Carnitine-induced senescence in glioblastoma cells

Abstract

Carnitine is essential for lipid metabolism in cells and is known to possess antioxidant properties. Previous reports have suggested that antioxidants are able to induce senescence in glioblastoma cells, consequently, in the present study, we investigated the effect of carnitine on glioblastoma cells. Under conditions of hyponutrition (undernutrition), the proliferation of glioblastoma cells was attenuated and the level of intracellular carnitine was increased. Glioblastoma cell proliferation was also attenuated in cultures that were supplemented with exogenous carnitine, where the induction of senescence was detected by senescence-associated β-gal (SA-β-gal) staining. However, there was no evidence of the induction of apoptosis. These effects were not detected when cells were cultured with carnitine plus an inhibitor of p38 mitogen-activated protein kinase (MAPK). It, therefore, appears that carnitine has antioxidant actions in normal cells but induces senescence, which may be regarded as an opposite phenomenon, in glioblastoma cells. Senescence has been reported in cells exposed to temozolomide, which is a standard drug used for the treatment of glioblastoma. Carnitine could, therefore, represent an attractive alternative therapy for glioblastoma.

Introduction

Glioblastoma is the most common malignant type of primary brain tumor found in humans, and the prognosis for patients remains poor despite multimodal therapy including surgery, radiotherapy and chemotherapy (1,2). The median patient survival time following glioblastoma diagnosis is only 12 months owing to characteristic diffuse infiltrations into the surrounding central nervous system tissue (3,4). Therefore, there is an urgent need to develop new approaches to its management.

Cellular senescence leads to the permanent growth arrest of proliferating somatic cells in response to damage and stress from exogenous and endogenous sources (5–7). It is also thought to contribute to a decrease in tissue renewal (that is, the replacement of aged cells), and has recently been recognized as a mechanism of tumor suppression (5,6,8). Several studies have attempted to induce replicative senescence in cancer cell lines using genetic, chemical, or biological treatments (9–11), providing preliminary evidence that senescence has potential as an anticancer therapy.

Carnitine is essential for the β-oxidation of fatty acids in mitochondria to generate adenosine triphosphate (ATP) in living cells (12,13). Under normal conditions, 70–80% of human carnitine is obtained through dietary means, although the liver, kidney and brain are capable of biosynthesizing carnitine from lysine and methionine. Carnitine is commonly regarded as an anti-aging agent, since it strongly suppresses the apoptosis of various cell types through the stabilization of mitochondrial membrane permeability (14–16). Furthermore, oxidative damage to mitochondria and cell death in the kidney and intestine, which may be induced by anticancer drugs such as cisplatin, is reported to be inhibited by carnitine (17). It is therefore widely regarded as having a protective effect on cells and tissues. However, few reports to date have documented the effects of carnitine on cancer cell senescence.

Glioblastoma cells in which senescence has been induced by reduced fetal bovine serum (FBS) levels (that is, hyponutrition) show increased amounts of intracellular carnitine. The present study therefore investigated the effects of carnitine on glioblastoma cells in vitro. The addition of exogenous carnitine to the culture attenuated the proliferation of glioblastoma cells and increased the number of senescent cells.

Materials and methods

Cells

The murine GL261 glioblastoma cell line was provided by A. Natsume of the Department of Neurosurgery at Nagoya University (Nagoya, Japan). The cell culture was maintained in an atmosphere of 5% CO₂ and 95% humidified air at 37°C in Dulbecco’s modified Eagle’s medium (DMEM; Life Technologies, Grand Island, NY, USA) supplemented with 10% FBS (Cellgro, Manassas, VA, USA), 2 mM L-glutamine, 100 U/ml penicillin and 100 mg/ml streptomycin. Cells were grown to 80–90% confluence in 75-cm² culture flasks (Corning, Acton, MA, USA) and were subcultured at a ratio of 1:2.

Culture

GL261 cells (approximately 1x10⁶) were seeded into 60-mm dishes and cultured for 72 h in DMEM with FBS at concentrations of 1, 2 and 10%. Hyponutrition was defined as a culture condition with 1 or 2% FBS. For some of the experiments, GL261 cells were cultured for 72 h in DMEM with 10% FBS in the presence of carnitine (100 or 500 μM).

Viable cell count

Following washing with phosphate-buffered saline (PBS) to remove dead floating cells, living cells were harvested by trypsinization. Following trypan blue staining, the total number of viable cells was determined by the Vi-XR cell viability counter (Beckman Coulter, Brea, CA, USA) in triplicate.

Intracellular carnitine measurement

Following washing with PBS, GL261 cells were treated with radio-immunoprecipitation assay (RIPA) buffer (Funakoshi, Tokyo, Japan). The cell lysate was collected in a microcentrifuge tube and centrifuged at 20,000 x g for 5 min. The supernatant was assayed using the enzymatic cycling method (Kainos, Tokyo, Japan), and the carnitine concentration was determined from the amount of accumulated thio-dihydronicotinamide adenine dinucleotide (NADH).

Senescence-associated β-galactosidase (SA-β-gal) activity assay

SA-β-gal activity was measured with a β-gal staining kit (BioVision, Mountain View, CA, USA) according to the manufacturer’s instructions. Briefly, GL261 cells were washed in PBS, fixed for 10 min at room temperature with 0.5 ml fixative solution, washed and incubated overnight at 37°C with the staining solution mix. Blue staining was observed under a microscope, and the absolute number of β-gal-positive cells in a sample of 200 cells was determined.

SB203580

SB203580, a specific inhibitor of p38 mitogen-activated protein kinase (MAPK), was dissolved in dimethyl sulfoxide (DMSO) and added to the GL261 cell culture at a final concentration of 10 μM to determine its effects.

Statistical analysis

Data are expressed as the mean ± standard deviation (SD) of five independent experiments. Comparisons between two groups with one variable were made using a Tukey-Kramer test for all data, with the exception of cell counts at 48 h cultured under hyponutrition or with carnitine, which did not show a normal distribution. Instead, Dunnett’s test was used to analyze these data.

Data were analyzed using Predictive Analytics SoftWare (PASW) version 18.0.0 (SPSS Japan Inc., IBM, Tokyo, Japan). A P-value less than 0.05 was considered statistically significant.

Results

Hyponutrition attenuates GL261 cell proliferation and increases GL261 cell senescence (Fig. 1)

Figure 1.

Effect of hyponutrition on cell proliferation and SA-β-gal-positive senescence. GL261 cells (1x10⁶/dish) were seeded into 60-mm dishes and cultured in DMEM supplemented with FBS at concentrations of 1, 2 and 10%, and cultivated for 72 h. (A) Number of viable cells over time. (B) Percentage of SA-β-gal-positive cells according to FBS concentration. ^*P-value of <0.05. (C) Cytochemical staining for SA-β-gal activity of GL261 cells after cultivation for 72 h. Microphotograph shows positive (blue) cells.

The proliferation of GL261 cells was attenuated in cells cultured in DMEM supplemented with 1 and 2% FBS compared with 10% FBS (the standard concentration) for 72 h. This effect was dose-dependent. Greater numbers of SA-β-gal-positive senescent GL261 cells were found in those cultures incubated with 1 and 2% FBS than in those cultivated with 10% FBS after 72 h.

Hyponutrition increases intracellular carnitine levels (Fig. 2)

Figure 2.

Effect of hyponutrition on intracellular carnitine. GL261 cells were cultured in DMEM with FBS at concentrations of 1, 2 and 10%. After cultivation for 72 h, the cells were collected and the amount of intracellular carnitine was assessed. ^*P-value of <0.05.

Increased levels of carnitine were observed in cells cultured under conditions of hyponutrition compared with cells cultured with the standard concentration of FBS.

Carnitine attenuates cell proliferation and induces cellular senescence (Fig. 3)

Figure 3.

Effect of carnitine on cell proliferation and senescence. GL261 cells were cultured in the presence of carnitine in DMEM with 10% FBS for 72 h. (A) Viable cells. (B) Cytochemical staining for SA-β-gal activity of GL261 cells. Microphotograph shows positive (blue) cells. ^*P-value of <0.05. (C) SA-β-gal-positive cells.

Increased intracellular carnitine levels were detected in the cultured cells that demonstrated hyponutrition-induced senescence. We therefore added exogenous carnitine to the culture and examined the effects on cell proliferation and senescence. Proliferation was attenuated by carnitine in a dose-dependent manner, while increased numbers of SA-β-gal-positive cells were observed in the culture supplemented with exogenous carnitine.

SB203580 inhibits the carnitine-induced attenuation of cell proliferation (Fig. 4A)

Figure 4.

Effect of SB203580 and the result of flow cytometry for GL261 cells cultured under hyponutrition. (A) Effect of SB203580 on the proliferation of GL261 cells treated with carnitine. ^*P-value of <0.05. (B) Number of Annexin V-FITC/PI double-positive cells among the GL261 cells cultured in DMEM supplemented with 1, 2 and 10% FBS.

The addition of the specific p38 MAPK inhibitor SB203580 reversed the inhibition of GL261 cell proliferation induced by carnitine. The carnitine-induced attenuation of GL261 cell proliferation therefore appeared to be mediated by the p38 MAPK signaling pathway.

Role of apoptosis in hyponutrition-induced GL261 cell senescence (Fig. 4B)

Flow cytometry with Annexin V conjugated to fluorescein (Annexin V-FITC)/propidium iodide (PI) double staining was used to investigate whether apoptosis was involved in the attenuation of proliferation by hyponutrition. No morphological changes were observed under transmission electron microscopy and the number of apoptotic cells did not increase in 1 or 2% FBS cultures compared with the 10% culture, suggesting that apoptosis did not play a role in the hyponutrition-induced senescence.

Discussion

Carnitine is an essential substance for the β-oxidation of fatty acids in mitochondria and is recognized as an anti-aging nutrient (12,18). Several reports have shown that it acts protectively in cells and tissues against various stresses and damage, including the side effects of anticancer chemo-therapy (14–17,19). However, few studies have documented the carnitine-induced changes to cancer cells. The present study revealed, for the first time, that carnitine induces senescence in glioblastoma cells. The addition of exogenous carnitine to the culture media attenuated cell proliferation and increased the number of SA-β-gal-positive senescent cells, suggesting that carnitine promotes cellular senescence. Carnitine shows antioxidant activity in normal cells, which suggests that it plays a crucial role in the prevention of aging. However, it induces senescence in glioblastoma cells, thus it appears to have opposing effects in different target cells.

The attenuation of proliferation and the increase in SA-β-gal-positive cells induced by exogenous carnitine have been confirmed in the U87MG glioblastoma cell line (Yamada et al, unpublished data). The absence of an increase in apoptosis among glioblastoma cells cultured with carnitine also supports the theory that carnitine induces senescence. The suppression of proliferation by a recognized inhibitor of p38 MAPK, which is part of the common senescence-signaling pathway (20,21), further indicates that carnitine induces senescence in glioblastoma cells.

Treatment-induced senescence (TIS) is of interest in conventional anticancer therapy. Although initially identified in tumors following radiation or genotoxic chemotherapy (9–11), TIS might also be induced at lower drug doses, in contrast to the higher doses at which DNA damage and apoptotic responses are elicited. Temozolomide is widely used for the treatment of glioblastoma (22,23), and has been reported to induce senescence without apoptosis in melanoma cells (24). The present study demonstrated that carnitine induced senescence in glioma cells. Considering its beneficial effects on aging and the side effects of anticancer drugs, the use of carnitine in combination with chemotherapy could represent an attractive alternative therapy for glioblastoma, which currently lacks an effective treatment.

In addition to carnitine, the polyphenolic phytoalexin resveratrol, found in grapes and other foods such as nuts, has well-known effects on aging, metabolic disorders, and inflammation (25,26). Indeed, it was recently reported to induce cellular senescence in carcinoma cells, including glioblastoma cells (27). Notably, its activity increased when it was administered in combination with the senescence-inducing nutrient quercetin. Although it is not yet known how resveratrol performs in association with carnitine, combining food nutrients with chemotherapy and radiation therapy might further improve outcomes in the treatment of glioblastoma.