated-VDACs to the autophagosome [21,25,26]. On the other hand, Nix interacts with GABARAPL1, and GABARAPL1 then brings the mitochondria to the autophagosome during the CCCP-induced mitophagy [22]. CCCP is the uncoupler that induces the fragmentation of mitochondria, which precedes mitophagy [23]. Therefore, we examined the effects of CCCP on the activation and expression of GABARAPL2. CCCP induced the upregulation of both GABARAPL2-II and total GABARAPL2. In contrast, the treatment of CCCP resulted in LC3-II upregulation, which is the indicator of the formation of the autophagosome, while CCCP did not affect the levels of expression of total LC3B. Recent studies have shown that LC3B plays a role in the early stage of autophagy (elongation of the phagophore membrane) and that GABARAPL2 is necessary for the late stage of autophagy (autophagosome closure) [20]. Therefore, GABARAPL2 may function in autophagosome closure during mitophagy, and each member of the LC3 subfamily and GABARAP subfamily may have distinct roles in the process of autophagy.

In conclusion, we demonstrated that both GABARAPL2-II and total GABARAPL2 were upregulated by CCCP in C6 glioma cells. GABARAPL2 possibly functions in the segregation of damaged mitochondria that occurs to protect against the dysfunction and death of astrocytes. The mechanism involving GABARAPL2 in the clearance of damaged mitochondria in astrocytes and the functions of GABARAPL2 require further investigations.

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Editorial Information

Editor-in-Chief

Masayoshi Yamaguchi
Emory University School of Medicine

Article Type

Research Article

Publication history

Received: April 04, 2015
Accepted: April 24, 2015
Published: April 27, 2015

Copyright

©2015 Kiriyama Y. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Citation

Kiriyama Y, Ozaki A, Kino K, Nochi H (2015) Effects of CCCP on the expression of GABARAPL2 in C6 glioma cells. Integr Mol Med 2: DOI: 10.15761/IMM.1000133

Corresponding author

Hiromi Nochi

Tokushima Bunri University, Kagawa School of Pharmaceutical Sciences, Shido 1314-1, Sanuki, Kagawa 769-2193, Japan; Tel: +81-87-899-7100; Fax: +81-87-894-0181.

E-mail : nochi@kph.bunri-u.ac.jp

Figure 1. The expression of mRNAs for the members of LC3 subfamily and GABARAP subfamily in C6 glioma cells. Total RNA was isolated from C6 glioma cells and LC3A, LC3B, GABARAP, GABARAPL1, and GABARAPL2 mRNA expression were detected by RT-PCR for 45 cycles. All primer sets spanned more than one intron of the target gene and were designed to amplify between 300 bp and 400 bp.

Figure 2. GABARAPL2 expression by CCCP in C6 glioma cells. (A) C6 glioma cells were treated with the indicated concentrations of CCCP for 4h. (B) C6 glioma cells were treated with 120 µM of CCCP for the indicated times. Cell lysates were subjected to a western blot analysis with an anti-GABARAPL2 antibody. The expression levels of GABARAPL2 were compared with those of actin, which was used as an internal control. The results are the ratios of the treated to control levels (means ± SEM, n = 3). p values <0.05 were considered statistically significant.

Figure 3. LC3B expression and the change in mitochondrial morphology in response to CCCP. (A) C6 glioma cells were treated with 120 µM of CCCP for the indicated times. Cell lysates were subjected to a western blot analysis with an anti-LC3B antibody. The expression levels of LC3B were compared with those of actin, which was used as an internal control. Results are the ratios of treated to control levels (means ± SEM, n = 3). p values <0.05 were considered statistically significant. (B) C6 glioma cells were treated with vehicle or 120 µM of CCCP for 4h, and the morphology of mitochondria was visualized with mitotracker. Corresponding DIC images are shown. Scale bars, 10 µm.