Published online before print June 16, 2005, doi: 10.1161/01.ATV.0000174130.75958.b7
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© 2005 American Heart Association, Inc.
Vascular Biology |
Vascular Endothelium Has a Local Anti-Adenovirus Vector System and Glucocorticoid Optimizes Its Gene Transduction
From the Department of Veterinary Pharmacology (T.M., M.H., H.O., H. K.), Graduate School of Agriculture and Life Sciences, The University of Tokyo, Japan; and the Department of Molecular and Cellular Pharmacology (S.L., A.N., K.K.), Gunma University Graduate School of Medicine, Gunma 371-8511, Japan.
Correspondence to Masatoshi Hori, DVM, PhD, Department of Veterinary Pharmacology, Graduate School of Agriculture and Life Sciences, The University of Tokyo, Bunkyo-ku, Tokyo 113-8657, Japan. E-mail ahori{at}mail.ecc.u-tokyo.ac.jp
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Abstract |
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Objective— Although adenovirus is a powerful tool for vascular research and therapy, endothelial impairment after infection has been reported. We investigated the mechanisms of this impairment and the effect of dexamethasone (DEX) on gene transfer into the vascular endothelial cells.
Methods and Results— ß-Galactosidase gene encoding adenovirus vector (ß-gal-Ad) (7.5x108 plaque-forming units/mL) transduced ß-gal into the rabbit organ–cultured pulmonary endothelium, followed by an apoptosis and an impairment of endothelium-dependent relaxation (EDR). Endothelial cell infected by ß-gal-Ad expressed proinflammatory genes mRNAs and suppressed endothelial nitric oxide synthase (eNOS) mRNA. Treatment with DEX dramatically increased ß-gal protein expression in the endothelium, attenuated ß-gal-Ad–induced apoptosis, and prevented the impairment of EDR. DEX also suppressed the mRNAs expressions of proinflammatory genes and recovered eNOS mRNA expression in organ-cultured vascular endothelium. In addition, we confirmed the DEX’s beneficial effects in an endothelial cell line (in vitro) and rat femoral artery (in vivo) experiments.
Conclusion— These results suggest that adenovirus vector induces host-immune responses and apoptosis in vascular endothelial cells. DEX is found to be a useful and potent tool to prevent the Ad-induced impairments of the endothelium and to optimize gene expression efficiency by adenovirus vector at the protein translation level in both in vitro and in vivo experiments.
We investigated the mechanisms of this impairment and the effect of DEX on adenovirus-mediated gene transfer into the vascular endothelial cells using organ-cultured pulmonary endothelium. Based on these results, we applied DEX treatment to in vitro and in vivo gene transfection.
Key Words: adenovirus • apoptosis • endothelial cells • gene therapy • inflammation
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Introduction |
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Vascular endothelium plays important roles in local regulation of vascular tone and smooth muscle cell proliferation via the release of vasoactive products such as nitric oxide (NO). Impairment of endothelium has long been considered to be a pathogenic mechanism of various vascular diseases, such as arteriosclerosis.1
A number of methods for delivering recombinant genetic material to vascular endothelial cells have been investigated in vitro and in vivo.2–4 Because they allow an effective transient gene expression in proliferating and nonproliferating cells, first-generation (E1/E3-deleted) adenovirus (Ad) vectors have become the most popular choice for use in arterial gene therapy and basic vascular experiments. However, in use of the vascular wall, high-titer E1/E3-deleted Ad vector infection has a number of disadvantages, such as the production of inflammatory reactions, resulting in transient recombinant protein expression, significant endothelial injury, and neointimal proliferation.5–7 These disadvantages seriously hamper its clinical application, and researchers have been struggling to alter the vector genome to reduce its toxicity.8,9
Several studies have demonstrated that these disadvantages are largely attributable to Ad-induced systemic cellular and humoral immune responses.7,10 However, the mechanism of direct adenoviral toxicity to endothelial cells remains to be clarified in detail. Further investigation and modification of the direct toxicity to vascular endothelial cells, along with optimization of gene expression efficiency, will be needed to advance the efficiency of arterial gene therapy.
In this study, we hypothesized that the vascular endothelium may exert a specific antiviral immuno-activity that results in endothelial impairment and low efficiency of transgene expression. To examine this possibility, we focused on the direct effects of Ad vector on the vascular endothelium using organ-cultured pulmonary arteries. In addition, we investigated the effects of 2 respective immunosuppression regimens, dexamethasone (DEX) and cyclosporine A (CSA), on gene transfer into the vascular endothelium to evaluate the usefulness of the Ad vector in gene therapy for vascular diseases. The organ culture method makes it possible to dissociate the influence of systemic cellular and humoral immune responses so that the direct effect of the Ad vector on the vascular endothelium can be investigated, and to easily examine the tissue for both morphological and functional changes. In this study, based on results from the organ culture procedure, we applied the technique to in vitro and in vivo gene transfer into endothelium.
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Materials and Methods |
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Adenovirus Construction and Purification
We made ß-galactosidase gene-encoding Ad vector (ß-gal-Ad) as previously described.11 Briefly, a nuclear-targeted bacterial ß-gal transgene fragment was inserted into a cosmid vector pAxCAwt with CAG promoter (Takara Shuzo, Japan) derived from adenovirus stereotype 5 with the E1 and E3 regions deleted at the SwaI site. Recombinant adenoviruses containing the insert were constructed by the COS/TPC (terminal protein complex) method using an adenovirus expression vector kit (Takara Shuzo, Japan). The concentration of ß-gal-Ad in the stock was 3x1010 plaque forming units (PFU)/mL, as determined by plaque titration on 293 cells. An Ad vector (5.3x1010 PFU/mL) (Takara Shuzo, Japan) without a transgene (Null-Ad) was used as a control vector.
Organ Culture Procedure and Gene Transfer
Animal care and treatment were conducted in conformity with the institutional guidelines of the University of Tokyo. Male Japanese White rabbits (2 to 2.5 kg) were euthanized. The organ culture procedure was performed as described previously.12 In brief, the main branches of the intrapulmonary arteries were isolated. Each artery was cut into rings with 
1.3 to 1.4 mm diameter and 1.3 to 1.4 mm width. Each arterial ring was then placed in 100 µL of DMEM and exposed to the respective adenoviral vectors in 1.5x108 to 1.5x109 PFU/mL in the presence or absence of 1 to 10 µmol/L DEX (Sigma) or 1 to 10 µmol/L CSA (Wako, Japan) for 2 hours (infection period). After infection, the mediums containing the viruses were removed. The arterial rings were rinsed 3 times with fresh DMEM and incubated in 100 µL DMEM for a period between 6 hours and 21 days in the presence or absence of these compounds (expression period) to induce the transfected ß-gal protein. The incubators were maintained at 37°C under an atmosphere of 95% air and 5% CO2.
Cell Culture Procedure and Gene Transfer
The human umbilical vein endothelial cell (HUVEC) line was purchased from the American Type Culture Collection and cultured in 1 mL DMEM containing 10% fetal bovine serum using a 20-mm well plate as previously reported.13 Subconfluent (1.8x104 cells/cm2) HUVECs at passage 31 to 34 showing cobblestone-like morphology were used for the experiments. Cells were cultured in 1% fetal bovine serum DMEM in the presence or absence of 0.3 to 3 µmol/L DEX 24 hours before the 3x105 to 3x107 PFU/mL Ad infection and during the infection period (2 hours) and the expression period (48 hours).
In Vivo Gene Transfer
Six hours before the surgery, 0.1 mg/kg DEX-containing physiological salt solution or DEX-free physiological salt solution was injected into Sprague-Dawley rats (280 to 310 grams) subcutaneously. Rats were anesthetized by pentobarbital (40 mg/kg), and the 1-cm segments of the right (for mock infection) and left (for Ad infection) femoral arteries were surgically exposed. For each artery, 20 µL of 3x108 to 3x1010 PFU/mL Ad containing DMEM or Ad-free DMEM was infected for 30 minutes. After the infection, 0.1 mg/kg DEX was injected subcutaneously every 24 hours. Two days after the infection, the femoral arteries were used for each experiment.
Vasomotor Studies
After the expression period, vascular muscle tension was recorded by a method described elsewhere.12 In brief, muscle tension was recorded isometrically with a force-displacement transducer under a resting tension of 10 mN. Data are shown as the percent relaxation of the steady-state preconstruction.
Histological Methods: ß-Gal Staining
After the expression period, arterial rings or HUVECs were rinsed 3 times with phosphate-buffered saline and fixed with 4% formaldehyde. Subsequently, arterial rings or HUVECs were stained for ß-gal by incubation at room temperature in X-gal solution, and then the ring was opened. Images were captured using a light microscope, and the number of ß-gal–positive endothelial cells was counted.
Cross-Section Hematoxylin and Eosin Staining and Terminal Deoxynucleotidyl Transferase-Mediated dUTP Nick End-Labeling Staining
After the ß-gal staining, arterial rings were embedded in paraffin. The 4-µm-thick sections were stained with hematoxylin and eosin. For the detection of apoptosis, the transferase-mediated dUTP nick end-labeling (TUNEL) method was applied to the sections using an In Situ Apoptosis Detection Kit-POD (Roche Diagnostics, Japan). For visualization, the sections were treated with 0.05% DAB solution with hematoxylin and eosin counterstaining.
Whole-Mount Immunostaining and TUNEL Staining
Whole-mount immunostaining was performed as previously described.13 After the fixation, arteries were probed with anti-CD31 monoclonal antibody (1:10 dilution) (Dako, Denmark). In the other experiment for the detection of apoptosis, fixed arteries were subjected to the TUNEL method using fluorescein isothiocyanate (FITC)-labeled dUTP. The images were captured using a confocal laser scanning microscope LSM510 imaging system (Carl Zeiss, Germany).
Semi-Quantitative Reverse-Transcription Polymerase Chain Reaction
After the incubation, the endothelial cells were scraped, and total RNA was extracted from the endothelial cells. Reverse-transcription polymerase chain reaction (RT-PCR) was performed as described previously.14 In some target genes, we performed partial sequence cloning (accession numbers in DDBJ; GAPDH; AB128158, endothelial nitric oxide synthase [eNOS]; AB128159, IL-1ß; AB128152, tumor necrosis factor [TNF]-
; AB128153, vascular cell adhesion molecule [VCAM]-1; AB128156, intercellular adhesion molecule-1 [ICAM-1]; AB128157, interferon [IFN]-; AB128154). The oligonucleotide primers were designed, as follows: GAPDH; sense, TCCCTCAAGATTGTCAGCAA; antisense, AGATCCACAACGGATACATT; eNOS: sense, ATAGAATTCACCAGCACCTTTGGGAATGGCGAT; antisense, ATAGAATTCGGATTCACTGTCTGTGTTGCTGGACTCCTT; IL-1ß: sense, CTGTCCTGCGTGATGAAAGA; antisense, CAGGAAGACGGGCATGTACT; TNF-: sense, ATGGTCACCCTCAGATCAGC, antisense, TTGACCGCTGAAGAGAACCT; IFN: sense, AGGACTCATCTGCTGCTTGG; antisense, TCTCATGATTTCTGCTCTGAC; VCAM-1: sense, AGAACCCAGATAGACAG; antisense, TAAAGGTTACTTCCAAACTC; ICAM-1: sense, TCCGTGCAGGTGAACT; antisense, GCATGAGAAATTGGCTCC; LacZ: sense, GTTAACCGTCACGAGCATCA; antisense, TCACACTCGGGTGATTACGA; h1-calponin: sense, AGGCCAATGATGTTCTGCCTTCTC; antisense, CTGGCACCAGCTGGAGAACATAGG. PCR products in 28 to 38 cycles (5-cycle interval) were electrophoresed. To exclude the possibility that the products contained RNA from sources other than endothelial cells, we confirmed that h1-calponin (smooth muscle marker) mRNA was not detectable in the purified total mRNA by RT-PCR procedure for 38 cycles (data not shown).
Real-Time PCR Analysis
The primers and probes were designed as follows: GAPDH: sense, TGCACCACCAACTGCTTAGC; antisense, TCTTCTGGGTGGCAGTGATG; probe, TCATCCACGACCACTTCGGCATTG; eNOS: sense, GAGTTACAAAATCCGCTTCAACAG; antisense, TCCGCCGCCAAGAAGAC; probe, CTCCTGCTCAGACCCGCTGG; IL-1ß: sense, CCTACCCTGCAGCTGGAGAGT; antisense, TTGTTGAAGACAAATCGTTTTTCC; probe, AGACCCCAACCGTTACCCAAAGAAGAAG; TNF- : sense, GGTCACCCTCAGATCAGCTTCT; antisense, CCACTTGCGGGTTTGCTACT; probe, CCCTGAGTGACGAGCCTCTAGCCCAC; interferon-: sense, GGATGCAACCCTCCTAGATTCA; antisense, ACAGGCTTGCAGACCACTCA; probe, TCTGCAATGACCTCCAG; VCAM-1: sense, GGAAAAAGGAGTTCAGGTGGAA; antisense, CCAAAGGGCCACTCAAATGA; probe, TCTACTCATTCCCCAAGGATCCAGA; ICAM-1: sense, GCACCGTGAATGTGATCTCCTT; antisense, CCGTGGGAATGAGACACTGA; probe, TCCCCATCCACTGCCTGGCG; LacZ: sense, TCCTGCTGATGAAGCAGAACA; antisense, AGCGGATGGTTCGGATAATG; probe, CTTTAACGCCGTGCGCTGTT. The mRNA expressions of the unknown samples were divided by the endogenous reference (GAPDH) amount to obtain a normalized target value. All PCR reactions were performed using an ABI Prism 7000 Sequence Detection System (Perkin-Elmer Applied Biosystems).
Statistical Analysis
The results of the experiments are expressed as the means±SEM. Statistical evaluation of the data were performed by analysis of variance (ANOVA), followed by the Tukey post-test for comparison between groups using Prism 3.0. P<0.05 was regarded as statistically significant.
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Results |
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The Effects of DEX and CSA on Transgene Expression in Organ-Cultured Pulmonary Arterial Endothelium
In the pulmonary artery infected with 7.5x108 PFU/mL ß-gal-Ad for 2 hours, ß-gal–positive cells were observed in the endothelium (Figure 1A). As expected, the predominant staining was intranuclear, and a nuclear dominant blue staining was not seen in null-Ad–infected arteries (n=4, data not shown). We first sought to assess the effect of virus-titer on Ad gene transfer in the pulmonary endothelium. In the pulmonary arteries infected with ß-gal-Ad at various concentrations (1.5x108 to 1.5x109 PFU/mL) for 2 hours, ß-gal–positive endothelial cells increased in a titer-dependent manner (1.5x108 PFU/mL; 108.2±2.1 cells/mm2, 7.5x108 PFU/mL; 199.5±4.3 cells/mm2, 1.5x109 PFU/mL; 470.2±3.1 cells/mm2; n=10 each).
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We next examined the effect of treatment with the immunosuppressive agents DEX and CSA on ß-gal-Ad–mediated gene expression into endothelium (Figure 1). DEX (1 to 10 µmol/L) and CSA (1 to 10 µmol/L) treatments during both the infection and the expression period optimized the ß-gal expression efficiency (the maximum increase in efficiency was 3.5-fold and 2.8-fold by 3 µmol/L DEX and 3 µmol/L CSA, respectively; n=10 each).
In an attempt to further enhance the DEX-induced increase in gene transfer into the endothelium, we investigated the effects of different treatment regimens. Treatment with 3 µmol/L DEX during the ß-gal-Ad infection period alone (before DEX treatment; Figure 1C) did not improve ß-gal-Ad–mediated gene expression in comparison with pulmonary endothelium infected with 7.5x108 PFU/mL ß-gal-Ad under a DEX-free condition (n=8; Figure 1C). In response to 3 µmol/L DEX treatment only during the expression period after the infection (after DEX treatment; Figure 1C), optimization of gene expression efficiency was observed similar to that in the DEX-treated endothelium during both the infection and the expression periods (before and after DEX treatment; n=8 each).
We next conducted an experiment to assess the optimal length of DEX treatment for stable ß-gal expression. We infected pulmonary arteries with 7.5x108 PFU/mL ß-gal-Ad for 2 hours in the presence of DEX (during a 2-hour infection and a 48-hour expression period), washed out the medium, and incubated the infected arteries in the DEX-free DMEM for 2 or 3 weeks. In these arteries, ß-gal expression was maintained at a high level at both 2 and 3 weeks after infection (2 weeks: 564.3±15.8 ß-gal–positive cells/mm2; 3 weeks: 540.3±19.2 ß-gal–positive cells/mm2; n=8 each).
Endothelial Cell Death and Denudation
Figure 2A shows a paraffin section of the vascular tissues stained first with ß-gal and then hematoxylin and eosin, and Figure 2B shows a whole-mount of CD31 (endothelium marker)-immunostained tissues. ß-gal–positive cells have blue-stained nuclei. In the nontreated pulmonary artery, no ß-gal–positive cells were observed, and the endothelial cells attached tightly to the tunica interna (n=5) (Figure 2A) and were tightly blocked like cobblestones (n=5) (Figure 2B). In the arteries infected with 7.5x108 PFU/mL ß-gal-Ad, in contrast, a few ß-gal–positive cells were observed in the endothelium; the excoriation of endothelial cells from the tunica interna was observed in some regions; and apoptosis-like concentrated and rounding endothelial nuclei were often observed (n=5). The 7.5x108 PFU/mL null-Ad–infected pulmonary artery had no ß-gal–positive endothelial cells (n=5), but in these arteries, similar morphological endothelial impairments were observed (n=5). In the arteries infected with 7.5x108 PFU/mL ß-gal-Ad in the presence of 3 µmol/L DEX during the infection and expression periods, many ß-gal–positive cells were observed in the endothelium (Figure 2A). No conspicuous changes, such as excoriation or apoptosis-like changes, were observed (n=5 each). We confirmed by ß-gal and CD31 double-staining that the morphology of ß-gal–expressing cells was completely intact (n=4; data not shown). In the arteries infected with 7.5x108 PFU/mL ß-gal-Ad and treated with 3 µmol/L CSA during the infection and expression periods, in contrast, many ß-gal–positive cells were observed in the endothelium (Figure 2A), and excoriation and apoptosis-like changes were often observed (n=5 each).
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We also performed a TUNEL assay in paraffin-sectioned and whole-mounted tissues to label apoptosis-induced DNA strand breaks (Figure 3A and 3B, respectively), and counted TUNEL-positive endothelial cells by whole-mount TUNEL assay (Figure 3C). In the nontreated arteries, there were no TUNEL-positive endothelial cells (n=5). In the arteries infected with 7.5x108 PFU/mL ß-gal-Ad, many TUNEL-positive endothelial cells were visible (n=5 each). Treatment with 3 µmol/L DEX during both the infection and expression periods significantly inhibited ß-gal-Ad–induced endothelial apoptosis (n=5); 3 µmol/L CSA treatment also inhibited ß-gal-Ad–induced endothelial apoptosis significantly, but its inhibitory effect was not pronounced as that of 3 µmol/L DEX (n=5).
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To assess the optical regimen length of DEX treatment for the inhibition of ß-gal-Ad (7.5x108 PFU/mL)-induced apoptosis, we also investigated the effects of different treatment regimens. Treatment with 3 µmol/L DEX during the ß-gal-Ad infection period alone (before DEX treatment) did not inhibit ß-gal-Ad–induced endothelial apoptosis (n=5) (Figure 3D). Treatment with 3 µmol/L DEX during the expression period only (after DEX treatment) significantly inhibited Ad-induced apoptosis, but this inhibitory effect was smaller than that by treatment during both the infection and expression periods (before and after treatment) (n=5).
Impairment of Endothelium-Dependent NO Production
In the nontreated pulmonary arteries with endothelium, substance P (0.1 to 30 nmol/L) caused vasorelaxation of the muscle contraction elicited by 1 µmol/L prostaglandin F2 in a concentration-dependent manner (n=5) (Figure 4A). The substance P (100 nmol/L)-induced endothelium-dependent relaxation was abolished by treatment with NG-monomethyl-L-arginine, a NOS inhibitor (200 µmol/L, 30 minutes before the addition of prostaglandin F2) (n=4 each; data not shown). Taken together, these results indicate that the substance P-induced vasorelaxation of the cultured arteries may be attributable mainly to NO production. In the ß-gal-Ad–infected pulmonary arteries, the substance P-induced endothelium-dependent relaxation was almost completely abolished (Figure 4A) (n=5). The 3 µmol/L DEX treatment, but not the 3 µmol/L CSA treatment (during both the infection and expression periods), significantly improved the ß-gal-Ad–induced endothelium-dependent relaxation impairment (n=5 each). In all of the arteries, the impairments in smooth muscle contractility and susceptibility to NO were not observed (n=5 each; data not shown)
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Endothelial Inflammation and Antivirus Reaction
In the pulmonary endothelial cells, the elevation of proinflammatory cytokines, TNF-, IL-1ß, and interferon- gene expressions were observed from 6 hours after infection, reached a peak at 12 hours after infection, as measured by semiquantitative RT-PCR analysis (n=4; data not shown). Figure 4B shows typical traces of semiquantitative RT-PCR analysis for GAPDH, eNOS, IL-1ß, TNF-, interferon-, VCAM-1, ICAM-1, and LacZ (ß-gal) in the pulmonary endothelial cells at 12 hours after infection with ß-gal-Ad (7.5x108 PFU/mL) in the presence or absence of 3 µmol/L DEX. In addition, we performed real-time RT-PCR analysis of these molecules for quantification (Figure 4C). The eNOS mRNA expression slightly decreased, whereas proinflammatory cytokines and the related gene expressions were increased in ß-gal-Ad–transfected endothelial cells (n=4 each). LacZ (ß-gal) mRNA expression was increased by ß-gal-Ad transfection. DEX treatment suppressed the elevation of the cytokines and those related genes expressions completely without any change in LacZ (ß-gal) or eNOS expression (n=4 each); eNOS mRNA expression was restored by DEX treatment (n=4).
The Effect of DEX on Transgene Expression in the Endothelial Cell Line
We next examined the effect of DEX on Ad-mediated gene transfer into HUVECs (Figure 5). In the HUVECs infected with ß-gal-Ad at various concentrations (3x105 to 3x107 PFU/mL) for 2 hours under the nontreated condition, a few ß-gal–positive endothelial cells were observed. However, even in the low-titer ß-gal-Ad–infected cells, morphological changes in HUVECs, such as apoptotic rounding, blebbing, and denudation from the plate (Figure 5A), were observed, and the number of the excoriated cells increased in a titer-dependent manner (Figure 5B).
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We next examined the effect of treatment with DEX on ß-gal-Ad–mediated gene expression in HUVECs. The transforming efficiency was increased 2.7-fold by 1 µmol/L DEX in the 3x106 PFU/mL ß-gal-Ad–infected HUVECs (Figure 5B; n=16). The higher (3 µmol/L) and lower (0.3 µmol/L) concentration of DEX slightly decreased the efficiency of gene expression (n=12 each; data not shown). In addition, ß-gal–positive HUVECs treated with 1 µmol/L DEX maintained their morphological characteristics (Figure 5A).
The Effect of DEX on Transgene Expression in Rat Femoral Artery
Finally, we examined the effects of DEX on in vivo transgene expression using rat femoral artery and found that 0.1 mg/kg DEX treatment increased the number of ß-gal–positive endothelial cells significantly in a titer-dependent manner (3x108 to 3x1010 PFU/mL) (Figure 6B). However, in the endothelium of femoral artery treated with Ad-free DMEM, no ß-gal–positive stained or impaired endothelial cells were observed (data not shown). In the 0.1-mg/kg DEX-treated rat, the submaximum transfection efficiency of ß-gal was obtained by 3x109 PFU/mL ß-gal-Ad infection (Figure 6B). Morphological study revealed that in the arteries infected with 3x109 PFU/mL ß-gal-Ad, most endothelial cells were excoriated at 2 days after infection (Figure 6A) (n=4). The degree of severity of these impairments was dependent on ß-gal-Ad titer (data not shown). In the 3x109 PFU/mL ß-gal-Ad–infected femoral arteries of 0.1 mg/kg DEX-treated rats, 325.4±16.1 cells/mm2 ß-gal–positive stained cells were detected in the endothelium (Figure 6B) (n=4). Additionally, no excoriation of endothelial cells from the tunica interna was observed in the DEX-treated arteries.
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Significantly different from the non-DEX–treated/3x108 PFU/mL ß-gal-Ad–infected or non-DEX–treated/3x109 ß-gal-Ad–infected artery; P<0.01. ##Significantly different from the non-DEX–treated/ß-gal-Ad (each virus titer)–infected artery; P<0.01. |
Discussion |
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In the present study, we found that ß-gal-Ad infection into the endothelium induced impairment of endothelium-dependent relaxation and morphological abnormality with proinflammatory cytokines and related genes mRNA expressions. Because the organ culture method to vascular tissues is a reliable means of distinguishing between the influence of systemic cellular and/or humoral immunoresponse and the direct effects of Ad infection into the endothelial cells, we concluded, based on the present results, that endothelial cells have an endothelium-specific antivirus system.
Another important finding of this study is that the immunosuppressive agents DEX and CSA can increase foreign gene transfection efficiency via improvement of the antiviral responses in endothelial cells. DEX, but not CSA, can prevent apoptosis of endothelial cells. These beneficial effects of DEX were confirmed in both in vitro and in vivo experiments. Taken together, these results suggest that DEX treatment during both the virus infection period and the protein expression period has good potential for use in the design of preclinical and clinical gene therapy experiments for vascular diseases.
Tripathy et al reported that host immune responses are directed predominantly against foreign transgene-encoded proteins.5 In this study, however, infection with an empty Ad vector yielded results similar to those by the bacterial ß-gal-Ad in morphological studies (Figure 2), demonstrating that our results are not unique to the ß-gal transgene, but rather occurred as a result of the direct effects of Ad infection itself.
Cytokines such as TNF-, IL-1ß, and interferon- play prominent roles in the host defense against viruses. Our results demonstrated that 7.5x108 PFU/mL ß-gal-Ad infection immediately induced these cytokines in endothelial cells. TNF- and IL-1ß are multifunction cytokines with many proinflammatory properties.15 TNF- is particularly important in the induction of apoptosis and in the upregulation of adhesion molecules such as ICAM-1 and VCAM-1, which recruit leukocytes to the site of inflammation.16 As mentioned, in an in vivo study, the Ad-induced T cell infiltration was reported to play an important role as a hindrance factor in vascular impairments. In this study, we did not examine the Ad-induced T cell infiltration, but it is expected that in the in vivo treatments, the inhibition of ICAM-1 and VCAM-1 expression observed in DEX-treated pulmonary arteries might lead to the attenuation of Ad-induced T cell infiltration and secondary impairment.
Interferon-/interferon-ß are secreted by virus-infected cells and inhibit virus replication through cessation of the protein translation of infectious viral RNA.17,18 In the present study, endothelial cells released interferon- at 6 to 12 hours after infection. In fact, 7.5x108 PFU/mL ß-gal-Ad without DEX did not result in a large expression of ß-gal protein even though a similar amount of LacZ mRNA was induced by ß-gal-Ad with or without DEX, suggesting that interferon- released from endothelial cells may protect against Ad transfection at the protein translation level.
Ad vector (subgroup C adenovirus) infection is mediated via 2 cell surface receptors. The fiber protein of Ad first binds to the cell surface of coxsackievirus and adenovirus receptor.19 Virus internalization is then mediated through cell surface 
ß3 or ß5 integrins. We observed that post-DEX treatment (in which DEX was absent during ß-gal-Ad infection) resulted in transfer of ß-gal protein into the endothelium at a level similar to that by DEX treatment during both the infection and the expression period. Taken together, these findings suggested that DEX optimizes the Ad transfection efficiency not by increasing viral cell adhesion and entry, but by protecting against viral ß-gal RNA translation. These results are also consistent with the mechanism of interferon action.
DEX prevented Ad-induced apoptosis and maintained endothelial function. Previous reports suggest TNF- upregulates FAS receptor and resulted in inducing apoptosis in lymphocytes.20 In the present study, TNF- was induced in endothelial cells by infection with Ad, indicating that similar apoptosis signaling with lymphocytes may be induced in endothelial cells. The actions of glucocorticoids are mediated by alteration of the expression of specific target genes.21,22 Suppression of some genes and/or cell survival signal activations may contribute to the inhibition of Ad-induced endothelial cell death by DEX treatment. We found a slight inhibitory effect of CSA against Ad-induced endothelial apoptosis, but CSA could not prevent the impairment of endothelial function significantly. A possible explanation is that most apoptosis negative endothelial cells treated with CSA may be just before or in the middle stage of the apoptosis cascade. Further experiments are needed to clarify this point. Additionally, we observed that post-DEX treatment is not sufficient in terms of Ad-induced apoptosis inhibition, even though post-DEX treatment can increase the Ad transfection efficiency.
NO and related molecules reduce the expression of adhesion molecules and proinflammatory cytokines23,24 and directly inhibit vascular smooth muscle cell proliferation25 and migration.26 Thus, the protective effects of DEX against Ad-induced endothelial injury may contribute to long-term protection from vascular injury induced by recombinant Ad.
Considering the differences between in vivo and in vitro experimental models, including various experimental conditions, we cannot make an accurate evaluation of the efficiency of Ad infections in the present study relative to that of those in other studies. However, our results indicate that high transfection efficiency can be achieved by quite low concentrations of Ad (in vitro isolated cells: 3x106 PFU/mL organ culture; 7.5x108 PFU/mL; in vivo: 3x109 PFU/mL) in the presence of DEX. Because the host response to Ad vector can vary depending on the dose of Ad,7 treatment with a relatively small amount of Ad may also help protect against the liver inflammation observed in in vivo Ad treatment.
Ad was rarely transduced into smooth muscle cells both in organ culture experiments and in vivo experiments. One probable explanation is that smooth muscle cells do not express enough coxsackievirus and adenovirus receptor as reported.27
Previous studies in endothelial cells in vitro have shown that gene expression peaks at 7 days after infection and persists for at least 14 days, and the same is true in endothelial cells in vivo.5–7 Our results using the organ culture procedure indicated that transient DEX treatment during and after infection could achieve enhanced and prolonged gene expression. Considering the side effects induced by long-term steroid treatments, these results have several potentially important implications for the design of preclinical and clinical gene therapy experiments.
In conclusion, we have shown that the vascular endothelium exhibits unique antivirus reactions, including apoptotic cell death and cytokine production in an autocrine and/or paracrine manner, and provided a simple method by which to markedly improve adenoviral delivery to endothelial cells using the immunosuppressive agent DEX. The present results have several potentially important implications for the design of preclinical and clinical gene-therapy experiments for vascular disease.
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Acknowledgments |
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This work was partly supported by a grant-in-aid for Scientific Research from the Ministry of Education of Japan, by research fellowships of the Japan Society for the Promotion of Science for Young Scientists, and by the Program for the Promotion of Basic Research Activities for Innovative Biosciences.
Received January 15, 2005; accepted March 30, 2005.
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