Age‑dependent increase in the expression of antioxidant‑like protein‑1 in the gerbil hippocampus.

Antioxidant-like protein-1 (AOP-1) reduces the intracellular level of reactive oxygen species. In the present study, the age‑related change in AOP‑1 expression in the hippocampus among young, adult and aged gerbils was compared using western blot analysis and immunohistochemistry. The results demonstrated that the protein expression of AOP‑1 was gradually and significantly increased in the hippocampus during the normal aging process. In addition, the age‑dependent increase in AOP‑1 immunoreactivity was also observed in pyramidal neurons of the hippocampus proper; however, in the dentate gyrus, AOP‑1 immunoreactivity was not altered during the normal aging process. These results indicated that the expression of AOP‑1 is significantly increased in the hippocampus proper, but not in the dentate gyrus, during the normal aging process.

Introduction

Antioxidant-like protein-1 (AOP-1) is an antioxidant protein with 93.3% homology to SP-22, a mitochondrial antioxidant protein (1). AOP-1, which is expressed in the cytoplasm, as well as in the mitochondria, has been known to reduce intracellular levels of reactive oxygen species (ROS) by co-operating with mitochondrial thioredoxin and is important in the maintenance of mitochondrial mass and membrane potential (1–3). In addition, AOP-1 is associated with various biological processes, including cell proliferation, differentiation, apoptosis and gene expression (4).

Aging leads to neuroanatomical and neurophysiological alterations in the central nervous system (5–7). In the brain, age-related changes are closely associated with alterations in DNA damage, synaptic vesicle transport, autophagic degradation and neuronal activity (8–12). In particular, oxidative stress, which accumulates with age, is considered to be one of the major causes of aging and age-associated cognitive impairment (8,13–16). Certain previous studies have demonstrated that antioxidant supplementation, which reduces oxidative stress in the brain, ameliorates histopathological alterations, as well as learning and memory deficits in animal models for brain aging (17–19). In addition, it is well established that marked increases in oxidative stress occur in the brain during the normal aging process (16,20). However, age-related changes in AOP-1 in the brain remain to be fully elucidated. Since the hippocampus, which is an important region associated with learning and memory, is the most vulnerable brain region to the aging process (21–24), the present study aimed to investigate age-related changes in AOP-1 in the hippocampus of the Mongolian gerbil, which is a suitable model for research on aging (20,25).

Materials and methods

Experimental animals

A total of 42 male Mongolian gerbils (Meriones unguiculatus) were obtained from the Experimental Animal Center, Kangwon National University (Chuncheon, South Korea). As previously described (9), the animals were divided into the following three groups (n=14/group): Young (3–4 months old; weighing 65–72 g), adult (10–12 months old; weighing 77–83 g) and aged (18–24 months old; weighing 85–95 g). The animals were housed in a conventional state under an adequate temperature (23±3°C) and relative humidity (55±5%) with a 12 h light/dark cycle, and were allowed free access to food and water. All experimental procedures for animal handling and use were approved by the Institutional Animal Care and Use Committee at Kangwon National University (approval no. KW-130424-3).

Western blot analysis

To examine alterations in the protein expression of AOP-1 in the hippocampus during normal aging, the animals (n=7/group) were used, and western blot analysis was performed, as previously described (9,10,26). Briefly, the hippocampus was homogenized and centrifuged, at 16,000 × g for 20 min at 4°C and the supernatants were subjected to western blot analysis. Following centrifugation, the protein level in the supernatants was determined using a micro bicinchoninic acid protein assay kit (Sigma-Aldrich, St. Louis, MO, USA) with bovine serum albumin as a standard (Pierce Biotechnology, Inc., Rockford, IL, USA). Aliquots containing 20 μg total protein were boiled in loading buffer containing 150 mM Tris (pH 6.8, Sigma-Aldrich), 3 mM dithiothreitol, 6% sodium dodecyl sulfate, 0.3% bromophenol blue and 30% glycerol. The aliquots were then loaded onto a 12% polyacrylamide gel. Following electrophoresis, the proteins were transferred to nitrocellulose transfer membranes (Pall Corporation, East Hills, NY, USA). To reduce background staining, the membranes were incubated with 5% non-fat dry milk (Sigma-Aldrich) in phosphate-buffered saline (PBS) containing 0.1% Tween-20 (PBST; Sigma-Aldrich) for 45 min at room temperature. Membranes were incubated with monoclonal mouse anti-AOP-1 (cat. no. A7674; dilution, 1:2,500; Sigma-Aldrich) or monoclonal mouse anti-β-actin (cat. no. A53161; dilution, 1:2,500; Sigma-Aldrich) overnight at 4°C. Following washing with PBST three times, the membranes were incubated with peroxidase-conjugated goat anti-mouse (cat. no. sc-2031; dilution, 1:1,000; Santa Cruz Biotechnology, Inc., Dallas, TX, USA) for 1 h at room temperature. An enhanced chemiluminescence kit (Pierce ECL Western Blotting Substrate; Thermo Fisher Scientific, Inc., Waltham, MA, USA) The result of the western blot analysis was scanned and densitometric analysis for the quantification of the bands was performed using Image J 1.49 software (National Institutes of Health, Bethesda, MD, USA), which was used to count the relative optical density (ROD). The expression of AOP-1 was normalized against that of β-actin, which was used as the internal control protein. A ratio of the ROD was calibrated as a percentage, with the young group designated as 100%. Western blot analysis was performed with three replicates.

Immunohistochemistry

To examine age-related changes in AOP-1 immunoreactivity in the gerbil hippocampus, immunohistochemical staining was performed, as previously described (9,10,26). In brief, the animals (n=7/group) were anesthetized with Zoletil 50 (30 mg/kg; Virbac, Carros, France) and perfused transcardially with 4% paraformaldehyde (Sigma-Aldrich) in 0.1 M phosphate-buffered saline (pH 7.4; Sigma-Aldrich). The brains were postfixed with the same solution for 6 h and sectioned with a cryostat at 30 μm. Immunohistochemical staining for AOP-1 was performed using monoclonal mouse anti-AOP-1 (cat. no. A7674; dilution, 1:500; Sigma-Aldrich) as a primary antibody. The brain tissues were subsequently incubated with biotinylated goat anti-mouse immunoglobulin G (cat. no. BA-9200; 1:200; Vector Laboratories, Burlingame, CA, USA) and streptavidin peroxidase complex (cat. no. SA-5004; 1:200; Vector Laboratories). A negative control test was performed using pre-immune serum instead of primary antibody in order to establish the specificity of the immunostaining. The negative control resulted in the absence of immunoreactivity in all structures.

A total of six sections with 90 μm intervals per animal were selected to quantitatively analyze AOP-1 immunoreactivity. Digital images of the hippocampal subregions were captured with an AxioM2 light microscope (Carl Zeiss, Oberkochen, Germany) equipped with a digital camera (Axiocam; Carl Zeiss) connected to a PC monitor. According to our previous method (27), AOP-1 immunoreactivity was evaluated using digital image analysis software (MetaMorph 4.01; Universal Imaging Corp., Bedford Hills, NY, USA). The immunoreactivity was measured using a 0–255 gray scale system (white to dark signal between 255 and 0). AOP-1 immunoreactivity levels of experimental groups were calibrated with the background in the same section. Subsequently, the ratio of the immunoreactivity was calibrated as a percentage, with the young group designated as 100%.

Statistical analysis

The data are expressed as the mean ± standard error of the mean. The data were evaluated by a two-way analysis of variance using SPSS software (version 12.0; SPSS, Inc., Chicago, IL, USA) and the means were assessed using Duncan's multiple-range test. P<0.05 was considered to indicate a statistically significant difference.

Results

AOP-1 protein level in the hippocampus

Western blot analysis demonstrated that the protein expression of AOP-1 was gradually and significantly increased in the hippocampus with normal aging. The protein expression of AOP-1 in the adult hippocampus was significantly increased (147.0%, F=9.914) compared with the young group. In the aged group, the protein expression of AOP-1 in the hippocampus was significantly higher (124.7%, F=8.107) compared with that in the adult group (Fig. 1).

Figure 1

Western blot analysis of AOP-1 (~25 kDa) in the hippocampus derived from the young, adult and aged groups. The ROD of the immunoblotting bands is shown as the percentage (n=7/group; *P<0.05, compared with the young group; #P<0.05, compared with the adult group). The data are presented as the mean ± standard error of the mean. AOP-1, antioxidant-like protein-1; ROD, relative optical density.

AOP-1 immunoreactivity in the hippocampus proper

Age-related changes in AOP-1 immunoreactivity (Fig. 2) in the hippocampus proper (CA1-3 regions) were found to be generally similar to the result of western blot analysis. In the hippocampus proper, weak AOP-1 immunoreactivity was primarily detected in pyramidal neurons of the stratum pyramidale of the young group (Figs. 2A, D, G and 3). In the adult group, AOP-1 immunoreactivity in the pyramidal neurons of the hippocampus proper was increased, compared with that in the young group (Figs. 2B, E, H and 3; F=34.407 in the CA1 region and F=25.579 in the CA3 region, respectively). In the aged group, AOP-1 immunoreactivity was significantly increased in the pyramidal neurons of the hippocampus proper (Figs. 2C, F, I and 3; F=24.753 in the CA1 region and F=51.553 in the CA3 region, respectively), compared with the young group.

Figure 2

AOP-1 immunohistochemistry in the (A–C) hippocampus, (D–F) hippocampal CA1 region, (G–I) CA3 region and (J–L) dentate gyrus of the young (left), adult (middle) and aged groups (right). AOP-1 immunoreactivity is increased in the SP (indicated by asterisks) of the CA1 and CA3 region during the aging process. However, no marked difference was observed in AOP-1 immunoreactivity in the DG among all groups. Scale bar, 400 μm (A–C) and 50 μm (D–L). GCL, granule cell layer; ML, molecular layer; PL, polymorphic layer; SO, stratum oriens; SR, stratum radiatum; SP, stratum pyramidale; DG, dentate gyrus; AOP-1, antioxidant-like protein-1.

Figure 3

Relative immunoreactivity as a percentage of AOP-1 immunoreactive cells in the CA1 region, CA3 region and DG of the young, adult and aged groups (n=7/group; *P<0.05, compared with the young group; #P<0.05, compared with the adult group). The data are presented as the mean ± standard error of the mean. AOP-1, antioxidant-like protein-1; DG, dentate gyrus.

AOP-1 immunoreactivity in the dentate gyrus

In the young group, AOP-1 immunoreactivity was observed predominantly in granule cells of the granule cell layer and in polymorphic cells of the polymorphic layer (Fig. 2J). AOP-1 immunoreactivity in those cells of the dentate gyrus was not altered in the adult and aged groups, compared with that in the young group (Figs. 2K, L and 3).

Discussion

Our previous study demonstrated no marked age-related histopathological alterations in the hippocampus between adult and aged gerbils, as determined by terminal deoxynucleotidyl transferase dUTP nick end labeling staining and Fluoro-Jade B histofluorescence staining, although a marked activation of microglia was observed in the aged group (28). However, in the present, western blot analysis revealed that the protein expression of AOP-1 was significantly increased during the normal aging process. It can be postulated that the significant increase in AOP-1 protein level occurs due to the age-dependent increases in oxidative stress in the hippocampus.

Numerous previous studies have reported a significant increase in oxidative stress in the brain during the aging process (14,15,20). On the basis of previous studies (8,14–16,20), which demonstrated the age-related decrease in antioxidant enzymes in the brain, the basal levels of oxidative stress markers and the production of ROS in the hippocampus at various stages of aging was not measured in the present study. In particular, Selaković et al (20) reported that basal levels of certain types of oxidative stress, including superoxide anion production, superoxide dismutase activity and the index of lipid peroxidation, were significantly increased in the hippocampus of the 10-month-old gerbil, compared with those of the 3-month-old gerbil. It was also reported that the level of lipid peroxidation was increased and the levels of antioxidant enzymes, including catalase, superoxide dismutase and glutathione peroxidase, were decreased in the brain of aged rats compared with those of young controls (16). The authors suggested that the age-related decrease in antioxidant enzymes in the brain is due to deficient antioxidative enzyme defense against ROS (16).

The present study also found that AOP-1 immunoreactivity was significantly increased in the hippocampus proper, not in the dentate gyrus and among hippocampal subregions during the aging process. Therefore, it can be hypothesized that the age-dependent increase in AOP-1 occurs primarily in the hippocampus proper. However, it is difficult to explain exactly why the age-dependent increase in AOP-1 immunoreactivity occurs in the hippocampus proper and not in the dentate gyrus, since, to the best of our knowledge, this is the first study regarding the age-dependent change in AOP-1 protein expression in the hippocampus. Among the hippocampal subregions, the dentate gyrus is known as the most sensitive and vulnerable region during the normal aging process, whereas the hippocampus proper is relatively resistant (29). In addition, our previous study demonstrated that FoxO3a, which is strongly associated with the aging process and senescence (30,31), was significantly decreased in the dentate gyrus, not in the hippocampus proper, of the aged gerbil hippocampus (26). On the basis of the present and other previous studies, it is likely that the expression patterns of biomarkers for brain aging are different according to brain areas. In this regard, enhanced AOP-1 expression in the hippocampus proper, not in the dentate gyrus, may be one of the possible mechanisms explaining why the dentate gyrus is more sensitive to oxidative stress compared with the other hippocampal subregions during the normal aging process.

In conclusion, the present study indicated that AOP-1 expression is significantly increased in the aged hippocampus, particularly in the hippocampus proper, during the normal aging process and suggests that age-related increases in AOP-1 may be a compensatory process against the elevation of oxidative stress in the aged hippocampus.