Although rapamycin is a well-known conformational inhibitor of mTORC1, it is now widely used for treating arterial restenosis. Various rapamycin analogues (rapalogue) have been made for applying to drug-eluting stents. Here we show that two major rapalogues, everolimus and biolimus, exert a differential effect on the mTORC1-mediated signaling pathways in vascular smooth muscle cells. In balloon-injured carotid arteries, both rapalogues strongly inhibit neointimal hyperplasia. Signaling pathway analyses reveal that everolimus exert cytotoxicity by increasing cellular reactive oxygen species and consequently reduce energy metabolism. By contrast, biolimus confers a preferential induction of autophagy by more strongly activating major autophagy regulator, ULK1, in vascular smooth muscle cells than everolimus does. As a consequence, the implantation of biolimus-eluting stent reduces endothelial loss, which in turn reduces inflammation, in porcine coronary arteries. Thus, this study reveals that a chemical derivatization can cause a change among mTORC1-dependent signaling pathways in vascular smooth muscle cells, thereby enabling to elicit a differential efficacy on arterial restenosis.
Balloon angioplasty and stent implantation have been applied to extend arterial vessels narrowed by atherosclerosis1. However, through the procedure, endothelial cells are denuded and thus the underlying vascular smooth muscle cells (VSMC) are exposed to blood stream containing macrophage/monocytes. As a result, VSMCs de-differentiate and aggressively proliferate, thereby causing in-stent restenosis2. To prevent such complications, drug-eluting stents coated with cytostatic/cytotoxic drugs that inhibit VSMC proliferation have been developed and widely used in clinics3. Nonetheless, those drugs also suppress re-endothelialization and thus induce inflammation and thrombosis.
Rapamycin is one of the most widely used drugs for drug-eluting stent4. Rapamycin was identified from soil bacterium S. hygroscopicus and it was initially known for its broad immunosuppressive and anti-proliferative effects5,6. Later, it was found that TOR protein (mTOR in mammals) is the target of rapamycin7,8. mTOR, a Ser/Thr protein kinase with many substrates, is a central regulator of cell proliferation, metabolism, and autophagy9,10. The mTOR kinase forms functionally distinct two complexes, mTORC1 and mTORC2, of which only mTORC1 is sensitively suppressed by rapamycin10. In mammalian cells, rapamycin firstly binds to a FKBP12 protein and then this complex allosterically inhibits mTORC1 by binding to the FRB domain next to the kinase domain of mTOR11. Recent studies have shown that some mTORC1 substrates are resistant to rapamycin in several cell types12,13. The p70S6K, a mTORC1 substrate involved in protein translation14, is fully inhibited by rapamycin in most cell types, while the multiple phosphorylation sites15 of another protein translation regulator 4E-BP116 show a differential degree of de-phosphorylation responding to the rapamycin-induced mTORC1 inhibition13. Also, the mTORC1-dependent phosphorylation of autophagy-inducing kinase ULK1 at S75817,18 is resistant to rapamycin12.
To date, many rapamycin analogues (rapalogue) have been developed to improve drug delivery and lower toxicity19. In general, rapamycin was broadly modified on C40 branch that does not bind to either the FRB domain of mTOR or the FKBP12 protein11. Those analogues exhibit different bioavailability and stability in vivo20. For example, the natural rapamycin sirolimus has a disadvantage of causing thrombosis4,21, whereas everolimus prevents such in-stent thrombosis22. The latest version of rapalogues is biolimus that shows an improved drug delivery capacity as it has more lipophilic properties23. Nonetheless, the differential signaling impact among rapalogues has not been evaluated seriously in VSMCs.
In this study, we found that biolimus is unexpectedly preferential to autophagy induction by enhancing the dephosphorylation of ULK at S758. Mechanistically, sirolimus and everolimus were cytotoxic by inducing cell death, while biolimus was rather cytostatic by inducing autophagy. More importantly, biolimus-eluting stents lowered inflammation score when it was implanted in porcine coronary arteries. Overall, our signaling study implicates the importance of structure-activity relationship for drug derivatization.
Materials and Methods
Sirolimus (Cat No. 37094), everolimus (Cat No. 07741), anti-LC3B antibody (Cat No. L7543) were purchased from Sigma-Aldrich. Biolimus (Cat No. sc-391515) and anti-pRb antibody (Cat No. sc-50) were purchased from Santa Cruz Biotechnology. Anti-p-mTOR (pS2448) (Cat No. 5536 S), Anti-mTOR (Cat No. 2972 S), Anti-p-ULK1 (pS758) (Cat No. 14202 S), Anti-ULK1 (Cat No. 6439 S), Anti-p-4EBP1 (pS65) (Cat No. 9451 S), Anti-4EBP1 (Cat No. 9644), Anti-p-P70S6K (pT389) (Cat No. 9205 S), Anti-P70S6K (Cat No. 9202 S) antibodies were purchased from Cell Signaling Technology. Anti-Ki67 antibody (Cat No. 550609) was purchased from BD Pharmingen. Alexa Fluor 488 (Cat No. A21206) and 568-conjugated donkey anti-rabbit secondary antibodies (Cat No. A10042) and Alexa Fluor 568-conjugated donkey anti-mouse secondary antibodies (Cat No. A10037) were purchased from Invitrogen. pRb (pThr373) antibody (Cat No. 9306 S) was purchased from New England Biolabs.
Human aortic SMCs (HASMC) were purchased from Lonza. Cells were cultured using Smooth Muscle Cell Growth Medium (SmGM) containing 5% fetal bovine serum with growth factors and antibiotics (Lonza, Cat no. cc-4149) in humidified incubator containing 5% CO2 at 37 °C. All experiments were performed with HASMCs at passages 5–7.
Cells were rinsed twice with ice-cold phosphate-buffered saline (PBS) and were frozen on liquid nitrogen. Then, they were lysed in a lysis buffer containing 20 mM HEPES (pH 7.0), 1% Triton X-100, 150 mM NaCl, 10% glycerol, 1 mM EDTA (pH 8.0), 2 mM EGTA (pH 8.0), 1 mM DTT, 5 mM Na3VO4, 5 mM NaF, 1 mM AEBSF, 5 μg/ml aprotinin, and 5 μg/ml leupeptin. The cell lysates were centrifuged at 15,000 ×g for 15 min, and the protein concentrations were determined by Bradford assay (Pierce). Protein samples were mixed with SDS sample buffer and boiled for 5 min. The proteins were separated by SDS-PAGE and transferred onto nitrocellulose membranes by electroblotting for 1 hr. The membranes were blocked with 5% bovine serum albumin (BSA) or 5% dry skimmed milk in Tris-buffered saline containing 0.05% (v/v) Tween-20 (TBST) for 2 hr ar room temperature and then incubated with the appropriate primary antibody (1:1,000 dilution) in blocking buffer at 4 °C overnight. After washing three times with TBST, membranes were incubated with horseradish peroxidase-conjugated secondary antibody (Amersham Biosciences) in blocking buffer. The immune-reactive bands were detected with an enhanced chemiluminescence kit (AbFrontier, Korea) and quantified by a LAS-3000 imaging system (Fuji Film, Japan). When necessary, the membranes were stripped by shaking them for 60 mins at 37 °C in 67 mM Tris (pH 6.7), 2% SDS, and 100 mM β-mercaptoethanol and reprobed with the appropriate pan-antibody.
Cell viability assay
HASMCs (3,000 cells) were seeded in 100 μl of complete media on white flat bottom 96-well plate (3917, Corning Costar). After 24 hr, rapalogues in ethanol were treated to cells at indicated concentrations and incubated for additional 24 hr. Cellular ATP concentration was measured using CellTiter-Glo Luminescent Assays kit (Promega) according to manufacturer’s protocol. Luminescence was measured by MicroLumat Plus LB96V (Berthold Technologies, USA).
Flow cytometry Analysis
HASMCs (1 × 105 cells) were cultured on 35-mm tissue culture dish (153066, Nunc) for 24 hr and then treated with rapalogues for additional 24 hr. For cell cycle analysis, cells were detached and permeabilized in 70% ethanol for overnight at −20 °C. The cells were treated with RNase A (100 μg/ml in PBS) for 1 hr at 37 °C and then stained with propidium iodide (final conc. 10 μg/ml).
For determination of S-phase cells, cells were incubated with 10 μM BrdU for 2 hr at 37 °C and then analyzed using BrdU Flow Kits (BD Biosciences) according to manufacturer’s protocol. Briefly, cells were fixed and permeabilized, and incubated with 300 μg/ml of DNase for 1 hr at 37 °C. FITC-conjugated anti-BrdU antibody was incubated with cells for 20 min at room temperature in the dark. Then, 7-AAD was treated just before analysis for total DNA contents. The percentages of G0/G1 diploid cells were analyzed by Modfit LT software (Verity Software House, Topsham, ME) in FACSCalibur system (BD biosciences). The percentages of BrdU-positive cells were analyzed by FlowJo software (Tree Star).
Balloon-induced injury procedure in rat carotid artery
Animal experiments were approved by the Institutional Animal Care and Use Committee (IACUC) of Ewha Womans University and conformed to Guide for Care and Use of Laboratory Animals published by the US National Institutes of Health (The National Academies Press, 8th Edition, 2011). The ten-week-old male Sprague-Dawley rats were used for a balloon-induced injury model. A balloon injury was created using an infiltrated 2 F Fogarty balloon embolectomy catheter in the left common carotid artery as previously described12. In brief, the rats were anaesthetized by inhalation of isoflurane gas (N2O: O2 / 70%: 30%). Then, the left external carotid artery was exposed and arterial branches were electro-coagulated. A catheter was inserted through the transverse arteriotomy of the external carotid artery and positioned in 1 cm distance from a cut-down site. The catheter was then inflated and moved back and forth three times along the common carotid artery. For catheter-mediated intramural delivery of drugs24, the solutions of rapalogues (20 μM in 200 μl of PBS) were infused into the injured carotid lumen and then incubated for 15 min to allow the efficient drug diffusion. The lumen was flushed once with saline before the catheter was removed. After the removal of catheter, the punched area was sealed and the clap in the common carotid artery was released to reestablish blood flow. Unless otherwise stated, the rats were then recovered in the cages for 10 days.
Paraffin sections of balloon injured carotid Arteries were de-paraffinized in xylene and rehydrated in ethanol. The rehydrated tissue sections were boiled for 20 min in citric acid-based antigen unmasking solution (Vector Laboratories) for antigen retrieval and then blocked with 5% normal donkey serum in PBST (0.3% Triton X-100 in PBS) for 1 hr. Then, the samples were incubated with anti-LC3B antibody (1: 200 dilution) or anti-Ki67 antibody (1: 50 dilution) overnight at 4 °C. After washing with PBST three times, the samples were incubated with Alexa Fluor 488 - or 568 - conjugated donkey anti-rabbit IgG antibodies for LC3B and Alexa Fluor 568 - conjugated donkey anti-mouse IgG antibodies for Ki67 for 2 hr at room temperature in the dark. Nuclear DNA was labeled with DAPI. Fluorescence image were obtained using LSM 510 META confocal microscope (Carl Zeiss).
De-paraffinized, rehydrated and antigen retrieved paraffin sections were incubated with TUNEL reaction mixture for 60 min at 37 °C using In Situ Cell Death Detection Kit (Roche Diagnostics), according to the manufacturer’s instructions. Nuclear DNA was labeled with DAPI.
Purification and quantification of rapalogues
HASMCs (8 × 105 cells) were seeded on 60 - mm tissue culture dishes (245389, Nunc). After 24 hr, rapalogues in ethanol were treated for 2 hr to the cells at final concentrations of 2 μM or 10 μM in 2.5 ml culture media. The cells washed with PBS quickly and extracted with 1 ml methanol for 2 hr at −20 °C. After centrifugation at 12,000 × g for 10 min, Supernatants were dried using a savant SPD121P Speedvac Concentrator (Thermo Fisher Scientific), dissolved in the 200 μl of 50% Acetonitrile with 0.1% trifluoroacetic acid solution. Samples were separated by a reverse-phase high performance liquid chromatography (Agilent Series 1100 HPLC system with diode array). 100 μl of each samples were injected to a C18 column (4.6 × 250 mm ID, 5 μm spherical packing; Vydac) and eluted through 50–95% Acetonitrile with 0.1% trifluoroacetic acid mobile phase solution at a rate of 1.2 ml/min. Amounts of extracted drugs from cells were calculated by using each standard curves gained from standard drug solutions (1.25, 2.5, 5, 10, 20 μM). Drugs were detected by UV absorbance at 278 nm.
Coating of drug on metal stent
Coating method was used by an ultrasonic spray method as described previously25. Briefly, 20 mg of sirolimus, evolimus, or biolimus with 20 mg of poly lactic acid (PLA, 0.80 ~1.2 dL/g of inherent viscosity in chloroform at 0.1 w/v% at 25 °C) were dissolved in 5 mL of tetrahydrofuran (THF), respectively. The coating solutions were spray-coated on the metal stent (SoniCoater, Noanix Co., Korea) and then were vacuum-dried for 24 hr. Coating thickness measured by reflection spectrometry (F40, Filmetrics, Inc., USA) was 6.5 ± 2.46 μm.
Stent implantation procedure
The animal study was approved by the Ethics Committee of Chonnam National University Medical School and Chonnam National University Hospital, and conformed to Guide for Care and Use of Laboratory Animals published by the US National Institutes of Health (The National Academies Press, 8th Edition, 2011). The mini-pigs weighing 25–30 kg were anesthetized with zolazepam and tiletamine (2.5 mg/kg, Zoletil50, Virvac, Caros, France), xylazine (3 mg/kg, Rompun, Bayer AG, Leverkusen, Germany) and azaperone (6 mg/kg, Stresnil, Janssen-Cilag, Neuss, Germany). They received supplemental oxygen continuously through an oxygen mask. After subcutaneous administeration of 2% lidocaine at the cut-down site, the left carotid artery was surgically exposed. A 7 French (F) sheath was inserted. Also, heparin (5,000 U) was administered intravenously as a bolus prior to the procedure. The target coronary artery was engaged using standard 7 F guide catheters and control angiograms of both coronary arteries were performed using nonionic contrast agent in two orthogonal views. The stent was deployed by inflating the balloon and the resulting stent-to-artery ratio was 1.3:1. Coronary angiograms were obtained immediately after stent implantation. All equipment was removed and the carotid artery ligated. The bare metal stent (BMS) and drug coated BMS were implanted in the left or right femoral arteries alternatively in each pig. Continuous hemodynamic and surface electrocardiographic monitoring was maintained throughout the procedure. To prevent acute thrombosis after stenting, aspirin 100 mg and clopidogrel 75 mg were administered daily for 5 days before the procedure, which was continued until sacrifice stage. After day 28 post-implantation, stenting, the animals underwent follow-up angiography in the same orthogonal views before sacrifice with 5 ml of potassium chloride via the intracarotid artery. The part of the arteries surrounding the stent were removed carefully and processed for histological analysis.
The balloon-injured rats were anesthetized and the common carotid arteries were excised after transcardiac perfusion-fixation with heparinized saline containing 3.7% formaldehyde. The vessels were paraffin embedded and sectioned by rotary microtome (Leica RM2255). The two serial tissue sections (4 μm in thickness) were obtained from the middle area of common carotid arteries and stained with haematoxylin and eosin (HE). The luminal, internal elastic laminal, and external elastic laminal areas were measured using NIH Image v 1.62. The intimal and medial areas were determined by subtraction of the luminal area from the internal elastic area and by subtraction of the internal elastic area from the external elastic area. The values from two serial sections per rat were averaged for analysis.
The stented coronary arteries were dissected and histopathological analysis was performed by cardiovascular pathologists. The specimens were cut 50–100 µm in thickness, and stained with hematoxylin and eosin (HE). Quantitative measurements of the samples were performed using a calibrated microscope, digital video imaging system, and a microcomputer program (Visus 2000 Visual Image Analysis System, IMT Tech). Borders were manually traced for lumen area, area circumscribed by the internal elastic lamina, and the innermost border of the external elastic lamina (external elastic lamina area). Morphometric analysis of the neointimal area for a given vessel was calculated as the measured internal elastic lamina (IEL) area minus lumen area. The measurements were made on five cross-sections from the proximal, middle, and distal ends of each stented segment. Histopathological stenosis was calculated as 100 × (lesion neointimal area/lesion internal elastic lamina area). Injury, inflammation, and fibrin scores were determined by methods of Schwartz26, Kornowaski27, and Suzuki28, respectively. Ordinal data for the inflammation, fibrin, and endothelial scores were collected on each stent section using a scale of 0 to 3. The endothelial score for evaluation of artery healing was as follows: 0 = no generation, 1= <25%, 2 = 20~75%, 3= complete circumferential endothelialization.
All the graphs shows the mean values with error bars from three or more repeated experiments. Student’s t-test was performed to determine the statistical significance between two groups. One-way ANOVA with Turkey’s test was used to determine the overall statistical significance of three drug groups. Two-way ANOVA with Turkey’s test was used when concentration or time parameters were involved. A P < 0.05 was considered to be statistically significant.
A rapamycin analogue biolimus exhibit a cytostatic, not cytotoxic, effects in VSMCs
To understand the molecular mechanism underlying the differential clinical outcome of rapalogues, we performed the signaling pathway analysis in VSMCs using two major rapalogues, everolimus, and biolimus. We also include the rapamycin (also known as sirolimus) as a standard drug. These drugs equally act as the conformational inhibitor of the mTORC1 complex29 but have different chemical moiety at C40 residue (Fig. 1a). Thus, we primarily tested the drug uptake by VSMCs30. When standard compounds were analyzed on C18 reverse-phase column by high-performance liquid chromatography, biolimus was eluted much later than other rapalogues (Fig. 1b), which confirmed that it is a more lipophilic version of rapamycin. To quantify the cellular uptake of drugs, VSMCs were incubated with drugs (2 or 10 μM in 2.5 ml culture media) for 2 hr and subjected to the methanol extraction. The methanol extracts of drug-treated VSMCs ran through C18 reverse-phase column for analysis. As a result, sirolimus and two other rapalogues showed a similar intracellular uptake in VSMCs (Fig. 1c). Although everolimus seemed to be slightly less permeable, the result indicated that cellular uptake does not matter to determine the efficacy of drugs tested in the study.
Next, we analyzed cell cycle progression in drug-treated VSMCs. As expected, drug treatments similarly elicited cell cycle G1 arrest in proliferating VSMCs (Supplementary Figure S1a). Consistently, the BrdU incorporation assay also showed that, along with sirolimus, two rapalogues effectively reduced the cell number in S phase (Fig. 2a). To see the cell cycle arrest by rapalogues in a molecular level, we examined the inhibitory phosphorylation of pRb, a tumor suppressor that inhibits G1-S cell cycle progression31,32. The inhibitory phosphorylation on Thr373 residue was evidently reduced by the drug treatments (Supplementary Figure S1b). However, it was noted that biolimus was likely to be less effective on cell cycle arrest than the other drugs. To further see the cytotoxic effect of drugs tested, we examined the SMC viability following treatment with increasing drug concentrations. Sirolimus and everolimus induced severe cell death at higher concentrations relative to the concentrations eliciting cell cycle arrest (IC50 = 54.24 μM for sirolimus, 29.50 μM for everolimus) (Fig. 2b). In contrast, biolimus did not exert cytotoxicity to VSMCs even at the highest concentrations tested (up to 100 μM of treatment concentration). Consistent with the tryphan blue assay, the ATP-based viability assay also revealed that sirolimus and everolimus drastically induced a necrotic death above 25 μM, while biolimus still had a modest effect on it (Fig. 2c). Indeed, sirolimus and everolimus significantly increased intracellular level of reactive oxygen species (ROS) in VSMCs, whereas biolimus did not (Fig. 2d). Collectively, the data indicated that sirolimus and everolimus, not biolimus, preferentially induce cell death by reducing energy metabolism and consequent ROS production.
Biolimus preferentially induces autophagy
We postulated that biolimus may elicit cell cycle arrest through a distinct signaling pathway. Since the mTORC1 complex is involved in various signaling pathways for protein translation, metabolism, and autophagy33, we examined the activation level of key signaling molecules downstream of mTORC1 in the drug-treated VSMCs. Sirolimus and two rapalogues all similarly reduced the mTOR phosphorylation and completely inhibited the activation of p70S6K, a central regulator of protein synthesis, which might be the underlying mechanism for the similar effect on cell cycle arrest among drugs (Fig. 3a). It is noted that complete de-phosphorylation of Thr 389 residue on p60S6K was confirmed by electrophoretic mobility in total p70S6K blot34. However, the activation of another protein synthesis regulator 4E-BP1, represented by mTORC1-dependent phosphorylation at Ser65 residue, was more effectively inhibited by biolimus compared to sirolimus and everolimus. Moreover, the level of inhibitory phosphorylation at Ser758 site on ULK1 was also decreased to a greater extent by biolimus (Fig. 3a). Thus, the data suggested that biolimus is certainly distinct, while sirolimus and everolimus are very similar, in term of signaling pathway specificity.
Since the previous studies have emphasized the importance of autophagy in the vascular environment35, we focused the distinct effect of biolimus on ULK1 as a key autophagy inducer. Therefore, we examined the autophagy induction in the drug-treated VSMCs. LB3B is a key molecular marker for autophagosome formation because the cytosolic form of LC3B (LC3B-I) is converted to phosphatidylethanolamine conjugate (LC3B-II) recruited to autophagosomal membranes36. As a result, biolimus treatment preminently increased LC3B-II level in both a dose- and time-dependent manner compared to other drugs (Fig. 3b and c). In addition, level of LC3B-II was similar between sirolimus and everolimus treatments. Subsequently, we measured the number of autophagosomes by immunofluorescence staining of LC3B in VSMCs. Indeed, biolimus treatment markedly increased the number of LC3B-positive punctas compared to those in sirolimus and everolimus treatments (Fig. 3d). Overall, these results demonstrate that biolimus preferentially induces autophagy, thereby resulting in the inhibition of VSMC proliferation.
Biolimus inhibits neointimal hyperplasia via autophagy induction in injured carotid arteries
We evaluated the in vivo efficacy of rapalogues in a balloon injury model of rat carotid artery. As expected, everolimus and biolimus effectively inhibited the SMC hyperplasia in intimal lesion of the injured rat carotid arteries (Fig. 4a). It is noted that the inhibition of SMC hyperplasia exhibited a dose dependency proportional to the increasing concentrations of everolimus. Thus, we examined the cell proliferation and death in the tissue sections of the injured carotid arteries. Immunostaining of Ki-67 as a proliferation marker indicated a marked reduction of the neointimal VSMC proliferation in the rapalogue-treated arteries compared to untreated control arteries (Fig. 4b). Subsequently, we measured the number of apoptotic cells by a terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay. While everolimus treatment strongly induced the apoptosis in the injured arteries compared to untreated control, biolimus treatment did not induce it (Fig. 4c). This unexpected result indicated that biolimus might inhibit the SMC hyperplasia through autophagy induction. To see it, we examined the autophagosome formation in the balloon-injured carotid arteries. Immunofluorescence images of injured carotid tissue sections clearly revealed that biolimus treatment significantly increased the number of LC3B puntas compared to control and everolimus treatment (Fig. 4d).
Biolimus prevents inflammation in porcine aorta with stent implantation
To validate the differential signaling impact of rapaloues in a porcine model, we performed the percutaneous transluminal angioplasty using the metal stents coated with sirolimus and rapalogues. Drugs were coated on the metal stent by an ultrasonic spray method25. As a result, the drug amount per metal stent was 140 ± 8.5, 136 ± 5.9, 159 ± 7.1 μg and coating thickness was 6.5 ± 2.46, 5.8 ± 4.15, 5.9 ± 6.41 μm for sirolimus, everolimus, and biolimus, respectively. Drug release kinetics were also similar between sirolimus-eluting stent (SES) and everolimus-eluting stent (EES) during 32 days (Supplementary Figure S2). However, the drug release from the biolimus-eluting stent (BES) was significantly slow compared to other coating stents. The stents were crimped onto the balloon delivery system and sterilized with EO gas. Fifteen stents (5 SES, 5 EES and 5 BES) were successfully implanted in the porcine coronary arteries. These coronary arteries with stents were isolated to histopathological analysis (Fig. 5a). The hematoxylin and eosin staining analysis showed absolutely no difference in injury score and area stenosis among the implanted stents (Fig. 5b,c). However, biolimus-eluting stents tended to have better endothelial score (Fig. 5d) and hence slightly lower fibrin and inflammation scores than other drug-eluting stents (Fig. 5e–g). Collectively, the results suggest that autophagy-dependent VSMC arrest by biolimus might promote endothelialization and hence reduce vascular inflammation.
Sirolimus, also known as rapamycin, has been used in the first-generation drug-eluting stents to inhibit smooth muscle cells proliferation4. When metal stents are implanted to arteries, a complication of in-stent thrombosis occurs due to direct contact of circulating blood with metal stents unless the denuded endothelial cells are recovered21,37. Thus, advanced drug-eluting stents have been developed to alleviate the thrombosis complication22 or to increase the efficiency of drug delivery23. In general, chemical derivatization of rapamycin has been pursed at the C40 residue which does not interfere rapamycin binding to mTOR or FKBP1238. Although clinical studies were conducted to evaluate effects of advanced drug-eluting stents on atherosclerotic arteries39,40, there have been no mode of action studies to define a biological effect of such chemical derivatization on VSMC signaling.
In this study, we found that the latest rapalogue, biolimus, which has the hydrophobic C40 branch, acts on mTORC1-mediated signaling differently from the current widely used rapalogue, everolimus. The mTORC1 complex mediate activation of mRNA translation and inhibition of autophagy33. Our signaling pathway analyses reveal that sirolimus, everolimus, and biolimus all similarly inhibit the S6K1 activation that promotes protein translation. However, sirolimus and everolimus strongly induce intracellular ROS production and thereby cell death in VSMCs, whereas biolimus favorably activates 4E-BP1 and induces autophagy in VSMCs (Fig. 6). It is likely that sirolimus and everolimus dominantly target the signaling branch of mTORC1 complex that promotes the pentose phosphate pathway (PPP) that produces the reducing power NADPH41. By contrast, biolimus preferentially targets the mTORC1-dependent inhibition of the autophagy initiator ULK1 in VSMCs, which thus strengthens cell cycle arrest rather than the ROS-dependent cell death. Hence, our study provides an important message that a chemical derivatization can change the mode of drug action. It is noteworthy that the hydroxyl group of C40 residue is directed toward the kinase domain, when rapamycin binds to mTOR. This feature provided a logic for development of a dual inhibitor linking rapamycin and mTOR kinase inhibitor at C40 branch42. When rapalogues were fitted onto mTOR structure using an autodock modeling tool43, we confirmed that the C40 branches are extended toward the kinase domain of mTOR (Supplementary Figure S3). This molecular docking data implicates that the modification of C40 residue may interfere with interaction of mTORC1 with substrates. Although the C40 branch in biolimus did not directly reach the kinase domain, it may sufficiently influence overall function of large mTORC1 complex interacting with diverse downstream targets. Hence, our finding provides a critical aspect on chemical derivatization strategy for designing small-molecule inhibitors that target a large protein complex.
We also revealed that biolimus inhibits neointimal hyperplasia as efficient as other drugs, although it does not provoke cell death. Unlike sirolimus and everolimus, biolimus preferentially activates ULK1-dependent autophagy process in VSMCs. Autophagy is a dynamic recycling system for maintaining cellular homeostasis by degrading cytoplasmic materials44. In the process of autophagy, cytoplasmic substances and organelles are encircled by membrane to form autophagosome. Then, outer membrane of autophagosome is combined with lysosome. Internal materials are degraded by lysosomal enzymes in the autolysosome45. Defective autophagy is associated with various diseases including cancer, neurodegeneration, and metabolic diseases46. Autophagy has been broadly studied in VSMCs35. For example, insulin-like growth factor-1 and TNF-α inversely regulate autophagy in human VSMCs47. Autophagy induced by PDGF-BB promotes contractile-to-synthetic phenotype transition and increases proliferation of VSMCs by degrading contractile proteins48. Sonic hedgehog, another secretory factor, also induces autophagy and thus promotes VSMC proliferation49. By contrast, it was shown that rapamycin induces VSMC differentiation through the inhibition of mTORC1/S6K1 axis50,51. However, the precise regulatory action of rapalogues on VSMC autophagy remains unclear. In our study, cellular ROS and ATP levels remains unchanged after biolimus treatment, which indicates that biolimus is unlikely to induce autophagic cell death. Instead, the biolimus-induced autophagy contributes in enhancing cell cycle arrest and consequently inhibiting neointimal hyperplasia in vivo as effectively as do sirolimus and everolimus. Similarly, we have shown that a chemical compound targeting monoamine transporter induces autophagy in VSMCs, which sufficiently inhibits neointimal hyperplasia in the injured carotid vessels52. In addition, we cannot exclude a possibility that the enhanced 4E-BP1 function also contributes to cytostatic effect of biolimus because the 4E-BP1 de-phosphorylation inhibits cell proliferation53. Overall, our in vitro and in vivo data demonstrate that a distinct feature of biolimus selective to autophagy induction is clinically beneficial by lowering thrombotic complication.
In summary, our in-depth signaling study reveals that a minor chemical modification on rapamycin can elicit an unexpected effect in the mTORC1-mediated signaling pathways. Thus, this evidence provides an insight on medicinal chemistry for drug candidates targeting protein complexes that orchestrates diverse signaling pathways.
Lemos, P. A., Serruys, P. W. & Sousa, J. E. Drug-eluting stents: cost versus clinical benefit. Circulation 107, 3003–3007, https://doi.org/10.1161/01.CIR.0000078025.19258.28 (2003).
Cercek, B., Sharifi, B., Barath, P., Bailey, L. & Forrester, J. S. Growth factors in pathogenesis of coronary arterial restenosis. Am J Cardiol 68, 24C–33C (1991).
Marx, S. O., Totary-Jain, H. & Marks, A. R. Vascular smooth muscle cell proliferation in restenosis. Circ Cardiovasc Interv 4, 104–111, https://doi.org/10.1161/CIRCINTERVENTIONS.110.957332 (2011).
Sousa, J. E. et al. Lack of neointimal proliferation after implantation of sirolimus-coated stents in human coronary arteries: a quantitative coronary angiography and three-dimensional intravascular ultrasound study. Circulation 103, 192–195 (2001).
Martel, R. R., Klicius, J. & Galet, S. Inhibition of the immune response by rapamycin, a new antifungal antibiotic. Can J Physiol Pharmacol 55, 48–51 (1977).
Houchens, D. P., Ovejera, A. A., Riblet, S. M. & Slagel, D. E. Human brain tumor xenografts in nude mice as a chemotherapy model. Eur J Cancer Clin Oncol 19, 799–805 (1983).
Brown, E. J. et al. A mammalian protein targeted by G1-arresting rapamycin-receptor complex. Nature 369, 756–758, https://doi.org/10.1038/369756a0 (1994).
Heitman, J., Movva, N. R. & Hall, M. N. Targets for cell cycle arrest by the immunosuppressant rapamycin in yeast. Science 253, 905–909 (1991).
Schmelzle, T. & Hall, M. N. TOR, a central controller of cell growth. Cell 103, 253–262 (2000).
Laplante, M. & Sabatini, D. M. mTOR signaling in growth control and disease. Cell 149, 274–293, https://doi.org/10.1016/j.cell.2012.03.017 (2012).
Benjamin, D., Colombi, M., Moroni, C. & Hall, M. N. Rapamycin passes the torch: a new generation of mTOR inhibitors. Nat Rev Drug Discov 10, 868–880, https://doi.org/10.1038/nrd3531 (2011).
Kang, S. A. et al. mTORC1 phosphorylation sites encode their sensitivity to starvation and rapamycin. Science 341, 1236566, https://doi.org/10.1126/science.1236566 (2013).
Choo, A. Y., Yoon, S. O., Kim, S. G., Roux, P. P. & Blenis, J. Rapamycin differentially inhibits S6Ks and 4E-BP1 to mediate cell-type-specific repression of mRNA translation. Proc Natl Acad Sci USA 105, 17414–17419, https://doi.org/10.1073/pnas.0809136105 (2008).
Magnuson, B., Ekim, B. & Fingar, D. C. Regulation and function of ribosomal protein S6 kinase (S6K) within mTOR signalling networks. Biochem J 441, 1–21, https://doi.org/10.1042/BJ20110892 (2012).
Herbert, T. P., Tee, A. R. & Proud, C. G. The extracellular signal-regulated kinase pathway regulates the phosphorylation of 4E-BP1 at multiple sites. Journal of Biological Chemistry 277, 11591–11596, https://doi.org/10.1074/jbc.M110367200 (2002).
Gingras, A. C., Kennedy, S. G., O’Leary, M. A., Sonenberg, N. & Hay, N. 4E-BP1, a repressor of mRNA translation, is phosphorylated and inactivated by the Akt(PKB) signaling pathway. Genes Dev 12, 502–513 (1998).
Jung, C. H., Ro, S. H., Cao, J., Otto, N. M. & Kim, D. H. mTOR regulation of autophagy. FEBS Lett 584, 1287–1295, https://doi.org/10.1016/j.febslet.2010.01.017 (2010).
Kim, J., Kundu, M., Viollet, B. & Guan, K. L. AMPK and mTOR regulate autophagy through direct phosphorylation of Ulk1. Nat Cell Biol 13, 132–141, https://doi.org/10.1038/ncb2152 (2011).
Kalra, A. et al. New-Generation Coronary Stents: Current Data and Future Directions. Current atherosclerosis reports 19, 14, https://doi.org/10.1007/s11883-017-0654-1 (2017).
MacKeigan, J. P. & Krueger, D. A. Differentiating the mTOR inhibitors everolimus and sirolimus in the treatment of tuberous sclerosis complex. Neuro Oncol 17, 1550–1559, https://doi.org/10.1093/neuonc/nov152 (2015).
Daemen, J. et al. Early and late coronary stent thrombosis of sirolimus-eluting and paclitaxel-eluting stents in routine clinical practice: data from a large two-institutional cohort study. Lancet 369, 667–678, https://doi.org/10.1016/S0140-6736(07)60314-6 (2007).
van Boven, N. et al. Stent thrombosis in early-generation drug-eluting stents versus newer-generation everolimus-eluting stent assorted by LVEF. Heart 101, 50–57, https://doi.org/10.1136/heartjnl-2014-305743 (2015).
Grube, E. & Buellesfeld, L. BioMatrix Biolimus A9-eluting coronary stent: a next-generation drug-eluting stent for coronary artery disease. Expert Rev Med Devices 3, 731–741, https://doi.org/10.1586/174344126.96.36.1991 (2006).
Cyrus, T. et al. Intramural delivery of rapamycin with alphavbeta3-targeted paramagnetic nanoparticles inhibits stenosis after balloon injury. Arteriosclerosis, thrombosis, and vascular biology 28, 820–826, https://doi.org/10.1161/ATVBAHA.107.156281 (2008).
Park, J. K. et al. Blood-compatible and biodegradable polymer-coated drug-eluting stent. Macromol Res 23, 237–244, https://doi.org/10.1007/s13233-015-3023-3 (2015).
Schwartz, R. S. et al. Restenosis and the proportional neointimal response to coronary artery injury: results in a porcine model. Journal of the American College of Cardiology 19, 267–274 (1992).
Kornowski, R. et al. In-stent restenosis: contributions of inflammatory responses and arterial injury to neointimal hyperplasia. Journal of the American College of Cardiology 31, 224–230 (1998).
Suzuki, T. et al. Stent-based delivery of sirolimus reduces neointimal formation in a porcine coronary model. Circulation 104, 1188–1193 (2001).
Yip, C. K., Murata, K., Walz, T., Sabatini, D. M. & Kang, S. A. Structure of the human mTOR complex I and its implications for rapamycin inhibition. Mol Cell 38, 768–774, https://doi.org/10.1016/j.molcel.2010.05.017 (2010).
Zhu, W., Masaki, T., Cheung, A. K. & Kern, S. E. In-vitro Release of Rapamycin from a Thermosensitive Polymer for the Inhibition of Vascular Smooth Muscle Cell Proliferation. Journal of bioequivalence & bioavailability 1, 3–12 (2009).
Giacinti, C. & Giordano, A. RB and cell cycle progression. Oncogene 25, 5220–5227, https://doi.org/10.1038/sj.onc.1209615 (2006).
Lents, N. H., Gorges, L. L. & Baldassare, J. J. Reverse mutational analysis reveals threonine-373 as a potentially sufficient phosphorylation site for inactivation of the retinoblastoma tumor suppressor protein (pRB). Cell Cycle 5, 1699–1707, https://doi.org/10.4161/cc.5.15.3126 (2006).
Zoncu, R., Efeyan, A. & Sabatini, D. M. mTOR: from growth signal integration to cancer, diabetes and ageing. Nature reviews. Molecular cell biology 12, 21–35, https://doi.org/10.1038/nrm3025 (2011).
Krause, U., Bertrand, L., Maisin, L., Rosa, M. & Hue, L. Signalling pathways and combinatory effects of insulin and amino acids in isolated rat hepatocytes. Eur J Biochem 269, 3742–3750, https://doi.org/10.1046/j/1432-1033.2002.03069.x (2002).
Salabei, J. K. & Hill, B. G. Autophagic regulation of smooth muscle cell biology. Redox Biol 4, 97–103, https://doi.org/10.1016/j.redox.2014.12.007 (2015).
Mizushima, N., Yoshimori, T. & Levine, B. Methods in mammalian autophagy research. Cell 140, 313–326, https://doi.org/10.1016/j.cell.2010.01.028 (2010).
Virmani, R. et al. Localized hypersensitivity and late coronary thrombosis secondary to a sirolimus-eluting stent: should we be cautious? Circulation 109, 701–705, https://doi.org/10.1161/01.CIR.0000116202.41966.D4 (2004).
Claessen, B. E., Henriques, J. P. & Dangas, G. D. Clinical studies with sirolimus, zotarolimus, everolimus, and biolimus A9 drug-eluting stent systems. Curr Pharm Des 16, 4012–4024 (2010).
Smits, P. C. et al. Abluminal biodegradable polymer biolimus-eluting stent versus durable polymer everolimus-eluting stent (COMPARE II): a randomised, controlled, non-inferiority trial. Lancet 381, 651–660, https://doi.org/10.1016/S0140-6736(12)61852-2 (2013).
Windecker, S. et al. Biolimus-eluting stent with biodegradable polymer versus sirolimus-eluting stent with durable polymer for coronary revascularisation (LEADERS): a randomised non-inferiority trial. Lancet 372, 1163–1173, https://doi.org/10.1016/S0140-6736(08)61244-1 (2008).
Dibble, C. C. & Manning, B. D. Signal integration by mTORC1 coordinates nutrient input with biosynthetic output. Nat Cell Biol 15, 555–564, https://doi.org/10.1038/ncb2763 (2013).
Rodrik-Outmezguine, V. S. et al. Overcoming mTOR resistance mutations with a new-generation mTOR inhibitor. Nature 534, 272–276, https://doi.org/10.1038/nature17963 (2016).
Forli, S. et al. Computational protein-ligand docking and virtual drug screening with the AutoDock suite. Nature protocols 11, 905–919, https://doi.org/10.1038/nprot.2016.051 (2016).
Mizushima, N. & Komatsu, M. Autophagy: renovation of cells and tissues. Cell 147, 728–741, https://doi.org/10.1016/j.cell.2011.10.026 (2011).
Feng, Y., He, D., Yao, Z. & Klionsky, D. J. The machinery of macroautophagy. Cell Res 24, 24–41, https://doi.org/10.1038/cr.2013.168 (2014).
Jiang, P. & Mizushima, N. Autophagy and human diseases. Cell Res 24, 69–79, https://doi.org/10.1038/cr.2013.161 (2014).
Jia, G. H., Cheng, G., Gangahar, D. M. & Agrawal, D. K. Insulin-like growth factor-1 and TNF-alpha regulate autophagy through c-jun N-terminal kinase and Akt pathways in human atherosclerotic vascular smooth cells. Immunology and Cell Biology 84, 448–454, https://doi.org/10.1111/j.1440-1711.2006.01454.x (2006).
Salabei, J. K. et al. PDGF-mediated autophagy regulates vascular smooth muscle cell phenotype and resistance to oxidative stress. Biochem J 451, 375–388, https://doi.org/10.1042/BJ20121344 (2013).
Li, H. et al. Sonic hedgehog promotes autophagy of vascular smooth muscle cells. Am J Physiol Heart Circ Physiol 303, H1319–1331, https://doi.org/10.1152/ajpheart.00160.2012 (2012).
Martin, K. A. et al. Rapamycin promotes vascular smooth muscle cell differentiation through insulin receptor substrate-1/phosphatidylinositol 3-kinase/Akt2 feedback signaling. J Biol Chem 282, 36112–36120, https://doi.org/10.1074/jbc.M703914200 (2007).
Martin, K. A. et al. The mTOR/p70 S6K1 pathway regulates vascular smooth muscle cell differentiation. Am J Physiol Cell Physiol 286, C507–517, https://doi.org/10.1152/ajpcell.00201.2003 (2004).
Cho, Y. S. et al. Antidepressant indatraline induces autophagy and inhibits restenosis via suppression of mTOR/S6 kinase signaling pathway. Sci Rep 6, 34655, https://doi.org/10.1038/srep34655 (2016).
Rousseau, D., Gingras, A. C., Pause, A. & Sonenberg, N. The eIF4E-binding proteins 1 and 2 are negative regulators of cell growth. Oncogene 13, 2415–2420 (1996).
This study was supported by grants from the National Research Foundation of Korea (NRF-2017M3A9G2077885 and 2012R1A5A1048236). This study was also supported by a grant from the Korean Health Technology R&D Project (H16C0094). D.H.K was a recipient of a Basic Science Research Program Award from the National Research Foundation of Korea (NRF-2014R1A6A3A04058006).
The authors declare no competing interests.
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Kim, Y., Park, J.K., Seo, J. et al. A rapamycin derivative, biolimus, preferentially activates autophagy in vascular smooth muscle cells. Sci Rep 8, 16551 (2018). https://doi.org/10.1038/s41598-018-34877-8
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