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Redox effector protein-1 (Ref-1) plays an essential role in DNA repair and redox regulation of several transcription factors. In the present study, we examined the role of Ref-1 in maintaining the redox status and survivability of adult cardiac stem cells challenged with a subtoxic level of H2O2 under inhibition of Ref-1 by RNA interference. Treatment of cardiac stem cells with a low concentration of H2O2 induced Ref-1–mediated survival signaling through phosphorylation of Akt. However, Ref-1 inhibition followed by H2O2 treatment extensively induced the level of intracellular reactive oxygen species (ROS) through activation of the components of NADPH oxidase, like p22phox, p47phox, and Nox4. Cardiac differentiation markers (Nkx2.5, MEF2C, and GATA4), and cell death by apoptosis were significantly elevated in Ref-1 siRNA followed by H2O2-treated stem cells. Further, inhibition of Ref-1 increased the level of p53 but decreased the phosphorylation of Akt, a molecule involved in survival signaling. Treatment with ROS scavenger N-acetyl-L-cysteine attenuated Ref-1 siRNA-mediated activation of NADPH oxidase and cardiac differentiation. Taken together, these results indicate that Ref-1 plays an important role in maintaining the redox status of cardiac stem cells and protects them from oxidative injury–mediated cell death and differentiation. Antioxid. Redox Signal. 11, 589–599.
Reactive oxygen species (ROS), including H2O2, superoxide anions, and hydroxyl radicals, are generated intracellularly though various sources including mitochondria and plasma membrane–associated oxidases like nicotinamide adenine dinucleotide phosphate (NADPH) oxidases (41). Several receptor-mediated generations of ROS have been shown to regulate many cellular functions such as growth inhibition, cytotoxicity, apoptosis, mitogenesis, differentiation, and cell hypertrophy (41).
Numerous studies have shown ROS as important chemical mediators in the regulation of cell growth and differentiation (15, 33). Oxidative stress resulting from various ROS-generating agents induces differentiation in a wide variety of cell types that include neuronal (23), monocytic (52), erythroid (9), osteoclast (43), and cardiac cells (39). The cellular redox state and the activity of antioxidant enzyme superoxide dismutase (SOD) are greatly altered during the differentiation of many types of cells (5, 9). Consequently, these changes bring about an increased rate of oxidant production, which cause induction of gene expression, leading to cell differentiation (1). This indicates that the cellular environment becomes more pro-oxidizing during differentiation (1).
The intracellular redox state regulates cellular signaling events by controlling many upstream and downstream molecules (17, 18, 22, 50). Normally, the intracellular redox state in the cell is maintained through many enzymatic and nonenzymatic molecules like SOD, catalase, redox effector factor-1 (Ref-1), thioredoxin, etc. Ref-1 is sensitive to changes in redox status and stimulates a rapid adaptive response to subtoxic level of variety of ROS induced by H2O2, superoxide anion and gamma rays (36). Injuries resulting from ROS generated by UV-radiation or H2O2 treatment remarkably induced the levels of Ref-1, which corresponds with the increase in endonuclease and redox activities of Ref-1 (45). ROS may regulate Ref-1 via activation of several transcription factors involved in oxidative stress such as AP-1, CREP, ATF, and p53 (16). Ref-1 facilitates the DNA binding and activation of transcription factors through reduction of a cysteine residue (16, 28). It also has been shown that ROS affects the functions of Ref-1 by altering the redox status of Ref-1. Oxidative stress or replacement of cysteine in Ref-1 severely affects both DNA repair and the redox regulation activities of Ref-1 (28, 48). Ref-1 deficiency caused many cells to undergo apoptosis induced by ionizing radiation, alkylating agents, and oxidative stress (3). Moreover, Ref-1 was shown to be associated with differentiation in the developing retina (10, 11).
The present study was designed to examine the role of Ref-1 in maintaining the redox status and survivability of adult cardiac stem cells under subtoxic levels of H2O2 treatment. To study the role of Ref-1, Ref-1 expression was blocked in cardiac stem cells by treating them with Ref-1–specific small interference RNA (siRNA). We found that subtoxic levels of hydrogen peroxide under inhibition of Ref-1 caused excessive production of ROS via activation of NADPH oxidase, leading to cardiac differentiation and cell death by apoptosis in adult cardiac stem cells. These results indicate that Ref-1 plays an important role in maintaining the redox status of cardiac stem cells and protects them from oxidative injury–mediated cell death and differentiation.
Control and Ref-1 siRNAs were obtained from Santa Cruz Biotechnology, Santa Cruz, CA. Primary antibodies of α-actinin and p53 were obtained from Cell Signaling Technology (Danvers, MA). Ref-1, Akt, p-Akt, and GAPDH antibodies were obtained from Santa Cruz Biotechnology. Redox-sensitive dye 5-(and−6)-chloromethyl-2′,7′-dichlorodihydrofluorescein diacetate acetyl ester (CM-H2DCFDA), and fluorescent conjugated secondary antibodies such as Alexa Fluor 488 and Alexa Fluor 594, and the nuclear stain To-Pro 1 iodide were obtained from Molecular Probes Inc. (Eugene, OR). N-acetyl-l-cysteine and H2O2 were obtained from Sigma (St. Louis, MO).
Clonogenic adult cardiac stem cells were a generous gift of Dr. Piero Anversa, and the cells were grown in modified neural stem cell medium (mNSCM), as mentioned earlier (6), at 37°C in a humidified chamber with 5% CO2. Cells were not allowed to grow beyond 70% confluency. Cells were treated with H2O2 at a 10μM concentration for 24h. Treatment with N-acetyl-L-cysteine at 1mM concentration was performed 20min before H2O2 treatment.
To each well of a six-well tissue culture plate, 2×105 cells were seeded with 2ml growth medium. Plates were incubated for 18–24h until 60–70% confluency was reached. Ref-1 and control siRNAs were used at the final concentration of 25 nM. siRNA transfection was done by using TransPass R2 Transfection Reagent (New England BioLabs), as mentioned in the kit. Cells were grown in complete growth medium for an additional period of 24h. Follow-up experiments like treatment with H2O2 and N-acetyl-L-cysteine were performed at the end of the 24-h incubation period.
At the end of experimentation, cells were washed with PBS and further treated with CM-H2DCFDA at 5μM concentration and incubated at 37°C incubator for 30min. At the end of incubation, cells were washed with PBS and observed immediately under a fluorescent confocal microscope, Zeiss LSM 510 (Thornwood, NY). Fluorescence intensity was measured by using Metamorph 7.2 software (Molecular Devices, Sunnyvale, CA) from 10 random confocal images of each group.
Total RNA was isolated from cells with TRIzol reagent (Invitrogen, Carlsbad, CA), according to the manufacturer's instructions, and dissolved in 20μl of DEPC-treated water. Total RNA concentration was determined by measuring the optical density at 260nm. Reverse transcription and polymerase chain reaction (RT-PCR) was performed with RETROscript (Ambion, Austin, TX), according to the manufacturer's instructions. RNA, 2μg, was used to prepare cDNA. The following primers were used in our study.
The PCR products were visualized on a UV-transilluminator and digitalized after electrophoresis on 2% agarose gel containing ethidium bromide.
At the end of experimentation, cells were washed with phosphate-buffered saline and lysed in RIPA buffer (Boston Bioproducts, Boston, MA) supplemented with protease inhibitor cocktail (Sigma) and a phosphatase inhibitor (100mM sodium orthovanadate) on ice for 1h. Lysate was centrifuged at 8,000g for 10min at 4°C, and the supernatant was mixed with sample buffer and heated at 95°C for 5min. Thus, prepared cell lysates were used for Western immunoblotting.
Proteins were separated in SDS-PAGE and transferred to nitrocellulose filters. Filters were blocked in 5% nonfat dry milk and probed with a primary antibody overnight. Primary antibodies such as α-actinin, p53, and GAPDH were used at 1:500 dilutions. Protein bands were identified with horseradish peroxidase conjugated secondary antibody (1:2,000 dilution) and Western Blotting Luminol Reagent (Santa Cruz Biotechnology). The resulting blots were digitized, subjected to densitometric scanning by using a standard NIH Image program, and normalized against loading control.
Cells were washed with phosphate-buffered saline (PBS) and fixed by using 4% paraformaldehyde solution for 20min. After a wash with PBS, the slides were blocked with Powerblock (BioGenex, San Ramon, CA) for 10min. Slides were washed with PBS and incubated with primary antibody (1:25 dilution) in PBS containing 1% BSA for 60min (overnight incubation for α-actinin). Slides were washed and incubated with fluorescein-conjugated secondary antibody (1:500 dilution) in the dark for 45min. Nuclear staining was done with To-Pro 1 iodide (1:500 dilution) for 45min in the dark. The slides were washed, covered with mounting medium, and examined under a fluorescence microscope. Confocal microscopic images were obtained by using a Zeiss LSM 510 (Thornwood, NY) confocal laser scanning microscope with×40 1.3 oil-immersion objective by simultaneous recording in the 488 λ, 530 λ, or 560 λ channels, or a combination of these, as appropriate.
Cell-death analysis was performed for the release of the cell-death marker enzyme lactate dehydrogenase (LDH) by using the spent culture medium as the substrate with the LDH Cytotoxicity Assay kit (Cayman Chemical Company, Ann Arbor, MI) as instructed.
Immunohistochemical detection of apoptotic cells was carried out with terminal deoxynucleotidyl transferase nick-end labeling (TUNEL) by using the DeadEnd Fluorometric TUNEL System (Promega, Madison, WI). Cells were fixed by immersion in 4% paraformaldehyde, and then stored in 4°C in PBS. The TUNEL experiment was done according to the manufacturer's instructions. The fluorescence staining was viewed with a fluorescence microscope (Axioplan2 Imaging; Carl Zeiss Microimaging, Inc., New York) at 520±20nm for the green fluorescence of fluorescein and at>620nm for the red fluorescence of propidium iodide. The number of apoptotic cells was counted and expressed as a percentage of the total myocyte population.
All values were expressed as the mean±standard error of the mean (SEM). Analysis-of-variance test, followed by Bonferroni's correction, was first carried out to test for any differences between the mean values of all groups. If differences were established, the values of the treated groups were compared with those of the control group with a modified t test. The results were considered significant at p<0.05.
A pro-oxidative environment has been shown to induce differentiation in many cell types (15, 33). Treatment with H2O2 alters the cellular redox status and induces differentiation in many cell types (9, 40, 43). Because Ref-1 plays an important role in the regulation of cellular redox status, we examined the role of Ref-1 in the regulation of cellular redox status and its effect on the differentiation of adult cardiac stem cells when the cells were challenged with pro-oxidative treatment with hydrogen peroxide. Adult cardiac stem cells were treated with various concentrations of hydrogen peroxide (10, 25, 50, 100, and 200μM) for different time periods (30min, 60min, 120min, 24h, and 48h). We found that Ref-1 protein expression was induced by 10μM concentration of H2O2 at two different time points [i.e., 120min and 24h (data not shown)]. However, cardiac differentiation markers like GATA4 and MEF2C were found to be induced more during the 24-h time period (data not shown). In subsequent experiments, we examined the role of Ref-1 by challenging cells with a 10μM concentration of H2O2 for 24h under the inhibition of Ref-1 by RNA interference.
Our Western immunoblotting results (Fig. 1A) show that treatment with Ref-1 siRNA followed by H2O2 significantly attenuated the H2O2-mediated induction of Ref-1 compared with control siRNA treatment. Ref-1 siRNA treatment alone did not show any significant changes in the alteration of Ref-1 protein expression when compared with normal cells (Fig. 1A). Further, confocal microscopic analysis (Fig. 1B) showed that the expression of Ref-1 is significantly attenuated when the cells are treated with Ref-1 siRNA followed by H2O2, compared with other groups.
To examine the cellular redox status, the cells were treated with cell-permeable dye CM-H2DCFDA, which itself is a nonfluorescent dye, but on entering the cell, it is cleaved by intracellular esterases and oxidized to a fluorescent compound by intracellular pro-oxidants. The fluorescence intensity is directly proportional to the level of ROS present in the cell. Our confocal microscopic analyses showed that the fluorescence intensity was slightly higher on treatment with H2O2 compared with normal cells (Fig. 1C–D). However, Ref-1 siRNA followed by H2O2 treatment massively increased the level of intracellular ROS compared with control siRNA followed by H2O2 treatment (Fig. 1C–D). Ref-1 siRNA treatment alone did not show any significant changes in the alteration of ROS production when compared with normal cells (data not shown). These results indicate that ROS production was significantly increased on challenging the cardiac stem cells with pro-oxidant under inhibition of Ref-1.
ROS-mediated intracellular signaling events are triggered through the activation of NADPH oxidase components like p22phox, p47phox, and NOX4, leading to the production of superoxide and affecting various cellular functions (8). In the present study, we tested whether Ref-1 inhibition-mediated induction of ROS activates NADPH oxidase. Our RT-PCR analyses show that NOX4, p22phox, and p47phox were slightly but insignificantly induced by hydrogen peroxide treatment alone at the end of the 24-h treatment period (Fig. 2). However, Ref-1 siRNA followed by H2O2 treatment significantly induced the expression of NOX4, p22phox, and p47phox compared with control siRNA followed by H2O2 (Fig. 2). Ref-1 siRNA treatment alone did not show any significant changes in the expression of NOX4, p22phox, and p47phox when compared with normal cells (data not shown). These results show that Ref-1 inhibition–mediated induction of ROS further activates NADPH oxidase components in cardiac stem cells.
ROS plays an essential role in the induction of differentiation in many cell types including neuronal (23), monocytic (52), erythroid (9), osteoclast (43), and cardiac cells (39). We tested whether the ROS produced through Ref-1 inhibition mediates cardiac differentiation in adult cardiac stem cells. RT-PCR analyses showed that cardiac differentiation markers like Nkx2.5, MEF2C, and GATA4 were slightly but insignificantly induced on treatment with H2O2 alone (Fig. 3A). However, Ref-1 siRNA followed by H2O2 treatment significantly induced Nkx2.5, MEF2C, and GATA4 compared with control siRNA followed by H2O2 treatment (Fig. 3A). Further, our Western immunoblotting results showed that the expression of another cardiac differentiation marker protein, α-sarcomeric actinin, was slightly but not significantly induced by H2O2 treatment alone, but Ref-1 siRNA followed by H2O2 treatment significantly induced the expression of cardiac sarcomeric actinin compared with control siRNA followed by H2O2 treatment (Fig. 3B). Ref-1 siRNA treatment alone did not show any significant changes in the expression of these differentiation markers when compared with normal cells (data not shown). Moreover, our confocal microscopic images show coexpression of NOX4 and the differentiation marker Nkx2.5 in cells treated with Ref-1 siRNA followed by H2O2 (Fig. 3C). Furthermore, coexpression of Nkx2.5 and α-sarcomeric actinin was found in cardiac stem cells under inhibition of Ref-1 and H2O2 treatment (Fig. 3D). These results clearly indicate the induction of cardiac differentiation on treating cells with Ref-1 siRNA followed by H2O2.
Cell differentiation is mostly accompanied by cell death by apoptosis in many cell types (37, 38). In the present study, the occurrence of cell death is confirmed by the release of cell-death marker enzyme LDH into the culture medium. Figure 4A shows that the release of LDH into the culture medium was significantly increased when the cells were treated with Ref-1 siRNA and H2O2 compared with other groups of cells. Furthermore, TUNEL apoptotic analysis show that Ref-1 siRNA followed by H2O2 treatment significantly increased the number of apoptotic cells compared with other groups of cells (Fig. 4B–C). Ref-1 siRNA treatment alone did not show any significant changes in LDH release and the percentage of apoptotic cells when compared with normal cells (data not shown). These results indicate that the induction of cardiac differentiation and cell death occurred simultaneously when the cells were treated with Ref-1 siRNA followed by H2O2.
Tumor-suppressor protein p53 plays an inevitable role in cell-cycle arrest, apoptosis, and differentiation (2). Moreover, p53 also is shown to be regulated by Ref-1 (21). In the present study, we examined the role of p53 protein under Ref-1 inhibition with low levels of H2O2 treatment. Our Western immunoblotting and RT-PCR analysis showed that p53 protein was expressed at high levels in normal cardiac stem cells. However, treatment with hydrogen peroxide decreased the level of p53 protein in the total cell lysate compared with normal cells (Fig. 5A and B). Conversely, Ref-1 siRNA treatment followed by H2O2 significantly increased the level of p53 protein compared with normal cell levels (Fig. 5A and B). Akt activation by serum stimulation was shown to inhibit p53; however, proapoptotic stimuli–induced p53 was shown to inhibit the activation of Akt (4, 16). Based on these data, in the present study, we examined the activation of Akt, which is known as a molecule involved in survival signaling. Our Western immunoblotting analysis (Fig. 5A) showed that the phosphorylation of Akt (i.e., activation of Akt) was induced after treating cells with H2O2, but H2O2-induced activation of Akt was almost completely abolished by Ref-1 siRNA treatment as compared with control siRNA treatment (Fig. 5A). Ref-1 siRNA treatment alone did not show any significant changes in the expression of p53 and the phosphorylation of Akt when compared with normal cells (data not shown). These results, in accordance with previous studies (4, 16), show that phosphorylation of Akt is negatively correlated with the level of p53. Our results indicate that a low level of H2O2 treatment–induced survival signaling is attenuated by Ref-1 siRNA treatment, leading to the increased level of p53, which may play an important role in the Ref-1 siRNA-mediated induction of cardiac apoptosis and differentiation.
In the present study, we found that H2O2 treatment under Ref-1 inhibition increased the level of intracellular ROS, which corroborates the induction of cardiac differentiation and apoptosis. To test the role of ROS in the Ref-1 siRNA-mediated induction of differentiation, the cells were pretreated with ROS scavenger N-acetyl-L-cysteine (1mM) 20min before treating the cells with H2O2. Our RT-PCR results show that treatment with N-acetyl-L-cysteine significantly attenuated the Ref-1 siRNA treatment–mediated induction of NADPH oxidase components such as p22phox, p47phox, NOX4, and cardiac transcription factors like Nkx2.5, GATA4, and MEF2C (Fig. 6). These results clearly indicate that ROS produced under Ref-1 inhibition and H2O2 treatment in cardiac stem cells play an essential role in the induction of cardiac differentiation.
The salient finding of the present study is that subtoxic level of H2O2 treatment under inhibition of Ref-1 caused excessive production of ROS via activation of NADPH oxidase, leading to cardiac differentiation and cell death by apoptosis in adult cardiac stem cells.
Ref-1 protein has two major functions: (a) repairing DNA base-pair excision produced through either oxidative damage or DNA glycosylases; and (b) redox regulation of many transcription factors like AP1, HIF1α, NF-κB, and p53 (14). In addition to these two major functions, Ref-1 was shown to suppress intracellular oxidative stress and apoptosis through modulation of Rac1-regulated NADPH oxidase (3, 46). Ref-1 promotes survival of neuronal cells from oxidative stress–induced injury (46), and the increased level of Ref-1 is associated with survival of cells during cold injury–induced brain lesions (31). Moreover, depletion of Ref-1 renders cells more sensitive to hyperoxia (47). Loss of Ref-1 was shown to precede DNA fragmentation in apoptotic neurons (49). Furthermore, Ref-1 was found to be associated with differentiation in developing retina (10, 11), and Ref-1 immunoreactivity was decreased with hippocampal development (10).
Stem cells in organs are usually sheltered in specialized structures called niches (i.e., stable microenvironments that control stem cell behavior) (44). A stem cell niche provides a microenvironment that preserves the survival and replication potential of stem cells (42). Recently, it was shown that ROS play a major role in induction of the exit of hematopoietic stem cells from the niche in bone marrow (20). A delicate balance between intracellular oxidizing and reducing equivalents allows ROS to function as second messengers in signaling cascades involved in cell proliferation and differentiation (18, 41). Low concentrations of hydrogen peroxide were shown to induce components of NADPH oxidase and cardiac transcription factors like Nkx2.5, MEF2C, and GATA4 in mouse embryonic stem cells (26). A cardiac-specific gene regulatory network has revealed that MEF2C, Nkx2.5, and GATA4 proteins are vital transcriptional regulators for the development of heart cells (7). The role of NADPH oxidase and NOX4 in the regulation of differentiation of mouse embryonic stem cells has been documented (3, 26). Downregulation of NOX4 caused suppression of cardiogenesis, but this was reversed by treatment with a low concentration of hydrogen peroxide (26). In our study, when the cells were treated with hydrogen peroxide at 10μM concentration, we found a slight but insignificant activation of NADPH oxidase components like p22phox, p47phox, and Nox4, leading to a slight but insignificant induction of cardiac differentiation markers like Nkx2.5, MEF2C, and GATA4. Moreover, the high proliferative capacity of murine embryonic stem cells was shown to be closely correlated with the high activity of different glycolytic enzymes, elevated glycolytic flux, and low mitochondrial oxygen consumption (25). In leukemic cells, glucose transport is activated by stem cell factor and H2O2, suggesting a potential role for ROS in leukemia proliferation (29). NADPH oxidase plays an important role in promoting the proliferation of skeletal muscle precursor cells (30). Long-term self-renewing hematopoietic stem cells (HSCs) have low levels of intracellular ROS. However, when intracellular ROS levels become excessive, they cause senescence or apoptosis, resulting in a failure of HSC self-renewal (32). Genes that are involved in either DNA-damage responses or longevity-related signaling are shown to play a role in the maintenance of the HSC self-renewal (32).
Adult cardiac stem cells treated only with Ref-1 siRNA showed a slight but not significant increase in the level of intracellular ROS (data not shown), but further treatment with 10mM H2O2 for 24h (under Ref-1 inhibition) induced the production of ROS compared with control siRNA-treated cells (Fig. 1C and D). This ROS production in Ref-1 siRNA-treated cells corresponded to the significant increase in the mRNA levels of NADPH oxidase components p22phox, p47phox, and NOX4. Moreover, elevated levels of ROS and NADPH oxidase components in Ref-1 siRNA-treated cells was further accompanied by an enhanced level of cardiac differentiation markers Nkx2.5, MEF2C, GATA4, and a-sarcomeric actinin. To validate the role of ROS in the induction of cardiac differentiation in our study, we treated cardiac stem cells with antioxidant N-acetyl-l-cysteine before treating them with H2O2. N-Acetyl-L-cysteine treatment abolished the Ref-1 siRNA-mediated induction of NOX4, p22phox, p47phox, and cardiac transcription factors Nkx2.5, MEF2C, and GATA4. Our results are in accordance with those of Buggisch et al. (8), who found that ROS and NADPH oxidase–mediated signaling cascades are involved in the proliferation and differentiation of embryonic stem cells. Furthermore, a role for phosphatidylinositol-3-kinase has been identified in ROS-mediated cardiac differentiation of embryonic stem cells (39).
Embryonic stem cell differentiation could recapitulate the in vivo differentiation process, including the occurrence of apoptosis accompanying differentiation (37, 38). Tumor-suppressor protein p53 regulates the cell-cycle checkpoint at G1-S phase transition, differentiation, and induces cell apoptosis. p53 was shown to be involved in the simultaneous induction of apoptosis and differentiation in primary granulose cells (24), neurons, and oligodendrocytes (13). A high level of p53 was shown to induce apoptosis, whereas low levels caused cell-cycle arrest (12). Undifferentiated embryonic stem cells express high levels of p53, followed by a decrease in the level of p53 as differentiation proceeds (2, 37, 38). The addition of retinoic acid, a physiologic regulator of embryonic development, to 8 to 10 days of differentiating murine embryonic stem cells caused an increase the level of p53 followed by accelerated neural differentiation and apoptosis (38). The basal level of p53 functions as an antioxidant, whereas hyperphysiologic levels of p53 behave as a prooxidant (27). p53 was shown to be regulated by both redox-dependent and redox-independent mechanisms (14). Ref-1 was found to be a potent activator of p53 (21). Activation of p53 plays an important role in copper- and zinc-induced generation of ROS, and activation of downstream targets of p53 like PIG3 and Bax leads to increased generation of ROS and apoptosis in epithelial cells (34). Induction of endogenous p53 was found to be associated with differentiation in mouse cultured keratinocytes (51), mouse embryonic stem cells (53), and hematopoietic and muscle cells (19). Taken together, these findings indicate that p53 plays an important role in determining the fine balance between growth, differentiation, and cell death.
In our study, when the cardiac stem cells were treated with low concentrations of H2O2, the level of p53 was decreased more than normal cellular levels. At the same time, H2O2 treatment increased the activation of survival kinase Akt and led to the protection of cells from oxidative injury–mediated apoptosis and differentiation (Fig. 7). Ref-1 siRNA followed by H2O2 treatment almost completely abolished the activation of survival-signaling molecule Akt; and at the same time, the level of p53 was significantly higher than normal levels, leading to enhanced levels of ROS production and ROS-mediated cell death and differentiation (Fig. 7). These results are in accordance with previous findings (4, 16), in which survival signaling–mediated activation of Akt inhibited p53, and proapoptotic stimuli–induced p53 inhibited Akt.
In conclusion, our results show that inhibition of Ref-1 followed by a low level of H2O2 treatment increased the intracellular level of ROS and p53, leading to the induction of cardiac differentiation and cell death by apoptosis in adult cardiac stem cells. Further, these results imply that Ref-1 plays an important role in maintaining the redox status of cardiac stem cells and protects them from oxidative injury–mediated cell death and differentiation.
This study was supported in part by NIH HL 34360, HL22559, and HL 33889. The authors have no conflicting financial interests.
CM-H2DCFDA, 5-(and-6)-chloromethyl-2′,7′-dichlorodihydrofluorescein diacetate, acetyl ester RT-PCR, reverse transcription and polymerase chain reaction; GAPDH, glyceraldehyde 3-phosphate dehydrogenase; HSC, hematopoietic stem cells; LDH, lactate dehydrogenase; NADPH, nicotinamide adenine dinucleotide phosphate; PBS, phosphate-buffered saline; ROS, reactive oxygen species; SEM, standard error of the mean; siRNA, small interference RNA; SOD, superoxide dismutase; TUNEL, terminal deoxynucleotidyl transferase nick-end labeling.
No competing financial interests exist.