Comparison of Magnetic Intensities for Mesenchymal Stem Cell Targeting Therapy on Ischemic Myocardial Repair: High Magnetic Intensity Improves Cell Retention but Has no Additional Functional Benefit

Magnet Cylinder

Three cylindrical NdFeB magnets (Shanghai Yahao Instrument Equipment Co., Shanghai, China) with 0.15 T, 0.3 T, and 0.6 T (diameter 8 mm) were used in this study. The magnetic flux density (B) of the magnet surface is measured using a model 51,662 Leybold Tesla meter (Beijing Zhuo Sheng Jia Magnetic Technology Co. Ltd., Beijing, China). The distribution of the magnetic flux density was calculated by a finite element analysis.

Rat MSCs, SPIOs, and DiR Labeling

Animal experiments were approved by the Animal Care and Use Committee of Fudan University and were in compliance with the Guide for the Care and Use of Laboratory Animals published by the National Academy Press (1). Femurs of 4-week-old male Sprague–Dawley (SD) rats, obtained from Shanghai animal administration center, were excised under sterile conditions. MSCs were cultured from bone marrow plugs explanted from 4-week-old male SD rats, as previously described (34). All used cells were harvested by 0.25% trypsin (Gibco, Grand Island, NY, USA) and 0.038% EDTA (Gibco) when they reached 80–90% confluence at passage 4. MSCs were labeled with superparamagnetic oxide nanoparticles (SPIOs; 100 mg/ ml; Schering, Berlin, Germany), as previously described (14). For cell tracking in vivo, cells were labeled with 1,1-dioctadecyl-3,3,3,3-tetramethyl indotricarbocyanine iodide (DiR; AAT Bioquest, Inc., Sunnyvale, CA, USA) according to the manufacturer's protocol. Labeled cells are hereafter called SPIOs-DiR-MSCs or DiR-MSCs for brevity. To evaluate the labeling efficacy, Prussian blue staining (potassium ferrocyanide and HCl solution from Jueshen Bio-Technology Co. Ltd., Shanghai, China) and electron microscopy (Phillips CM120, Philips FEI, Eindhoven, Netherlands) were undertaken to indicate the presence and localization of intracellular iron particles, and DiR staining was observed by fluorescence microscopy using the XF112-Omega optical filter after cell nuclei were counterstained with 4′,6-diamidino-2-phenylindole (DAPI; Sigma-Aldrich, St. Louis, MO, USA) (16).

Effects of SPIO Labeling on MSC Differentiation Capacity

Our previous study demonstrated that SPIO labeling had no significant effect on the proliferation and viability of MSCs (16). Here we further determined the differentiation capacity of SPIOs-MSCs. The MSCs and SPIOs-MSCs were, respectively, cultured in adipogenic (SR811D250, Amsbio, Abingdon, UK) or osteogenic (SR417D250, Amsbio) media for 21 days with media replenishment every 3 days. To demonstrate adipogenic differentiation, the cells were stained with 0.3% Oil red O (O0625; Sigma-Aldrich) in isopropanol for 30 min and rinsed with PBS. For osteogenic differentiation, the cells were stained with 1% Alizarin red (500-4; RiccaChem, Arlington, TX, USA) for 15 min (2).

To determine the myocardium-like cell differentiation, the MSCs and SPIOs-MSCs were cultured in culture medium-added 5-aza-2′-deoxycytidine (5-azaC; Sigma-Aldrich) for 24 h. Incubation then continued in complete medium lacking 5-azaC, with medium changes every 3 days. Undifferentiated cells and normal mature rat cardiomyocytes were, respectively, used as negative and positive controls. Total RNA was extracted from cultured cells using TRIzol reagent (Invitrogen, Carlsbad, CA, USA) according to the manufacturer's protocol. RT-PCR primers (synthesized by Sangon, Shanghai, China) were as follows: GATA-4, 5′-CTG TCA TCT CAC TAT GGG CA-3′ and 5′-CCA AGT CCG AGC AGG AAT T T-3′; α-actin, (F) 5′-TCC TTT ATC GGT ATG GAG TCT G-3′ and (R) 5′-TGA TCT TGA TCT TCA TGG TGC T-3′; cTnT, 5′-AGA GGA CTC CAA ACC CAA GC-3′ and 5′-ATT GCG AAT ACG CTG CTG TT-3′; Cx43, 5′-TCC TTG GTG TCT CTC GCT TT-3′ and 5′-GAG CAG CCA TTG AAG TAG G C-3′; GAPDH, 5′-GAC ATG CCG CCT GGA GAA AC-3′ and 5′-AGC CCA GGA TGC CCT TTA GT-3′. Transcriptional expressions of GATA-4, cTnT, α-actin, and Cx43 genes from the MSCs and SPIOs-MSCs were determined by real-time PCR according to the manufacturer's instructions. Transcript levels were standardized to the corresponding rat GAPDH level.

In Vitro Magnetic Capture of Flowing SPIOs-MSCs

To test the magnetic responsiveness of MSCs labeled with SPIOs (SPIOs-MSCs), the accumulation of SPIOs-MSCs was observed, while cells flowed through a tube served as a model of blood vessels in a magnetic field. A total of 20 ml SPIOs-MSCs suspension, at a concentration of 5 × 10⁴ cells/ml, was placed in a 50-ml syringe (Shanghai Boguang Biotechnology Co. Ltd., Shanghai, China) and flowed through a quartz tube (ID 2.3 mm, OD 4.3 mm, length 20 cm) (Shanghai Puya Quartz Glass Factory, Shanghai, China). Cell suspension circulated at flows of 5 mm/s to mimic circulatory conditions in animals and human beings. The aforementioned 0.15-T magnet cylinder was placed tightly at the midsegment of the tube. The cell suspension flowed through the magnet field was collected in a centrifuge tube (Shanghai Boguang Biotechnology Co. Ltd.) 1#. The remaining cells within the quartz tube were washed using PBS and collected in centrifuge tube 2#. The numbers of SPIOs-MSCs in centrifuge tube 1# and 2# were counted using a counting plate and referred to quantity of captured cells (Q₁) and quantity of uncaptured cells (Q₂). The capture efficiency (CE) was calculated by C E = Q 1 Q 1 + Q 2 × 100 % . Then, the effects of the 0.3-T and 0.6-T magnets on the accumulation of SPIOs-MSCs in turn were observed. The magnetic responsiveness of MSCs unlabeled with SPIOs was tested according to the method mentioned above. All experiments were performed in six copies for each condition.

Animal Model and Magnetic Targeting

To make our experiment more relevant to reperfused acute myocardial infarction (AMI), a rat I/R model was developed in female SD rats (150-200 g). Rats were anesthetized with ketamine (100 mg/kg, IP) (Beijing Zizhu Pharmaceutical Co. Ltd., Beijing, China) and xylazine (10 mg/kg, IP) (Shanghai Ruicong Laboratory Equipment Co. Ltd., Shanghai, China) and were ventilated with a rodent ventilator using room air at 80 breaths per minute. Female SD rats (n = 236 total), obtained from Shanghai animal administration center, underwent a left thoracotomy in the fourth intercostal space under general anesthesia. The heart was exposed, and myocardial infarction was produced by a 90-min ligation of the left anterior descending coronary artery (LAD) using a 7-0 silk suture (Unik Surgical Sutures Mfg. Co. Ltd., Suzhou, China). The suture was then released to allow coronary reperfusion. Twenty minutes later, cells were injected into the left ventricle cavity during a 5-s temporary aorta and main pulmonary artery occlusion, as previously described (18,19). Cell delivery was confirmed by the temporary observation of bradycardia and epicardial blanching.

For magnetic targeting, three cylindrical NdFeB magnets with 0.15 T, 0.3 T, and 0.6 T were separately placed above the injured myocardium during and after cell injection for 10 min, which was determined to be the optimal time (5,6). The 217 survivors were randomized into six groups according to the strength of the magnetic field (n = 37 for 0.3 T group, n = 36 for other groups): 0 T group, 0.15 T group, 0.3 T group, 0.6 T group, MSC group, and PBS group. All magnets were close to the target site, that is, within 0–1 mm, during and after infusion in the three magnetic targeting groups. Except for the PBS group, which was intraventricularly injected with vehicle (PBS) only, the other treatment groups were intraventricularly injected with 1 × 10⁶ SPIOs-DiR-MSCs (0 T, 0.15 T, 0.3 T, and 0.6 T group) or DiR-MSCs (MSC group). All animals received humane care in compliance with the Guide for the Care and Use of Laboratory Animals.

Fluorescence Imaging

After assessment of cardiac function using trans-thoracic echocardiography, six animals were randomly selected from each treatment group and were euthanized 24 h after cell injection for fluorescence imaging. Extensive PBS washing was performed to remove any cells adherent to the surface of organs. Hearts, lungs, livers, spleens, and kidneys were placed in a Carestream In-Vivo Multispectral Imaging System FX PRO (Carestream Health, Toronto, Canada) to detect DiR fluorescence under 748 nm of excitation and 780 nm of emission. Exposure time was set at 3 s and kept the same during the entire imaging session. Organs from the PBS group (i.e., the animals receiving normal saline) were also imaged as controls for background noise. Fluorescence signals (photon/s) from a fixed region of interest (ROI) were measured as described (36).

Quantification of Engraftment by Real-Time PCR

Quantitative PCR was performed 24 h (after fluorescence imaging and assessment of cardiac function), 10 days, and 3 weeks (after fluorescence imaging and assessment of cardiac function) after cell injection in six animals from each cell-injected group to quantify cell retention/engraftment. We injected MSCs from male donor SD rats into the left ventricle of female recipients, utilizing the sex-determining region Y (SRY) gene located on the Y chromosome as a detection target (28). The whole heart was harvested, weighed, and homogenized. Genomic DNA was isolated from aliquots of the homoge-nate corresponding to 12.5 mg of myocardial tissue using commercial kits (DNA Easy minikit, Qiagen, Hilden, Germany). The TaqMan® assay (Applied Biosystems, Carlsbad, CA, USA) was used to quantify the number of transplanted cells with the rat SRY gene as a template [forward primer: 5′-GAG CTT TGG GAG CAG TGA C-3′ (TM 55.1), reverse primer 5′- ATG AGG CTG ATA TTT ATA GTT TGG-3′ (TM 51.5), Taq Man probe: 6 FAM CAA CAG AAT CCC AGC ATG CAG AAT TCA G TAMRA; Applied Biosystems]. A standard curve was generated with multiple dilutions of genomic DNA isolated from male hearts to quantify the absolute gene copy numbers. All samples were spiked with equal amounts of female genomic DNA as a control. The copy number of the SRY gene at each point of the standard curve was calculated with the amount of DNA in each sample and the mass of the rat genome per cell. For each reaction, 50 ng of template DNA was used. Real-time PCR was performed using an Applied Biosystems 7900 HT Fast real-time PCR System. All experiments were performed in triplicate. Cell numbers per milligram of heart tissue and percentages of retained cells of the total injected cells (1 × 10⁶) were calculated.

Assessment of Cardiac Function

Postinfarct cardiac function was evaluated by transtho-racic echocardiography using a Vevo 770 high-resolution imaging system (Visual Sonics, Toronto, Canada) with a 17.5-MHz probe 24 h and 3 weeks after I/R and treatment (n = 13 for the 0.3 T group, n = 12 for other groups). After the induction of light general anesthesia, hearts were imaged in 2D and M-mode. The recordings were obtained from the parasternal long axis view at the level of the greatest LV diameter. The LV internal end-diastolic diameter (LVIDd) and LV internal end-systolic diameter (LVIDs) were measured from M-mode recordings. The LV ejection fraction (LVEF) was calculated as follows: LVEF (%) = [(LVIDd)³ - (LVIDs)³]/(LVIDd)³ × 100. All echocardiographic measurements were averaged from at least five separate cardiac cycles.

Immunohistochemistry and Morphometric Heart Analysis

At 72 h after cell injection, six representative recipient hearts from each group embedded in paraffin were cut into 5-μm slices, which were stained with Prussian blue (Shanghai HuaYi Bio Technology Co. Ltd., Shanghai, China). The representative hearts were harvested and frozen in OCT compound (Leica JUNG, Wetzlar, Germany) 72 h after transplantation and 3 weeks subsequent to echocardiography of the rat. Cryostat sections (8 mm thickness) were obtained for immunofluorescence staining to evaluate cardiomyocyte or endothelial differentiation of injected MSCs. Potential transdifferentiation of myocardium-like cells from implanted MSCs was verified by antibody immunostaining for troponin T (cTnT). Briefly, frozen tissue sections were fixed in acetone at 4°C for 10 min and incubated separately with a mouse anti-rat cTnT (TnT, cardiac isoform Ab-1; Laboratory Vision Corp, Chicago, IL, USA) diluted 1:100 for 60 min at room temperature. After washing with PBS solution, sections were incubated with a goat anti-mouse-conjugated FITC IgG (Molecular Probes, Inc., Eugene, OR, USA) diluted 1:200 for cTnT. Goat anti-rat CD31 (BD Biosciences, San Diego, CA, USA) was diluted 1:100 to check for evidence of angiogenesis. Secondary antibody of donkey anti-goat IgG conjugated with FITC (Molecular Probes) diluted 1:200 was used. Cell nuclei were counterstained with DAPI. Capillary density was also assessed by staining with anti-CD31 antibody as previously described (31). A total of 10 visual fields where a cross-section of capillaries was clearly visible were randomly selected in the peri-infarct zone, and the number of capillaries was counted under 200× magnification by a Leica Fluorescence microscope (Leica DM LB2).

For morphometric analysis, representative recipient hearts in each group were harvested at 3 weeks (after cardiac function assessment) and embedded in paraffin. Masson's trichrome staining was performed as described by the manufacturer's instructions [HT15 Trichrome Staining (Masson) Kit; Sigma-Aldrich]. To determine the infarct size, the average ratio of infarct size per LV was measured for all paraffin slides after staining with Masson's trichrome as previously described (21). All analyses were performed in a blinded manner.

Statistical Analysis

Animal numbers used in each experiment are shown in Table 1. All data are shown as mean ± standard deviation (SD). The difference between mean values was determined with one-way analysis of variance (ANOVA) and Bonferroni post hoc test. The correlation analysis was based on the Pearson correlation coefficient. Statistical significance was set at p < 0.05.

OPEN IN VIEWER

Table 1.

Study Protocol and Rat Numbers Used in Each Experiment

	24 Hours	72 Hours		10 Days	21 Days
	Heart Fluorescence/ PCR for SRY	Prussian Blue Staining	Cell Fluorescence	PCR for SRY	Masson Staining/ Immunofluorescence	PCR for SRY
PBS group	6	6	6	6	6	6
MSC group	6	6		6	6	6	6
0 T group	6	6		6	6	6	6
0.15 T group	6	6		6	6	6	6
0.3 T group	6	6		6	6	7	6
0.6 T group	6	6		6	6	6	6

Twelve animals from each group (except for 13 animals in 0.3 T group) underwent echocardiography at 24 h and 21 days after injection, respectively. SRY, sex-determining region Y gene; PBS, phosphate-buffered saline (control); MSC, mesenchymal stem cell; T, Tesla (magnetic field strength).

Labeling of Rat MSCs with SPIOs and DiR

The fourth passage of MSCs was characterized by fusiform or spindle-shaped morphology (Fig. 1A). The SPIOs-DiR-MSCs had a strong red fluorescence signal (Fig. 1B). The Prussian blue staining of the MSCs showed intracytoplasmic iron inclusions as dense blue-stained vesicles, and the magnetic nanoparticles were distributed evenly around the nucleus of the MSCs as a spherical shell (Fig. 1C). The labeling efficiency was approximately 100% reproducible using a very low concentration of iron oxide (50 μg/ml). Transmission electron microscopy of labeled cells indicated the presence of anionic magnetic nanoparticles exclusively in polydisperse vesicles in the cytoplasm, and no obvious change in the ultramicrostructure was observed (Fig. 1D).

OPEN IN VIEWER

Figure 1.

SPIOs and DiR labeling of rat MSCs. (A) The fourth passage of MSCs used in the present study. (B) MSCs were labeled with DiR, and cell nuclei were counterstained with DAPI. (C) Prussian blue staining of MSCs labeled with SPIOs on cover glass. (D) Transmission electron microscopy demonstrated the presence of numerous iron-containing vesicles in the cytoplasm of MSCs. SPIOs, superparamagnetic oxide nanoparticles; DiR, 1,1-dioctadecyl-3,3,3,3-tetramethyl indotricarbocyanine iodide; MSCs, mesenchymal stem cells; DAPI, 4′,6-diamidino-2-phenylindole.

Characterization of SPIOs-MSCs

To determine the adipogenic and osteogenic differentiation, the MSCs and SPIOs-MSCs were cultured for 21 days in media that promote differentiation into adipogenic and osteogenic lineages. As shown in Figure 2A and B, both MSCs and SPIOs-MSCs differentiated into the two lineages, as demonstrated by staining for Oil red O and Alizarin red, respectively. Following myocardial differentiation, real-time PCR showed that myocardial genes GATA-4, cTnT, α-actin, and Cx43 were both detected in differentiated MSCs and SPIOs-MSCs (all p > 0.05) (Fig. 2C). The expression of these myocardial genes was comparable in differentiated MSCs and SPIOs-MSCs (Fig. 2D). The results from RT-PCR suggested that low concentration of SPIO labeling did not affect MSC differentiation.

OPEN IN VIEWER

Figure 2.

Differentiation capacity of SPIOs-MSCs. (A) Oil red O staining for adipogenic differentiation. (B) Alizarin red staining for osteogenic differentiation. (C) Real-time PCR for myocardial gene GATA-4, cTnT, α-actin, and Cx43. (D) Quantitative gene expression analysis showed no difference between MSCs and SPIOs-MSCs, suggesting low concentration of SPIO labeling did not affect MSCs differentiation. NC, negative control; PC, positive control.

In Vitro Theoretical Analysis of the Magnetic Targeting

The magnetic field lines around the magnet were mapped by point-by-point magnetic field measurements using a model 51662 Leybold Tesla meter. The center magnetic flux densities of three cylindrical magnet poles were 0.15 T, 0.3 T, and 0.6 T, and the peripheral strengths of the corresponding magnetic poles were 0.40 T, 0.56 T, and 0.93 T, respectively. As shown in Figure 3A–C, the magnetic field strength gradually declines with the shortened distance from periphery to center of the magnetic pole in the horizontal direction. Line 1 and line 2, respectively, represent magnetic field lines from the center and periphery of the magnetic pole in the vertical direction (Fig. 3D). According to the principle of magnetic attenuation, when the magnetic pole radius is 4 mm, the density of magnetic flux is attenuated by 47%, 43%, and 40% at 2 mm from the magnetic poles with 0.15 T, 0.3 T, and 0.6 T and is further decreased by 83%, 80%, and 76% at 6 mm from the three magnets, respectively (Fig. 3E–G). Thus, it is critical not only to overcome the magnetic attenuation but also to make magnetic field lines cover the target site for administering a specific strength of magnetic targeting. We controlled the movement ranges of magnets with the heartbeat to within 1 mm to maximally overcome magnetic attenuation. The actual measured working strengths of the magnets with 0.15 T, 0.3 T, and 0.6 T were at least 0.12 T, 0.23 T, and 0.49 T, respectively. All magnets used here were 8 mm in diameter and approximately the size of a MI in rats. We managed to cover the infarct area and infarct border zone with the strongest area of the magnetic field, thus ensuring target homing of magnetic-responsive cells.

OPEN IN VIEWER

Figure 3.

Theoretical analysis of magnetic fields. (A-C) Distribution of magnetic field lines from three magnets. In the horizontal direction, the magnetic field strength gradually declines along the radius from the periphery to the center. (D-G) Schematic diagram of magnetic attenuation in the vertical direction. Lines 1 and 2 represent magnetic decay curves of central and peripheral of magnetisms, respectively, in the vertical direction.

Magnetic Capture of Flowing SPIOs-MSCs

The flowing SPIOs-MSCs were substantially attracted to the site where the magnetic pole was positioned. The flowing SPIOs-MSCs in the absence of an applied magnetic field demonstrated minimal accumulation (0.26% ± 0.04%), while the CEs reached 42.92% ± 4.76%, 70.53% ± 6.53%, and 80.2% ± 4.79% when the magnetic intensities were 0.15 T, 0.3 T, and 0.6 T, respectively (all p < 0.001 among groups) (Fig. 4A–C). The capture efficiency of cells increased as the magnetic intensity enhanced, indicating that the flowing SPIOs-MSCs can be significantly magnetically attracted in a magnetic flux density-dependent manner. In contrast, the flowing unlabeled MSCs exposed to the varying intensities of magnetic fields only showed minimal accumulation (0.22% ± 0.04%, 0.21% ± 0.02%, 0.21% ± 0.02% and 0.22% ± 0.03% for 0 T, 0.15 T, 0.3 T, and 0.6 T, respectively; all p > 0.05 among groups), indicating that MSCs without SPIOs were not magnetically responsive.

OPEN IN VIEWER

Figure 4.

Magnetic concentration of the flowing SPIOs-MSCs. (A) A schematic illustration of the microfluidic system. The SPIOs-MSCs were injected into the tube, and the flow rate was controlled using a syringe pump. Cells were captured by use of three NdFeB magnets located beside the tube. (B) Representative images of cell accumulation in the segment close to the magnet at velocities of 5 mm/s. (C) The efficiency of magnetically capturing flowing SPIOs-MSCs with different magnetic intensities. (#p < 0.001 vs. the 0 T group; Δp < 0.001 vs. the 0.15 T group; ☆p < 0.01 vs. the 0.3 T group).

Magnetic Strength Influences Cell Distribution After Retention

Because vascular-delivered cells reportedly translocate into the parenchyma after 48–72 h (29), a subpopulation of animals was histologically examined at 72 h. Representative hearts were cryosectioned and analyzed for covisualization of CD31⁺ blood vessels (green) and DiR-labeled MSCs (red). Cells were found residing in the infarct area and peri-infarct border zone in the groups treated with SPIOs-DiR-MSCs or DiR-MSCs. Not surprisingly, the numbers of DiR-MSCs were indistinguishable in the 0 T and MSC groups (p > 0.05) (Fig. 5A, B). Three magnetic targeting groups exhibited more SPIOs-DiR-MSCs compared to either the 0 T group or the MSC group (all p < 0.001) (Fig. 5A–E). DiR fluorescence from MSCs suggested that the 0.15 T, 0.3 T, and 0.6 T groups demonstrated 2.18-, 3.95-, and 2.31-fold cell distribution, respectively, outside vascular structures relative to the 0 T group (all p < 0.001, respectively) (Fig. 5F). Interestingly, comparable results were found in the 0.6 T and 0.15 T groups (p > 0.05).

OPEN IN VIEWER

Figure 5.

Microembolization at 72 h after intraventricular infusion (n = 6 for each group). (A–E) Representative fluorescence image of heart sections from MSC group (A), 0 T group (B), 0.15 T group (C), 0.3 T group (D), and 0.6 T group (E). CD31 antibody (green) stained for detecting blood vessels. MSCs were visualized by red fluorescence, and cell nuclei were counterstained with DAPI. (F) MSC numbers from 10 randomly selected high-power fields (five from the infarct area and five from the border zone) in each group were quantified by fluorescence microscopy. Data are mean ± SD. (#p < 0.001 vs. the MSC group or the 0 T group; Δp < 0.001 vs. the 0.15 T group; ☆p < 0.001 vs. the 0.3 T group). HPF, high power field.

Meanwhile, microemboli were detected in the groups treated with MSCs (Fig. 6A, B). The percentage of blocked vessels was comparable in the MSC and 0 T groups (2.93 ± 1.12% vs. 3.16 ± 1.36%, p > 0.05), indicating that MSCs can induce microvascular obstruction as has been reported previously (13,30). More importantly, the percentage of blocked vessels was 4.3% ± 0.98%, 8.24% ± 1.12%, and 15.12% ± 2.09% when the magnetic intensities were 0.15 T, 0.3 T, and 0.6 T, respectively, indicating that the external magnetic field may exacerbate magnetically responsive MSCs obstructed in microvascular, and the microembolisms further worsened with the escalating magnetic intensity (Fig. 6C).

OPEN IN VIEWER

Figure 6.

Microembolization at 72 h after intraventricular infusion (n = 6 for each group). (A) Representative heart frozen sections were stained for CD31 antibody (green) to detect blood vessels. SPIOs-DiR-MSCs were visualized by red fluorescence, and cell nuclei were counterstained with DAPI. The 0.6 T groups showed blood vessel completely blocked by cell clumps, whereas the 0 T, 0.15 T, and 0.3 T groups exhibited that blood vessels containing cells were still patent. (B) Prussian blue staining confirmed that blood vessels were blocked by cell clumps in the 0.3 T and 0.6 T groups (arrows), but most blood vessels containing cells were still patent in the 0 T and 0.15 T groups (arrows). (C) Quantitative analysis of blocked vessels by frozen sections stained with CD31 antibody. (#p < 0.001 vs. the MSC group or the 0 T group; Δp < 0.001 vs. the 0.15 T group; ☆p < 0.001 vs. the 0.3 T group).

The Relationship Between Magnetic Strength and Short-Term Cell Retention

Fluorescence imaging of hearts excised 24 h after cell infusion revealed more fluorescence signals in hearts from the three magnetic targeting groups than the 0 T and MSC groups. The enhanced fluorescence from three magnetic targeting groups was dependent on magnetic strength. As a negative control, excised hearts from the PBS group were also imaged. No signals were detectable (Fig. 7A, B).

OPEN IN VIEWER

Figure 7.

Short-term cell retention and long-term cell engraftment in hearts and other organs. (A) Representative fluorescence imaging of hearts harvested 24 h after cell injection. (B) Quantificative analysis of fluorescence intensities. (*p < 0.001 vs. the PBS group; #p < 0.001 vs. the MSC group or the 0 T group; Dp < 0.001 vs. the 0.15 T group; ☆p < 0.001 vs. the 0.3 T group). (C) Cell retention in other organs by fluorescence imaging 24 h after cell injection. (#p < 0.001 vs. the MSC group or the 0 T group; Dp < 0.001 vs. the 0.15 T group; ☆p < 0.001 vs. the 0.3 T group). (D) Cell detection 24 h, 10 days, and 3 weeks after injection in the heart by quantitative PCR of the male-specific SRY gene (n = 6 for each group).

To compare off-target migration, lungs, livers, spleens, and kidneys from the same animals were also harvested to detect fluorescence signals of transplanted MSCs. Not surprisingly, fluorescence signals were detectable in these organs, but less so in the organs from three magnetically targeted groups than in those from the MSC and 0 T groups (Fig. 7C). Moreover, there is a trend that fluorescence signals in the off-target organs from three magnetically targeted groups decreased with the enhancement of strength of heart magnetic targeting (Fig. 7C).

Quantitative PCR for the male-specific SRY gene was performed 24 h after cell infusion. Consistent with the fluorescence imaging results, magnetic targeting enhanced short-term cell retention in a magnetic strength-dependent manner: the 0.15 T, 0.3 T, and 0.6 T groups exhibited 1.45-, 2.76-, and 3.86-fold greater cell retention rates, respectively, than the 0 T group (all p < 0.001) (Fig. 7D). The relationship between magnetic intensity and retained cell numbers is a positive linear correlation (r = 0.983, p = 0.017).

Different Magnetic Strengths Induce Varying Long-Term Cell Engraftment

To examine the effects of magnetic targeting on long-term engraftment, quantitative PCR for the male-specific SRY gene was performed 10 days and 3 weeks after cell infusion. Consistent with previous findings (4,6,19,20), quantitative PCR revealed that the five groups treated with MSCs experienced a substantial drop in surviving cells 10 days after cell infusion. The surviving cells furthered reduced 3 weeks after cell infusion; however, the three magnetic targeting groups still exhibited enhanced cell engraftment relative to the 0 T group (all p < 0.001) (Fig. 7D), which is consistent with previous findings (5,6), indicating that magnetic targeting can enhance MSC homing and engraftment. At 3 weeks after cell infusion, the 0.15 T, 0.3 T, and 0.6 T groups exhibited 1.88-, 3.06-, and 1.90-fold greater cell engraftment rates, respectively, than the 0 T group (Fig. 7D). Interestingly, cell engraftment rates in the 0.6 T group were lower than the 0.3 T group (p < 0.001) (Fig. 7D). Compared with the 0.15 T group, the 0.6 T group exhibited comparable cell engraftment rates (p > 0.05) (Fig. 7D).

Magnetic Strength Affects Therapeutic Benefits of Cell Transplantation and Left Ventricular Remodeling

To investigate functional outcomes mediated by magnetic targeting, LVEF was assessed by echocardiography at baseline (24 h after I/R and treatment) and for a subsequent 3 weeks. The 0.6 T group had the lowest LVEF at baseline, but LVEF did not differ between treatment groups (Fig. 8A), indicating a comparable degree of initial injury. Over the next 3 weeks, LVEF declined progressively in the PBS group, but it did not decline in the four MSC-treated groups. Both the 0.15 T and 0.3 T groups exhibited better therapeutic outcome, with LVEF superior to the 0 T group (all p < 0.001) (Fig. 8A) at 3 weeks. Not surprisingly, the 0.3 T group had a higher LVEF than the 0.15 T group (p < 0.001) (Fig. 8A). Notably, LVEF was comparable among the 0.6 T, 0 T, and MSC groups (all p > 0.05) (Fig. 8A). To facilitate comparisons, we calculated the treatment effect, that is, the change in LVEF at 3 weeks relative to baseline, in each group.

OPEN IN VIEWER

Figure 8.

Functional benefits of cell transplantation. (A) LVEF measured by echocardiography 24 h and 3 weeks after cell injection (n = 13 for 0.3 T and n = 12 for other groups). (B) Changes in LVEF from 24 h to 3 weeks in each group. (*p < 0.001 vs. the PBS group; #p < 0.001 vs. the MSC group or the 0 T group; Δp < 0.001 vs. the 0.15 T group; ☆p < 0.001 vs. the 0.3 T group). (C–D) Changes in LVEF are plotted against changes in LVIDs (C) and LVIDd (D). Change reflects the difference between parameters measured 24 h and 3 weeks after therapy. LVEF, left ventricular ejection fraction; LVIDs, left ventricular internal end-systolic diameter; LVIDd, left ventricular internal end-diastolic diameter; ΔLVEF, Changes in LVEF from 24 h to 3 weeks.

The PBS group had a negative treatment effect, with LVEF decreasing over time. In contrast, the 0.15 T and 0.3 T groups exhibited a sizable positive treatment effect that was greater than the 0 T and 0.6 T groups (Fig. 8B). The similar changes were also observed in LVIDd and LVIDs. Compared with the MSC, 0 T, and 0.6 T groups, the 0.15 T group exhibited the greater reduction in LVIDd and LVIDs (0.21 mm and 0.15 mm, 0.19 mm and 0.13 mm, 0.21 mm and 0.14 mm vs. 0.59 mm and 0.40 mm, respectively, all p < 0.001). More importantly, the 0.3 T group exhibited the greatest reduction in LVIDs (1.4 mm) and LVIDd (0.90 mm) among three magnetic targeting groups (all p < 0.001). The percentage of change in the LVEF at 3 weeks, as a function of the LVIDs (Fig. 8C) or LVIDd (Fig. 8D) percentage of change indicated that appropriate intensity of magnetic targeting mediating cell therapy extended the therapeutic benefit of cell therapy for cardiac function and structure.

Morphometry at 3 weeks showed more infarct size in the PBS group than the five MSC-treated groups. The 0.15 T and 0.3 T groups showed significantly smaller infarct size than the 0 T group and the MSC group. Furthermore, the infarct size was 4.7% lower in the 0.3 T group than the 0.15 T group (p < 0.001) (Fig. 9A, B). Again, LV infarct size was indistinguishable among the 0.6 T, 0 T, and MSC groups (p > 0.05) (Fig. 9A, B).

OPEN IN VIEWER

Figure 9.

Left ventricular remodeling. (A) Representative Masson's trichrome stained myocardial sections from a subgroup of animals 3 weeks after treatment (n = 7 for 0.3 T and n = 6 for other group). (B) Quantitative analysis of fibrosis size. (*p < 0.001 vs. the PBS group; #p < 0.001 vs. the MSC group or the 0 T group; δp < 0.001 vs. the 0.15 T group; ☆p < 0.001 vs. the 0.3 T group).

Different Intensities of Magnetically Targeted Cell Delivery Induce Varying Angiogenesis

To determine the mechanisms underlying the beneficial effects of cell transplantation, we investigated the effects of cell transplantation on angiogenesis in the post-I/R hearts. At 3 weeks after cell transplantation, immunofluorescence staining for CD31 antibody indicated significant angiogenesis in MSC-treated hearts, with more CD31-expressing capillaries being present in the peri-infarct region of MSC-treated groups compared with the PBS group (all p < 0.05) (Fig. 10A, B). Quantitative evaluation of CD31-positive capillary numbers indicated that the PBS group exhibited the lowest capillary density. In contrast, both the 0.15 T and 0.3 T groups had more capillary density than the 0 T and 0.6 T groups (all p < 0.01) (Fig. 10A, B). Not surprisingly, the 0.3 T group had the most capillary density. Also, no significant difference was found among the 0.6 T, 0 T, and MSC groups (p > 0.05) (Fig. 10B). However, few cells stained positive for both the endothelial cell marker CD31 or the cardiomyocyte marker TnT and DiR in the five MSC-treated groups. These data suggest that transplanted MSCs may promote angiogenesis through a paracrine effect, contributing to the observed cellular therapy-associated beneficial effects.

OPEN IN VIEWER

Figure 10.

Angiogenesis 3 weeks after cell infusion. (A) Frozen sections of representative hearts were stained for CD31 antibody (green) to detect capillary densities in the peri-infarct region 3 weeks after MSC transplantation. (B) Quantitative analysis of CD31-containing capillaries in the peri-infarct region (n = 7 for 0.3 T and n = 6 for other group). (*p < 0.05 vs. the PBS group; #p < 0.05 vs. the MSC group or the 0-T group; Δp < 0.01 vs. the 0.15-T group; ☆p < 0.001 vs. the 0.3-T group).

Study Limitations

Although it describes a new and promising method, the present study has a number of limitations. The optimized magnet strength obtained from the small animal studies may not be directly extrapolatable to large animals. Additionally, we did not include a magnet targeting group without cell infusion and hence did not explore the effects of magnet targeting on a rat model of acute ischemia/ reperfusion. Furthermore, instead of optimizing basal cell dosage and magnetic exposure time, we chose cell dose and duration consistent with previous studies that showed functional benefits in small animals (5,6,9,18,19,25). Further dosage and exposure time optimization would be valuable, to inform future clinical studies. Finally, we did not investigate whether the SPIO movement guided by the magnetic field damaged the MSCs’ micro- and ultrastructures. Future studies will be designed to capture any changes caused by magnetic targeting in transplanted cell micro- and ultrastructures.