Zinc ions regulate opening of tight junction favouring efflux of macromolecules via the GSK3β/snail-mediated pathway

Ruyue Xiao a, Lan Yuan a, Weijiang He b and Xiaoda Yang *a
aState Key laboratories of Natural and Mimetic Drugs and Department of Chemical Biology, School of Pharmaceutical Sciences, Peking University Health Science Center, Beijing 100191, China. E-mail: xyang@bjmu.edu.cn; Fax: +86-10-62015584; Tel: +86-10-82805611
bState Key Laboratory of Coordination Chemistry, Coordination Chemistry Institute, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210093, P. R. China

Received 17th October 2017 , Accepted 13th December 2017

First published on 13th December 2017


Zinc is an essential trace element presenting in particularly high concentration in the brain. In some regions, e.g. lateral amygdala, subiculum and hippocampus, rapidly-exchangeable zinc may transiently reach even up to 600 μM. To explore the possible roles of high-concentration Zn2+ in regulating the blood–brain barrier (BBB), we investigated the effects of Zn2+ on the functions and structures of the tight junction (TJ) with an in vitro model of a Madin-Darby canine kidney (MDCK) cell monolayer. The experimental results indicated that high concentrations (>200 μM) of Zn2+ can affect the TJ integrity in a polarized manner. Basolateral addition of Zn2+ led to reversible TJ opening with pore paths of r ∼ 2 nm or more depending on Zn2+ concentration. The efflux/influx ratios of different sized probes were found to be ∼4.6 for FD4 (MW 4000) and ∼1.8 for Eu–DTPA (MW 560), suggesting that the Zn2+-induced paracelluar channels favour efflux especially for macromolecules. Further mechanistic studies revealed that the elevated intracellular Zn2+ taken from the basolateral side can increase phosphorylation of glycogen synthase kinase (GSK) 3β, primarily due to the inhibition of calcineurin (CaN), thus resulting in the elevation of the snail transcriptional repressors. Subsequently, Zn2+ can cause the down-regulation of claudin-1, breakage of occludin and ZO-1 rings, and collapse of basolateral F-actin structures. These overall factors result in the formation of a trumpet-like paracellular channel, which allows asymmetric solute permeation. The ERK1/2 and JNK1/2 pathways may also be involved in the Zn2+-induced TJ opening process, while the activation of matrix metalloproteinase was not observed. Our results may suggest a potential role of zinc in regulation of BBB permeability associated with brain clearance of metabolites through the glymphatic system.

Significance to metallomics

Zinc is a well-known essential element with some as-yet-unclear biological functions. The present work investigated the biological significance of high concentrations of Zn2+ for the tight junction (TJ), which is a critical structural element of the blood–brain barrier. Our results showed that high concentrations (>200 μM) of zinc caused reversible TJ opening in a polarized manner through the GSK3β/snail-mediated pathway. Zn2+-Induced asymmetric paracellular pore paths favour the efflux of molecules, especially macromolecules. The present work may indicate a new role of Zn2+ in regulating BBB permeability and potential role of Zn2+ in brain clearance of metabolites through the glymphatic system.


As an essential micro-nutrient, zinc (Zn) is very important in a variety of biological processes due to its indispensable catalytic, structural and regulatory functions. The roles and the underlying mechanisms of Zn in biological systems have fascinated researchers for decades.1 With significant abundance in the brain, zinc has the second highest concentration after iron among all transition metals. However, the exact concentration of free Zn2+ in the brain is controversial.2–9 While some researchers reported relatively low concentrations of Zn (nanomolar level),2–4 others showed evidence of higher concentrations of Zn (more than 100 μM).5–9 Some cytoarchitectonic regions of the brain, for example the neuropil of the lateral amygdala, subiculum, and the mossy fiber neuropil of the hippocampus, are speculated to contain 200–600 μM of mobile Zn.2,5–8 During neuronal activity, Zn2+ ions are released into the synaptic cleft, resulting in transient local Zn2+ concentrations in the range of 100–300 μM.9 In certain pathological conditions, such as brain ischemia and reperfusion injury, a significant and sustained increase of extracellular Zn2+ concentration has been observed.2,10 Overall, the biological significance of the high concentration of Zn2+ in the brain has so far remained mysterious;11 in particular, it is of interest to establish how temporarily high levels of Zn2+ would affect the structure and functions of the blood–brain barrier (BBB).

It is well described that the BBB controls the flux and transport of liquids, ions and larger solutes into and out of the central nervous system (CNS) and protects the CNS from toxins and pathogens.12 The tight junction (TJ) between endothelial cells of brain capillaries is one of the most important structural elements of the BBB.13 Structurally, the TJ is an intricate complex consisting of transmembrane proteins and cytoplasmic accessory proteins primarily including claudins, occludin, zonula occludens (ZO) proteins and junctional adhesion molecules (JAMs).14 These TJ proteins are linked to an actin-based cytoskeleton, allowing the formation of TJ seals.15 Alterations in TJ structures and functions are associated with many diseases16,17 and metal toxicities.18–21 Previous studies indicated that low concentrations of Zn2+ strengthened the TJ,22–26 for example, 100 μM of Zn2+ enhanced the TJ functions that operate through the PI3K/AKT/mTOR signalling pathway in caco-2 cells.24 Nevertheless, considering the apico-basal polarization of epithelial cells and potential site-dependent action of Zn2+,27–30 it is appropriate to investigate the actions of Zn2+ in a bilateral manner, particularly at higher concentrations (100–300 μM).

In the present work, we investigated the effects of Zn2+ on the TJ. The experimental results showed that Zn2+ can cause alteration of TJ structures and functions in a polarized manner, and >200 μM concentrations of Zn2+ could increase the paracellular permeation favouring efflux of macromolecules via the GSK3β/snail-mediated pathway. Our results may suggest a potential role of zinc in regulation of BBB permeability associated with brain clearance of metabolites through the glymphatic system.

Materials and methods


Madin-Darby canine kidney (MDCK) cells were obtained from the Cell Culture Center of Peking Union Medical College, high glucose Dulbecco's modified Eagle's medium (DMEM) was from HyClone, penicillin–streptomycin was from Gibco (USA), fetal bovine serum (FBS) was from PAN (Germany), and Transwells (12 wells, pore diameter of 3 μm, polycarbonate) were from Corning Costar (USA). The MTS tetrazolium compound was from Promega (USA). All the other reagents were of analytical grade and came from commercial sources.

Eu–DTPA was prepared according to the previous method.31 Briefly, 1 mL 10 mM EuCl3 solution was added to 1 mL 10 mM DTPA solution in Hank's balanced salt solution (HBSS; pH 7.0) under vigorous stirring. The mixture was centrifuged at 4000 rpm for 10 min, then the supernatant (Eu–DTPA) was collected.

Non-fluorescent DMEM (NF-DMEM) was prepared by excluding some amino acids (tryptophan, tyrosine, and phenylalanine) and vitamins (folic acid, pyridoxine hydrochloride, and riboflavin) from media preparation according to our previous method.32

MDCK cell culture and monolayer preparation

MDCK cells were cultured in high glucose DMEM supplied with 10% FBS, 1% nonessential amino acids, and penicillin–streptomycin (100 μg mL−1) at 37 °C in a 5% CO2 atmosphere. Cultured MDCK cells were used at passage 15–50 in all experiments. MDCK cell monolayers were prepared by plating the cells onto Transwell filters (aperture, 3 μm; diameter, 12 mm) at a density of 2.5 × 104 cells per well and allowing growth and differentiation for 2–3 d. The transepithelial electrical resistance (TEER) was measured with an EVOM Voltohmmeter (World Precision Instruments, USA). The cell monolayers with TEER of >200 Ω cm2 were used for later studies.

Cytotoxicity assay

Cell viability was measured by MTS assay according to the manufacturer's instructions. Briefly, MDCK cells were seeded in 96-well plates at a density of 5 × 103 cells per well and left to grow for 24 h. The cells were then incubated with various concentrations of ZnSO4 (0–800 μM) diluted in DMEM with 5% FBS for 12 h. Then the cells were incubated with MTS solution for another 2 h at 37 °C. Finally, the absorbance at 490 nm was measured on a Thermo Multiskan Ascent plate reader (Thermo, USA). Cell viability was calculated as Atest/Acontrol × 100%. The 50% inhibition concentration (IC50) was calculated by plotting the cell viability versus Zn2+ concentrations and fitting the data to the Hill model using the MicroCal™ Origin program (Lab Corporation, USA).

Measurement of apparent permeability coefficient (Papp) of paracellular permeation probes

MDCK cell monolayers were prepared as above. After rinsing twice with NF-DMEM, the apical (donor) chambers were supplied with 0.5 mL NF-DMEM containing 10 μM Eu–DTPA and 0.5 mM fluorescein isothiocyanate-dextran 4 kDa (FD4) while the basolateral (receiver) chambers were supplied with 1.5 mL NF-DMEM. For the bilateral flux tests, the basolateral chambers were supplied with 2 mL NF-DMEM to mimic the dynamic flux process in the brain.33,34 Samples were collected in the opposite receiver chambers after 1 h incubation. Then the Papp values of Eu–DTPA and FD4 were calculated using the following formula:
Papp = (ΔQt)/(AC0)
where ΔQt is the flux of probes across the monolayer (mol transported per s), A is the surface area of the cell monolayers (1.12 cm2 in this study), and C0 is the initial concentration of Eu–DTPA (or FD4) in the donor chamber.

The concentration of FD4 was determined by fluorescence spectrometric measurement on a Flexstation 3 microplate reader (Molecular Devices, USA) at λEx/Em = 490/525 nm. The concentration of Eu–DTPA in the samples above was determined by a time-resolved fluorescence assay. Briefly, samples were mixed with equal volumes of 2 × β-NTA fluorescence enhancement solution (30 μM β-NTA, 10 mM TOPO, 0.2% Triton X-100, and 0.1 M potassium hydrogen phthalate buffer, pH 3.0) and left at 37 °C for 1 h. Then the fluorescence intensity was measured on a Flexstation 3 microplate reader at λEx/Em = 340/616 nm with a measurement window from 600 to 1000 ms.

Calculation of TJ pore size and the retention capacity upon incubation with ZnSO4

MDCK cell monolayers were treated with various concentrations of ZnSO4 (added on the apical side or basolateral side or both sides) for 12 h. After rinsing with NF-DMEM, fluorescent probes (10 μM Eu–DTPA and 0.5 mM FD4) were added in the donor chamber and the Papp values were determined as described above.

The calculation of TJ pore size and the retention capacity was performed according to the previous method.32 Briefly, the diffusion coefficient of a solute (Dp) was obtained by the following equation:

image file: c7mt00288b-t1.tif
where h is the thickness of the membrane and Km/f is a constant for the membrane. The scale factor a for a certain fluorescent probe can be estimated using the following equation:
image file: c7mt00288b-t2.tif
Given that the diffusion of the probes in tight junction channels is similar to that in porous medium and there is no specific interaction among the solutes, solvents and tight junction channels, the diffusion of the probes can be described by the amended Knudsen equation:
image file: c7mt00288b-t3.tif
in which
image file: c7mt00288b-t4.tif
where ε and τ represent the porosity and tortuosity of the porous medium, respectively; r is the radius of the pores; MA is the molecular mass of the solute. The ratio ε/τ is an overall reflection of the retention capacity of the porous medium for the solutes. Considering the size exclusion effect, the relationship between the ε/τ values of Eu–DTPA and FD4 is described as:
(ε/τ)Eu–DTPA = (ε/τ)·10tr(Eu–DTPA)/tr(FD4)
where the retention time (tr) of the probes was measured on a size exclusion gel column (DEAE Sephadex A-25). Then, the Knudsen equations for the two fluorescent probes were obtained as:
image file: c7mt00288b-t5.tif

image file: c7mt00288b-t6.tif
By assigning the size (r ∼ 4 Å) of primary TJ pores35 as the average size of sealed TJ pores, the calibration constant k was calculated to be 8.47 × 10−4. Then, the change of pore size (r) and retention capacity (ε/τ) could be calculated using the above equations.

Cellular zinc uptake

The cellular uptake of Zn2+ was measured using a Zn2+ fluorescent sensor (NBD-TPEA).36 Briefly, MDCK cell monolayers on Transwell filters were incubated with 250 μM ZnSO4 (in the apical chamber or basolateral chamber or both) in DMEM containing 5% FBS for 12 h. Then the cell monolayers were rinsed with Ca2+/Mg2+-free PBS buffer (0.0067 M) and incubated with 25 μM NBD-TPEA for 30 min at room temperature. After rinsing, the cells were observed under a confocal microscope (Leica TCS SP8 STED 3X; Leica, Wetzlar, Germany).

Matrix metalloproteinase (MMP) activity assay

The MMP activity of MDCK cells upon Zn2+ treatment was measured with an Amplite™ Universal Fluorimetric MMP Activity Assay Kit (AAT Bioquest, USA) according to the manufacturer's instructions. Briefly, MDCK cells were seeded in 96-well plates at a density of 5 × 103 cells per well and incubated for 24 h. Then the cells were incubated with 0, 100, 250, 350 μM ZnSO4 in 50 μL of DMEM with 5% FBS for 12 h. Then 50 μL of MMP Green substrate solution was added. The fluorescence signal was read on a microplate reader (Thermo, USA) at λEx/Em = 490/525 nm. Cells pre-treated with 1 mM 4-aminophenylmercuric acetate (APMA) for 2 h were used as positive control.

Calcineurin (CaN) activity assay

MDCK cells were seeded in 6-well plates at a density of 2 × 105 cells per well and incubated for 24 h. Then the cells were incubated with 0, 100, 250, 350 μM ZnSO4 in 2.5 mL of DMEM with 5% FBS for 12 h. After incubation with ZnSO4, the cells were lysed by lysis buffer (50 mM Tris, pH 7.5, 0.1 mM EDTA, 0.1 mM EGTA, 1 mM DTT, 0.2% NP-40) containing protease inhibitor cocktails and centrifuged at 12[thin space (1/6-em)]000 rpm at 4 °C for 20 min. Then the intracellular CaN activity was measured using an assay kit (Nanjingjiancheng, China) following the manufacturer's instructions.

Western blotting

Cells were lysed by RIPA buffer containing protease and phosphatase inhibitor cocktails and then centrifuged at 12[thin space (1/6-em)]000 rpm at 4 °C for 20 min. The supernatant protein concentration was determined using a BCA protein assay reagent kit (Beyotime Biotechnology, China). Samples containing 30 μg total protein were applied to an SDS-polyacrylamide gel electrophoresis instrument and the bands were transferred to polyvinylidene difluoride membranes (Millipore, USA). The membranes were blocked for 1 h with 5% skim milk, and then incubated overnight at 4 °C with the corresponding primary antibodies, i.e. antibodies against claudin-1 (Bioworld), occludin and ZO-1 (Invitrogen), p-Akt, p-ERK1/2, p-JNK1/2, and snail (Cell Signaling Technology), p-GSK3β (Abcam), and GAPDH (BioEasy). After washing with TBS containing 0.05% Tween-20, the membranes were incubated with horseradish peroxidase (HRP)-conjugated secondary antibodies (BioEasy, China) at room temperature for 1 h. Finally the protein bands were developed and analysed on a MiniChemi Imaging and Analysis System (Sage Creation Science Co., Ltd, China) using an ECL western blot substrate kit (Pierce, USA) according to the manufacturer's instructions.

RT-PCR assay for claudin-1 expression

The total RNA of the harvested MDCK cells was extracted with TransZol Up (Transgen Biotech, China) according to the manufacturer's instructions. The purity and concentration were determined by measuring the absorbance (A) at 260 nm and 280 nm (A260/A280). Then 2 μg of total RNA was reverse transcribed into the first-strand cDNA using a RevertAid First Strand cDNA Synthesis Kit (Thermo, USA) and quantitative PCR reactions were carried out using 2 × SYBR Green qPCR Mix (Aidlab, China) according to the manufacturer's protocols. Genes of interest were normalized to GAPDH expression.


Immuno-fluorescence imaging

MDCK cell monolayers were prepared on 6-well plates containing coverslips for 2–3 days. After incubation with different concentrations of ZnSO4 for 12 h, the coverslips were washed with cold PBS, fixed in 4% paraformaldehyde for 15 min at 4 °C and permeabilized with 0.1% Triton X-100 in PBS for 4 min. After blocking with PBS containing 1% bovine serum albumen (BSA) for 1 hour at room temperature, the cells were then incubated with the primary antibody in PBS containing 1% BSA solution overnight at 4 °C. After washing with PBS three times, AlexaFluor 488-conjugated goat anti-rabbit secondary antibodies in PBS were applied for 1 h at room temperature in the dark. Finally the cells were stained with DAPI (5 μg mL−1 in PBS) for 10 min at room temperature, washed with PBS and mounted with a drop of glycerol and placed on coverslips. The slides were observed on a confocal microscope (Leica TCS SP8 STED 3X; Leica, Wetzlar, Germany).

Transmission electron microscopy (TEM)

MDCK cell monolayers on Transwell filters were incubated with 250 μM ZnSO4 in the basolateral chamber for 12 h. Then the cell monolayers were fixed in glutaraldehyde and treated with 1% osmium tetroxide. Samples were dehydrated with graded ethanol and propylene oxide, and embedded in pure epoxy resin. Ultrathin sections were stained with uranyl acetate, and observed in a JEM 1400 transmission electron microscope (JEOL, Japan).

Statistical analysis

All the experiments were repeated at least three times. Results are presented as means ± SE. The differences between the groups were compared using one-way analysis of variance (ANOVA). A P-value less than 0.05 was considered as statistically significant.


The effect of ZnSO4 on cell viability and monolayer permeability

Zn2+ below 200 μM did not affect cell viability; however, at higher concentrations, treatment of MDCK cells with ZnSO4 for 12 h caused a dose-dependent decrease of cell viability (Fig. 1A). The IC50 value was calculated to be 347 ± 6 μM.
image file: c7mt00288b-f1.tif
Fig. 1 The effect of ZnSO4 on cell viability and monolayer permeability. (A) MTS assay of MDCK cell viability upon treatment with ZnSO4 for 12 h. (B) Alteration of TEER of MDCK cell monolayer upon Zn2+ treatment. ZnSO4 was added to the apical, the basolateral or both chambers and incubated for 12 h at 37 °C. (C) Recovery of Papp of Eu–DTPA after removal of Zn2+. 250 μM of Zn2+ was added to the basolateral side of the MDCK cell monolayer for 12 h and removed. 24 h after Zn2+ was removed, the Papp of Eu–DTPA returned to the control level. Data are means ± SE (n = 3). *P < 0.05, **P < 0.01 vs. control.

The alteration of MDCK cell monolayer integrity was monitored by TEER measurement upon treatment with 100, 250 and 350 μM of Zn2+, corresponding to the residual cell viability of 100%, >80% and ∼50%, respectively. The results (Fig. 1B) showed that Zn2+ could cause paracellular leakage in both concentration and action-site-dependent manners: (i) Zn2+ at the apical chamber enhanced the TJ seal in the tested range of concentrations; (ii) Zn2+ at the basolateral chamber caused a significant decline of TEER at concentrations above 200 μM and (iii) compared with Zn2+ at both apical and basolateral chambers, Zn2+ at only the basolateral chamber had a similar effect on the TJ.

It was observed that 250 μM of Zn2+ on the basolateral side could cause a ∼50% decrease of the TEER value. However, when Zn2+ was removed from the media, TEER recovered completely in 24 h. The full recovery of the TJ seal was also verified by the permeability of the Eu–DTPA probe (Fig. 1C). The Papp of Eu–DTPA increased by three-fold upon incubation with 250 μM Zn2+ at the basolateral chamber, but returned to the control level after removal of Zn2+.

Alterations of TJ pore size and retention capacity

The changes of TJ pore size and retention capacity upon Zn2+ treatment were investigated using Eu–DTPA and FD4 as double probes as described.32 Zn2+ (Table 1) at the apical side did not affect TJ pore size but increased the retention capacity, which is consistent with the enhancement of TEER (Fig. 1B). The presence of 250 μM Zn2+ at the basolateral side increased the pore size to r ∼ 2 nm, which would allow the leakage of most biological macromolecules. Higher Zn2+ concentrations induced larger pores. Markedly, Zn2+ present at the basolateral side caused a significant decreasing of the retention capacity (ε/τ) of paracellular pathways, indicating that the TJ was open.
Table 1 The TJ pore size (r) and retention capacity (ε/τ) upon treatment with Zn2+
Zn2+ location Apical side Basolateral side Both sides
[Zn2+] (μM) 0 100 250 350 100 250 350 100 250 350
r (nm) (SD) 0.4 (0.1) 0.2 (0.1) 0.7 (0.2) 0.4 (0.1) 0.9 (0.1) 1.8 (0.2) 6.1 (0.3) 0.6 (0.1) 2.6 (0.4) 52.4 (3.0)
τ/ε (SD) 0.03 (0.01) 0.04 (0.01) 0.24 (0.05) 0.12 (0.03) 0.10 (0.01) <0.01 <0.01 0.14 (0.01) <0.01 <0.01

Effects of Zn2+ on TJ architecture of MDCK cell monolayer

The change of spatial distribution of major TJ proteins, e.g. claudin-1, occludin, ZO-1 and F-actin,37–40 revealed the alteration of the TJ architecture. As shown in Fig. 2A, treatment with 250 μM Zn2+ caused TJ structural changes including: (i) significant decrease of the claudin-1 level; (ii) breakage and condensation of occludin and ZO-1 ring structures; (iii) re-arrangement and scattering of F-actin structure at the basolateral side. TEM observation (Fig. 2B) indicated the formation of a trumpet-like paracellular pathway with the bell mouth facing the basolateral side.
image file: c7mt00288b-f2.tif
Fig. 2 Effects of Zn2+ on TJ architecture of MDCK cells. (A) The expression of major TJ proteins shown by immunofluorescence staining. MDCK cells were incubated with indicated concentrations of ZnSO4 for 12 h. (B) TEM image of the paracellular paths of MDCK cells. The yellow arrows indicate the TJ. Zn2+ induced a trumpet-like paracellular channel with the bell mouth at the basolateral side. MDCK cells were treated with 250 μM ZnSO4 for 12 h. (C) The bilateral permeability of Eu–DTPA and FD4 showed that the Zn2+-induced TJ opening favoured efflux especially for macromolecules. Zn2+ (250 μM) was added to the basolateral side of the MDCK cell monolayer for 12 h. Data are means ± SE (n = 3). *P < 0.05, **P < 0.01 vs. control.

Bilateral flux of Eu–DTPA and FD4 probes upon Zn2+-induced TJ opening

The asymmetric paracellular pathway structure upon Zn2+ treatment indicates potential discrimination between transmembrane efflux (basolateral-to-apical) and influx (apical-to-basolateral). Thus, the changes of bilateral flux of two different sized probes upon opening of the TJ by treatment with 250 μM Zn2+ on the basolateral side for 12 h were investigated under dynamic conditions mimicking those in the brain, as previously described.33,34 The results (Fig. 2C) revealed that both influx and efflux of the Eu–DTPA and FD4 probes increased markedly. For the small probe (Eu–DTPA, MW 560), the ratio of efflux/influx changed from 1.0 ± 0.5 (TJ closed) to 1.8 ± 0.3 (TJ); however, for the large probe (FD4, MW 4000), the ratio of efflux/influx changed from 1.9 ± 1.1 (TJ closed) to 4.6 ± 0.6 (TJ). These results clearly indicate that the Zn2+-induced TJ pore path favoured efflux, especially for macromolecules.

The levels of claudin-1, occludin and ZO-1 expression in MDCK cells upon treatment with Zn2+

To further clarify the TJ protein alteration induced by Zn2+, the levels of claudin-1, occludin and ZO-1 expression were examined by western blot analysis and the results are shown in Fig. 3. It is observed that: (i) Zn2+ caused a dose-dependent decrease in both protein and mRNA levels of claudin-1; (ii) neither occludin nor ZO-1 protein levels were affected significantly by Zn2+ treatment.
image file: c7mt00288b-f3.tif
Fig. 3 Effects of Zn2+ treatment on expression levels of claudin-1, occludin and ZO-1. (A) Protein levels of claudin-1, occludin and ZO-1; (B) mRNA levels of claudin-1. MDCK cells were treated with 0–350 μM ZnSO4 for 12 h. Protein levels were estimated by western blotting and mRNA levels were quantified by RT-PCR assay. Data are means ± SE (n = 3). **P < 0.01 vs. control.

Cellular uptake of zinc

As shown in Fig. 4, the cellular Zn2+ level increased significantly upon incubation with 250 μM of ZnSO4. Addition of Zn2+ to the apical chamber (A), basolateral chamber (B) and both chambers (AB) caused elevation of intracellular Zn2+ levels to 204.2 ± 4.2%, 268.3 ± 7.4%, and 324.3 ± 7.5% respectively.
image file: c7mt00288b-f4.tif
Fig. 4 Change of intracellular Zn2+ levels upon 12 h treatment with 250 μM of extracellular Zn2+. 250 μM of ZnSO4 was added to the apical chamber (A), basolateral chamber (B) and both chambers (AB). Data are means ± SE (n = 3). **P < 0.01 vs. control.

The mechanism underlying Zn2+-induced TJ opening

MMPs are normally responsible for the tissue remodeling and degradation of the extracellular matrix. Activation of MMPs has been shown to enhance BBB permeability.41,42 However, the present results (Fig. 5A) showed that the treatment of Zn2+ did not affect the MMP activity in MDCK cell monolayers.
image file: c7mt00288b-f5.tif
Fig. 5 The signalling pathways involved in Zn2+-induced TJ opening. (A) MMP activity. MDCK cells were incubated with 0–350 μM ZnSO4 for 12 h before MMP activity assay. Untreated MDCK cells were incubated with 1 mM APMA for 2 h before MMP activity assay as positive control; (B) alteration of snail expression and phosphorylation of GSK3β, JNK1/2 and ERK1/2 upon incubation with 0–350 μM of Zn2+ for 12 h; (C) temporary changes of snail, p-GSK3β and claudin-1 levels upon treatment with 250 μM Zn2+ for 0–12 h; (D) CaN activity assay. MDCK cells were incubated with 0–350 μM ZnSO4 for 12 h before CaN activity assay. Data are means ± SE (n = 3). *P < 0.05, **P < 0.01 vs. control.

Zn2+ and its transporters are known to be involved in regulating cell adhesion in the epithelial–mesenchymal transition (EMT).43–45 Amongst these, snail is a transcriptional repressor that plays an important role in the EMT46 and modulation of tight junction proteins.47,48 Thus, the changes of snail and related signal transduction were observed. The results (Fig. 5B–D) revealed that: (i) Zn2+ at 250 μM or higher concentrations significantly increased the levels of snail, p-GSK3β, p-JNK1/2 and p-ERK1/2 in a dose-dependent way; (ii) the levels of snail, p-GSK3β and claudin-1 were significantly altered at ∼6 h after Zn2+ treatment; (iii) both the increase of snail and p-GSK3β and decrease of claudin-1 were well correlated; (iv) Zn2+ above 250 μM significantly inhibited the CaN activity.


High concentration of Zn2+ causes reversible TJ opening favouring efflux of macromolecules by inducing a trumpet-like paracellular channel

The effect of Zn2+ on MDCK cell viability was tested over the entire potential physiological concentration range (0–600 μM) in neural systems. As Zn2+ caused a decline of cell viability in the range of 250–450 μM (Fig. 1A), the effects of Zn2+ on the TJ function of MDCK monolayers were observed at Zn2+ concentrations of 100, 250 and 350 μM, corresponding to 100%, >80%, and ∼50% of cell viability, respectively. The results (Fig. 5C) and preliminary tests suggested that the transcriptional effect of Zn2+ (not Zn2+ signalling) reached its maximal extent after 12 h. Hence, the effects of Zn2+ were most clearly observed at 12 h.

The MDCK cells in the monolayer were apparently more resistant to Zn2+ toxicity because Zn2+ (0–350 μM) on the apical side actually improved the TJ seal, as indicated by the increase of TEER (Fig. 1B) and paracellular path retention capacity (τ/ε) (Table 1). Very interestingly, Zn2+ on the basolateral side caused a concentration-dependent reversible opening of the TJ (Fig. 1B and C). It is noteworthy that the TJ pore size (r ∼ 2 nm or more) induced by Zn2+ may allow the leakage of various biological macromolecules.

The changes of TJ architecture (Fig. 2A and B) and the major building proteins (Fig. 3) revealed that the Zn2+ treatment caused different effects on the two ends of the polarized MDCK cell monolayer. On the apical end, the TJ seal was broken, possibly due to loss of claudins. On the basolateral end, the collapse of F-actin structure probably indicated large expansion of the paracellular space. Also, the TEM observation (Fig. 2B) revealed the formation of a trumpet-like paracellular channel with the bell mouth at the basolateral side. This Zn2+-induced channel may be similar to the tapered nanopores, which allow asymmetric ion transport.49

Then, to further explore the Zn2+-induced preferential direction of solute diffusion, bilateral flux assays were conducted under conditions mimicking dynamic flux. In the BBB, the apical side of cerebral capillary endothelial cells faces the blood while the basolateral side faces the cerebral interstitial fluid. According to the Bernoulli principle,50 a faster blood flow leads to a lower pressure in vivo on the apical side. As shown in Fig. 2C, upon Zn2+ treatment, the bilateral permeability of the probes increased significantly, especially the rate of outgoing flux (efflux). Compared with the small Eu–DTPA probe, the efflux/influx ratio of FD4 (MW ∼ 4000) was increased greatly to c.a. 4.6, suggesting that the barrier favours efflux of macromolecules.

Zn2+ induces TJ opening via the GSK3β/snail-mediated signal transduction

The effect of elevating the intracellular Zn2+ level (Fig. 4) suggested that Zn2+ may exert effects either inside or outside the cells. However, Zn2+ treatment did not change the activity of MMPs in MDCK cells (Fig. 5A), ruling out the involvement of MMPs in Zn2+-induced TJ opening.

Among the signal transduction modulating TJ proteins, the level of snail, a zinc finger (ZnF) transcription factor, was herein observed to be up-regulated significantly by Zn2+ in both a time- and dose-dependent manner (Fig. 5B and C). It has been revealed that the increase of snail not only suppresses expression of claudin-1, but also causes F-actin re-arrangement.51–53 The nuclear localization of snail is dependent on both the ZnF domain and the Zn transporter ZIP6,54 while the level of snail is regulated by GSK3β.55 Snail can be phosphorylated by GSK3β, leading to nuclear exportation of snail protein and subsequent degradation. Conversely, phosphorylation inhibition of GSK3β causes elevation of snail expression.55,56 As the snail expression upon Zn2+ treatment synchronized well with the increase of phosphorylated GSK3β (p-GSK3β) and decease of claudin-1, it can be concluded that the Zn2+-induced TJ opening is activated through the GSK3β/snail-mediated pathway.

The GSK3β phosphorylation is known to be primarily up-regulated by Akt57,58 and down-regulated by calcineurin (CaN).59,60 CaN is a calmodulin-dependent serine/threonine protein phosphatase and Zn2+ is a potent inhibitor of CaN.61,62 Meanwhile, in TJ-related pathways, Akt is regulated by integrin linked kinase (ILK).63,64 We have found that inhibition of ILK caused Akt inactivation but did not affect p-GSK3β (data not shown) in MDCK cells. Therefore, phosphorylation of GSK3β was elevated due to inhibition of CaN (Fig. 5D).

In addition to the snail pathway, ERK1/2 and JNK1/2 are also reported to down-regulate claudin-1 expression,65–68 but the mechanisms are not clear yet. The results (Fig. 5B) suggested that activation of ERK1/2 and JNK1/2 by Zn2+ should be involved in TJ opening, which needs to be further investigated. To conclude, a putative mechanism for Zn2+-induced TJ opening is summarized in Fig. 6.

image file: c7mt00288b-f6.tif
Fig. 6 Putative mechanisms for zinc-induced tight junction opening. High concentrations (>200 μM) of basolateral zinc inhibit the activity of CaN thus increasing phosphorylation of GSK3β. Snail was stabilized by inhibition of GSK3β, thus causing: (i) down-regulation of claudin-1 and (ii) re-arrangement of occludin, ZO-1 and basolateral F-actin. ERK1/2 and JNK1/2 pathways were also involved in zinc-induced TJ opening and need to be further investigated.

Why Zn2+ affected TJ only from the basolateral side remains a mystery for further research. Nevertheless, it was observed (Fig. 4) that the sum amount of Zn2+ uptake from either the apical or the basolateral side individually almost equalled that from both sides combined. This may suggest that Zn2+ taken from the basolateral side largely remains in different cellular compartments compared with Zn2+ taken from the apical side. This is possibly because the differentiated MDCK cells exhibit an apicobasal polarization characterized by the polarization of the microtubule network in cytoplasm and polarized distribution of enzymes and transport systems to the two ends of the plasma membrane.69 Thus, Zn2+ taken from the basolateral side could inhibit CaN activity and trigger downstream events, but Zn2+ from the other side could not.

Speculation on the potential role of Zn2+ in brain clearance of metabolites through the glymphatic system

To date, the physiological/pathological significance of high concentration synaptic Zn2+ release is poorly understood. It was postulated that Zn2+ release during ischemia may exert either neuroprotective or neurotoxic effects.70 In contrast to intracellular accumulation, the extracellular actions of Zn2+ after accumulation during ischemia may serve to limit neuronal injury by inhibiting NMDA channels and acid-sensing ion channels.71–73 The present results may indicate a new role of Zn2+ to accelerate brain clearance of toxins/wastes through the glymphatic system during pathological conditions such as ischemia (or even possibly in certain physiological processes) by regulating BBB TJ opening.

The glymphatic system is a recently discovered macroscopic waste clearance system in the brain.74–76 It has been proposed that primarily during sleep, the gaps between vascular endothelial cells and astroglial cells are opened and a unique system of perivascular channels is formed. The cerebrospinal fluid (CSF) and interstitial fluid (ISF) flow through the perivascular channels and wash out various kinds of metabolic wastes, such as Aβ and its soluble oligmers.77 The failure of glymphatic function might contribute to pathology in neurodegenerative disorders, traumatic brain injury and stroke.78–80 In fact, borneol was proposed to play an important role in treatment of cerebral ischemia through opening the BBB intercellular tight junctions.81,82 Inspired by all the above, we speculate that opening of the perivascular gaps might be regulated by the high-concentration synaptic Zn2+ release. Moreover, the Zn2+-induced flared TJ channels in the vascular endothelial cells would facilitate the excretion of pathological products, particularly macromolecular toxins, out of the brain. The high Zn2+ concentration needed to effectively open the intercellular junction may provide a hint for why the brain needs to keep such a high level zinc deposit. Overall, the complex roles of Zn2+ in neural systems, particularly in glymphatic function, could be a fascinating new issue for future research in bioinorganic chemistry.


In summary, the present work studied the effects of Zn2+ on TJ structures and functions in the MDCK cell monolayer model. Our results demonstrated that high concentrations (>200 μM) of Zn2+ can reversibly open TJ pore paths, favouring efflux of macromolecules. Further investigation revealed that Zn2+ uptake from the basolateral side caused inhibition of CaN activity, resulting in phosphorylation inactivation of GSK3β, which in turn elevated the level of snail transcription suppressors. Consequently, via the snail-mediated signal transduction, Zn2+ caused the rearrangement of basolateral F-actin and down-regulation of claudin-1 expression, leading to the formation of asymmetric paracellular channels. The present work may indicate new roles of Zn2+ in regulating the BBB function, further suggesting a potential role of Zn2+ in brain clearance of metabolites through the glymphatic system.

Conflicts of interest

There are no conflicts of interest to declare.


Project (No. 21571006 and 21271012) supported by NNSFC. The National Key Research and Development Program of China (2016YFC0103605 and 2016YFC0103600).


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