Introduction
The blood-brain barrier (BBB), a dynamic interface between systemic circulation and brain, precisely regulates the CNS microenvironment [
1]. The BBB selectively restricts blood-borne and xenobiotic entities from entering the CNS, thus maintaining cerebral homeostasis. These restrictive properties are bestowed upon the BBB by unique features of the microcapillary endothelium such as: 1) expression and organization of intercellular tight junction (TJ) complexes [
2,
3]; 2) polarized expression of specialized carrier systems for selective transport of essential nutrients; 3) non-selective drug efflux pumps [
4,
5]. Thus, BBB integrity is critical to ensure optimal CNS function and its disruption during cerebrovascular pathologies can be prodromal to the onset and progression of major neurological disorders [
6].
Increasing evidence indicts BBB dysfunction as a major cerebrovascular complication in diabetes mellitus that underlies the pathogenesis of a host of CNS disorders [
7,
8]. Both hypoglycemia and diabetes-dependent chronic hyperglycemia have profound impact on cerebrovasculature in terms of endothelial dysfunction, increased vascular permeability, and altered gene expression, thus leading to potential neuronal injuries. Chronic hyperglycemia has been shown to affect BBB permeability, although conflicting evidence exists between animal [
9,
10] and human studies [
11,
12]. Similarly, disparate evidence from clinical and experimental studies has been reported in relation to the effects of hyperglycemia on BBB glucose transporters (mainly GLUT-1) expression and nutrient transport. While some studies have shown long-standing hyperglycemia being prodromal to a decreased GLUT-1 expression, others have reported an unaltered cerebral glucose metabolism and no changes in the expression of glucose transporter under similar conditions. Chronic hypoglycemia has been shown to elicit BBB over-expression of GLUT-1 perhaps to compensate for low circulating blood glucose levels [
13]. However, the issue of whether altered glycemic conditions may impact other BBB glucose transporters has only been marginally addressed. Potential effects of altered glycemia on TJ expression/redistribution and endothelial oxidative/inflammatory responses are other under-investigated areas. Notably, inter-species variations in the expression of BBB phenotypic markers further impact the translational significance of a large number of such studies [
14].
Reliable
in vitro models that closely mimic the human BBB microenvironement are essential to understand the cellular/molecular basis of brain microvessel endothelial physiology [
15], thus facilitating the identification and characterization of BBB regulatory mechanisms potentially impaired in diseased states [
16,
17]. Recently, an immortalized brain microvascular endothelial cell line, hCMEC/D3, was derived from isolated human primary BBB ECs by lentiviral vector-mediated co-expression of human telomerase and SV40 T antigen [
18]. This stable cell line exhibits robust proliferation while retaining the morphological and known biochemical phenotype of differentiated human BBB ECs over many passages [
18,
19]. This cell line has been extensively characterized for its utility as a model of human BBB for CNS drug delivery and translational neurovascular research focusing on BBB function [
16,
20‐
22].
Given the increased public attention to diabetes and its relevance to the pathogenesis of major CNS disorders (e.g., Diabetic neuropathy, Alzheimer’s, Dementia, Stroke, Depression, etc.), the objective of this study is to assess and characterize the independent impact of diabetes-associated hyper and hypoglycemic conditions on BBB integrity and endothelial function using hCMEC/D3 cell line.
Methods
Materials and reagents
The antibodies used in this study were obtained from the following sources: Rabbit anti-ZO-1 (#D7D12) and anti-VE-cadherin (#D87F2) from Cell Signaling Technology (Danvers, MA, USA); Rabbit anti-GLUT-1 (#ab15309) and anti-SGLT-1 (#ab14686) from Abcam (Cambridge, MA, USA); Rabbit anti-GLUT-4 (#sc-7938) from Santa Cruz Biotechnology (Santa Cruz, CA, USA); Donkey anti-rabbit (#NA934) and sheep anti-mouse (#NA931) HRP-linked antibodies from GE Healthcare (Piscataway, NJ, USA); Mouse anti-Claudin 5 (#35-2500), goat anti-mouse (#A11001) and anti-rabbit (#A21428) conjugated to Alexa Fluor® 488 and 555 from Invitrogen (Camarillo, CA, USA). Sterile culture ware was obtained from Fisher Scientific (Pittsburgh, PA, USA), while other reagents and chemicals were purchased from Sigma-Aldrich (St. Louis, MO, USA) or Bio-Rad laboratories (Hercules, CA, USA). Fluorescein isothiocyanate (FITC) and Rhodamine B isothiocyanate (RITC) dextrans were purchased from Sigma-Aldrich, while Cascade Blue®-dextran was obtained from Invitrogen (Eugene, OR, USA).
Cell culture
The immortalized hCMEC/D3 cell line was donated by Dr. Couraud (INSERM, Paris). The hCMEC/D3 cells (passage 28-32) were seeded on collagen-coated culture flasks (2.5-3 × 10
4/cm
2) or glass slides (4 × 10
4/cm
2) in EBM-2 basal medium (Lonza, Walkersville, MD, USA) supplemented with 5% FBS (Atlanta Biologicals, Lawrenceville, GA, USA), chemically defined lipid concentrate (Life technologies, Carlsbad, CA, USA), growth factors, antibiotic/antimycotic (1:1) and HEPES (10 mM) and maintained at 37°C with 5% CO
2 exposure. Medium was changed every 2-3 days until the cells reached confluence. Monolayer integrity of hCMEC/D3 cells at confluence was confirmed by the expression of endothelial cell-specific phenotypic markers at cell-cell junctions, as previously described [
18].
Co-culture setup
HCMEC/D3 cells were co-cultured with juxtaposed human astrocytes (ScienCell Research Laboratories, San Diego, CA, USA) grown on the abluminal side of semipermeable Transwell® inserts [
16,
23]. The Transwell® apparatus allows for the BBB endothelium to remain in anatomical contact with astrocytes thus closely mimicking the BBB anatomical structure [
17]. Briefly, Transwell® inserts (clear polyester membranes with 0.4 μm pore size) were seeded with human primary astrocytes (HA, passage no. 3-4) on the abluminal side of the microporous membrane and cultured in DMEM/F12 media with 10% FBS. After 72 h, hCMEC/D3 cells were loaded on the apical side and grown in EBM-2 basal medium containing the supplements mentioned above. Cells in co-cultures were grown in their respective media for one week before treatment. Confluence and integrity were checked by phase contrast microscopy and trans-endothelial electrical resistance (TEER) measurements.
Treatment
HCMEC/D3 cells in monocultures or co-cultures were maintained overnight in media containing 1% human serum with no growth factors (referred as low serum media). The next day, cells were exposed to fresh low serum media containing 5.5 mM (normal/control), 2.2 mM (hypoglycemic) or 35 mM (hyperglycemic) D-glucose for 3-24 h. These concentrations were selected based on previously published reports
in vitro[
24,
25] and
in vivo[
13]. Additional osmotic control experiments were performed by exposing hCMEC/D3 cells to media containing 5.5 mM D-glucose + 4.5 mM L-glucose, 2.2 mM D-glucose + 7.8 mM L-glucose or 30 mM D-mannitol. Note that this mannitol concentration was significantly lower than the 1.4 M used for transient opening of BBB [
26].
Cell viability
Following exposure to normal, hypo or hyperglycemic (5.5, 2.2 or 35 mM D-glucose respectively) media for 3 and 24 h, cell viability was determined by lactate dehydrogenase (LDH) measurements in the culture medium by a colorimetric enzymatic reaction (Pierce LDH cytotoxicity assay kit - Thermo Scientific, Rockford, IL), according to the manufacturer guidelines.
BBB integrity
Acute effects of altered glycemia on BBB integrity were assessed by measuring concomitant paracellular permeability (luminal to abluminal) to labeled dextrans (4-70 kDa) and TEER (Ω.cm
2) measurement by EVOM 2 (World Precision Instruments, Sarasota, FL, USA), as described earlier [
16,
23]. For paracellular permeability studies, hCMEC/D3 cell monolayers seeded on Transwell inserts were exposed to normal, hyper or hypoglycemic media for 30 min at 37°C in humidified incubator prior to the addition of a mixture of labeled dextrans in PBS (FITC- 4 kDa, 7 mg/ml; Cascade Blue®- 10 kDa, 5 mg/ml; and RITC - 70 kDa, 7 mg/ml) to the luminal compartment. Abluminal samples (50 μL) were collected over 60 min and replaced with equal volume of fresh media to allow sink conditions. Dextran flux was determined by fluorescent measurements at appropriate excitation and emission wavelengths for each fluorescent dye. Media-only samples with no added dextrans and cell-free inserts with added dextrans served as reference. Similarly, following 24 h treatment, TEER values were measured across hCMEC/D3 cell monolayers. Cell-free inserts were used to calculate the final resistance.
ELISA
Following treatment, the respective conditioned media from either mono or co-cultures of hCMEC/D3 cells were analyzed by Quantikine ELISA kits (R&D systems, Minneapolis, MN, USA) for vascular endothelial growth factor (VEGF), platelet derived growth factor (PDGF-BB) and interleukin-6 (IL-6) according to the manufacturer’s protocol.
Immunofluorescence
HCMEC/D3 cells cultured on chamber slides were rinsed in PBS and fixed with ice-cold acetone (10 min at -20°C). After PBS washes, fixed cells were blocked with 5% goat serum in PBS at room temperature (RT) for 30 min, followed by incubation with rabbit (1:200) or mouse (1:150) primary antibodies overnight at 4°C. After 3 rinses with PBS, cells were incubated for 1 h at RT with Alexa Fluor® 488 or 555 conjugated goat anti-mouse or anti-rabbit antibodies, respectively (1:1000). Thereafter, cells were rinsed and counterstained with DAPI in Prolonged Gold Anti-fade reagent (Invitrogen, OR, USA). Slides were cover slipped, cured overnight in dark and examined with EVOS digital inverted fluorescence microscope. Cell staining devoid of primary antibodies served as negative controls.
Western blotting
Briefly, cells were lysed in ice-cold RIPA buffer containing Complete Protease Inhibitor (Roche Diagnostics, Indianapolis, IN, USA) and centrifuged at 14000 rpm, 4°C for 30 min. Protein concentration was determined by bicinchoninic acid assay [
27]. Denatured samples containing equal amounts of protein (12 or 15 μg) were subjected to SDS-PAGE (7.5 or 10%) and electrotransferred to PVDF or nitrocellulose membranes. Membranes were blocked for 2 h (RT) with 5% non-fat dry milk in TBS containing 0.1% Tween-20 (TTBS) and subsequently incubated with rabbit (1:500) or mouse (1:350) primary antibodies. After 3 washes (10 min each) with TTBS, membranes were incubated with anti-rabbit or anti-mouse (1:7000) HRP-conjugated secondary antibodies (2 h, RT) and washed with TTBS. Bands were detected by enhanced chemiluminescence using Amersham ECL™ Prime with ChemiDoc™ XRS system. Membranes were subsequently stripped and probed for β-tubulin (1:500), as a loading control. Band densities were analyzed by Quantity One Software.
Statistical analyses
Data from all experiments were expressed as mean ± standard error of mean (S.E.M) and analyzed by one or two-way ANOVA using GraphPad Prism Software Inc. (La Jolla, CA, USA). Post hoc multiple comparison tests were performed with Tukey’s or Dunnett’s test. P value less than 0.05 was considered statistically significant.
Discussion
In vivo experiments are currently the gold standard in basic and translational studies; however several factors generally hinder the utility of animal models to dissect out the impact of complex pathophysiological stimuli down to molecular mechanisms. In addition, marked inter-species differences make it difficult to extrapolate
in vivo data to humans. In this context, development of reliable
in vitro platforms for basic and translational study is supported by the National Research Council [
33]. Recent studies have shown inter-species variations related to the expression and distribution of BBB transporters, thus advocating for the use of humanized models to study
in vitro the physiological/pathological responses of the human BBB endothelium
in vivo[
14,
17,
34]. Although, various immortalized endothelial cell lines have been developed, the hCMEC/D3 cell line stands out as the most well characterized
in vitro human BBB model till date [
20]. It has been shown to retain known structural and functional aspects of differentiated human BBB endothelium [
16,
20] over multiple passages [
18,
20]. However, the expression of specific TJ molecules and transporters on hCMEC/D3 cells, though comparable to primary BMECs [
18,
35], remained relatively 3-5 fold lower than in isolated human brain microvessels [
36]. Recently, Luissint and colleagues [
37] have investigated the molecular partners of claudin-5 and their putative involvement in regulation and maintenance of BBB TJ integrity in this cell line. Nevertheless, hCMEC/D3 endothelial cells maintain a restrictive barrier with expression of functional transporters and intercellular TJs that can be further enhanced by various stimuli and culture conditions including exposure to astrocytes and shear stress.
Both claudin-5 and ZO-1 have previously been shown to play a critical role in BBB TJ formation and organization [
16,
38,
39]. Our data demonstrate a progressive down-regulation of claudin-5 expression at cell-cell contacts following hypoglycemic exposure, while exposure to hyperglycemia did not alter its immunoreactivity, in accordance with previous reports [
24]. Surprisingly, an increased expression of cytosolic ZO-1 was observed at 3 and 24 h under hypoglycemic conditions. However, prolonged exposure (72 h, data not shown) resulted in significant reduction of ZO-1, suggesting a time-dependent dysregulation of ZO-1 at cell-cell contacts by hypoglycemia. It is plausibly explained that hypoglycemic exposure for 3-24 h induces a significant translocation of ZO-1 away from membrane, thus affecting the barrier integrity, as discussed below. On the other hand, hyperglycemia for 24 h did not alter ZO-1 expression, as reported earlier [
40], although a significant alteration in its localization (a pronounced cytosolic distribution) was observed.
VEGF - an endothelial specific mitogen and a potent mediator of vascular permeability [
28], was shown to alter BBB integrity
in vitro[
41] and
in vivo[
38] by affecting TJ protein expression and organization including phosphorylation. In addition, our findings are also supported by previous studies performed in brain [
24,
41] and retinal ECs [
42]. Notably, our results have shown significant differences in endothelial response to hypo or hyperglycemic conditions which manifested through differential release of VEGF when ECs were cultured with or without abluminal astrocytes (Figure
3). Specifically, VEGF release in response to hypoglycemic media was significantly enhanced when ECs were co-cultured with astrocytes as compared to endothelial monocultures. Interestingly, hyperglycemic exposure showed a two-fold increase in VEGF release by endothelial cells co-cultured with astrocytes (Figure
3B), while no significant effects were observed in monocultures when compared to controls (Figure
3A). However, while no significant TEER changes were observed within 24 h treatment (despite the initial increase of VEGF), we observed a significant increase in permeability to dextran molecules. A statistically significant TEER decrease was observed only at 72 h which was paralleled by a larger increase in VEGF release (data not shown) compared to both controls and 24 h exposure (Figure
3C). While we might have expected a decline in TEER even at 24 h this is not surprising since characteristically relatively low TEER values commonly obtained (with few exceptions) in Transwell setups may not provide enough sensitivity to detect minimal yet significant changes in paracellular permeability. Such is the case here where relative loss of BBB integrity was instead demonstrated by changes in dextran permeability. Nevertheless, hypo and hyperglycemia differentially regulate the TJ protein distribution and expression in a time-dependent manner and thus negatively affect the BBB integrity and corresponding selective permeability. While the mechanism(s) for the observed effects at this point are still unknown it is possible that the increase in VEGF expression can be responsible for these phenomena although other mechanisms (e.g. oxidative/inflammatory stress as mentioned below) cannot be ruled out and need to be further investigated.
In line with these findings, our results demonstrate that hypoglycemia, and hyperglycemia (to some extent), potentially compromise BBB integrity, as evidenced by a significant increase in paracellular permeability (abluminal accumulation) to dextrans in a time-dependent and size-selective manner in hCMEC/D3 cells co-cultured with astrocytes, with a significant increase in permeability to all labeled dextrans at 60 min following treatment (vs. controls, Figure
3C). These results are supported by a recent finding in which rapid normalization of plasma glucose in diabetic rats with acute insulin injection (mimicking acute hypoglycemia) increased the sucrose permeability at 20 min [
43]. Note that similar to sucrose, dextrans cross the BBB mainly by a paracellular pathway, but not through cell transcytosis [
44]. Moreover, hypoglycemia induced a similar increase in paracellular flux of all labeled dextrans at 60 min (data not shown). However, a closer analysis of permeability at later time points indicates that the paracellular fluxes of all dextrans inclined towards steady state dynamics and therefore, permeability was assessed at 30 min following the addition of dextran markers.
Brain microvascular endothelium is highly enriched with stereospecific glucose transporters, mainly GLUT-1 (~55 kDa), that selectively facilitate the diffusion of glucose to the CNS [
45]. Existing evidence indicates a decreased GLUT-1 activity and glucose clearance in chronic hyperglycemia, with a parallel decrease in expression of GLUT-1 at BBB [
46], as confirmed by subsequent studies [
47,
48]. On the other hand, chronic hypoglycemia increased BBB glucose transport resulting from a concomitant increase in GLUT-1 transcription and expression on lumenal side of brain capillaries [
49]. In line with these observations, we found opposite effects of hypo and hyperglycemia on GLUT-1 expression on hCEMC/D3 cells following 3-24 h exposure. Specifically, GLUT-1 expression was progressively up-regulated by hypoglycemia (24-72 h), following an initial down-regulation at 3 h. Given the differential regulation of GLUT-1 expression by hypoglycemia in a time-sensitive manner, additional studies investigating the effects of hypoglycemia on glucose transport kinetics would be important, as GLUT-1 impairment was previously linked to loss of BBB integrity [
50]. Our results also indicate a marginal decrease in membrane GLUT-1 expression by prolonged hyperglycemia (slow onset). Interestingly, 24 h hyperglycemia (but not hypoglycemia) significantly increased the expression of insulin-responsive GLUT-4. Divergent evidence has been reported on the expression of this insulin-sensitive glucose transporter across various brain regions and the cerebral vasculature. However, GLUT-4 was shown to be expressed in fore brain microvessel endothelium [
51], while Ngarmukos and colleagues reported its expression and co-localization with GLUT-1 and other endothelial marker (such as ZO-1) in brain glucose-sensing region [
52] and could be involved in glucose uptake in hCMEC/D3 cells [
53]. Nevertheless, the functional relevance of this finding is not well understood given the evidence that GLUT-4 expression at brain microvasculature remains stable during long-standing diabetes [
51].
Importantly, we show for the first time, the differential regulation of BBB SGLT-1 (~75 kDa isoform) expression by hypo and hyperglycemia in hCMEC/D3 cells. Data indicate an induction of this sodium-dependent glucose transporter (2Na
+/Glucose) expression specifically by hypoglycemic exposure from 3-24 h. These findings corroborate previous studies demonstrating an increased activity of SGLT-1 in bovine brain artery ECs during low glucose conditions [
54], in addition to its role at cerebrovasculature during oxygen-glucose deprivation [
55]. Overall, the present study highlights the concomitant alterations in BBB endothelial expression of GLUT-1 and SGLT-1 under hypoglycemic conditions and further studies are required to dissect out the relative functional significance of each transporter.
Existing evidence implicates the potential role of oxidative and inflammatory stress, through overproduction of reactive oxygen species (ROS), in the development of various CNS complications in diabetes [
56‐
58]. In fact, the cerebrovascular endothelium is highly vulnerable to the oxidative stress resulting in the loss of BBB function and integrity,
via altered composition of the intercellular TJ complexes as one of the mechanisms [
59‐
61]. Recent studies have demonstrated the potential role of Nrf-2 in preventing the BBB dysfunction and preserving its integrity, by protecting the BBB endothelium from oxidative and inflammatory stress [
30,
62,
63]. Here in, we demonstrate for the first time a progressive and significant loss of Nrf-2 expression by hypoglycemic insult at 24 h suggesting loss of potential protective mechanisms against oxidative stress thereby leading to increased production of ROS as previously reported by others [
25] (Figure
5A), although, it cannot be ruled out that the observed decrease in Nrf-2 can be related to decrease in cellular metabolism following hypoglycemia. It is logical to assume that hypoglycemia-induced dysregulation of TJ proteins is possibly mediated through the down-regulation of Nrf-2 expression, as Nrf-2 activation was shown to partially restore TJ proteins and prevent BBB permeability [
63]. In contrast, hyperglycemic exposure for 24 h did not affect Nrf-2 expression (relative to control), while previous studies indicate Nrf-2 down-regulation following chronic hyperglycemic exposure over 4 days [
64].
Interestingly, we observed a significant decline in BBB endothelial IL-6 release following 3 and 24 h exposure to hypoglycemic (but not hyperglycemic) conditions (Figure
5B) which could be attributed to the down-regulation of Nrf-2. This notion is supported by a recent finding from Wruck and colleagues [
65] that demonstrates the role of Nrf-2 in regulation of IL-6 gene transcription and suggests a possible role for IL-6 in oxidative stress defense. Moreover, our data indicate disruption and relocation of VE-cadherin with a concomitant increase in the soluble VCAM-1 expression, by hypo and hyperglycemia in hCMEC/D3 cells, effects that are critical to progression of BBB inflammation and augmented leukocyte infiltration in diabetes [
31,
59,
66,
67]. Interestingly, VE-cadherin was shown to positively regulate the transcription of claudin-5 [
32], thus providing an alternative explanation for loss of claudin-5 by hypoglycemia. In addition, hypoglycemic exposure was shown to down-regulate the PDGF-BB release from hCMEC/D3 cells (Figure
5C). While the role of PDGF-BB in BBB physiology and function is emerging, existing evidence indicates the importance of PDGF-BB/PDGFR-β signaling for optimal function of pericytes [
68], an inherent constituent of neurovascular unit that regulates the BBB function [
6]. Taken together, these results suggest that immunological function of BBB is compromised following altered glycaemia and, thus may lead to subsequent neuroinflammation.
In summary, our in vitro study suggests that hypo and hyperglycemia differentially impact and potentially impair BBB integrity and function through altered expression/distribution of TJ proteins including various glucose transporters. In addition, hypoglycemic exposure affected the BBB endothelial expression of oxidative and inflammatory stress markers including VCAM-1 and Nrf-2. In conclusion, this study provides further insights into the role and modality of hypoglycemia-induced BBB dysfunction.
Competing interests
No competing interests are perceived to exist for any of the authors listed on this manuscript.
Authors’ contributions
RS contributed to the experimental design, conducted the experiments and had written the manuscript; SP contributed to design and performing the experiments including the revision of the manuscript; LC contributed to experimental design, manuscript writing and revision as well as supporting this study. All authors have read and approved the final version of the manuscript.