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发表于 2009-4-21 13:48 |只看该作者 |倒序浏览 |打印

作者：Douglas V. Cancherini, Leonardo G. Trabuco, Nancy A. Rebouças,  Alicia J. Kowaltowski作者单位：1 Departamento de Fisiologia e Biofísica, Instituto de Ciências Biomédicas, and Departamento de Bioquímica, Instituto de Química, Universidade de São Paulo, 05508-900 São Paulo, Brazil , i0 r/ q2 T0 w  j6 D) f


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      【摘要】7 _; ^: E1 u' H1 K7 E  ?! a% `
   Isolated kidney mitochondria swell when incubated in hyposmotic solutions containing K salts in a manner inhibited by ATP, ADP, 5-hydroxydecanoate, and glibenclamide and stimulated by GTP and diazoxide. These results suggest the existence of ATP-sensitive K channels in these mitochondria, similar to those previously described in heart, liver, and brain. Renal mitochondrial ATP-sensitive K uptake rates are 140 nmol·min -1 ·mg protein -1. This K transport results in a slight increase in respiration and decrease in the inner membrane potential. In addition, the activation of ATP-inhibited K uptake using diazoxide leads to a decrease of ATP hydrolysis through the reverse activity of the F 0 F 1 ATP synthase when respiration is inhibited. In conclusion, we characterize an ATP-sensitive K transport pathway in kidney mitochondria that affects volume, respiration, and membrane potential and may have a role in the prevention of mitochondrial ATP hydrolysis.
      【关键词】 kidney mitochondria K transport ischemic preconditioning uncoupling6 f% B. W- p% y2 G
   TO MAINTAIN THE inner membrane potential ( ) and achieve effective ATP synthesis through oxidative phosphorylation, mitochondria must present very limited permeability to cations ( 31 ). It was thus surprising to find that ATP-sensitive K uniporters (mitoK ATP ) exist in the inner membrane of mitochondria isolated from heart, liver, and brain ( 23, 32 ). Mitochondrial K transport in these tissues is composed of at least three distinct components: 1 ) mitoK ATP, which transports K from the cytosol into the mitochondrial matrix in a manner driven by and regulated by adenine and guanosine nucleotides ( 23, 32, 33 ); 2 ) the K leak through the inner membrane, also driven by ( 17 ); and 3 ) the electroneutral K /H exchanger, which removes excess K from the mitochondrial matrix in a manner stimulated by mitochondrial swelling ( 15 )." l2 H0 ^1 b9 N- J- J( w1 a& W

The concomitant activity of K uptake through mitoK ATP and removal by the K /H exchanger would be expected to result in a decrease of the inner membrane electrochemical H gradient, which could hamper oxidative phosphorylation. However, mitoK ATP activity was found to be compatible with the maintenance of oxidative phosphorylation because K transport rates through this channel in all mammalian tissues studied to date are very limited ( 4, 28 ). Indeed, mitoK ATP activation seems to be directly involved in the regulation of more effective oxidative phosphorylation, because the small increments in K transport promoted by this channel are accompanied by substantial increases in mitochondrial matrix volume, resulting in more efficient respiration ( 21 ), oxidative phosphorylation ( 11 ), and less ATP loss when respiration is inhibited ( 6 ). MitoK ATP may also be involved in the regulation of mitochondrial reactive oxygen species generation ( 7, 12, 14, 29 )./ W1 T5 [- B/ v: V

The specific effects of mitoK ATP on mitochondrial structure and function gained interest when Garlid et al. ( 18 ) demonstrated that diazoxide (DZX), a K ATP agonist used at concentrations that activate mitoK ATP but not plasma membrane K ATP channels, protected heart tissue against ischemic damage. The protective effect of mitoK ATP opening was later confirmed by independent groups, both in heart tissue and in brain ( 10, 18 ). MitoK ATP was also shown to participate in heart ischemic preconditioning (the protective effect of short, nondeleterious ischemic episodes on a longer, potentially damaging ischemic event), because this process was inhibited by mitoK ATP antagonists such as 5-hydroxydecanoate and glibenclamide ( 3, 20, 24 ). The cardioprotective effect of mitoK ATP is probably related to the ability of this channel to prevent ATP loss during ischemia and increase the efficiency of postischemic oxidative phosphorylation ( 6, 11 ).

Renal tissue is also protected by ischemic preconditioning ( 30, 37 ), suggesting that mitoK ATP may be present in this tissue. However, to our knowledge, no previous attempt to characterize mitoK ATP and establish its regulatory properties in renal mitochondria has been made. In this manuscript, we describe a K transport pathway inhibited by adenine nucleotides in kidney mitochondria and measure ATP-sensitive K transport rates and the effects of this transport on mitochondrial function.& j' c! `8 E. S  b+ S

MATERIALS AND METHODS

Mitochondrial isolation. Kidneys were rapidly removed from male Wistar rats weighing between 150 and 250 g, finely minced, and homogenized in ice-cold buffer containing 210 mM mannitol, 70 mM sucrose, 5 mM Na -HEPES, 2 mM Na -EGTA, and 0.1% BSA, pH 7.2. The suspension was then centrifuged at 800 g for 4 min, the resulting supernatant was centrifuged at 12,000 g for 7 min, and the pellet was resuspended in the same buffer. Both centrifugations were repeated, and the final pellet was resuspended in 300-500 µlof buffer. Mitochondrial protein concentration was determined using the Biuret reaction.

Mitochondrial swelling. Changes in light scattering, reflecting changes in mitochondrial volume ( 5, 24, 36 ), were followed using a temperature-controlled Hitachi F4500 spectrofluorometer, operating with continuous stirring at excitation and emission wavelengths of 520 nm, with 2.5-nm slits.6 ]3 n% r: E& C

Mitochondrial membrane potential estimation. Mitochondrial membrane potentials were estimated by following safranin O (5 µM) fluorescence ( 1 ) at 495-nm excitation and 586-nm emission on a Hitachi F4500 spectrofluorometer. A calibration curve was constructed using the K ionophore valinomycin (0.1 µg/ml) and known concentrations of K  , assuming matrix K concentration to be 150 mM ( 1 ).
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Measurement of mitochondrial respiration. Respiration was measured using a computer-interfaced Clark-type oxygen electrode from Hansatech equipped with magnetic stirring. Oxygen solubility at 37°C was taken to be 203 nmol/ml. When fixed potentials were needed ( Fig. 3 ), 0.1 µg/ml valinomycin and known K concentrations were used to manipulate, calculated using the Nernst equation, assuming matrix K concentration to be 150 mM ( 27 ).
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Fig. 3. Relationship between and respiration in renal mitochondria. Isolated mitochondria ( 0.1 mg/ml) were added to a reaction medium at 37°C containing 250 mM sucrose, 10 mM inorganic phosphate, 0.1 mM EGTA, 1 mM Mg 2 , 5 mM HEPES, 2 mM succinate, pH 7.4 (NaOH), 1 µg/ml oligomycin, 1 µM rotenone, 0.1 µg/ml valinomycin, and variable K concentrations to vary as predicted by the Nernst equation. Oxygen consumption was measured as described in MATERIALS AND METHODS./ x- \6 o( H$ d2 V
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ATP measurements. ATP concentrations were determined by light emission at 560 nm on a Hitachi F4500 spectrofluorometer using a commercial luciferin-luciferase kit (Promega FF2021). Light emission during the first 120 s following the addition of luciferin-luciferase was integrated, and data were calibrated using known concentrations of ATP.4 [; c8 H7 Q* m" Z, u" q
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Reagents. Safranin O, EGTA, succinate, BSA, FCCP, rotenone, valinomycin, cyclosporin A, oligomycin, glibenclamide, diazoxide, 5-hydroxydecanoic acid, ADP, ATP, GTP, and antimycin A were purchased from Sigma.
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Data analysis. Replicate experiments were performed in mitochondria isolated from separate animals, each representing an n of 1. Data are expressed as means ± SE. The inhibition of mitochondrial swelling promoted by ADP and ATP was normalized to control and analyzed by comparison to one using t -tests for a single sample. The remaining swelling data were analyzed with one-way ANOVA multiple t -tests for planned comparisons between mean values. Planned comparisons were DZX ATP vs. ATP; glibenclamide DZX ATP vs. DZX ATP; 5-hydroxydecanoate DZX ATP vs. DZX ATP; and GTP ATP vs. ATP. and oxygen consumption variation data ( Fig. 2 ) were compared with zero, and ATP measurements were normalized to control and compared with one using t -tests for a single sample." e0 {" h, w8 D5 B# T. v* l

Fig. 2. ATP-sensitive K transport promotes small changes in inner membrane potential ( ) and respiration. Isolated renal mitochondria ( 0.5 mg/ml) were added to a reaction medium at 37°C containing 150 mM KCl, 10 mM inorganic phosphate, 0.1 mM EGTA, 1 mM Mg 2 , 5 mM HEPES, 2 mM succinate, pH 7.4 (KOH), 1 µg/ml oligomycin, and 1 µM rotenone in the presence (ATP) or absence (control) of 200 µM ATP. ( A ) and oxygen consumption ( B ) were measured as described in MATERIALS AND METHODS. FCCP (1 µM) was added where indicated.
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RESULTS, L) s5 x5 u0 O  I

Regulation of renal mitochondrial K transport. Mitochondrial isolation promotes K loss and contraction of the matrix, a process reversed when the organelles are incubated in a medium containing physiological concentrations of K ( 24, 28 ). We measured increases in mitochondrial volume promoted by K uptake and the entrance of osmotically obligated water by following light scattering in isolated kidney mitochondrial suspensions incubated in hypotonic media rich in K  . K uptake increased mitochondrial volume, decreasing light scattering in a time-dependent manner. Swelling due to K uptake was complete after 20 to 60 s and was followed by mitochondrial contraction, probably due to the activity of the mitochondrial K /H antiporter (results not shown). ATP significantly decreased the swelling rate compared with control ( P Fig. 1 A and averages in Fig. 1 B ). The K for ATP inhibition of K uptake was 20 µM (data not shown), and 200 µM ATP was sufficient to attain the maximal inhibitory effect. These results indicate that an ATP-sensitive pathway for K uptake is present in kidney mitochondria. This pathway is selective for K  , because swelling in Li or Na salts, which are not transported by mitoK ATP ( 28 ), was less extensive and unaltered by ATP (empty and hatched columns). K uptake in kidney mitochondria was also prevented by ADP ( P ATP in brain, liver, and heart ( 4 ).9 V8 w2 M6 \& i/ V# {! _( S0 Y

Fig. 1. Kidney mitochondria transport K in an ATP-sensitive manner. Isolated renal mitochondria ( 0.2 mg/ml) were added to a reaction medium at 37°C containing 80 mM KCl, 10 mM inorganic phosphate, 0.1 mM EGTA, 1 mM Mg 2 , 5 mM HEPES, 2 mM succinate, pH 7.4 (KOH), 1 µg/ml oligomycin, 1 µM rotenone, and the additions specified below. Decreases in light scattering due to mitochondrial K and water uptake were measured. A : representative traces. B : averages ± SE of swelling rates. One millimolar ADP, 200 µM ATP, 100 µM GTP, 20 µM diazoxide (DZX), 1 µM glibenclamide (GLB), or 300 µM 5-hydroxydecanoate (5-HD) were added as shown. In the last 2 bars, K salts in the media were substituted with Na or Li  , as indicated, both for the control (100%) and ATP-containing samples. * P P P; c0 `/ c; ?0 R* R' e5 ~6 G7 B

The inhibitory effect of ATP on mitochondrial swelling in K salts was reversed by GTP ( P ATP activator ( 33 ), and DZX ( P ATP agonist that acts selectively on mitochondrial channels at the concentration used ( 19 ). As previously described ( 24 ), GTP and DZX had no effect in the absence of ATP and/or K (data not shown). The DZX effect could be prevented by the concomitant presence of glibenclamide ( P ATP antagonist ( 24 ), demonstrating that renal ATP-sensitive K transport is also regulated by sulphonylureas, and must, therefore, be mediated by a channel similar to previously described mitoK ATP s ( 4, 19, 24, 32, 33 ). Another effective inhibitor of the DZX-induced swelling was 5-hydroxydecanoate ( P to be specific for mitoK ATP ( 24 ). These inhibitors were also ineffective in the absence of ATP and DZX (data not shown), as previously seen ( 24 ).

Effect of ATP-sensitive K transport on respiration and. With the use of safranin O fluorescence to measure, we found an increase of 11.4 ± 1.5 mV ( n = 4; P mV) when 200 µM ATP was added to the reaction medium to inhibit mitoK ATP ( Fig. 2 A ). An increment of 16.2 ± 4.9 mV ( n = 5; P P 0.05 vs. the previous group) in after a 200 µM ATP addition was measured in a similar reaction mixture containing fatty acid-free BSA (1 g/l), demonstrating that the ATP effect was not due to an inhibition of fatty acid-stimulated uncoupling ( 26 ). Cyclosporin A, an inhibitor of the mitochondrial permeability transition ( 38 ), also did not eliminate the ATP effect (data not shown), suggesting that our increases were not due to prevention of permeability transition by ATP. In addition, 200 µM ATP did not significantly increase (0.8 ± 2.0 mV, n = 4; P 0.05 vs. 0 mV) when added to a reaction medium that did not contain K  . Thus K transport through an ATP-sensitive pathway results in decreases of 10 mV. In all experiments, the proton ionophore FCCP was added at the end of the run to dissipate and ensure that safranin O fluorescence returned to similar levels.1 k( c) C; }( S

Associated with the changes in, we found that mitochondria incubated in K salts in the absence of ATP presented higher respiratory rates than those in which K transport was inhibited by ATP ( Fig. 2 B ), in a manner unaltered by the presence of BSA (not shown). With the use of succinate as a respiratory substrate, ATP-sensitive increments in respiration observed in K -rich media were 11.9 ± 1.4 nmol O 2 ·min -1 ·mg protein -1 ( n = 10; P to an estimated K transport rate of 143 nmol O 2 ·min -1 ·mg protein -1, considering that K /H exchange is electroneutral and 6 protons are pumped per oxygen atom consumed ( 4 ).

A verification of the compatibility of our data for and respiration rate changes promoted by mitoK ATP was conducted by measuring oxygen consumption rates in the presence of fixed s, as described in MATERIALS AND METHODS and shown in Fig. 3. By fitting the data obtained with respiratory rates lower than the maximal rates, we found that respiration and are related by a slope of 1.067 ± 0.012 nmol O 2 ·mV -1 ·min -1 ·mg protein -1, a result fully compatible with the finding that mitoK ATP alters respiration and by 1.04 ± 0.18 nmol O 2 ·mV -1 ·min -1 ·mg protein -1.
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Effect of K transport on the reverse activity of the F 0 F 1 ATP synthase. Opening ATP-sensitive K channels in heart mitochondria changes ADP and ATP transport across mitochondrial membranes, increases the efficiency of oxidative phosphorylation, and preserves tissue ATP levels during ischemia ( 6, 11 ). To verify whether the same effect was present in kidney, we incubated renal mitochondria in the presence of antimycin A (a complex III inhibitor), to simulate an ischemic condition, and measured ATP loss promoted by hydrolysis through the reverse activity of the F 0 F 1 ATP synthase. Initially, ATP hydrolysis by the F 0 F 1 ATP synthase was measured by following the generated by proton pumping by this protein. We observed that the sustained by ATP hydrolysis was lower and more rapidly lost when K transport was stimulated by the presence of DZX (a representative trace of 6 independent experiments is shown in Fig. 4 ). The addition of 2 µg/ml oligomycin completely abolished generation by ATP in the presence or absence of DZX (not shown), confirming that the generated was related to ATP hydrolysis by the F 0 F 1 ATP synthase. We also measured ATP concentrations in the reaction buffer after 120-s incubation in the presence or absence of DZX. We found that ATP concentrations in the DZX group were 1.86 ± 0.21 times greater ( n = 8; P = 0.005 vs. 1) than those found in the control group, confirming that DZX decreases mitochondrial ATP hydrolysis by the F 0 F 1 ATP synthase in the absence of respiration.
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Fig. 4. Renal mitochondrial K transport reduces the reverse activity of the F 0 F 1 ATP synthase. Isolated renal mitochondria ( 0.2 mg/ml) were added to a reaction medium at 37°C containing 150 mM KCl, 10 mM inorganic phosphate, 0.1 mM EGTA, 1 mM Mg 2 , 5 mM HEPES, pH 7.4 (KOH), 200 µM ATP, and 2 µg/ml antimycin A in the absence (control) or presence of 10 µM DZX. ATP hydrolysis-supported was measured as described in MATERIALS AND METHODS.
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DISCUSSION

We characterized a regulated K import pathway in renal mitochondria that promotes mitochondrial swelling. This swelling is inhibited by ATP and ADP, in a manner reversed by the K ATP agonists DZX and GTP. The DZX and GTP effect is prevented by 5-hydroxydecanoate and glibenclamide ( Fig. 1 ). Although the specificity of these drugs toward mitoK ATP and validity of light-scattering measurements of mitochondrial volume have recently been challenged ( 9, 22, 28 ), we found the mitoK ATP agonists and antagonists used here to be effective only when mitochondria were suspended in K -containing buffers, a strong indication that they change mitochondrial light-scattering characteristics by altering K transport. Furthermore, we found our light-scattering data to be reproducible and statistically significant, whereas measurements of mitochondrial volume used previously ( 9 ) probably present errors larger than the volume changes promoted by these channels. Indeed, our findings regarding ATP-sensitive K uptake in renal mitochondria are comparable to those described in mitochondria isolated from liver, heart, and brain ( 4, 19, 24, 32, 33 ), in which mitoK ATP has been isolated and reconstituted and strongly support the idea that kidney mitochondria present a mitoK ATP similar to that described in other tissues.  ?/ M) ?5 M# G& S5 m) L
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ATP-sensitive K transport in renal mitochondria results in mild respiratory rate enhancement and a partial decrease in ( Fig. 2 ), as would be expected for the uptake of a cation into the negatively charged mitochondrial matrix. Changes promoted by ATP in renal mitochondria (10-20 mV) were somewhat greater than those described in heart (1-2 mV; 28 ) and in brain (3-6 mV; 4 ). On the other hand, kidney mitoK ATP transport rates ( 140 nmol·min -1 ·mg protein -1 ), estimated by measuring respiratory rate differences, were larger than those found in heart ( 30 nmol·min -1 ·mg protein -1; 28 ) and slightly lower than brain K transport rates ( 170 nmol·min -1 ·mg protein -1; 4 ), suggesting that renal tissue expresses intermediate mitoK ATP protein levels. In kidney and all other tissues studied to date ( 4, 24 ), the respiration and effects of mitoK ATP activation were small and certainly insufficient to hamper oxidative phosphorylation or Ca 2  uptake, indicating that large-scale and respiratory regulation must not be the central role of mitoK ATP. On the other hand, a major role of mitoK ATP may be to regulate mitochondrial volume, which can change up to 20% in response to ATP-regulated K uptake rates as limited as those found in heart ( 7, 24, 28 ).3 y+ g$ o* p0 Z7 _' |0 T+ k
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In addition to altering volume, respiration, and in respiring mitochondria, DZX-stimulated K transport in renal mitochondria was associated with lower ATP hydrolysis through the reverse activity of the F 0 F 1 ATP synthase under nonrespiring conditions ( Fig. 4 ). We previously obtained a similar result in heart mitochondria ( 6 ), and there is evidence that this effect is linked to volume changes ( 11 ). Indeed, we found that perfused hearts subjected to ischemia presented higher ATP levels when treated with DZX, atractyloside (an inhibitor of nucleotide transport into the mitochondrial matrix), or oligomycin (which inhibits the mitochondrial F 0 F 1 ATP synthase). This is strong evidence that limitation of ATP hydrolysis by the F 0 F 1 ATP synthase can be relevant for the maintenance of high-energy phosphate levels during ischemia and that mitoK ATP may contribute to ischemic protection by preventing ATP hydrolysis secondarily to changes in mitochondrial volume ( 6, 11 ).) k9 ?8 m. f: h) e2 k% z
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The reproduction of this finding in kidney mitochondria suggests that this channel may also have a protective effect in renal ischemia. Unfortunately, although we attempted to obtain a protective effect against ischemic damage using DZX in renal tissue and cell lines, we have not yet been able to confirm this hypothesis due to the toxic effect of this drug on these models (Cancherini, Trabuco, Kowaltowski, and Rebouças, unpublished observations). Pinacidil, another mitoK ATP agonist frequently used to study the protective effects of this channel ( 2, 8, 25, 34 ), previously failed to protect the kidney against ischemia ( 30 ).7 y9 \9 l% @7 C5 d) `/ ]  H. T

Although a possible protective role for renal mitoK ATP under pathological conditions remains to be verified, our data clearly indicate that this channel may have important functions under physiological conditions. We found that renal mitoK ATP can increase mitochondrial matrix volume by stimulating K uptake rates ( Fig. 1 ). This provides a regulated mechanism through which renal mitochondria can swell and counteracts the contraction promoted by the K /H exchanger ( 16 ), which appears to be highly active in this tissue (results not shown). MitoK ATP activation thus allows for the maintenance of mitochondrial volume when K leak through the inner membrane is decreased due to oxidative phosphorylation ( 28 ). In fact, the maintenance of adequate matrix volume and a narrow intermembrane space is important to ensure the preferential transport of creatine phosphate in relation to ATP across mitochondrial membranes in heart ( 11 ). Matrix swelling can also significantly activate the electron transport chain ( 21 ).) a. w5 [6 V2 J( }% [. O$ `

The concomitant activity of both mitoK ATP and the K /H exchanger also results in a small decrease in mitochondrial and increased respiration, which may be another important function for this channel. Although insufficient to hamper oxidative phosphorylation or Ca 2  uptake ( 28 ), mild uncoupling such as that promoted by mitoK ATP may be important to generate heat, regulate metabolism, and even prevent reactive oxygen species generation by mitochondria ( 12, 35 ). Indeed, uncoupling proteins, whose sole known function is to promote mild uncoupling, exist ubiquitously ( 13, 26 ), attesting to the importance of limited physiological regulation./ G% c* v: O# |* H% V+ ^, o
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In conclusion, we characterized a controlled K import pathway in renal mitochondria similar to mitoK ATP previously described in other tissues. These putative renal mitoK ATP channels regulate mitochondrial volume, respiration,, and F 0 F 1 ATP synthase activity. The possible importance of the regulation of these mitochondrial functions in cellular physiology and pathology remains to be determined.
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DISCLOSURES7 N$ _% R+ [, a( D% U

This work was supported by Fundação de Amparo a Pesquisa do Estado de São Paulo (FAPESP) and Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) grants to A. J. Kowaltowski and N. A. Rebouças. D. V. Cancherini and L. G. Trabuco are students supported by FAPESP and CNPq-PIBIC scholarships, respectively.
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