Significance of MDR1 and multiple drug resistance in refractory human epileptic brain
© Marchi et al; licensee BioMed Central Ltd. 2004
Received: 19 April 2004
Accepted: 09 October 2004
Published: 09 October 2004
The multiple drug resistance protein (MDR1/P-glycoprotein) is overexpressed in glia and blood-brain barrier (BBB) endothelium in drug refractory human epileptic tissue. Since various antiepileptic drugs (AEDs) can act as substrates for MDR1, the enhanced expression/function of this protein may increase their active extrusion from the brain, resulting in decreased responsiveness to AEDs.
Human drug resistant epileptic brain tissues were collected after surgical resection. Astrocyte cell cultures were established from these tissues, and commercially available normal human astrocytes were used as controls. Uptake of fluorescent doxorubicin and radioactive-labeled Phenytoin was measured in the two cell populations, and the effect of MDR1 blockers was evaluated.
Frozen human epileptic brain tissue slices were double immunostained to locate MDR1 in neurons and glia. Other slices were exposed to toxic concentrations of Phenytoin to study cell viability in the presence or absence of a specific MDR1 blocker.
MDR1 was overexpressed in blood vessels, astrocytes and neurons in human epileptic drug-resistant brain. In addition, MDR1-mediated cellular drug extrusion was increased in human 'epileptic' astrocytes compared to 'normal' ones. Concomitantly, cell viability in the presence of cytotoxic compounds was increased.
Overexpression of MDR1 in different cell types in drug-resistant epileptic human brain leads to functional alterations, not all of which are linked to drug pharmacokinetics. In particular, the modulation of glioneuronal MDR1 function in epileptic brain in the presence of toxic concentrations of xenobiotics may constitute a novel cytoprotective mechanism.
Failure to respond to therapeutic concentrations of antiepileptic drugs (AEDs) is the usual basis for defining multiple drug resistant epilepsy, but the mechanisms underlying resistance to AEDs are still largely unknown. It is generally believed to be a multifactorial phenomenon, depending on both pharmacodynamic and pharmacokinetic mechanisms. The electrical and synaptic properties of neurons in epileptic human tissue are reported to undergo changes that may result in decreased susceptibility to some AEDs . Multidrug resistance in epilepsy may also result from inadequate intraparenchymal AED concentrations due to poor penetration of the blood-brain barrier (BBB).
Recent findings suggest that the molecular mechanisms of clinically defined multiple drug resistance involve drug-efflux transporters such as the ATP-binding cassette subfamily B member 1 (ABCB1), also known as MDR1 or P-glycoprotein (P-gp) [2–4]. Specifically, in epileptic brain, genes associated with multiple drug resistance are overexpressed in the endothelial cells that constitute the BBB [5, 6]. MDR1 is also overexpressed in neurons [4, 7] and astrocytes (in which MDR1 is normally not measurable) from lesions associated with active epileptogenic foci in human and rodent brain [8–10].
The link between MDR1 overexpression and drug resistance in epilepsy is still poorly understood [6, 11]. Thus, while localization of the drug extrusion pump in the BBB is consistent with reduced penetration of AEDs into the CNS, it is not known if or how the presence of MDR1 in the parenchyma affects drug delivery and distribution, or whether it is involved in different cellular functions. Evidence from several groups suggests that MDR1 diminishes the apoptotic response induced by growth factor withdrawal , decreases complement-mediated cytotoxicity ( and impairs the activation of caspase-dependent cell death pathways [14, 15]. Reports indicate that all these events occur in epileptic tissue, and they are thought to be at least partly responsible for seizure-associated neuronal cell death. In addition, we recently found that epileptic astrocytes that overexpress MDR1 are devoid of p53, a proapoptotic factor .
In this study we have evaluated the relationship between neuronal and astrocytic MDR1 expression and the capacity of the cells to survive cytotoxic insults, using drug resistant epileptic human specimens. Our results suggest that overexpression of MDR1 leads to functional alterations in the CNS that may be linked to both drug pharmacokinetics and neuroglial survival in injured brain.
Information on patients affected by various forms of epilepsy whose brain specimens were used for the experiments (ICC = Immunocytochemistry and Immunohistochemistry, TOX = Phenytoin toxicity, UP = drug uptake).
Parieto-Occipital-Frontal cortical dysplasia, Right Hemispherectomy
Temporal Lobe Epilepsy, Hippocampal atrophy
Left Hippocampal sclerosis
Cortical Dysplasia, Right Hemispherectomy
Left Cortical Dysplasia
Right Frontoparietal Epilepsy
Left Frontal Lobe Epilepsy
Right Temporal Lobe Epilepsy
Temporal Lobe Epilepsy
Temporal Lobe Epilepsy
Left Frontal Lobe Epilepsy
Left Temporal/Frontoparietal Epilepsy
Cell isolation and primary cultures
Astrocyte cell cultures were established, as described by Marroni et al. [8, 9, 16], from cerebral cortical tissue obtained during temporal lobectomies (n = 3) conducted to relieve medically intractable seizures (see Table 1 for details on patients, ID# 12, 13, 14). The cells were passaged up to three times before use. MDR1 expression was not affected by the number of passages [8, 9, 16].
Commercially available normal human astrocytes were used as controls (ACBRI 371, Applied Cell Biology Research Institute, Kirkland, WA, USA, and Clonetics, Biowhitaker, Walkersville, MD, USA).
To investigate MDR1 protein expression and cellular distribution in human epileptic tissue, slide-mounted sections (10 μm thickness) from frozen brain tissue (Table 1, patient ID# 1–11; 3 slices per patient) were double immunostained as previously described [8, 9, 16]. The primary antibodies used were mouse monoclonal anti-P-Glycoprotein (C494) (1:40, Calbiochem-Novabiochem Corporation, San Diego, CA, USA), human polyclonal anti-P-Glycoprotein (1:100, Calbiochem-Novabiochem Corporation, San Diego, CA, USA), mouse monoclonal anti-neuronal nuclei (NeuN) (1:500, Chemicon International, Temecula, CA, USA), rabbit polyclonal anti-neurofilament (NF) (1:200, Chemicon International, Temecula, CA, USA) and rabbit anti-cow glial fibrillary acidic protein (GFAP) (1:200, DAKO Corporation, Carpinteria, CA, USA). Secondary antibodies were chosen according to the primary antibody hosts: Texas red dye-conjugated affinipure donkey anti-mouse IgG (1:50, Jackson Immunoresearch Laboratories Inc., West Grove, PA, USA), and Fluorescein isothiocyanate (FITC)-conjugated affinipure donkey anti-mouse and anti-rabbit IgG (1:200, Jackson Immunoresearch Laboratories Inc., West Grove, PA, USA). Sections were coverslipped on glass slides using Vectashield mounting medium with DAPI (Vector, Burlingame, CA, USA) and analyzed by fluorescent microscopy.
Astrocytes from epileptic tissue (Table 1, patient ID# 12, 13, 14) or commercially available control human astrocytes were cultured in 8-well chamber-slides. At confluence, the cells (approximately 8 × 104 per well) were treated overnight with 1μM XR9576, a specific MDR1 blocker [17, 18], or for 2 h with 50 μM verapamil, a non-specific MDR1 blocker [19, 20]. Further sets of astrocytes from epileptic tissue and controls were incubated as above but in the absence of blockers. Fluorescent red doxorubicin  was then added to all the cultures for 1, 2, 3, 5, 7 and 24 h. Incubation was stopped by rinsing twice with PBS and the cells were fixed overnight at 4°C in 4% formalin in PBS (pH 7.4). They were mounted and coverslipped the next day using Vectashield mounting medium. Doxorubicin uptake was analyzed by fluorescent microscopy (Leica Leitz DM-RXE, Wetzlar, Germany) using NIH Image Software. For each well, four fields (1600 μm2) were randomly analyzed and optical density measurements were averaged to obtain representative data. To quantify the doxorubicin in the cells, the fluorescence in each sample was compared with standard solutions of doxorubicin (10 nM-10 μM). Data were analyzed using Origin Lab 7 software.
14C-Phenytoin uptake was measured in cultured astrocytes from epileptic tissue (Table 1, patient ID# 12, 13, 14) and in control astrocytes, as described by Meyer et al. . The cells were cultured in 30-mm Petri dishes (approximately 106 cells) and incubated at 37°C with 1 ml of T3 cell buffer (Tris-HCl 50 mM, NaCl 120 mM, KCl 50 mM, pH 7.4) containing 10 μM 14C-Phenytoin (Specific activity = 9.57 μCi/μmol). The incubation was terminated after 10 s, 30 s, 1 min, 5 min or 10 min by adding 1 ml of ice-cold T3 buffer. The cells were washed with 1 ml of ice-cold T3 buffer and solubilized with 1% (w/v) Triton X-100 for 1 h at 37°C. Intracellular radioactivity was measured using a scintillation cocktail (Packard Ultima Gold, ECN, Costa Mesa, CA, USA).
Acute in vitro toxicity
Brain slices (500 μm) were cut using a vibratome from dysplastic human cortex and temporal lobe epilepsy brain specimens (Table 1, patient ID# 9,10,11). Slices (n = 6 per patient) were maintained in vitro as previously described [23, 24]. A further set of 6 slices was obtained from 3 naïve rats as previously described . Slices (n = 2 per patient per experimental condition) were incubated for 2 h in artificial CSF containing, in mM: NaCl 124; KCl 3; CaCl2 1; MgCl2 1.4; NaHCO3- 26; KH2PO4 1.25; glucose 10, with or without 3 μM XR9576. A toxic concentration (375 μM) of Phenytoin (PHE) was then added for 5 h . An additional set of slices was kept for 7 h in artificial CSF only, and electrophysiological measurement of activity was used to assess tissue viability throughout the experiment. Live/Dead Viability/Cytotoxicity solution (Molecular Probes L3224, Eugene, OR, USA) was used to quantify cell death or survival; EthD-1, a component of the solution, enters cell nuclei through damaged membranes, producing a bright red fluorescence in dead cells. The 2 mM EthD-1 stock solution (20 μl) was added to 10 ml of 1X sterile PBS. At the end of the experiment, each slice was washed with PBS and incubated with 2 ml of the above solution for 10 min under continuous oxygenation. The slices were then fixed in 4% formalin in PBS overnight at 4°C and cryoprotected by 30% sucrose. Three 20 μm slices were cryosectioned from each 500 μm slice and analyzed by fluorescent microscopy. DAPI was used to assess the total number of cells per slice, and GFAP and NeuN were used to identify glia and neurons (see 'Immunohistochemistry'). The number of EthD-1 positive cells was reckoned in 3 randomly chosen fields (1600 μm2) within each slice. These values were averaged for each slice and expressed as percentages of the average number of DAPI-positive cells in the chosen fields.
Evaluation of glioneuronal damage
Statistical analysis of data
Data were expressed as means ± SEM. The level of significance between means was estimated by ANOVA (Origin 6.0. Microcal). Differences with p < 0.05 were considered significant.
Results were obtained from 14 patients (50% female) affected by intractable seizures. The mean patient age was 16.4 years (range 8 months – 49 years; SE = 4.6). For details, see Table 1.
MDR1 expression in human epileptic brain tissue
Figure 1 shows representative micrographs of MDR1 expression in endothelial, glial and neuronal cells from epileptic human brain specimens (Table 1, patient ID# 1–11). The findings are consistent with previous work demonstrating that MDR1 expression in multiple drug resistant brains is confined to the cortical lesion site [4, 7–9, 16]; this was consistently observed in all epileptic samples in the present study. Thus, relatively normal brain distant from the dysplastic tissue can be used as "control". Abundant MDR1 immunopositive endothelial cells (thin arrows in A) were observed in epileptic cortex, as well as immunopositive parenchymal and perivascular astrocytes (arrowheads in A) double-labeled with GFAP, a specific glial marker. Out of 107 GFAP-positive astrocytes, 91 (85%) showed MDR1 staining (Figure 1B). We also examined MDR1 expression in neurons from epileptic tissue, identified by NeuN and NF immunoreactivity (Fig. 1C). Approximately 169 out of 264 NeuN-positive neurons (64%) showed MDR1 staining (Figure 1D).
Role of MDR1 expression in drug extrusion by astrocytes
Fig. 2B shows that uptake of 10 μM14C-Phenytoin was significantly lower in astrocytes from epileptic tissue than in control astrocytes, and the difference was maximal after 10 min incubation with the AED (p < 0.05). The difference was abolished in the presence of 1 μM XR9576, indicating MDR1-mediated efflux of PHE in epileptic astrocytes. The MDR1 blockers did not affect doxorubicin or Phenytoin uptake in control astrocytes (not shown). Neither Phenytoin nor doxorubicin treatment induced toxicity in cell cultures under our experimental conditions.
MDR1 and cell survival
MDR1 is involved in detoxification mechanisms that protect cells from xenobiotics , apoptosis  and other cellular stresses [13–15]. To investigate whether MDR1 expression in astrocytes and neurons from epileptic tissue enhances survival of toxic or injurious events, we exposed neocortical slices from human epileptic (Table 1, patient ID# 9, 10, 11) and rat brain to concentrations of PHE higher than those reported to induce toxicity in cultured rat astrocytes . Bar histograms (Figure 3A) indicate that slices of human epileptic cortex exposed for 5 h to 375 μM PHE showed no cellular toxicity, as assessed by co-localization of the nuclear marker DAPI with EthD-1, a marker of cell damage. Conversely, significant cell loss (p < 0.05) was observed in rat brain slices under these experimental conditions. When MDR1 activity was blocked by 3 μM XR9576, PHE induced cell damage in the human epileptic cortex to an extent similar to that in rat brain tissue. Neurons and astrocytes, identified using NeuN and GFAP respectively, were similarly affected by PHE (Fig. 3A). The MDR1 inhibitor XR9576 alone (3μM) did not affect tissue viability (data not shown).
Figure 3B shows a significant positive correlation (R = 0.4, p < 0.006) between MDR1 expression and cell integrity, as measured by morphological evaluation of nuclear condensation (DAPI staining) [29, 30]. Quantification of the cells retaining nuclear DNA integrity showed that no DNA damage occurred in 85% of glia and 66% of neurons expressing MDR1, suggesting a novel role for MDR1 in protecting neurons and glia from toxic agents.
The main finding was that MDR1 might have different roles depending on the location in the brain where it is expressed. Thus, in addition to overexpression in endothelial cells, which is likely to affect the penetration of AEDs into the brain, MDR1 is also overexpressed in the parenchyma, where it might have a cytoprotective role, extruding otherwise toxic concentrations of xenobiotics from the intracellular compartment.
MDR1 expression in epileptic brain
In agreement with previous findings, we report here that MDR1 is highly expressed in vessels of the BBB and in parenchymal cells (histochemically identified as astrocytes and neurons) in drug refractory epilepsy of different etiologies [4, 7–9, 11, 27]. Pharmacological evidence suggests that MDR1 overexpression in blood vessels of the BBB has the crucial role of extruding AEDs from brain to blood [19, 20, 27, 31], and this phenomenon may contribute to failure of antiepiletic treatments. In this study, we focused on the effects of MDR1 expression in parenchymal neurons and astrocytes from pharmacoresistant epileptic tissue.
MDR1 expression in astrocytes: drug uptake studies
MDR1 expression in neurons and parenchymal glia: relationship to cell survival
We show in this paper that MDR1 is expressed in immunocytochemically identifiable neurons and astrocytes in brain slices from refractory human epilepsy patients. We have previously reported that basic apoptotic mechanisms may be defective in glia from epileptic tissue, since the pro-apoptotic proteins p53 and p21 could not be detected in "epileptic" astrocytes [8, 9, 16]. This evidence, together with overexpression of MDR1, suggests that "epileptic" astrocytes have gained a distinct survival advantage. This is supported by the marked enhancement of Phenytoin cytotoxicity in both glia and neurons when MDR1 function is blocked. The conclusion is consistent with the findings of Bittigau et al.  that various AEDs induce apoptotic neuronal cell death in developing naïve rat brain at plasma concentrations relevant to seizure control in humans; activators of MDR1 transcription prevented these effects.
Finally, we found a positive correlation between neuronal and astrocytic expression of MDR1 and lack of nuclear condensation, a marker of apoptosis and irreversible cell damage. Thus, expression of MDR1 in glia and neurons may protect the cells against toxic xenobiotics or against endogenous compounds that enter the brain in pathological conditions.
In conclusion, as summarized in figure 4, our findings indicate a possible new function for MDR1. In normal brain, MDR1 operates at the blood-brain barrier, regulating the plasma/brain exchange of xenobiotics. In epileptic brain, the levels of astrocytic, neuronal and endothelial MDR1 are abnormal, possibly leading to altered brain penetration/distribution of drugs. Perivascular astrocytes may also contribute to this phenomenon. In addition to its drug extrusion effect at the BBB, which may be relevant for pharmacoresistance in epilepsy, this protein may have a role in neuroglial survival under hostile conditions such as those occurring in epileptic brain. The overexpression of multiple drug resistance could be the consequence of an altered mechanism of apoptotic cell death; this hypothesis is supported by the finding that changes in multiple drug resistance gene expression correlate with negative regulation of p53 and other pro-apoptotic genes .
NM and LC carried out the pharmacological experiments and data analysis.
KLH and KMK obtained surgical resections, established astrocytic cell cultures and performed the immunohistochemical and cell counting studies.
GM performed the acute in vitro toxicity experiments.
WB provided the surgical specimens.
GD provided additional input and editing.
AV and DJ designed and co-ordinated some of the experiments.
They also contributed equally to the preparation of the manuscript.
DJ, the PI of the study, co-ordinated and supervised most of the personnel involved in this project.
glial fibrillary acidic protein
multiple drug resistance protein
The authors would like to thank Drs. P. Schwartzkroin and J. Engel for their helpful comments on an earlier version of this manuscript. They would also like to thank Dr. David Norris from Xenova Limited for the MDR inhibitor. LC was supported in part by a grant from ARDF (Alternatives Research and Development Foundation). This work was supported by NIH-2RO1 HL51614, NIH-RO1 NS 43284 and NIH-RO1 NS38195 to DJ, and by FIRB (RBNE01NR34_007) to AV.
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