The hCMEC/D3 cell line was derived from human temporal lobe microvessels isolated from tissue excised during surgery for control of epilepsy. The primary isolate was enriched in CECs. In the first passage, cells were sequentially immortalized by lentiviral vector transduction with the catalytic subunit of human telomerase (hTERT) and SV40 large T antigen, following which CEC were selectively isolated by limited dilution cloning, and clones were extensively characterized for brain endothelial phenotype 1 .

The hCMEC/D3 cells form a contact-inhibited monolayer of elongated cells on collagen type I or type IV. They do not show adhesion-independent growth in soft agar but form capillary structures in Matrigel, a characteristic property of cultured endothelium. They were reported to have an apparently normal diploid human karyotype 1 , although a high-resolution multicolor fluorescence in situ hybridization (FISH) approach revealed a more complex karyotype at high passages than initially thought 2 . In addition, they stain positively for endothelial markers including CD34, CD31, CD40, CD105, CD144 (VE-cadherin) and von Willebrand factor, but not for CD36, which is absent from brain endothelium. They maintain stable growth and endothelial marker characteristics, at least until the 35^th passage.

In the context of endothelial cell junctions, hCMEC/D3 cells are positive for junction-associated Ig-like proteins such as PECAM-1 and JAM-A, for AJ and TJ structural proteins such as VE-cadherin, claudin-3,-5 and occludin as well as for scaffolding proteins such as beta catenin and zonula occludens (ZO)-proteins-1 and 2 1 3 . The small G-protein Gαi2, suggested as a TJ-associated protein, was indeed identified as a partner of claudin-5 and its presence was necessary for TJ formation in hCMEC/D3 cells 4 . Expression of claudins and occludin at intercellular junctions is best observed when the cells are confluent, treated with anti-inflammatory steroids such as hydrocortisone, anti-oxidant agents such as resveratrol, or the Wnt/β-catenin signaling activator, lithium chloride (LiCl). The Wnt/β-catenin pathway acts in hCMEC/D3 cells to induce/enhance the BBB phenotype by increasing expression of claudins as demonstrated in primary mouse CECs 5 . Similarly, all growth factors, particularly vascular endothelial growth factor (VEGF), should be removed from the culture medium with the exception of basic fibroblast growth factor (bFGF) to enhance expression of junctional proteins. The hCMEC/D3 cells express other newly identified junctional proteins such as annexins-1 and -2, which also appear to be important for maintenance of TJ integrity 6 .

Comparison of transcriptional profiles of hCMEC/D3 cells and primary human CEC with freshly isolated mouse CEC confirmed the expression by hCMEC/D3 cells of a substantial number of genes expressed by brain endothelium, but showed lower expression of claudin-5, occludin, JAM-2, glut-1 and the insulin receptor 7 . The authors concluded that in order to attain a mature brain endothelial phenotype, other cell types present in the neurovascular unit (e.g. astrocytes, pericytes) regulate gene expression by CEC, suggesting that a more complex in vitro model might be required to fully mimic the BBB. Alternatively, in line with the aforementioned differentiating action of the Wnt/β-catenin pathway, complementing the hCMEC/D3 culture medium with astrocyte- and/or pericyte-derived soluble factors might be sufficient for further differentiation towards a BBB phenotype.

Monolayers of hCMEC/D3 show restricted permeability to lucifer yellow (LY: a low molecular weight paracellular diffusion marker) and to many hydrophobic and hydrophilic low molecular weight drugs which correlate with in vivo permeability coefficients as demonstrated by Weksler et al 1 and confirmed by Poller et al 8 . They also show a restricted permeability to low and high molecular weight dextrans that is similar to primary CECs and lower than non-cerebral endothelium (e.g. human umbilical vein endothelial cells, HUVECs), particularly under conditions of flow 9 . Indeed, for compounds of MW>4000, the permeability profile is very similar to that of bovine and porcine CECs, hitherto the best characterized in vitro BBB models. As discussed above for TJ protein expression, the permeability barrier function is maximized in the presence of LiCl and corticosteroids (or resveratrol): in these conditions, the permeability coefficient (Pe) for LY, is: 1.55 +/- 0.16 10^-3 cm/min. For comparison, Pe values for 4 kDa- and 70 kDa-dextrans are: 0.72 +/- 0.07 10^-3 cm/min and 0.09 +/- 0.01 10^-3 cm/min, respectively.

Conversely, stress conditions and extracellular stimuli have been shown to increase paracellular permeability of hCMEC/D3 cells via signaling pathways such as JNK, PKC or NFκB. These include mannitol treatment, oxygen and glucose deprivation (OGD) and pro-inflammatory cytokines such as TNFα and chemokines such as CCL2. Cowan et al 10 examined the effects of OGD under static conditions in hCMEC/D3 cells. They observed a reversible increase in monolayer permeability to dextran after 1 h of OGD without cytotoxicity, but permanent changes in monolayer permeability and marked cytotoxicity after 12-24 h. The acute permeability changes involved the generation of nitric oxide and could be prevented by blocking inducible nitric oxide synthase. Other studies have demonstrated that cytokines/chemokines increase the paracellular permeability of hCMEC/D3 cells to dextrans via different mechanisms 11 . With pro-inflammatory stimuli, ZO-1, occludin and claudin-5 expression levels are decreased 11 12 , whereas JAM-A translocates away from tight junctions, without any expression changes 13 . The chemokine CCL2, which is elevated during CNS inflammation and is associated with endothelial dysfunction, transiently induces Src-dependent disruption of hCMEC/D3 AJs, translocation of β-catenin from the AJ to PECAM-1, and increases surface localization of PECAM-1 14 .

In brief, these studies illustrate the usefulness of the hCMEC/D3 model for unraveling the regulatory mechanisms of junctional integrity and BBB permeability in pathological conditions (for a review see 15 ).

Although the TEER of human cerebral microvessels has not been directly determined, it is widely accepted that mammalian systems such as the rat show high TEER values well above 1,000 Ω·cm², a characteristic of the BBB in vivo 16 . However, TEER values above 1,000 Ω·cm² are difficult to achieve in cultured CEC in vitro and this is particularly true for cell lines compared to primary cultures. Under static culture conditions, hCMEC/D3 monolayers develop only a low to medium-level TEER (around 30-50 Ω·cm²) in various reports. Interestingly, higher TEER values close to 300 Ω·cm², were observed in the presence of hydrocortisone, probably due to the modulatory activity of corticosteroids on the expression of TJ proteins such as occludin and claudin-5 12 . Another strategy targeted at increasing TEER values in hCMEC/D3 cells has involved co-culture with other cell types forming the neurovascular unit, as suggested above. In a recent paper, co-culture of hCMEC/D3 cells with astrocytes from different brain regions evoked a significant TEER increase from 30 to over 60 Ω·cm² 17 . In both monocultures and co-cultures of hCMEC/D3 with astrocytes, TEER values increased from baseline over an interval of 5 days, presumably due to TJ maturation with time. By far the most promising method to increase hCMEC/D3 cell TEER values has been exposure to flow-based shear stress. Indeed, in hCMEC/D3 monolayers subjected to pulsatile flow after seeding in a capillary cartridge system, the TEER was reported to rise to 1000-1200 Ω·cm², then to rapidly drop following flow cessation 8 . Co-culture with astrocytes did not induce any further increases in TEER values in this flow-based model suggesting that, at least in vitro, shear stress may be a more critical factor in inducing a mature barrier phenotype than interactions with other cell types.

hCMEC/D3 cells express functional efflux transporters (known as ABC transporters because they contain ATP-binding cassette(s) for active transport), typical for brain endothelium, as observed in freshly isolated human brain microvessels: these include P-glycoprotein (P-gp or MDR1 or ABCB1), breast cancer resistance protein (BCRP or ABCG2), and multidrug resistance-associated proteins (MRP) -4 and -5 (or ABCC4 and 5) 18 . In addition, hCMEC/D3 cells express MRP-1, as previously reported with primary human brain endothelial cells in culture, strongly suggesting that in vitro culturing may non-physiologically induce the expression of this gene 18 . Protein expression of P-gp/MDR1, MRP4, BCRP by hCMEC/D3 cells (grown on collagen-coated dishes) was further assessed by quantitative proteomic analysis 19 , whereas no expression of P-gp/MDR1 was detected in HUVECs, used as reference non-brain EC. Interestingly, expression levels of P-gp, BCRP and MRP4 were similar in hCMEC/D3 cells and in isolated human brain microvessels 19 . Moreover, these key transporters are functional in hCMEC/D3 cells as efflux transporter inhibition studies invariably leads to elevated intracellular levels of their substrates 1 8 18 . In addition, P-gp expression is polarized to the apical membrane as previously demonstrated in situ in human brain microvessels and appears to be stable for at least 40 passages 20 .

ABC transporter activity and/or expression levels may be modulated by extracellular stimuli. For example, Poller et al 21 noted that P-gp activity was not altered by TNF-α treatment, although P-gp expression levels increased after treatment. However, it is noteworthy that apparent increases in P-gp expression have been found in some cases to be due to selection of high Pgp-expressing hCMEC/D3 cells, for example, after exposure to potentially cytotoxic agents, and so may not reflect real increases in P-gp expression 22 . Substrates for P-gp can increase its level of expression and activity as demonstrated in hCMEC/D3 cells exposed to the HIV-1 protease inhibitors ritonavir and atazanavir, both substrates for P-gp. Inhibition of P-gp (but not of MRP-1) increased transport of these protease inhibitors. These drugs bind the xenobiotic receptor PXR which likely acts as a transcription factor for P-gp 23 . Concern about P-gp up-regulation during long-term administration of antiretroviral therapy, thus possibly blocking brain entry of these protease inhibitors (as well as of other therapeutic drugs) suggests that the hCMEC/D3 model may prove useful in designing newer antiretroviral therapies that use other means of crossing the BBB. Of interest, HIV-1 Tat can also lead to up-regulation of P-gp expression and hence contribute to decreased entry of antiretroviral therapy into the CNS 24 .

In contrast to P-gp, BCRP expression and activity are decreased by inflammatory cytokines, in particular IL-1β and TNFα 21 . Conversely, agonists of the peroxisome proliferator-activated receptor alpha (PPARα) up-regulate BCRP in hCMEC/D3 cells, and can significantly decrease accumulation of drugs that are BCRP substrates (e.g. mitoxantrone). PPARα antagonists down-regulate BCRP in these CECs 25 suggesting new targeting strategies for either improving drug brain bioavailability or increasing neuroprotection. Along the same lines, BCRP was shown, using hCMEC/D3 cells, to mediate the transport of nifurtimox, an anti-trypanosomal drug 26 . These observations indicate that BCRP inhibitors potentially could improve the activity of anti-trypanosomal drugs and confirm that the hCMEC/D3 model is appropriate to test novel drugs.

Brain endothelium is known to express a large number of membrane receptors and transporters that specifically control the blood-to-brain transport of nutrients, including insulin, transferrin and LDL receptors as well as glucose, amino-acids and organic ion transporters, all members of the solute carrier family (SLC) of transporters. Accordingly, hCMEC/D3 cells were tested for expression of these receptors and transporters by immunochemical analysis, RT-PCR and/or quantitative proteomic analysis. First, they were shown to express at a high level the glucose transporter Glut-1 and the transferrin receptor. Indeed, Glut-1 expression was found by quantitative proteomic analysis to be 15-fold higher in hCMEC/D3 cells than in HUVECs and similar to that of human brain microvessels 19 . Influx transporters such as the cation transporter OCT-1, and to a lesser extent OCT-2 and -3 are expressed and functional in hCMEC/D3 cells. OCT-1 is responsible for CEC uptake of the antiepileptic drug lamotrigine, a process blocked by the selective inhibitor prazosin 27 . Also, hCMEC/D3 cells express the neutral and cationic amino acid transporter (ATB⁰,⁺), which may be involved in the brain uptake of the anti-influenza compounds amantadine and rimantadine 28 . In addition, Carl et al 29 reported the expression by hCMEC/D3 cells of the monocarboxylate transporters SLC16A1 and SLC16A3 (MCT1 and MCT3), while little or no expression of SLC16A2 (MCT2) was noted. In agreement with these data, a high level of SLC16A1 expression at the protein level was detected by quantitative proteomic analysis of hCMEC/D3 cell extracts 19 . Regarding the proton-coupled oligopeptide transporter superfamily (POT, SLC15A) transporters, Carl et al also reported that hCMEC/D3 cells express both hPHT1 and hPHT2, while little to no expression of either hPepT1 or hPepT2 was observed, in line with previous data in the human BBB in vivo 29 .

The hCMEC/D3 cells respond to inflammatory stimuli by increasing paracellular permeability to tracers (see previous section) and are able to support adhesion and migration of leukocytes by increased expression of adhesion proteins like ICAM-1 and VCAM-1 1 . They express functional cytokine and chemokine receptors such as TNFR1 and 2, IFNGR1 and CXCR1-5 and CCR3-6 1 37 . Indeed, Fasler-Kan et al 38 demonstrated TNFα activation of NFκB signaling, whereas interferon gamma (IFNγ induced activation of JAK/STAT signaling pathways, and upregulated MHC Class I. In addition, secretion of chemokines by CECs may be an additional mechanism for modulating leukocyte extravasation. Furthermore, hCMEC/D3 cells secrete chemokines in a similar fashion to primary human brain endothelium both under basal conditions (CCL2 and CXCL8) or following stimulation by cytokines (CCL5, CXCL10, CX3CL1 or fractalkine) 39 40 .

Monocytes adhere to activated hCMEC/D3 cells and migrate across the monolayer. The interaction between human monocytes and hCMEC/D3 cells involves the generation of reactive oxygen species (ROS), release of tissue-plasminogen activator (tPA) from the endothelial cells and a subsequent increase in permeability of the endothelial monolayer to large molecules (>150 kDa). Degradation of occludin appears to mediate the opening of endothelial-endothelial TJs 41 . Blocking the ERK1/2 pathway can partly reverse the monocyte-induced opening of monolayer TJs and impede occludin degradation. The same mechanism as demonstrated in the hCMEC/D3 model underlies brain changes in experimental autoimmune encephalomyelitis in the rat, a model of multiple sclerosis, as well as in rat monocytes and rat brain endothelial cells in vitro, suggesting that it is a generalized mechanism and may be pertinent in multiple sclerosis pathology. The same authors recently reported that a modulator of the sphingosine-1-phosphate (S1P) receptor, known to reduce inflammatory lesions in multiple sclerosis (FTY720P or Gilenya®), actually maintains hCMEC/D3 cells in a state of immune quiescence associated with decreased transmigration of monocytes 42 . This result further validates the hCMEC/D3 model for investigating the regulatory mechanisms of inflammation at the BBB.

Monocyte adhesion to hCMEC/D3 cells is enhanced by endothelial treatment with TNFα or IFNγ and can be inhibited by antibodies to the integrin VLA-4. A role for the junction-associated prion protein PrP^C in monocyte transmigration through brain endothelial cells was demonstrated with hCMEC/D3 cells, using either the U937 monocytic cell line or fresh primary blood monocytes: antibodies to the prion protein inhibited monocyte transmigration across the endothelial layer, whereas anti-PECAM 1 antibodies had no effect 43 . This inhibition was also observed with mouse primary brain EC and with a rat brain endothelial cell line, suggesting, as above, a mechanism common to brain endothelium from several species.

Bahbouhi et al 44 used hCMEC/D3 cells as a BBB model to compare adhesion and transmigration across CEC by peripheral blood mononuclear cells (PMBC) or purified T cells from multiple sclerosis patients versus PBMC or T cells from healthy individuals. They observed that PBMC migration is dependent on PSGL-1 and LFA-1 present on the PBMC. Both CD4+ and CD8+ T cells utilize these ligands to adhere to brain endothelium via P-selectin and VLA-4, respectively, and adherence can be blocked by anti-ligand antibodies. In multiple sclerosis, the frequency of CD4+ T cells that are PSGL-1+ is significantly greater than in healthy individuals; CD8+ cell populations were similar in both MS patients and controls. Transmigration of PBMC from multiple sclerosis individuals was enhanced across both resting and TNFα-activated hCMEC/D3 cells. The absolute transmigration was much greater across TNFα-activated hCMEC/D3 cells. Interestingly, PMBC from individuals treated with IFNβ a widely used first-line treatment of multiple sclerosis) had lower rates of transmigration and demonstrated lower LFA-1 levels.

Whether human neutrophils induce permeability changes in brain endothelium was studied by Joice et al 45 using hCMEC/D3 monolayers. This study was undertaken to understand whether neutrophil accumulation contributes to vasogenic edema in stroke. Untreated neutrophils applied to the hCMEC/D3 monolayers for 30 min actually decreased baseline permeability to low molecular weight (4 kDa) dextran by 53%, whereas neutrophils preactivated with TNFα, LTB4 or PMA (treatments that induced marked release of ROS) had no effect on baseline permeability. The authors then showed, in rats injected intracerebrally with human neutrophils, that very similar changes in brain vascular edema were seen. The authors concluded that the hCMEC/D3 model was useful in evaluating potential contributions to vasogenic edema.

Studies related to retroviral infection have concerned two pathogens, HTLV-1 and HIV-1. HTLV-1 infects hCMEC/D3 cells via their receptors for viral entry, Glut-1 and neuropilin-1, an observation that has been confirmed in situ in necropsy material from patients with TSP/HAM (tropical spastic paraparesis/human T-lymphotropic virus type-I-associated myelopathy) 3 . CEC infection leads to increases in paracellular permeability and TJ disorganization, probably via expression of the viral protein Tax. An additional mechanism leading to BBB disruption is via secretion of TNFα and IL1α by HTLV-1 infected T cells 46 .

In the context of HIV-1, studies on hCMEC/D3 cells have focused on 1) mechanistic studies on HIV-1-induced BBB breakdown or 2) a model to investigate effects of anti-HIV therapeutics, particularly protease inhibitors, on BBB function (see previous section). For mechanistic studies, it has been demonstrated that HIV-1 and/or Tat protein induces disruption of claudin-5 and increases permeability of hCMEC/D3 cells in a similar fashion to effects on primary rodent BECs 47 . Tat-induced delocalization of ZO-1 from the membrane into the nucleus is mediated by Rho signaling and CREB 48 . In addition, Tat induces hCMEC/D3 cells into an activated inflammatory state by inducing increased expression of IL-1β, E-selectin, CCL-2, and IL-6 49 , an effect that is attenuated by PPARα and PPARγ agonists 50 via matrix metalloproteases 51 . As a result, HIV-1-infected monocytes, or Tat protein itself, have been shown to increase ICAM-1 expression and to favor transmigration of the infected monocytes across hCMEC/D3 cells by a mechanism that involved NFκB-induced release of MMP-9 52 .

HIV Tat also induces amyloid beta (Aβ) peptide accumulation in hCMEC/D3 cells which may contribute to its effect on BBB function 53 . Aβ accumulation and Tat-induced barrier dysfunction are lipid raft- and caveolae-dependent and involve caveolae-associated Ras signaling 54 55 . As mentioned above, Tat can also lead to up-regulation of P-gp expression and hence contribute to decreased entry of antiretroviral therapy into the brain 24 .

Adhesion to and penetration across a monolayer of hCMEC/D3 cells by the fungal pathogen Cryptococcus neoformans was demonstrated by Vu et al 56 , who found that a large polysaccharide capsule on the fungus plus CD44, the hyaluronic acid receptor present on the hCMEC/D3 cells, were both important for the adherence of fungal particles to endothelial cells. Upon adherence of Cryptococci, the endothelial cells developed microvilli that attached to the fungi and appeared to aid in their transcytosis. Conversely, removal of hyaluronic acid or use of non-encapsulated organisms blocked adherence. The authors pointed out that although the TEER of the monolayers was low—about half that of primary brain endothelial cells—it was not further lowered by the adherence of Cryptoccocci and appeared to constitute a genuine barrier.

Although meninogocci (Neisseria meningitidis) are commonly carried in the nasal and oral mucosa of humans, direct meningococcal infection of the brain, a devastating illness, is fortunately rare. How meningococci enter the brain has long been poorly understood, but hCMEC/D3 cells used as a model of the BBB have importantly contributed to the elucidation of this mechanism. Adhesion of meningococci on hCMEC/D3 monolayers induces translocation of multiple endothelial membrane proteins, including ezrin, moesin, and actin to form honeycomb cortical plaques beneath the meningococcal colonies. Coureuil et al 57 observed that type IV pili present on pathogenic meninogocci recruited to the site of bacterial colonies the Par3/Par6/PKCζ endothelial polarity complex. This complex normally plays a pivotal role in the establishment of eukaryotic cell polarity and governs the formation of intercellular junctions; its translocation to these cortical plaques led to the formation of ectopic intercellular junctional domains at the sites of bacteria-endothelial cell interactions and depleted junctional proteins at endothelial cell-cell interfaces. This response of hCMEC/D3 cells resulted in the opening of intercellular junctions, thus permitting paracellular bacterial infiltration across the endothelial barrier. Coureuil et al further 58 explored the hCMEC/D3 model to ascertain the signaling pathway that recruits the cortical plaques to meningococcal colony sites. They elegantly demonstrated that meningococci “hijack” another endothelial physiological pathway through activation of β-adrenergic receptors by their Type IV pili, followed by activation of the scaffolding protein β-arrestin and the tyrosine kinase Src. Activation of this pathway favors endocytosis of phosphorylated VE-cadherin, a normal component of TJs, further opening up endothelial TJs. Of note, these authors recently reported that this pathway is also used by non-brain microvascular endothelial cells, but is clearly distinct from that used by epithelial cells 59 .

Cerebral malaria, a common complication of Plasmodium falciparum infection particularly in children, is one of the most severe and often lethal manifestations of this common tropical disease. Induction of cerebral edema during cerebral malaria is among the most feared complications of this disease, yet the mechanisms are not well understood. The hCMEC/D3 cell line has provided an excellent in vitro model for studying the detailed interactions between P. falciparum parasites and brain endothelium. Jambou et al 60 evaluated the mechanism of P. falciparum-parasitized erythrocyte adhesion to hCMEC/D3 cells and showed for the first time that this process involved trogocytosis, the transfer of membrane material from one cell (malarial antigens on parasitized erythrocyte) to another cell (endothelial cell), followed by ingestion of the entire parasitized erythrocyte. These authors compared the hCMEC/D3 cell line with the HBEC-5i cell line and showed that the HBEC-5i line displayed a more activated phenotype when unstimulated, expressing much higher levels of ICAM-1, an important receptor in the interaction between parasitized erythrocytes and brain endothelial cells 60 . Blocking ICAM-1 or TNFα activation of endothelial cells prevented cytoadhesion of parasitized erythrocytes and their ingestion. More recently, hCMEC/D3 cells were used by Zougbede et al 61 to demonstrate that P. falciparum-parasitized red blood cells could alter BBB integrity also by a mechanism independent of cytoadhesion, namely, by induction of metabolic acidosis, which also resulted in opening TJs in the hCMEC/D3 monolayer, a process which also would favor development of cerebral edema.