Protective role of FKBP51 in calcium entry-induced endothelial barrier disruption

Reagents

All reagents were obtained from Sigma-Aldrich (St. Louis, MO, USA) unless otherwise noted. Cell culture medium was obtained from Thermo Fisher Scientific (Waltham, MA, USA) or Santa Cruz Biotechnology (Santa Cruz, CA, USA) and penicillin/streptomycin was obtained from Thermo Fisher Scientific. EquaFETAL® bovine serum (EBS) and fetal bovine serum (FBS) were purchased from Atlas Biologicals, Inc. (Fort Collins, CO, USA) and Thermo Fisher Scientific, respectively. Hank’s Balanced Salt Solution (HBSS) was purchased from Thermo Fisher Scientific. Monoclonal antibodies to FKBP51 and expression plasmids for human FKBP51 have been described previously.^15,16 β-actin antibody was purchased from Santa Cruz Biotechnology. Doxycycline was purchased from Clontech Laboratories, Inc. (Mountain View, CA, USA).

Cell culture

PAECs were isolated from Sprague-Dawley rats and characterized as described. ¹⁷ Cells are grown in high glucose DMEM supplemented with 10% FBS or EBS, penicillin G (50 U/mL), and streptomycin (0.05 mg/mL). Animal work was approved by the University of South Alabama Institutional Animal Care and Use Committee and was performed in compliance with the National Institutes of Health Guide for the Care and Use of Laboratory Animals.

FKBP51 overexpressing cells were generated by lentiviral transduction. Production of lentiviral supernatants and infection of target cells was performed as described previously. ¹⁸ Briefly, lentivirus containing supernatants were produced by CaPO₄-mediated transfection of HEK293FT cell lines using established protocols.^19,20 Gag, Pol, and Env functions for lentiviral constructs were provided in trans by cotransfection of the vector plasmid with two helper plasmids, psPAX2 and pMD2.G (both gifts from Didier Trono [École Polytechnique Fédérale de Lausanne; Addgene (Cambridge, MA, USA)] plasmid #12260 and #12259, respectively). Transduction of PAECs with the lentivirus encoding human FKBP51 (lv3899) was performed in 35-mm dishes at 50% confluence by incubating them overnight with corresponding supernatant in the presence of 10 µg/mL polybrene. The next day, supernatant was removed and cells were allowed to recover for 24 h in fresh DMEM after which they were selected with puromycin (1 µg/mL) for three days.

Quantitative polymerase chain reaction (qPCR)

Messenger RNA was prepared from PAECs using the RNeasy mini kit (Qiagen, Valencia, CA, USA) and reverse transcribed to complementary DNA (cDNA) using an iScript cDNA preparation kit (Bio-Rad Laboratories, Hercules, CA, USA). qPCR was performed by SYBR Green incorporation using a CFX Connect (Bio-Rad) thermocycler with the following primers:

rHPRT1qPCRf 5’-GACCTCTCGAAGTGTTGGATAC-3’

rHPRT1qPCRr 5’-TCAAATCCCTGAAGTGCTCAT-3’

hFKBP51qPCR-1f 5’-GCTGAGCAGGGAGAGGATATTA-3’

hFKBP51qPCR-1r 5’-TCTCCAATCATCGGCGTTTC-3’

Western blotting

Cells were lysed by scraping and sonification for 10 s (Branson Digital Sonifier model S-450D; Branson, Danbury, CT, USA) at 12% output in RIPA buffer (Boston Bioproducts; Ashland, MA, USA) with 1% protease inhibitor cocktail followed by centrifugation at 12,000× g for 20 min. Whole cell lysates were electrophoresed on 4–12% bis-Tris gels (Thermo Fisher Scientific). Proteins were transferred to nitrocellulose membranes at 100 V. Membranes were blocked with milk (5% non-fat dry milk/0.2% BSA in PBS supplemented with 0.1% Tween-20) for 1 h and then rocked with primary antibodies overnight at 4℃ and with secondary antibodies for 1 h at room temperature. Supersignal West Pico or West Femto chemiluminescent substrates (Thermo Fisher Scientific) were applied to membranes to allow for protein visualization.

Cytochemistry

Cells were seeded on coverslips and grown to 80–100% confluence in 35-mm dishes. Cells were either fixed immediately or were pretreated with thapsigargin (1 μM) for 5 min before fixation. For actin stress fiber analysis, the cells were fixed with 4% paraformaldehyde for 15 min at room temperature, washed with 100 mM glycine in PBS, then permeabilized with 0.1% Triton X-100 in PBS for 1–2 min. For microtubule analysis, monolayers were fixed and permeabilized with 90% ice-cold methanol in PBS for 3 min at −20℃. Following fixation/permeabilization, cells were incubated in blocking buffer (10% normal goat serum, 10% normal donkey serum, 1.5% glycine, 1% bovine serum albumin in HBSS) for 1 h at room temperature. To visualize filamentous actin, cells were incubated with AlexaFluor 568 phalloidin (Molecular Probes; Eugene, OR, USA) either diluted 1:100 in PBS for 15 min at room temperature or diluted 1:150 in milk (5% non-fat dry milk in PBS supplemented with 0.1% Tween-20) overnight at 4℃. Cells were incubated with Hoechst 33342 nuclear counterstain (500 μM; Thermo Fisher Scientific) under agitation for 20 min at room temperature. To visualize tubulin and EB-1, cells were incubated with primary antibodies diluted in milk (5% non-fat dry milk in PBS supplemented with 0.1% Tween-20) overnight at 4℃. Cells were treated sequentially with secondary antibodies, with a wash in between, for 1 h at room temperature. Dilutions used for primary antibodies were 1:200 for α-tubulin and 1:150 for EB-1. Secondary antibodies were used at 1:500 dilution and include goat anti-mouse IgG fluorescein-conjugated (Thermo Fisher Scientific; Pittsburg, PA, USA) and AlexaFluor 488 donkey anti-goat IgG (H&L) (Life Technologies, Grand Island, NY, USA). Cells were incubated with Hoechst 33342 nuclear counterstain (10 µg/mL; Thermo Fisher Scientific) under agitation for 20 min at room temperature. Cells were incubated with CellMask™ Orange cell membrane stain (5 µg/mL; Life Technologies) under agitation for 40 min at room temperature. Fluorescent images were obtained using a Nikon A1 confocal laser scanning microscope (NIH S10RR027535) fitted with a 60X water immersion objective or a Zeiss Observer.D1 widefield microscope (Carl Zeiss®, Germany) fitted with 40X oil immersion objective.

Global Ca²⁺ measurements and patch-clamp electrophysiology

Cells were seeded onto glass coverslips and grown to confluence in 35-mm dishes. Changes in cytosolic calcium concentration were determined using Fura 2-acetoxymethyl ester (Fura 2/AM; Thermo Fisher Scientific).^4–6,21 Patch-clamp electrophysiology recordings were performed in whole-cell configuration on electrically isolated cells as described. ⁴ Isolation of single cells was achieved via treatment of cell monolayers with a non-enzymatic cell dissociation solution in PBS (catalog no. C5789). Transmembrane current was measured with an Axopatch 200B Amplifier (Molecular Devices; Sunnyvale, CA, USA). PClamp10 software was used to record the current evoked by step depolarization in 20 mV increments from −100 to +80 mV. Currents were measured as the mean value of the current amplitude during the last 20 ms of each step. The standard pipette solution contained (in mmol/L) 130 N-methyl-D-glucamine, 10 Hepes, 2 Mg²⁺-ATP, 1 N-phenylanthranilic acid, 0.1 5-nitro-2 -(3-phenylpropylamino)benzoic acid, 2 EGTA, 1 Ca(OH)₂ (pH 7.2, adjusted with methane sulfonic acid). The bath (external) solution contained (in mmol/L) 120 aspartic acid, 5 Ca(OH)₂, 5 CaCl₂, 10 Hepes, 0.5 3,4-diaminopyridine (pH 7.4 adjusted with tetraethylammonium hydroxide). All solutions were adjusted to 290–300 mOsm/L with sucrose. The free [Ca²⁺] was estimated to be 100 nmol/L as previously described. ¹⁰ Recording pipettes are made of hemo capillaries (A-M Systems; Sequim, WA, USA) pulled by a micropipette puller (P-97; Sutter Instruments; Novato, CA, USA) and heat-polished by a microforge (MF-830; Narishige; Tokyo, Japan) to a final resistance of 3–5 megaohms when filled with standard pipette solution. All of the experiments were performed at room temperature (22–25℃). Data are expressed as mean ± SEM for the number of cells (n) in which whole-cell patch-clamp recordings were obtained. Average change in overall current was calculated by summing the average change at each testing potential and dividing by 10 (the number of testing potentials used).

Actin stress-fiber quantification

Cells were seeded onto triplicate 24-well plates and grown to confluence. Each cell type was seeded into ten wells of the respective 24-well plate. The corner wells were treated with cell-free endothelial cell media. The WT and constitutive FKBP51 overexpressing PAEC monolayers were treated with either 1 µM thapsigargin in DMSO or the equivalent volume of DMSO without thapsigargin in media for 20 min. The monolayers were paraformaldehyde-fixed, permeabilized, and subjected to cytochemistry using AlexaFluor 568 phalloidin as described above. Nuclear counterstain was also applied as an internal control for cell count. The cell-free corner wells were also treated with the above conditions. Fluorescence at 620-nm and 460-nm wavelengths was recorded in each well simultaneously with a Synergy 2 fluorescence plate reader (BioTek; Winooski, VT) using with Gen5 (BioTek) software. The mean fluorescence from the cell free corner treatments was subtracted from the average fluorescence of treatment at each wavelength measured.

EB-1 microtubule plus-end quantification

Cells were seeded onto glass coverslips in 35-mm dishes, grown to confluence and treated with either 1 µM thapsigargin in DMSO or the equivalent volume of DMSO without thapsigargin in media for 20 min. The monolayers were methanol-fixed, permeabilized, and subjected to immunocytochemistry for EB-1 as described above. In addition to the Hoechst nuclear counterstain, the monolayers were also treated with CellMask™ Orange cell membrane stain. Cell monolayers were imaged via a Nikon A1 confocal microscope. Images were analyzed with Image J software. Green fluorescent events above a constant threshold for all treatments were obtained. The relative distance of each detected event between the nuclear membrane (parameters determined by the nuclear counterstain) and the cell membrane (parameters determined by the cell membrane stain) of each image was calculated.

Gap formation studies and electric cell-substrate impedance sensing (ECIS®)

Constitutive FKBP51 overexpressing PAECs and WT PAECs were seeded onto 35-mm coverslips and grown to confluence. Cells were imaged (40X oil immersion) at 5-s intervals for 60 min using a Zeiss Observer.D1 widefield microscope and AxioVision Rel 4.8 Software. Thapsigargin (1 μM) was added 5 min after the beginning of experiments. Gap size was measured by outlining gap areas and using the pixel-to-micron conversion feature of the AxioVision Rel 4.8 Software.

ECIS® experiments were performed as previously described. ²² Baseline resistance measurements were obtained for at least 30 min. Thapsigargin (1 μM) was then added to each well to initiate calcium entry. Change in resistance was measured until a new baseline was obtained.

Transwell dextran-flux assays

Endothelial cells were cultured in growth medium on a porous polycarbonate membrane (Corning Incorporated; Corning, NY, USA; Costar Transwell #3413) to confluency. Experiments were initiated by adding 330 µg/mL of 40,000 Da FITC-Dextran or 330 µg/mL FITC-Dextran/1 µM thapsigargin mix to the upper chamber, and the increase in intensity of FITC-Dextran was measured in the lower chamber over time using the Synergy 2 (BioTek) multi-mode microplate reader.

In situ endothelial permeability measurement

FKBP51^–/– mice were purchased from The Jackson Laboratory (Bar Harbor, ME, USA). For these mice, a lacZ targeting vector replaces the first coding exon of the Fkbp5 gene. WT mice used in these experiments were litter-mates of the FKBP51^–/– mice.

Male and female mice aged 10–12-weeks (20–25 g) were used in this study. To perform the in-chest lung perfusion protocol, ²³ anesthetized mice were weighed and tracheostomized. Lungs were exposed by removal of the anterior chest wall and cannulas inserted in the pulmonary artery and left ventricle. Lungs were then perfused in situ under constant flow (2 mL/min) without recirculation with 4% bovine serum albumin (BSA) in HBSS buffer containing 2 mM Ca²⁺ at 37℃ for 15 min after which they were challenged with 30 nM thapsigargin for 15 min. Finally, 2.5 mL (0.1 g dye/5% BSA) albumin-bound Evans Blue were added to 45 mL perfusate for an additional 15 min. Lungs were then excised, blotted dry, weighed, and homogenized in PBS (1 mL·100 µg⁻¹ tissue) and incubated with two volumes of formamide (18 h, 60℃) followed by centrifugation at 12,000 × g for 20 min. Optical density of the supernatant was determined by spectrophotometry at 620 nm.

Statistical analysis

Statistical analysis was performed using GraphPad version 5.0 software (San Diego, CA, USA). Data are presented as mean ± SEM. Comparisons between multiple groups were performed using a two-way ANOVA and the Bonferroni post hoc test. Student’s t-tests were used elsewhere. Values were considered significantly different when P < 0.05. Sample size for in vitro experiments is the number of independent experiments using independently passaged cell cultures. For in situ experiments, we used the minimum number of animals required to achieve statistical significance.

Characterization of I_SOC and actin stress fiber formation in PAECs

Thapsigargin, a plant alkaloid, causes emptying of the endoplasmic reticulum calcium store by blocking the SERCA Ca²⁺/ATPase pump. ²⁴ In PAECs, thapsigargin treatment leads to global calcium entry that is sensitive to 2-aminoethoxydiphenyl borate (2-APB) and YM-58483. ²⁵ While both 2-APB and YM-58483 are SOC entry inhibitors, 2-APB is considered to be relatively non-specific, ²⁶ whereas YM-58483 is a potent inhibitor of the I_CRAC (calcium release activated calcium current). ²⁷ We were particularly interested in 2-APB because it blocks calcium entry through some TRPC channels,^28–30 and the endothelial ISOC channel is composed of at least TRPC1 and TRPC4 subunits.^5,31 Xu et al. ²⁵ showed that treatment of PAECs with 2-APB resulted in a ∼50% decrease in thapsigargin-induced global calcium entry. Similarly, YM-58483 decreased global calcium entry by ∼50%, overall suggesting that thapsigargin activates multiple calcium entry pathways in PAECs. Indeed, one of these pathways is I_SOC;^2,3,5–7 however, it is unknown whether I_SOC is sensitive to 2-APB or YM-58483. We thus performed patch-clamp electrophysiology to measure I_SOC in the presence of 2-APB or YM-58483. Thapsigargin treatment activated I_SOC, a small current of –22.8 ± 2.5 pA at –40 mV that has a reversal potential of ∼ + 32 mV (Fig. 1a), and lanthanum reduced the current to noise level, consistent with that previously reported. ⁴ 2-APB reduced I_SOC by ∼46% (average differences at all testing potentials) whereas YM-58483 had no appreciable effect. The observation that I_SOC is sensitive to 2-APB but not YM-58483 is consistent with TRPCs 1 and 4 contributing to the ISOC channel make-up. OPEN IN VIEWER

We next wanted to determine whether inhibition of I_SOC leads to decreased thapsigargin-induced stress fiber formation. It was previously shown that thapsigargin treatment of PAECs leads to downstream actin stress fiber and inter-endothelial cell gap formation. ⁸ As thapsigargin activates multiple calcium entry pathways, it was not clear whether the I_SOC pathway in particular is important for actin stress fiber formation. To address this question, we performed cytochemistry of thapsigargin-treated PAEC monolayers using Rhodamine-phalloidin to visualize actin filaments. To rule out contributions from other ionic currents, e.g. Cl⁻, K⁺ and Na⁺, the cells were bathed in the same solution (which we refer to as I_SOC solution) that is used for patch-clamp electrophysiology. In this way, any stress fiber formation that occurs will be the result of calcium current. Additionally, cells were treated with the I_SOC inhibitors, La³⁺ and 2-APB, or with the I_CRAC inhibitor YM-58483. In PAECs treated with thapsigargin, I_SOC was activated and actin stress fibers formed throughout the monolayer (Fig. 1b). In the presence of La³⁺ or 2-APB, both of which inhibited I_SOC, thapsigargin-induced actin stress fiber formation was abolished. In the presence of YM-58483, which did not inhibit I_SOC, actin stress fibers still formed, although at decreased levels compared to control PAECs. We also tested YM-58483 when the cells were bathed in HBSS with calcium instead of the I_SOC solution. Here in the presence of YM-58483, again we observed actin stress fiber formation. Overall, these observations suggest that calcium entry must occur through specific channels, one in particular being the ISOC channel, for actin stress fibers to form. As I_SOC activation leads to actin stress fiber and inter-endothelial cell gap formation, ⁷ inhibition of I_SOC should be protective to the endothelial barrier. Indeed, here we show that inhibition of I_SOC correlates with decreased stress fiber formation. A caveat however is that both La³⁺ and 2-APB can block other channels in addition to the ISOC channel. We have identified another I_SOC inhibitor, the immunophilin FKBP51, ¹⁰ although it has not yet been determined whether inhibition of I_SOC by FKBP51 is protective to the endothelial barrier

Increased FKBP51 expression inhibits I_SOC in PAECs

We have previously demonstrated that treatment of PAECs with dexamethasone upregulates FKBP51 expression leading to decreased thapsigargin-induced I_SOC. ¹⁰ In that study we also demonstrated FKBP51-mediated inhibition of I_SOC in doxycycline-inducible FKBP51 HEK293 cells. However, to be certain that the dexamethasone effect on I_SOC in PAECs was specifically due to FKBP51 upregulation, in the current study we generated via lentiviral construct a PAEC cell line that constitutively overexpresses FKBP51 (cFKBP51). This cell line also gave us a tool to study the effect of FKBP51 on endothelial barrier function. qPCR and western blot analysis confirmed upregulation of FKBP51 (Fig. 2a and b). At the protein level, FKBP51 expression was increased by 3.1 ± 0.5-fold compared to control cells. Using whole cell patch-clamp electrophysiology, I_SOC was decreased by ∼40% in the FKBP51 overexpressing cells compared to control cells (Fig. 2c). OPEN IN VIEWER

We then measured global calcium entry following thapsigargin treatment using the ratiometric dye Fura 2/AM. Using a calcium add-back approach, we observed that cFKBP51 PAECs exhibited calcium entry that was not statistically different from control cells (Fig. 2d and e). Whereas increased FKBP51 expression in PAECs does not change the global calcium entry, it does inhibit I_SOC. Taking into consideration that measurement of global calcium reflects calcium entry through all thapsigargin-activated calcium channels, these observations suggest that FKBP51 is principally acting on the ISOC channel and not other calcium entry channels.

Increased FKBP51 expression inhibits calcium entry-induced stress fiber formation

As we have shown that FKBP51 is principally inhibiting calcium entry through the ISOC channel in PAECs, we next went on to determine whether inhibition of I_SOC by FKBP51 decreases thapsigargin-induced stress fiber formation. Here, WT and cFKBP51 PAECs were grown to confluence, treated with thapsigargin to activate calcium entry, fixed, permeabilized, and stained with AlexaFluor 568 phalloidin to visualize filamentous actin. In control PAECs without thapsigargin treatment, actin was principally localized to the cell periphery as the cortical actin rim (Fig. 3a, top left). Following thapsigargin treatment, actin stress fibers appeared throughout the monolayer (Fig. 3a, bottom left). In cFKBP51 PAECs, there was very little thapsigargin-induced actin stress fiber formation (Fig. 3a, compare top and bottom right). Quantitation of filamentous actin (F-actin) using phalloidin revealed a 21 ± 7% increase in F-actin in control PAECs following thapsigargin treatment, reflective of stress fiber formation (Fig. 3b). On the other hand, thapsigargin had no effect on F-actin in cFKBP51 cells. Overall, these data indicate that inhibition of I_SOC by FKBP51 decreases calcium entry-induced actin stress fiber formation. OPEN IN VIEWER

Increased FKBP51 expression leads to increased microtubule polymerization in PAECs

We have shown that FKBP51 inhibits I_SOC and downstream actin stress fiber formation. In endothelial cells, there is cross-talk between the actin and microtubule networks where microtubule depolymerization precedes actin stress fiber formation^32,33 and microtubule stabilization decreases actin stress fiber formation.^34,35 Further, FKBP51 was shown to promote microtubule polymerization in a Xenopus oocyte system. ¹⁴ Thus, we questioned whether microtubules are playing a role in FKBP51’s effect on I_SOC. We first wanted to determine whether increased FKBP51 expression promotes microtubule polymerization in PAECs. Immunoblotting was performed for total and tyrosinated tubulin in control and cFKBP51 PAECs. Tyrosination is a post-translational modification that occurs on α-tubulin, ³⁶ and detyrosinated microtubules exhibit enhanced stability. ³⁷ While total tubulin levels did not differ between the two cell types, cFKBP51 cells exhibited decreased tyrosinated tubulin (46 ± 7%), suggesting more detyrosinated tubulin and increased microtubule stability (Fig. 4a). OPEN IN VIEWER

Immunocytochemistry was then performed to visualize the microtubule cytoskeletal network. In contrast to WT PAECs which showed microtubules extending from the centrosome partially into the cytosol, the cFKBP51 cells exhibited a much more extensive microtubule network throughout the entire cytosol, suggesting increased microtubule polymerization (Fig. 4b). To quantitatively confirm the more extensive microtubule network in cFKBP51 cells, the number of the microtubule plus-ends and their spatial orientation relative to the nucleus and the plasma membrane were measured. Here, microtubule plus-ends were identified using EB-1 antibody, and we observed that microtubules in cFKBP51 cells were more numerous and extended farther away from the nucleus as compared to control PAECs, overall revealing increased microtubule polymerization in the cFKBP51 cells (Fig. 4c and d). Further, following a 20-min thapsigargin treatment, the number and localization of microtubule plus-ends were not different than the respective vehicle treatment in both WT and cFKBP51 PAECs. Overall, we have determined that FKBP51 impacts microtubule dynamics in PAECs by increasing microtubule polymerization.

FKBP51 inhibits I_SOC through microtubule polymerization

We next wanted to determine whether microtubule polymerization by FKBP51 leads to inhibition of I_SOC. To address this question, we treated WT or cFKBP51 PAECs with nocodazole over a concentration range that effected limited to complete dissolution of the microtubule network. In the absence of nocodazole, cFKBP51 PAECs again exhibited a more extensive microtubule network than WT cells (Fig. 5a). With a 10-μM nocodazole treatment, the microtubule network in WT PAECs was dramatically reduced, and at 100 μM nocodazole, the network was completely disrupted. In cFKBP51 cells, at 10 μM nocodazole, the extended microtubule network was slightly retracted from the cell periphery, but was largely still intact. At 100 μM nocodazole, the microtubule network was mostly condensed to the perinuclear region. We then measured I_SOC under these same conditions to determine whether extended microtubules are required for the FKBP51-mediated inhibition of I_SOC. OPEN IN VIEWER

In the WT PAECs, in the absence of nocodazole, a normal I_SOC was recorded (Fig. 5b). In the presence of 1 and 10 μM nocodazole, I_SOC was decreased in a concentration-dependent manner. At 100 μM nocodazole, with complete dissolution of the microtubule network, the cells could not be patched because a gigaseal could not be attained. When WT PAECs were treated with taxol (10 μM) to stabilize microtubules, I_SOC was also decreased. Thus, we observed that I_SOC function is dependent on microtubules, which is in agreement with previous observation. ³ If the extended microtubules in cFKBP51 cells are required for inhibition of I_SOC, then we would expect that when microtubules are partially depolymerized, inhibition of I_SOC will be prevented. Indeed, we observed that when cFKBP51 cells were treated with 1 μM nocodazole, I_SOC inhibition was decreased, as evidenced by an increased current, and at 10 μM nocodazole I_SOC inhibition was completely prevented (Fig. 5c). To better visualize this, currents recorded at –60 mV holding potential under the conditions of 0 μM nocodazole and 10 μM nocodazole were plotted (Fig. 5d). At 0 μM nocodazole, the current in cFKBP51 PAECs was decreased compared to control cells revealing the FKBP51-mediated inhibition of I_SOC. However, at 10 μM nocodazole, FKBP51 was not able to inhibit I_SOC, as the current recorded in cFKBP51 cells in 10 μM nocodazole was not significantly different from the current recorded in WT cells with no nocodazole treatment. These data demonstrate that I_SOC in PAECs is dependent upon a delicate balance of microtubule polymerization, and that increased microtubule polymerization observed in cFKBP51 PAECs is required for the FKBP51-mediated inhibition of I_SOC.

Increased FKBP51 expression reduces calcium entry-induced endothelial permeability

Since we observed that increased FKBP51 expression promotes microtubule polymerization and decreases calcium entry-induced actin stress fiber formation, we next questioned whether inter-endothelial cell gap formation is also reduced. Here, confluent monolayers of control and cFKBP51 PAECs were treated with thapsigargin and inter-endothelial cell gap formation was monitored via videomicroscopy over 45 min (Fig. 6a). Time 0 min represents the cells under resting conditions, 5 min before the addition of thapsigargin. Quantitation of inter-endothelial cell gaps revealed that in the basal state, cFKBP51 cells exhibited fewer and smaller gaps compared to control PAECs, suggesting a tighter basal barrier in the cFKBP51 cells (Fig. 6b). Following thapsigargin treatment, there was an increase in inter-endothelial cell gaps in both cell types. However, the cFKBP51 PAECs exhibited fewer and smaller gaps than control cells, revealing a protective effect of FKBP51 on the endothelial barrier. We also performed ECIS® as a measure of endothelial barrier integrity. Following thapsigargin treatment, control PAECs exhibited a decrease in resistance of 17 ± 2% whereas cFKBP51 cells exhibited 7 ± 3% decrease in resistance (Fig. 7a–c), indicating less endothelial barrier disruption as compared to control cells. Finally, we performed dextran flux assays using 40 kD dextran to measure macromolecular permeability across the endothelial barrier. Treatment with thapsigargin resulted in increased permeability in control PAECs whereas there was no permeability increase in cFKBP51 cells (Fig. 7d). Overall, these data reveal that FKBP51 protects the endothelial barrier from calcium entry-induced disruption. OPEN IN VIEWER

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Fig. 7.

FKBP51 overexpression protects endothelial barrier integrity and decreases permeability. (a, b) ECIS® was performed to measure changes in endothelial barrier integrity upon activation of calcium entry with thapsigargin. Baseline resistance values were obtained for ∼30 min, at which time calcium entry was activated with thapsigargin (1 μM, arrow). (a) Absolute resistance values and (b) normalized, to baseline, resistance values. (c) Bar graph showing maximum change in resistance relative to baseline (0.1 s before addition of thapsigargin) for each cell type. The thapsigargin-induced decrease in resistance was inhibited in cFKBP51 cells. *P < 0.05 as determined by Student’s t-test; n = 11. (d) Endothelial permeability was measured using the Transwell dextran flux protocol. Calcium entry was activated with thapsigargin (1 μM). While control PAECs exhibited increased permeability following thapsigargin treatment, there was no increase in permeability in cFKBP51 cells. *P < 0.05 for thapsigargin-treated control cells vs. untreated control cells; n = 3–6.

Knockout of FKBP51 exacerbates calcium entry-induced endothelial permeability in situ

As we have shown that overexpression of FKBP51 reduces calcium entry-induced endothelial barrier disruption, we wanted to determine whether knockout of FKBP51 leads to increased endothelial barrier disruption. For this we used FKBP51^–/– mice and measured lung endothelial permeability in situ. Here, we performed an in-chest lung perfusion protocol ²³ in WT and FKBP51^–/– mice. Thapsigargin was perfused to activate calcium entry and was followed by perfusion of Evans Blue dye-conjugated albumin. Tissue permeation of Evans Blue dye-conjugated albumin was measured as an indicator of endothelial permeability. Lungs from FKBP51^–/– mice exhibited ∼3 times greater permeability following thapsigargin treatment compared to WT mice (Fig. 8), suggesting that the physiological role of the FKBP51-mediated inhibition of I_SOC is to limit calcium entry-induced endothelial barrier disruption. OPEN IN VIEWER