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doi:10.1369/jhc.6A7026.2006
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Volume 55 (2): 191-197, 2007
Copyright ©The Histochemical Society, Inc.
Expression of the MDR-1 Gene-encoded P-glycoprotein in Cardiomyocytes of Conscious Sheep Undergoing Acute Myocardial Ischemia Followed by Reperfusion
Department of Pathology (RPL,LAC,PMCM,GGY) and Department of Physiology (GLVJ,HFV,ECL,JAN,AJC), Favaloro University, Buenos Aires, Argentina; Department of Clinical Biochemistry, Faculty of Pharmacy and Biochemistry, Buenos Aires University, Buenos Aires, Argentina (AJL); and Scientific Investigation Commission of Buenos Aires Province, La Plata, Argentina (PMCM)
Correspondence to: Alberto Crottogini, Favaloro University, Solís 453, 1078 Buenos Aires, Argentina. E-mail: crottogini{at}favaloro.edu.ar
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Summary |
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We have recently reported that in chronic myocardial ischemia, adult mammalian cardiomyocytes express P-glycoprotein (P-gp). We now investigate if P-gp is also expressed in acute regional ischemia followed by reperfusion. Adult conscious sheep underwent 12-min occlusion of the mid-left anterior descending artery (inflatable cuff). Successful ischemia–reperfusion was confirmed by monitoring percent systolic left ventricular anterior wall thickening (sonomicrometry) during the whole ischemic period and every 10 min over 2 hr following cuff deflation. At 3, 24, and 48 hr after reperfusion, P-gp expression was investigated by immunohistochemistry and Western blot and MDR-1 mRNA by RT-PCR. Cardiomyocytes in the occluded artery territory (but not those in remote areas) consistently expressed P-gp at their sarcolemma. Whereas at 3 and 24 hr P-gp was mainly observed in the T tubules, at 48 hr it predominated in intercalated discs and gap junctions. RT-PCR and Western blot revealed higher expression in ischemic than in control myocardium. We conclude that in adult sheep with acute myocardial ischemia, the MDR-1 gene-encoded P-gp is expressed at the sarcolemma of the cardiomyocytes from 3 hr up to at least 48 hr after reperfusion. (J Histochem Cytochem 55:191–197, 2007)
Key Words: P-glycoprotein • MDR-1 • cardiomyocytes • stunning • acute myocardial ischemia • ischemia–reperfusion injury • sheep
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Introduction |
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TopSummaryIntroductionMaterials and MethodsResultsDiscussionLiterature Cited |
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THE P-GLYCOPROTEIN (P-gp), encoded by the multidrug resistance (MDR-1) gene, is a cationic efflux pump of the plasma membrane (Juliano and Ling 1976
; Thiebaut et al. 1987; Solbach et al. 2006) normally present in various tissues such as the epithelium of the small intestine, the proximal tubules of the kidney, and the capillaries of the blood–brain barrier (Cordon-Cardo et al. 1990). Although P-gp is not present under normoxic conditions in mammalian cardiomyocytes, we have recently shown that cardiomyocytes of pigs undergoing chronic myocardial ischemia express P-gp (Lazarowski et al. 2005). However, it is not known if P-gp is expressed in acute myocardial ischemia. In the present study we investigated if cardiomyocytes of adult conscious sheep undergoing acute, non-lethal regional myocardial ischemia followed by full reperfusion express P-gp.
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Materials and Methods |
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TopSummaryIntroductionMaterials and MethodsResultsDiscussionLiterature Cited |
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Surgical Preparation
Nine Corriedale sheep weighing 27 ± 2 kg were operated. All procedures were done in accordance with the Guide for the Care and Use of Laboratory Animals, published by the US National Institutes of Health (NIH publication No. 85-23, revised 1996). After premedication with acepromazine maleate (0.3 mg/kg), anesthesia was induced with sodium thiopental (20 mg/kg) and maintained with 3% enflurane carried in oxygen through a Bain tube connected to a volume-driven ventilator. A sterile thoracotomy was performed at the left fifth intercostal space, and the pericardium was opened. A pressure microtransducer (P7 transducer; Konigsberg Instruments, Inc., Pasadena, CA) was inserted in the left ventricle (LV) through a stab wound in the apex together with a fluid-filled catheter for later calibration of the microtransducer. The left anterior descending (LAD) artery was dissected free from surrounding tissue just distal to the emergence of the second diagonal branch, and a pneumatic cuff occluder was positioned around it.
To measure LV wall thickness, a pair of 5-MHz piezoelectric crystals (one sutured to the epicardium and the other lying in the subendocardium) was placed well within the zone to be rendered ischemic. Cables and catheters were tunneled SC to emerge between the scapulae, and the thoracotomy was repaired. The venous and LV catheters were flushed daily with heparinized saline. Cephalomycin (1 g) was given IV immediately after surgery and continued for 3 days (1 g/day IM).
Experimental Protocol
Seven to 10 days after surgery the animals were studied in the conscious, unsedated state. The Konigsberg transducer and the ultrasonic crystals were connected to a System 6 Physiological Monitoring System (Triton Technology; San Diego, CA), and the fluid-filled catheter was connected to a pressure transducer (DT-XX; Viggo-Spectramed, Oxnard, CA) previously calibrated using a transducer calibration system (Xcaliber; Viggo-Spectramed). The zero pressure point was set at the level of the right atrium, and the signal generated by the Konigsberg transducer was adjusted to match that of the external transducer. Ultrasonic crystals were calibrated in millimeters using the sonomicrometer internal calibration.
The experiment consisted of 20 min of stabilization and 12 min of ischemia followed by reperfusion. This duration of ischemia was previously shown to produce a significant degree of myocardial stunning without permanent cardiomyocyte injury (Negroni et al. 2002).
Measurements were acquired just before ischemia (basal condition), at the time of cuff deflation, every 10 min during the first hour, and every 20 min during the second hour of reperfusion. At each acquisition time, the signals of consecutive steady beats were digitized at 4-msec intervals over 15 sec using a personal computer equipped with an A/D converter (National Instruments Lab-PC; Austin, TX) and software developed in our laboratory.
At 3 (n=5), 24 (n=2), and 48 (n=2) hr after the onset of reperfusion the animals were killed with an overdose of sodium thiopental followed by a bolus injection of potassium chloride. The heart was excised for histological examination, assessment of P-gp expression by immunohistochemistry, and confirmation of correct crystal positioning. Western blot analysis for P-gp and RT-PCR for MDR-1 mRNA were performed in hearts excised at 3 (n=2), 24 (n=2), and 48 (n=2) hr.
Regional Function Measurements
End diastole was defined to occur at the onset of the rapid upstroke of the digitally obtained time derivative of left ventricular pressure (dP/dt). End systole was defined as the time point where the descending limb of the negative dP/dt reached 10% of its minimal value and end ejection was established to occur at peak negative dP/dt (del Valle et al. 2001). Percent regional wall thickening fraction (%WTh) was calculated as %WTh = 100x(WThe–WThd)/WThd, where WThe is maximum wall thickness between end systole and end ejection, and WThd is end diastolic wall thickness.
Signal processing and %WTh calculation were performed at each time of data acquisition from each recorded beat. The average of processed beats (15 to 30 beats) was the sample value assigned to the corresponding acquisition time. Ischemia and reperfusion recovery were expressed as percent of basal condition taken as 100%.
Histology and Immunohistochemistry
The LV was cut transversally at a plane lying 
0.5 cm above the epicardial crystal. Correct positioning of the endocardial crystal was assessed, and a 1-cm-thick slice of the whole LV wall close to (but not containing) the crystal pair was cut and fixed in 10% buffered formaldehyde for 48 hr. The slice was then sectioned into four pieces corresponding to the interventricular septum and the anterior, lateral, and posterior LV walls. Each piece was further divided into two halves. All eight fragments were embedded in paraffin. Four-µm-thick tissue sections were stained with hematoxylin–eosin, periodic acid-Schiff, and Masson's trichrome. For immunohistochemistry, antigen retrieval was done by incubating the hydrated sections in 10 mM sodium citrate buffer (pH 6) in a microwave oven during 5 min. To detect P-gp in a double-check fashion, we used two different specific monoclonal antibodies: clone C494 (1:100, 200 µg/ml; Signet Laboratories, Dedham, MA) or clone MDR88 (1:100, 10 mg/ml; Biogenex, San Ramon, CA). Clone C494 antibody detects an epitope present only in the MDR-1 isoform of the P-gp and cross-reacts with pyruvate carboxylase, a mitochondrial enzyme. Unequivocal plasma membrane patterns of immunostaining represent true P-gp expression. Clone MDR88 is a monoclonal antibody against a recombinant P-gp containing four tandem repeats of the amino acid sequence 1092–1252. All tissue sections were incubated for 1 hr at room temperature with either one of the described antibodies. For visualization of antibody binding, we used a commercial biotin–streptavidin–peroxidase kit, with EAC as chromogen (Biogenex) and counterstained with hematoxylin. As positive controls we used murine brain and kidney tissue sections.
Western Blot
In the six hearts submitted to Western blot analysis, an extra 1-cm slice immediately distal to the slice used for histological analysis was cut, divided into eight fragments as previously described, and deep frozen in liquid nitrogen. Protein extracts were obtained by the method of Maniatis (Sambrook et al. 1989) from ischemic–reperfused and control myocardial fragments. Samples containing 100 µg of protein (10 mM KCl, 1.5 mM MgCl2, 10 mM Tris Cl, pH 7.4, 0.5% SDS, 2 µg/ml leupeptin, 2 µg/ml aprotinin, and 1 µg/ml E64) were subjected to SDS-PAGE in 7% gels and then electroblotted to Hybond P membrane (Amersham Life Science; Arlington Heights, IL). The primary antibody used was the monoclonal C494 (Signet Laboratories) or anti-ß actin (Santa Cruz Biotechnology; Santa Cruz, CA) as internal protein loading control. The secondary antibody was a peroxidase-conjugated goat anti-mouse IgG (Dako; Carpinteria, CA) coupled with the detection system ECL reagent (Amersham) according to the manufacturer's instructions. Densitrometric analysis was performed using Gel-Pro Analyzer software (version 3.1; Media Cybernetics, Silver Spring, MD). Tissues with high constitutive expression of P-gp (liver, colon, and kidney from rat and sheep) were used as positive controls. Results obtained in control and ischemic–reperfused tissue samples were expressed in optical density (OD) units.
mRNA Isolation and RT-PCR Analysis
Total RNA was isolated (Trizol reagent; Gibco BRL, Grand Island, NY), treated with DNase I (Promega; Madison, WI), quantitated, and reverse transcripted (random hexamers; Perkin-Elmer, Boston, MA). Primers 5'-AGCCCATTCTGTTTGACTGC-3' and 5'-TCAAGTCTGCGTTCTGGATG-3' were designed to amplify the 3371- to 3742-bp region of the sheep MDR-1 cDNA (GenBank accession number U78609). A reaction mixture (25 µl) containing cDNA preparation (5 µl), 1X PCR buffer, 2.5 mM MgCl2, 200 µM dNTPs, primers (0.2 µM each), and 0.625 U Taq DNA polymerase (Applied Biosystems; Branchburg, NJ) was used. Cycling conditions were as follows: 94C for 1 min, then 30 cycles at 94C for 15 sec, 55C for 30 sec, 65C for 30 sec, and then a final step of 72C for 7 min. Primers for glyceraldehyde-3-phosphate dehydrogenase (GAPDH) cDNA (sense primer, 5'-CCCATCACCATCTTCCAGGAG-3'; antisense primer, 5'-GTTGTCATGGATGACCTTGGC-3') were used as internal control for the amount of RNA and RT efficiency. Samples were kept at 94C for 1 min and then subjected to thermocycling (25 cycles at 94C for 15 sec, 56C for 30 sec, and 65C for 30 sec, with a final extensionat 72C for 7 min). Each primer set was amplified using an optimized number of PCR cycles to ensure the linearity requirement for semiquantitative RT-PCR analysis. Specific MDR-1 amplicon was observed (372 bp), and its identity was confirmed by restriction mapping with BslI and MnlI. Ethidium bromide-stained gels were scanned (Fotodyne Inc.; Hartland, WI) and analyzed using Gel-Pro Analyzer 3.1 software (Media Cybernetics). The MDR-1 mRNA was normalized by GAPDH mRNA signal and expressed in OD units. Tissues with high constitutive expression of P-gp (liver, colon, and kidney from sheep) were used as positive controls.
Statistical Analysis
Percent WTh was compared at each time point using Student's one-sample t-test against 100. Western blot data for P-gp content and RT-PCR results for MDR-1 mRNA expression in control and ischemic–reperfused myocardium were compared using an unpaired t-test. Differences were considered significant when p<0.05. Results are expressed as mean ± SE.
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Results |
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Effect of Ischemia–Reperfusion on Regional Myocardial Function
In all animals, ischemia–reperfusion lead to myocardial stunning. Basal, preocclusion WTh was 39.6 ± 4%. Figure 1 shows the time course of wall thickening fraction expressed as a percent of basal wall thickening, from the moment of cuff deflation up to 2 hr of reperfusion. At the onset of reperfusion, systolic %WTh showed a negative value (–14.2 ± 5.9%), indicating regional dyskinesia. Following cuff deflation, %WTh recovered progressively, reaching 70.5 ± 5.1% of the basal value after 2 hr of reperfusion. We did not measure %WTh at the time of sacrifice. However, because no permanent ischemic damage occurs in this established model of myocardial stunning, complete recovery of regional myocardial function is to be expected, especially at the 24- and 48-hr time points, as previously reported (del Valle et al. 2001
; Negroni et al. 2002).
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p<0.001.Immunohistochemistry
In the five sheep killed at 3 hr after the onset of reperfusion, all cardiomyocytes in the tissue blocks corresponding to the LAD territory (anterior septum and anterior ventricular wall) displayed a positive reaction at their sarcolemma and T tubules (Figure 2A ). In contrast, cardiomyocytes from the lateral and posterior ventricular wall were consistently negative. In the tissue sections corresponding to the periphery of the ischemic area, transition was abrupt, and intensely P-gp-positive cardiomyocytes were observed alongside negative ones (Figure 2B). In this border zone, the capillaries (Figure 2B) as well as larger arterioles (Figure 2C) displayed a positive reaction.
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In sheep killed at 3 and 24 hr after reperfusion, distribution of P-gp in the sarcolemma and T tubules was mostly uniform. In the animals killed at 48 hr after occlusion, most of the P-gp was located in the intercalated discs (Figures 2D and 2E) and lateral gap junctions (Figure 2F).
Western Blot
P-gp content (pooled data for all three time points) was23.9 ± 3.9 OD in control myocardium and 78.4 ± 4 OD in ischemic–reperfused myocardium (p<0.001, Figure 3A
). At 3, 24, and 48 hr after reperfusion, P-gp was between two and seven times higher in the myocardium subjected to ischemia–reperfusion than in control myocardium in the two sheep studied at each time point (Figure 3B).
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RT-PCR
MDR-1 mRNA (pooled data for all three time points) was 15.9 ± 3.8 OD in control myocardium and 38.6 ± 1.9 OD in ischemic–reperfused myocardium (p<0.001, Figure 4A ). In the two sheep studied at each time point, MDR-1 mRNA was between 1.5 and 4 times higher in ischemic–reperfused than in control myocardium (Figure 4B).
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Discussion |
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TopSummaryIntroductionMaterials and MethodsResultsDiscussionLiterature Cited |
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We have recently reported that P-gp, which is not found in myocytes of mammalian normoperfused myocardium, is expressed when cardiomyocytes are subjected to chronic ischemia (Lazarowski et al. 2005
). In the present study we extend our previous observation by demonstrating for the first time that in the setting of acute, non-lethal myocardial ischemia, P-gp expression also occurs as soon as 3 hr after reperfusion and persists for at least 48 hr.
Among the variants of ischemic heart disease, ischemia–reperfusion injury is a condition increasingly observed in clinical practice, given the widespread use of primary and rescue coronary angioplasty. When reperfusion occurs early enough to prevent cell death, the resulting feature is myocardial stunning (Braunwald and Kloner 1982), a phenomenon characterized by delayed recovery of ventricular contractile function despite successful reperfusion (Kloner and Jennings 2001; Barnes and Khan 2003). The main mechanisms involved in this condition are oxidative stress with generation of free radicals, principally the hydroxyl radical (Bolli et al. 1987; Farber et al 1988) and perturbation of calcium homeostasis with intracellular free calcium overload (Bolli 1990).
Although it was not the aim of our study to determine the functional role of P-gp in this context, given that the main action of P-gp and other ATP binding cassette (ABC) transporters is to extrude a wide spectrum of cytotoxic compounds to the extracellular space (Litman et al. 2001), it is reasonable to speculate that P-gp may contribute to cardiomyocyte protection against the harmful products derived from ischemia–reperfusion.
In support of this hypothesis, it should be noted that many compounds and signal transduction pathways involved in myocardial stunning have been shown to induce expression of the MDR-1 gene. Diacylglycerol, an agonist of protein kinase C (PKC) that appears early after cardiomyocyte hypoxia in rabbit hearts (Gysembergh et al. 2000), induces MDR-1 gene expression. In fact, activation of PKC is directly related to P-gp function (Chaudhary and Roninson 1992). One of the isoforms of PKC that activates P-gp is the epsilon isoform (Idriss et al. 2000), the same that is translocated during myocardial ischemia (Ping et al. 1997). Furthermore, heat shock transcription factor 1, which plays a role in cell protection against myocardial ischemia–reperfusion injury, is also a transcription factor for the MDR-1 gene (Williams and Benjamin 2000).
The precocity of P-gp expression seen in our model has been previously reported for human lymphocytes after PKC stimulation with TPA (Chaudhary and Roninson 1992), where the MDR-1 mRNA was detected as early as 2 hr after induction. As suggested by Shtil and Azare (2005), MDR-1 can be regarded as an "immediate early" gene, whose activation plays a pivotal role for cell survival.
Interestingly, P-gp was located at different regions of the plasma membrane over time. At 3 and 24 hr after reperfusion, P-gp appeared preferentially located in the T tubules, but at 48 hr it was also (and predominantly) present in the intercalated discs and gap junctions. The reasons for these translocations are difficult to explain. However, one can speculate that the preferential presence of P-gp in the T invaginations may serve to extrude dangerous substances from the close vicinity of the contractile apparatus and therefore allow for a more rapid recuperation from stunning. Following the same reasoning, in the intercalated discs P-gp may protect the gap junctions by transporting products of anaerobic metabolism from neighboring myocytes to the narrow (1 to 2 nm) intercellular space between them. Another possibility is that these translocations may be the result of lateral diffusion, a phenomenon that describes trafficking of proteins in the membrane along the lateral surface. A known example for myocyte integral membrane proteins exhibiting significant lateral diffusion is the cardiac ryanodine receptor RyR2 (Peng et al. 2004). In other cell types, glycoproteins including CFTR, an ABC transporter with molecular structure similar to that of P-gp, have been shown to display lateral diffusion (Bates et al. 2006). Therefore, it is reasonable to expect similar behavior for P-gp in the cardiac sarcolemma. Given that in isolated cardiac myocytes hypoxia has been shown to accelerate lateral diffusion (Finch et al. 1985), the translocation pattern observed in our animals may have resulted from a similar influence of the hypoxic conditions on P-gp.
The reason for the persistency of P-gp expression for a relatively long time cannot be explained with the present data, especially because of the low number of animals studied at 24 and 48 hr. However, the possibility that it may be related to the delayed phase of ischemic preconditioning could be considered. The ischemic preconditioning mechanism was described as a phenomenon by which transient myocardial ischemia protects the heart from extensive necrosis (Murry et al. 1986). The protection vanishes in a couple of hours but reappears 24 to 96 hr later, helping to protect the cardiomyocyte from a new ischemic event (Yellon and Baxter 1995). This delayed phase of ischemic preconditioning (also termed second window of protection) may be at least in part afforded by P-gp, extruding from the myocyte the toxic compounds generated by the new ischemic episode.
Finally, our finding of low levels of P-gp expression by Western blot and MDR-1 mRNA by RT-PCR in the control, normoperfused myocardium without any localization by immunohistochemistry reflects the well-known differences of sensitivity between these methods (Volk et al. 2005). Expression of MDR-1 mRNA with immunostaining of the capillaries has been reported in human non-failing hearts (Meissner et al. 2002). However, these hearts were donor organs that were excised and preserved for transplantation and, therefore, probably subjected to a degree of ischemia, which could have raised P-gp expression to a level detectable by immunohistochemistry. In turn, this latter situation is likely comparable to our finding of vessels immunostained for P-gp in the close vicinity of the ischemic–reperfused area (Figures 2B and 2C).
In conclusion, in adult sheep undergoing acute, non-lethal myocardial ischemia followed by reperfusion, P-gp is expressed in the sarcolemma of the cardiomyocytes from 3 hr up to at least 48 hr after restoration of myocardial blood flow. Given the known role of P-gp as an extruder of cytotoxic compounds from the intracellular space, our results suggest that P-gp may afford cardioprotection in the setting of ischemia–reperfusion injury.
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Acknowledgments |
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This study was supported by grants from the René G. Favaloro University Foundation.
We thank veterinarians María Inés Besansón, Pedro Iguain, and Marta Tealdo for assisting in anesthesia, and animal house personnel Juan Ocampo, Osvaldo Sosa, and Juan Carlos Mansilla for dedicated care of the animals. We also thank Julio Martínez, Juan Gauna, and Marcela Álvarez for technical help. R.P.L. and A.J.C. are established investigators of Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Argentina.
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Footnotes |
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Received for publication June 2, 2006; accepted October 17, 2006
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