AP747 synthesis

One milligram of apelin-F13A (Merck Millipore, Burlington, USA) was added to 10 equivalents (14 mg) of NODA-GA-NHS ester (CheMatech, Dijon, France) solubilized in 700 µL of 0.2 mol/L bicarbonate buffer. The conjugate was then transferred to a tC18 cartridge (Sep-Pak, Waters, Milford, USA) and then eluted with 500 µL of HPLC-grade absolute ethanol (VWR, Radnor, USA). The solvent was evaporated at room temperature and 500µL HPLC-grade water (VWR, Radnor, USA) were added. Aliquots (10 µL) were stored at – 20 °C.

High-resolution mass spectrometry (HRMS) characterization

The characterization of the resulting AP747 was performed by HRMS, using a Waters SYNAPT G2 HDMS II (Manchester, United Kingdom) equipped with an electrospray source, operated under positive ionization mode [ESI—( +)], and a quadrupole/time of flight analyzer (QTOF). Capillary voltage was fixed at 2.8 kV, and the declustering potential was optimized at 30 V; N2 at 100 L/h flow and 35 °C was used as desolvation gas. The samples were diluted (1/100, v/v) in methanol doped with 1% formic acid and infused at 10 µL/min flow rate into the ESI source. The m/z values were calibrated by Mass Lock procedure using a methanolic solution of positively charged clusters of sodium acetate. The experimental data were acquired and processed using MassLynx 4.1 (Waters, Milford, USA).

Radiolabeling of AP747 and RGD2 with gallium-68

Fifty microliters of 4 mol/L ammonium acetate buffer (pH 7.4) were added to a 10 µL AP747 sample (1 μg/μL) or a 10 µL NODAGA-RGD dimer acetate sample (1 μg/μL, ABX, Radeberg, Germany). 500 µL of [68Ga]GaCl3 (200.6 ± 40.9 MBq/500 µL) were eluted from a commercial TiO2-based [68Ge]Ge/[68Ga]Ga generator (Galliapharm, Eckert & Ziegler Berlin, Germany) using 0.1 mol/L HCl and added to the reactor.

Final pH of the mixture was 6.0. Radiochemical purity (RCP) was determined by radio-thin-layer chromatography (radio-TLC) on a miniGITA radio-TLC scanner detector (Elysia-Raytest, Straubenhardt, Germany) using iTLC-SG plate as solid phase (Agilent, Les Ulis, France) and a mixture of 1 mol/L aqueous ammonium acetate solution and methanol 1:1 (v/v) as mobile phase 1 (free [68Ga]GaCl3 Rf = 0; [68Ga]Ga-AP747 Rf = 0.5; [68Ga]Ga-RGD2 Rf = 1) and trisodium citrate 0,1 mol/L pH = 5 as mobile phase 2 ([68Ga]Ga-AP747 or [68Ga]Ga-RGD2 Rf = 0; free [68Ga]GaCl3 Rf = 1). Radiochemical purity was also determined by radio-high pressure liquid chromatography (radio-HPLC) with an Ultimate 3000 pump (Dionex, ThermoFisher, Waltham, USA) using a reversed-phase C18-column (Luna LC Column 150 × 4.6 mm, Phenomenex, Torrance, USA), an in-line radioactivity detector (Gabi, Elysia-Raytest, Straubenhardt, Germany) and a gradient of water/acetonitrile with 0.1% trifluoroacetic acid (TFA) from 100/0 (v/v) to 0/100 (v/v) for 15 min at a flow rate of 2.5 mL/min (free [68 Ga]GaCl3 retention time: 1.0 min; [68Ga]Ga-RGD2 retention time = 3.5 min; [68Ga]Ga-AP747 retention time: 4.0 min). Radio-HPLC chromatograms were interpreted using Chromeleon software (ThermoFisher Scientific, Waltham, USA). The evaluation of [68Ga]Ga-AP747 radiochemical stability was performed as previously described [37] after incubating 100 µL of the radiotracer in 400 µL of physiological saline or in 400 µL of human serum. The radiochemical purity was checked 60 and 120 min after radiosynthesis by radio-TLC, at room temperature and at 37 °C.

Radiolabeling of AP747 with gallium-67

Gallium-67 was obtained from [67Ga]Ga-citrate (200 MBq, Curium, Paris, France) and converted into [67Ga]GaCl3 using two Light silica Sep-Pak (Waters, Milford, USA). Briefly, [67Ga]Ga-citrate was charged on the cartridges and then eluted using 1 mL 0.1 mol/L HCl (KT720P, Rotem Industries, Dimona, Israël) in form of [67Ga]GaCl3 and subsequently used for radiolabeling. The final product was formulated in 3 mL of Phosphate Buffer Saline (PBS, Eurobio-scientific, Les Ulis, France). This solution was then added to AP747 (1 μg/μL). The RCP was determined by radio-TLC and was performed using iTLC-SG plate as solid phase (Agilent, Les Ulis, France) and trisodium citrate 0.1 mol/L as mobile phase ([67Ga]Ga-AP747 Rf = 0, [67Ga]GaCl3 Rf ≥ 0.8, [67Ga]Ga-NODAGA Rf ≥ 0.8).

[67Ga]Ga-AP747 lipophilicity

Determination of logD value was realized by the shake-flask method [38]. Briefly, 50 µL of [67Ga]Ga-AP747 was added to a 1 mL solution of octanol and physiological serum (1:1). This solution was stirred and vortexed for two minutes and centrifugated (100 g, 5 min). Three 100 µL samples of each phase were collected, and the respective activity was measured using a gamma counter (Wizard 2480, Perkin-Elmer, Waltham, USA).

Cell culture

Human colon adenocarcinoma T84 cell line (RRID:CVCL_0555) was cultivated in filtrated DMEM-F12 (Gibco, ThermoFisher Scientific, Waltham, USA)/Glutamax (Gibco, ThermoFisher Scientific, Waltham, USA) medium. Human umbilical vein endothelial cells (HUVECs, gratefully from the Cell Therapy Laboratory, La Conception University Hospital, AP-HM, Marseille, France) were cultivated in filtrated Endothelial Cell Growth Medium MV (EGM-2 SupplementMix, Promocell, Heidelberg, Germany). Both media were supplemented with 10% decomplemented fetal bovine serum and 1% antibiotic–antimycotic mix (penicillin–streptomycin). Cell lines were maintained in a humidified 5% CO2 incubator at 37 °C. HUVECs activation was obtained by overnight incubation with Tumor Necrosis Factor alpha (TNF-alpha, 10 ng/mL, Euromedex, Souffelweyersheim, France).

APJ cell expression

APJ expression was evaluated by Western Blot. Cell lysates of human colon adenocarcinoma T84 cells and human umbilical vein endothelial cells (HUVECs) in TNF-activated or baseline (PBS) conditions were loaded on polyacrylamide gel (NuPAGE, 4–12%, Invitrogen, Waltham, USA). After migration, proteins were transferred to a nitrocellulose membrane and checked by Rouge-Ponceau. The membrane was saturated [Tris-buffered saline Tween 20% (TBST); bovine serum albumin (BSA) 3%], then an anti-APJ antibody (1 µg/mL, 5H5L9, rabbit monoclonal Invitrogen, Waltham, USA) was added overnight, under agitation at 4 °C. After three TBST washes, a secondary goat anti-rabbit horseradish peroxidase (HRP)-tagged antibody (1/2000, #31460, ThermoFisher, Waltham, USA) was added for one hour. Revelation was achieved with an enhanced chemiluminescent (ECL) kit (#32106, ThermoFisher, Waltham, USA) with an incubation of 5 min at room temperature. Membrane image acquisitions were realized through a Gbox system (Syngene, Cambridge, UK) with an exposure time of 1 min. After 10 min of stripping and three washes, the membrane was saturated [Tris-buffered saline Tween 20% (TBST); bovine serum albumin (BSA) 3%] and incubated with a GADPH antibody [#2118, (14C10) rabbit monoclonal, Cell Signaling Technologies, USA] at 4 °C overnight under agitation as the anti-APJ antibody. After three TBST washes, a secondary goat-anti-rabbit HRP-tagged antibody (1/2000, #31460, ThermoFisher, Waltham, USA) was added for half an hour. Revelation and membrane image acquisition were completed as described above with an exposure time of 30 s. The optical density of each band was measured using a specific software (GeneTools, Syngene, Cambridge, UK). APJ expression evaluation was normalized by division of GAPDH expression as protein load control.

In vitro saturation binding assay

T84 cells were seeded at a 250.103 cells per well density in 24-well plates (Corning, Corning, USA) and incubated overnight with complete medium. Plates were set on ice 30 min before the beginning of the experiment. [67Ga]Ga-AP747 was then added to the medium at a 0.1, 1, 10, 100, or 250 nmol/L concentration and cells were incubated for 2 h at 4 °C, in quadruplicate (n = 3). Incubation was stopped by removing the medium and washing cells twice with ice-cold PBS (Eurobio-scientific, Les Ulis, France). Finally, cells were treated with 1 mol/L NaOH, and the activity was measured using a gamma counter (Wizard 2480, Perkin-Elmer Waltham, USA). In order to assess non-specific affinity, an excess of non-radioactive apelin-F13A (final concentration 1 µmol/L) was added to selected wells.

In vitro evaluation of [ 68Ga]Ga-AP747 specificity

T84 cells were seeded at a 1.106 cells per well density in 24-well plates (Corning, Corning, USA) and incubated overnight with a complete medium. [68Ga]Ga-AP747 (1.7 MBq/10 µL) was added to each well. In 6 wells, a large excess (500 µg/500 µL) of apelin-F13A (Phoenix Pharmaceuticals, Burlingame, USA) was added to T84 cells 10 min before incubation with [68Ga]Ga-AP747 (triplicate, n = 6). After a 1 h incubation, the medium was removed and the cells were washed 3 times with PBS (Eurobio-scientific, Les Ulis, France) and their viability assessed. The wells were measured for [68Ga]Ga-AP747 signal by autoradiography using a phosphor-based Cyclone autoradiograph (Perkin-Elmer, Waltham, USA). The background signal was measured through [68Ga]Ga-AP747 activity in wells without cells.

Animal experiments

All procedures involving animals were approved by the Institution’s Animal Care and Use Committee (CE71, Aix-Marseille Université, projects #15790, #32157, #31843), conducted according to the 2010/63/EU European Union Directive and the ARRIVE guidelines 2.0 [39]. Mice were housed in enriched cages and placed in a temperature- and hygrometry-controlled room with daily monitoring, fed with water, and commercial diet ad libitum. Pigs were housed in enriched boxes with daily monitoring with water ad libitum and a commercial diet adapted with their nutritional requirements.

[68Ga]Ga-AP747 biodistribution in healthy mice

Nine-week-old male Swiss mice (Janvier Labs, n = 3) were injected in the lateral caudal vein with [68Ga]Ga-AP747 (4.45 ± 0.32 MBq/70 µL), and small animal PET images were continuously acquired right after, up to 2 h post-injection. The quantified PET signal in organs was presented as mean ± SD percentage of the decay-corrected injected dose (%ID). Acquisition of small animal dynamic PET/CT was performed for 120 min on a NanoScan PET/CT camera (Mediso, Budapest, Hungary) under 2% isoflurane in medical air anesthesia [PET parameters: numbers of iterations: 4, coincidence: 1–3, field of view (FOV): 10 cm]. CT parameters were fixed at 35 kV voltage, 300 ms exposure at medium zoom, acquired by semi-circular method on the same FOV as PET. CT attenuation-corrected reconstruction was performed using Nucline software (Mediso, Budapest, Hungary) on the following time frames: 0–5 min, 6–10 min, 11–15 min, 16–20 min, 21–25 min, 26–30 min, 31–45 min, 46–60 min, 61–75 min, 76–90 min, 91–105 min, and 106–120 min. Quantitative volume-of-interest (VOI) analysis of the small animal PET images was CT-based manually performed on attenuation- and decay-corrected PET images using VivoQuant software (v.3.5, InVicro, Boston, USA).

Three 9-week-old Swiss male mice were injected in the lateral caudal vein with [68Ga]Ga-AP747 (4.02 ± 0.16 MBq/70 µL) and maintained under isoflurane anesthesia (2%) for two hours. Blood was collected at 2, 5, 10, 15, 20, 30, 45, 60, 75, 90, 105, and 120 min post-injection and gamma counted with decay correction. Plasmatic half-life (t1/2) was estimated by nonlinear regression. At two hours post-injection, mice were euthanatized and the main organs (heart, liver, lungs, muscle, brain, spleen, intestines, bone, pancreas, and kidneys) were collected, washed in PBS, weighted, and gamma counted. Results were decay corrected and expressed as percentage of injected dose corrected by organ weight (%ID/g).

[68Ga]Ga-AP747 biodistribution in healthy swine

Six-month-old Pietrain pigs (n = 3, Blossin, Aubagne, France) were injected with [68Ga]Ga-AP747 (85 ± 30 MBq/5 mL in 0.9% NaCl) under 2% sevoflurane in medical air anesthesia. A series of six 15-min-long, static PET/CT acquisitions (Discovery PET/CT 710, GE Healthcare, Chicago, Illinois, USA) was started 15 min after the injection of [68Ga]Ga-AP747 and repeated at 45 min, 75 min, 90 min, 105 min, and 120 min post-injection (PET parameters: numbers of iterations: 4, coincidence: 1–1, FOV: 50 cm, reconstruction type: VPHD; CT parameters: 120 kV, 220 mA, slice thickness: 3,75 mm, number of pictures: 47, detector width: 40 mm). Attenuation-corrected images were reconstructed using ADW software v4.6 (GE Healthcare, Chicago, Illinois, USA), and PET signal quantifications were performed on CT-based manually drawn volumes of interest (VOIs) using VivoQuant software v.3.5 (InVicro, Boston, MA, USA). Results were decay corrected and expressed as mean ± sd percentage of the injected dose (%ID).

Human colon adenocarcinoma mouse model

Human colon adenocarcinoma xenografts were established by subcutaneous dorsal injections of 1.106 T84 cells (100 µL, PBS) to 6-week-old male Swiss nude mice (Charles River, Saint-Germain-Nuelles, France, n = 3) under 2% isoflurane anesthesia.

Matrigel plug mouse model

Matrigel plugs were established by subcutaneous dorsal injections of 300 µL Matrigel (Dutscher, Bernolsheim, France) supplemented with 10% fetal bovine serum, to 9-week-old male Swiss mice (Janvier Labs, Le Genest-Saint-Isle, France, n = 12) under 2% isoflurane anesthesia. Seven Matrigel mice underwent small animal PET follow-up, and five others were involved in the in vivo specificity study as described below.

In vivo specificity of [68Ga]Ga-AP747 PET signal

Mice bearing ectopic colon adenocarcinoma xenograft (n = 3, 1370 ± 167.3 mm3) or Matrigel plug (n = 5, 635 ± 146 mm3) were injected in the lateral caudal vein with [68Ga]Ga-AP747 (5.14 ± 0.60 MBq/80 µL) and underwent small animal PET imaging acquired 1 h p.i. followed by a CT scan. Small animal PET imaging acquisition lasted 20 min (number of iterations: 4, coincidence: 1–3) using a field of view (FOV) of 10 cm. CT parameters were fixed at 35 kV voltage, 300 ms exposure at medium zoom, acquired by semi-circular method on the same FOV as PET. CT attenuation-corrected reconstruction was performed using Nucline software (Mediso, Budapest, Hungary). The day after, the mice received an intravenous injection of a 100X excess of unconjugated peptide (apelin-F13A, 100 µg/100 µL) 30 min before the intravenous injection of 5.5 ± 0.20 MBq/80 µL [68Ga]Ga-AP747. PET images were acquired 1 h after [68Ga]Ga-AP747 injection. Tissue uptake values were expressed as a mean target-to-background PET signal ratio (TBRmean) with background represented by the left gastrocnemius muscle.

Hindlimb ischemia mouse model

Unilateral hindlimb ischemia (HLI) was induced on 9-week-old female Swiss mice (Janvier Labs, n = 8) after femoral artery excision under 2% isoflurane anesthesia as previously described [40]. LASER Doppler perfusion imaging (Perimed, Craponne, France) was used to assess revascularization from day 0 to day 21 after surgery. Perfusion measurements were expressed as an ischemic-to-contralateral ratio of hind limb blood flow normalized to the day of surgery.

In vivo longitudinal study using [6868Ga]Ga-AP747 PET compared with [Ga]Ga-RGD PET2

Matrigel plug mouse model (n = 7) and HLI mice (n = 8) were injected in the lateral caudal vein with [68Ga]Ga-AP747 (5.66 ± 0.57 MBq) and 11 h later with [68Ga]Ga-RGD2 (5.96 ± 0.95 MBq) on days 1, 3, 7, 10, 13, and 21 after ischemia (Fig. 1). Static PET images were acquired 1 h after intravenous injection of [68Ga]Ga-AP747 or [68Ga]Ga-RGD2 and followed by a CT. Small animal PET imaging acquisition lasted 20 min (numbers of iterations: 4, coincidence: 1–3) using a field of view (FOV) of 10 cm. CT parameters were fixed at 35 kV voltage, 300 ms exposure at medium zoom, acquired by semi-circular method on the same FOV as PET. CT attenuation-corrected reconstruction was performed using Nucline software (Mediso, Budapest, Hungary). Tissue uptake values were expressed as a target-to-background (Matrigel-to-muscle) or as an ischemic-to-contralateral hindlimb PET signal ratio.

Fig. 1

In vivo longitudinal study using [68Ga]Ga-AP747 PET compared with [68Ga]Ga-RGD2 PET on Matrigel and HLI mouse models

Immunofluorescence of APJ receptor in hindlimb ischemia tissue

After cervical dislocation of HLI mice, the skin of the hind limbs was gently removed, and the tendons were cut. The left (contralateral) and right (ischemic) gastrocnemius muscles were isolated and snap frozen in OCT with isopentane and liquid nitrogen, and 10 µm slices were realized using a cryostat and kept at − 80 °C. The slices were incubated in cold methanol (− 20 °C) for 5 min at RT, washed three times with PBS, and incubated in PBS with 10% of fetal bovine serum and 3% BSA for one hour. Primary anti-APJ antibody (rabbit monoclonal 5H5L9, 2 µg/mL in PBS and 3% BSA, Invitrogen, Waltham, USA) was incubated on the slices overnight at 4 °C in dark wet chamber. Five PBS washes were then realized and a secondary goat anti-rabbit antibody (Alexa fluor 488, 1/500 in PBS and 3% BSA, ThermoFisher, Waltham, USA) was added during 1 h in dark wet chamber. Slides were finally washed three times with PBS +/+ in the dark. Mounting medium (Fluoromount, Invitrogen, Waltham, USA) was added on histological sections. After overnight drying at 4 °C, slides were observed using a NIE microscope (Nikon, Tokyo, Japan) and analyzed using the NIS Elements Imaging software (Nikon, Tokyo, Japan).

Statistics

Statistical analyses were performed using Prism v9 (GraphPad, San Diego, USA), P ≤ 0.05 indicating statistical significance. Autoradiography results were submitted to an unpaired t test after checking the data for normal distribution with a Shapiro–Wilk test. In vivo specificity of [68Ga]Ga-AP747 PET signal results were submitted to a paired t test after checking the data for distribution normality with a Shapiro–Wilk test. Perfusion quantification data in HLI mouse model were compared using a one-way ANOVA test followed by a post hoc Tukey’s multiple comparisons test. PET quantification data of the in vivo longitudinal study were compared using a two-way ANOVA followed by a Sidak’s multiple comparisons post hoc test. Correlations were tested using the Pearson R correlation test.