Mitochondrial respiratory chain is involved in insulin-stimulated hydrogen peroxide production and plays an integral role in insulin receptor autophosphorylation in neurons
© Storozhevykh et al.; licensee BioMed Central Ltd. 2007
Received: 18 April 2007
Accepted: 08 October 2007
Published: 08 October 2007
Accumulated evidence suggests that hydrogen peroxide (H2O2) generated in cells during insulin stimulation plays an integral role in insulin receptor signal transduction. The role of insulin-induced H2O2 in neuronal insulin receptor activation and the origin of insulin-induced H2O2 in neurons remain unclear. The aim of the present study is to test the following hypotheses (1) whether insulin-induced H2O2 is required for insulin receptor autophosphorylation in neurons, and (2) whether mitochondrial respiratory chain is involved in insulin-stimulated H2O2 production, thus playing an integral role in insulin receptor autophosphorylation in neurons.
Insulin stimulation elicited rapid insulin receptor autophosphorylation accompanied by an increase in H2O2 release from cultured cerebellar granule neurons (CGN). N-acetylcysteine (NAC), a H2O2 scavenger, inhibited both insulin-stimulated H2O2 release and insulin-stimulated autophosphorylation of insulin receptor. Inhibitors of respiratory chain-mediated H2O2 production, malonate and carbonyl cyanide-4-(trifluoromethoxy)-phenylhydrazone (FCCP), inhibited both insulin-stimulated H2O2 release from neurons and insulin-stimulated autophosphorylation of insulin receptor. Dicholine salt of succinic acid, a respiratory substrate, significantly enhanced the effect of suboptimal insulin concentration on the insulin receptor autophosphorylation in CGN.
Results of the present study suggest that insulin-induced H2O2 is required for the enhancement of insulin receptor autophosphorylation in neurons. The mitochondrial respiratory chain is involved in insulin-stimulated H2O2 production, thus playing an integral role in the insulin receptor autophosphorylation in neurons.
Accumulated evidence suggests that hydrogen peroxide (H2O2) generated in cells during insulin stimulation plays an integral role in insulin receptor signal transduction [1–4]. Specific molecular targets of H2O2 identified to date include the insulin receptor kinase [5–7], protein tyrosine phosphatases (PTP) [8–11], and the lipid phosphatase PTEN , whose activity is modified via oxidative reactions with H2O2. Two distinct insulin-sensitive cellular H2O2 sources have been identified. A membrane-bound NADPH-oxidase is involved in insulin-induced H2O2 production in adipocytes [13–17] and vascular smooth muscle cells [18, 19]. The mitochondrial respiratory chain is implicated in insulin-induced H2O2 generation in liver and heart [20, 21]. There are experimental data that insulin-induced reactive oxygen species (ROS) and H2O2 play a role in the activation of insulin signaling in neuroblastomas [12, 22]. However, the role of insulin-induced H2O2 in neuronal insulin receptor activation and the origin of insulin-induced H2O2 in neurons remain unclear.
The aim of the present study is to test the following hypotheses (1) whether insulin-induced H2O2 is required for insulin receptor autophosphorylation in neurons, and (2) whether mitochondrial respiratory chain is involved in insulin-stimulated H2O2 production, thus playing an integral role in insulin receptor autophosphorylation in neurons.
Insulin-induced H2O2is required for the enhancement of the insulin receptor autophosphorylation in neurons
To determine whether insulin-induced H2O2 is involved in the enhancement of insulin receptor autophosphorylation, we next studied the effects of N-acetylcysteine (NAC), a H2O2 scavenger, on the insulin-stimulated autophosphorylation of the insulin receptor in CGN. As shown in Figure 1A, the pre-incubation of CGN with NAC abolished the insulin-stimulated H2O2 release from cells to undetectable levels (<7 nmol/L), indicating that NAC is a potent scavenger of insulin-induced H2O2 under these experimental conditions. Figure 1B shows that pre-incubation of CGN with NAC resulted in the significant inhibition of insulin-stimulated insulin receptor autophosphorylation (P < 1e-6 vs. insulin). These results suggest that insulin-induced H2O2 is required for the enhancement of insulin receptor autophosphorylation in neurons.
The mitochondrial respiratory chain is involved in insulin-stimulated H2O2production, thus playing an integral role in the insulin receptor autophosphorylation in neurons
Insulin signaling requires the autophosphorylation of the insulin receptor kinase at tyrosine residues in the activation loop of the kinase domain [23–28]. Upon autophosphorylation, the receptor undergoes a major conformational change resulting in unrestricted access of protein substrates and ATP to the kinase active site and an approximate two-order increase in kinase activity [29–31]. In the present study, we demonstrate that N-acetylcysteine, the H2O2 scavenger, inhibits both insulin-stimulated H2O2 generation and insulin-stimulated insulin receptor autophosphorylation in CGN. These results suggest that insulin-induced H2O2 is required for the enhancement of insulin receptor autophosphorylation in neurons.
We found that mitochondrial respiratory chain is involved in insulin-stimulated H2O2 production, thus playing an integral role in insulin receptor autophosphorylation in neurons. Mitochondrial respiration is a major cellular source of H2O2 that may convert up to 2% of total oxygen consumption into H2O2 in state 4 respiration (oxygen consumption in the absence of ADP) with succinate as a respiratory substrate . Among other respiratory substrates, the complex II substrate succinate provides the highest rates of mitochondrial H2O2 generation in brain mitochondria . Molecular mechanisms of H2O2 production in mitochondria are the subject of intense ongoing research. The respiratory chain reduces oxygen to superoxide anion, which dismutates to H2O2 spontaneously or by the action of superoxide dismutase . Although mitochondria produce H2O2 in all metabolic states, high mitochondrial membrane potential (ΔΨ) characteristic to the resting (State 4) respiration significantly promotes H2O2 generation [33, 35]. Substances that decrease (ΔΨ), e.g. malonate and FCCP, inhibit H2O2 generation [33, 35–37]. In the present study, we demonstrate that inhibitors of respiratory chain-mediated H2O2 production, malonate and the protonophore FCCP, inhibit both insulin-induced H2O2 generation and insulin-stimulated receptor autophosphorylation in neurons. The respiratory substrate succinate, taken in form of dicholine salt of succinic acid, significantly enhances the stimulatory effect of suboptimal insulin concentration on insulin receptor autophosphorylation. These results, together with our observations that the H2O2 scavenger (NAC) inhibited both insulin-stimulated H2O2 generation and insulin receptor autophosphorylation, suggest that the mitochondrial respiratory chain is involved in insulin-stimulated H2O2 production, thus playing an integral role in insulin receptor autophosphorylation in neurons.
Our prior studies provide evidence that a transient activation of succinate dehydrogenase (SDH) is a mode by which insulin increases the rate of mitochondrial H2O2 generation [20, 21]. Earlier, it has been demonstrated that insulin exhibits an immediate stimulatory effect on oxidation of [2,3-14C]-succinate in mitochondrial Krebs cycle, which is almost maximal within 30 sec [38, 39]. The results of the present study are consistent with these findings. Malonate, a competitive inhibitor of succinate dehydrogenase, inhibits both insulin-stimulated H2O2 production and the receptor phosphorylation in neurons, indicating a role of SDH in these processes. Although signaling pathways regulating insulin-stimulated SDH activation remain to be elucidated, these pathways seem to be distinct from those induced by autophosphorylated form of insulin receptor. The reason for it is that insulin-stimulated H2O2 burst enhances the autophosphorylation of the insulin receptor, since inhibitors of insulin-stimulated H2O2 generation abolish the receptor autophosphorylation.
A large body of evidence has accumulated that impairments in cerebral insulin receptor signaling may contribute to age-related cognitive decline and Alzheimer's disease [40–43]. In this context, our findings identify mitochondrial respiratory chain as a potential pharmacological target for the treatment of disorders associated with dysfunctional insulin receptor signal transduction in neurons.
Results of the present study suggest that insulin-induced H2O2 is required for the enhancement of insulin receptor autophosphorylation in neurons. The mitochondrial respiratory chain is involved in insulin-stimulated H2O2 production, thus playing an integral role in insulin receptor autophosphorylation in neurons.
PhosphoDetect™ Insulin Receptor (pTyr1162/1163) ELISA kit and Insulin Receptor (β-Subunit) ELISA Kit were from Calbiochem. Dicholine salt of succinic acid was prepared by a reaction of succinic acid with choline base in the Russian Scientific Center on Drug Safety (Staraya Kupavna, Moscow region). Other materials were purchased from Sigma, ICN, Gibco, Biosource, Invitrogen, or Acros.
Cerebellar granule neurons were prepared from 7- to 8-day-old Wistar rats as described [44, 45]. Cerebellum was dissected and placed in ice-cold Ca2+/Mg2+-free Hanks' buffered salt solution (HBSS) without Phenol Red (Gibco). After mincing the tissue with fine scissors, the tissue was placed in Ca2+/Mg2+-free HBSS with Phenol Red and 0.1% trypsin for 15 min at 36°C. Trypsin was inactivated by washing with normal HBSS. Cells were dissociated by trituration and pelleted in HBSS. Then, the cells were resuspended in Neurobasal Medium (Gibco) supplemented with B-27 Supplement (Gibco), 20 mmol/L KCl, GlutaMax (Gibco) and penicillin/streptomycin and plated with density 5 × 106 cells/ml onto 35 mm × 10 mm sterile cell culture dishes which had been previously coated with poly-D-lysine. The cultures were maintained at 36°C in a humidified atmosphere of 5% CO2 and 95% air and fed with supplemented Neurobasal Medium. Cultures were treated on day 3 with 10 μmol/L cytosine arabinoside (Sigma) for 24 h to prevent glial proliferation. Neurons at 7 to 9 days were used for experiments.
Measurement of hydrogen peroxide
H2O2 release from CGN cultures for 1 min was measured fluorimetrically employing the cell-impermeable Amplex Red dye (Invitrogen) in the presence of horseradish peroxidase (Sigma). With Amplex Red, it is possible to perform reliable measurements of H2O2 production by brain mitochondria under physiologically realistic conditions . CGN cultures were pre-incubated for 30 min in Hepes-buffered salt solution (145 mmol/L NaCl, 5.6 mmol/L KCl, 1.8 mmol/L CaCl2, 1 mmol/L MgCl2, 20 mmol/L HEPES, and 5 mmol/L glucose) at pH 7.4 and then exposed to insulin (100 nM) or vehicle. H2O2 release from CGN cultures for 1 min was measured. Where indicated, NAC (5 mmol/L) was added 30 min before the insulin stimulation. Malonate (2 mmol/L) or FCCP (0.5 μmol/L) were added 5 min before the insulin stimulation. In these experiments, the incubation medium was supplemented with 2 μmol/L Amplex Red and 4 IU/ml horseradish peroxidase. Fluorescence was measured with an epifluorescent inverted microscope Axiovert 200 (Carl Zeiss, Germany) equipped with a 20× fluorite objective using excitation at 550 ± 10 nm and fluorescence detection at 610 ± 30 nm. All imaging data were collected and analyzing using the Metafluor 6.1 software (Universal Imaging Corp., USA). Standard curves obtained by adding known amounts of H2O2 to the assay medium were linear up to 1500 nmol/L. Fluorescence values were converted to H2O2 values using these standard curves. The calculated detection limit of the assay was 7 nmol/L. Data were normalized by cell density and expressed as nmol/L H2O2.
Insulin receptor phosphorylation assay
Amounts of double phosphorylated β-subunit of insulin receptor (pYpY-IR) were measured by PhosphoDetect™ insulin receptor (pTyr1162/1163) ELISA kit (Calbiochem) suitable for studies with rat insulin receptor. CGN cultures were pre-incubated for 30 min in Hepes-buffered salt solution (145 mmol/L NaCl, 5.6 mmol/L KCl, 1.8 mmol/L CaCl2, 1 mmol/L MgCl2, 20 mmol/L HEPES, and 5 mmol/L glucose) at pH 7.4 and then exposed to insulin (100 nM) or vehicle for 20 min (the incubation time and the insulin concentration were determined from a time and dose response curves respectively; data not shown). Where indicated, NAC (5 mmol/L) was added 30 min before the insulin stimulation. Malonate (2 mmol/L) or FCCP (0.5 μmol/L) were added 5 min before the insulin stimulation. The experiment was terminated by removing the medium, washing with ice-cold PBS, and adding 120 μL per dish cell lysis buffer (Biosource) supplemented with 1 mmol/L PMSF, 50 mmol/L protease inhibitor set III (Sigma), and 2 mmol/L sodium ortovanadate as the inhibitor of tyrosine phosphatases at 4°C for 20 min. Lysates were centrifuged at 12,000 rpm at 4°C for 12 min. In each CGN lysate, pYpY-IR amounts were measured as described by the manufacturer's manual. Obtained values were normalized to total amounts of insulin receptor β-subunit (IR) measured by insulin receptor (β-subunit) ELISA kit (Calbiochem). The results are expressed as a percentage of the response produced to 100 nmol/L insulin.
Data were analyzed for statistical significance by one-way analysis of variance (ANOVA). Values are given as means ± SD. Differences were considered significant at P < 0.05.
cerebellar granule neurons
dicholine salt of succinic acid
Hanks' buffered salt solution
phosphatase and tensin homolog
protein tyrosine phosphatases
This work was funded by Biosignal Ltd., Moscow, Russia.
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