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Di et al., Sci. Adv. 2020; 6 : eaba9381 17 June 2020
S C I E N C E A D V A N C E S | R E S E A R C H A R T I C L E
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A P P L I E D S C I E N C E S A N D E N G I N E E R I N G
An orthogonally regulatable DNA nanodevice for spatiotemporally controlled biorecognition and tumor treatmentZhenghan Di1,2*, Bei Liu1*, Jian Zhao1,2*, Zhanjun Gu3, Yuliang Zhao1,2,4†, Lele Li1,2,4†
Despite the potential of nanodevices for intelligent drug delivery, it remains challenging to develop controllable therapeutic devices with high spatial-temporal selectivity. Here, we report a DNA nanodevice that can achieve tumor recognition and treatment with improved spatiotemporal precision under the regulation of orthogonal near-infrared (NIR) light. The nanodevice is built by combining an ultraviolet (UV) light–activatable aptamer module and a photosensitizer (PS) with up-conversion nanoparticle (UCNP) that enables the operation of the nanodevice with deep tissue–penetrable NIR light. The UCNPs can convert two distinct NIR excitations into orthogonal UV and green emissions for programmable photoactivation of the aptamer modules and PSs, respectively, allowing spatiotemporally controlled target recognition and photodynamic antitumor effect. Furthermore, when combined with immune checkpoint blockade therapy, the nanodevice results in regression of untreated distant tumors. This work provides a new approach for regulation of diagnostic and therapeutic activity at the right time and place.
INTRODUCTIONDNA is emerging as a highly programmable building block for the design of molecular nanodevices with specific functions, including sensors, motors, and circuits (1–3). Upon interfacing with biology, such DNA nanodevices can carry out versatile tasks such as biosensing and imaging (4–7), molecular information computing (8–10), and controllable cargo transport and release (11–21). In particular, recent work has demonstrated that DNA nanodevices could work as smart drug delivery systems (17–21). A key feature of such devices is that they can perform cell subtype–targeted delivery in response to specific biological cues. Because of their high affinity and specificity to specific targets, aptamers that can selectively bind diseased cell–associated receptors have been incorporated into DNA nanodevices for intelligent delivery (18–21). For example, an aptamer based DNA nanorobot permitted specific transport of molecular payloads to cancer cells in response to membrane epitopes (19). An aptamertethered DNA nanotrain was explored for tumorselective drug delivery (20). Recently, we designed an aptamerdriven nanorobot for controlled delivery of therapeutic protein to tumor blood vessels in response to specific receptors on the surface of tumor vascular endothelial cells (21). Despite the progress made, the cell surface receptors that these nanodevices recognize are not only exclusive to diseased cells but also expressed at a low level in normal cells (22). Therefore, such aptamerbased nanodevices can also bind with the same target on normal cells, leading to ontarget offtumor effects. The engineering of aptamerbased nanodevices with high spatial
temporal selectivity remains a challenge because of the lack of a design methodology.
Light has proven to be an appealing tool for precise regulation of chemical and biological activities both spatially and temporally (23, 24). For example, optogenetics has had a transformative impact in neurobiology and cell biology (25, 26). The engineering of biomolecules with photolabile groups allows controlled manipulation of gene expression (27), cell signaling (28), and therapeutic activity (29, 30). For example, a phototriggerable strategy was demonstrated for the spatiotemporal regulation of aptamer activity (31). However, most of these lightcontrolled systems are propelled with either ultraviolet (UV) or visible light and, thus, have shallow depth of tissue penetration and insufficient photoactivation efficiency, limiting their application in vivo. Recently, lanthanidedoped upconversion nanoparticles (UCNPs) have enabled the use of nearinfrared (NIR) photons for regulation of photosensitive moieties (32–37) owing to their unique conversion ability to absorb NIR light and emit tunable UV and visible light (38, 39). Most recently, UCNPs were leveraged as optogenetic actuators of NIR light for the regulation of deep brain neurons (34).
Inspired by the achievements, herein we present a conceptual approach for the design of NIR light–controlled DNA nanodevice that imparts biorecognition and tumor treatment with improved spatialtemporal selectivity. As a clinically approved treatment modality, photodynamic therapy (PDT) relies on the generation of cytotoxic reactive oxygen species (ROS) under irradiation of photosensitizers (PSs) (40). To date, its applications are still limited by low tissue penetration of UV/visible light and lack of spatial control over PSs (41). In our design, an orthogonal upconversion nanotechnology was used to achieve intended regulation of DNA nanodevice with deep tissue–penetrable NIR light, allowing efficient PDT with improved tumor specificity. Furthermore, the combination of the nanodevice with immune checkpoint blockade therapy elicited both synergistic and abscopal effects in tumorbearing mice by facilitating tumor infiltration of cytotoxic T cells.
1CAS Key Laboratory for Biomedical Effects of Nanomaterials and Nanosafety and CAS Center for Excellence in Nanoscience, National Center for Nanoscience and Technology, Beijing 100190, China. 2College of Materials Science and Optoelectronic Technology, University of Chinese Academy of Sciences, Beijing 100049, China. 3CAS Key Laboratory for Biomedical Effects of Nanomaterials and Nanosafety, Institute of High Energy Physics, Chinese Academy of Sciences, Beijing 100049, China. 4GBA Research Innovation Institute for Nanotechnology, Guangdong 510700, China.*These authors contributed equally to this work.†Corresponding author. Email: [email protected] (Y.Z.); [email protected] (L.L.)
Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC).
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RESULTSProgramming of the DNA nanodeviceWe choose an aptamer that recognizes nucleolin (NCL) overexpressed on the surface of various cancer cells (31, 42) to demonstrate our design. As shown in Fig. 1A, the nanodevice (PTUN) was constructed by controlled organization of UV light–activatable aptamer modules (LApt) and PSs on the surface of an orthogonal UCNPs. LApt is designed by hybridizing the aptamer with a complementary strand (LHD) containing a commercially available photocleavable 2nitrobenzyl linker (PC linker; fig. S1). In this duplex state, the recognition capability of the aptamer to NCL is inhibited. The UCNPs act as a photoregulator to locally convert two NIR lights of different wavelengths (808 and 980 nm) into orthogonal UV and green up conversion luminescence (UCL), respectively. UV UCL obtained under 808nm irradiation enables photolysis of the PC bonds and liberation of the aptamer at desired time and site, while green UCL achieved upon 980nm irradiation allows excitation of PSs for the production of cytotoxic ROS. After intravenous injection, PTUN could specifically bind the NCL on tumor cell surface upon 808nm NIR light–mediated local triggering, and subsequently generate ROS to induce tumor cell apoptosis under 980nm NIR light irradiation (Fig. 1B).
To achieve orthogonal UCL in response to two distinct NIR light (808 and 980 nm), we designed and synthesized the core multishell–structured UCNPs (NaGdF4:Yb,Er@NaYF4@NaYF4: Yb,Tm@NaYbF4:Nd@NaYF4) with lanthanide activators (Er3+ and Tm3+) and sensitizers (Yb3+ and Nd3+) doped in separate layers (fig. S2A). Er3+/Yb3+ were codoped in the core for producing green emission under 980nm excitation, while Tm3+/Yb3+ and Yb3+/Nd3+ were codoped in the second and third shell layers, respectively, to enable UV emission upon 808nm excitation (32). To prevent the energy migration between the two luminescent regions, an inert interlayer of NaYF4 without any dopant was introduced as the first shell layer. In addition, an NaYF4 shell layer was grown outermost to minimize surface quenching effect. Transmission electron microscopy (TEM) showed that the assynthesized UCNPs displayed uniform hexagonal platelike shape with a size of ∼50 nm by 25 nm (Fig. 2A and fig. S2, B to H). The interplanar lattice spacing of 0.52 nm revealed by
the highresolution TEM image was identified as (100) crystal plane of the hexagonal phase (fig. S2I) (43). The multishelled structure could be identified via image contrast in the highangle annular darkfield scanning TEM (HAADFSTEM) image (Fig. 2B). The fourshelled UCNPs with asdesigned distribution of lanthanide ions in different layers were further confirmed by linear energydispersive spectroscopy scanning (fig. S2J). Then, the UCNPs were coated with mesoporous silica shell for the modification of LApt on their external surface and loading of Rose Bengal (RB) PSs in the mesopores (fig. S3A). Each step of the construction was verified by the measurement of zeta potential and UVvisible absorbance of the resulted NPs (fig. S3, B and C). The average number of LApt conjugated on each NP was calculated to be 93. The resulting PTUN showed an average size of 60 nm by 35 nm (with a mesoporous silica layer of ~5 nm), standing on the TEM grid on either the bottom face or the side face (Fig. 2C). Figure 2 (D and E) shows the UCL spectra of the UCNPs upon irradiation with two NIR light of different wavelengths. Under 808nm NIR light irradiation, characteristic Tm3+ dominated UV (347 and 363 nm) and visible blue (452 and 475 nm) emissions were observed (Fig. 2D). In contrast, upon 980nm NIR light excitation, visible green (522 and 541 nm) and red (656 nm) emissions of Er3+ dominate the spectrum (Fig. 2E).
We then evaluated the 808nm NIR light–triggered activation of LApt. The AS1411 strand and LHD strand were modified with fluorophore Cy5 and black hole quencher (BHQ2), respectively, yielding fluorescence resonance energy transfer (FRET) pair–labeled LApt with a low fluorescence background. Upon 808nm NIR light irradiation (0.5 W cm−2), PTUN showed a notable increase in the Cy5 fluorescence intensity (Fig. 2F), indicating the liberation of the aptamer strand from the hybrid due to the photolysis of LHD. As a control, when the nanoconstruct was modified with a DNA probe that had the same sequence as LApt but without a PC linker (nPTUN), no obvious fluorescence change of Cy5 was observed under 808nm NIR light irradiation, indicating that the introduction of the PC bond was crucial for the design. Because the green UCL band of UCNPs under 980nm irradiation overlaps well with the absorbance spectra of RB PSs (Fig. 2G), the green UCL of the nanostructure was obviously quenched after loading of RB in the mesopores, while
Fig. 1. Schematic showing the orthogonal regulation of DNA nanodevice for programmed tumor cell recognition and treatment. (A) The orthogonal photo-activation behavior of the DNA nanodevice in response to two NIR light of different wavelengths. (B) Sequential activation of the nanodevice with orthogonal UCL for programmed tumor recognition and PDT.
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the red UCL was barely influenced (Fig. 2H). The energy transfer from the UCNP to the RB was further confirmed by the timeresolved photoluminescence measurement, which reveals a significantly decreased lifetime of Er3+ emission (from 487 to 317 s) upon the loading of RB in the nanostructure (fig. S4, A and B). Next, the capability of PTUN to produce single oxygen (1O2) under 980nm NIR light irradiation was examined using the dye 1,3diphenylisobenzofuran (DPBF) as an indicator of 1O2. As expected, the absorption intensity of DPBF in PTUN dispersion decreased upon 980nm irradiation, but exhibited negligible change with 808nm irradiation or without any irradiation (Fig. 2I), confirming that the photon energy absorbed by UCNP under 980nm laser irradiation was transferred to RB for 1O2 generation. In addition, no obvious leakage of RB from PTUN was observed (fig. S4C), which was important for the application of such system for PDT.
Orthogonally regulated target recognition and photodynamic effect in vitroNext, we examined the NIR light–triggered recognition of PTUN to 4T1 breast cancer cells with NCL on their surface. The nanostruc
tures were loaded with Cy5 dye instead of RB for the studies by confocal laser scanning microscopy (CLSM) and flow cytometry. As shown in Fig. 3A, CLSM images revealed much lower fluorescence signals in the cells treated with PTUN compared with cells exposed to TUN (wherein the system was modified with the aptamer strand only), indicating that formation of LApt blocked the recognition ability of the aptamer. Irradiation of PTUN with 808nm laser significantly increased their cellular uptake to a level comparable to that observed with TUN, demonstrating that 808nm NIR light irradiation liberated aptamer on the PTUN surface for cell targeting. In contrast, 4T1 cells whose surface NCL was blocked by antiNCL antibody exhibited no response to the photoactivated system, confirming that the NIRresponsive cellular uptake enhancement of PTUN is directed by NCLmediated binding. As a control, 808nm NIR light irradiation of inactive nPTUN led to no obvious change of their intracellular uptake, confirming the indispensable role of the PC element for the photoregulation design. The NIR light–controlled biorecognition was further confirmed by flow cytometry (Fig. 3B and fig. S5A). The cells treated with PTUN plus 808nm NIR light activation exhibited 2.3fold higher fluorescence than those without
Fig. 2. Characterization of the nanodevice. (A and B) TEM (A) and high-angle annular dark-field scanning TEM (HAADF-STEM) (B) images of the core-multishell UCNPs. (C) TEM image of PT-UN. (D and E) UCL spectra of the core-multishell UCNPs upon excitation of 808 (D) and 980 nm (E). Inset is the schematic illustration of UCL in response to different NIR excitation. (F) Relative fluorescence intensity of fluorescence resonance energy transfer (FRET) pair–labeled PT-UN and nPT-UN with or without 808-nm irradiation as a function of irradiation time. (G) UCL spectrum of the UCNPs under 980-nm excitation and UV-visible absorption (Abs.) spectrum of RB PSs. (H) UCL spectra of PT-UN before and after loading with RB under 980-nm NIR light excitation. (I) Normalized absorbance of 1,3-diphenylisobenzofuran (DPBF) in the presence of PT-UN upon different irradiations. a.u., arbitrary units.
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light irradiation, that is, to a level similar to that of cells incubated with TUN. The colocalization study revealed that the photoactivated PTUN mainly accumulated inside endo/lysosomes (fig. S5B).
Afterward, we investigated the orthogonal UCL–regulated photodynamic effect. Intracellular 1O2 generation was first examined by using a fluorescent ROS probe, 2,7dichlorodihydrofluorescein diacetate (H2DCFDA). Cells treated with PTUN displayed relatively
dim ROS signal compared with cells exposed to TUN under 980nm irradiation because of their inhibited celltargeting ability (fig. S6A). In contrast, sequential irradiation with 808 and 980nm NIR light notably enhanced ROS signal of cells incubated with PTUN (Fig. 3C), suggesting that the 808nm NIR light–mediated recovery of the recognition capability enhanced intracellular ROS production. Quantitatively, ROS signal in PTUN–treated cells with sequential
Fig. 3. Orthogonally regulated cell recognition and photodynamic effect in vitro. (A) CLSM images of 4T1 cells with indicated treatments. Scale bars, 20 m. (B) Flow cytometric quantification of the fluorescence intensity of 4T1 cells, with different treatments. Data are means ± SD (n = 3). (C) CLSM images of 4T1 cells treated with PT-UN and 2,7-dichlorodihydrofluorescein diacetate (H2DCFDA) upon different irradiation. Scale bars, 100 m. (D) Cell viability of 4T1 cells treated with different concentrations of PT-UN and irradiation. Data are means ± SD (n = 3). (E) Cell viability of 4T1 cells with indicated treatments. Data are means ± SD (n = 3). (F) CLSM images of PT-UN–treated 4T1 cells with different irradiation, and then costained with calcein AM and propidium iodide (PI). Scale bars, 200 m. (G) Flow cytometry analysis of cell apoptosis induced by PT-UN plus different irradiation using the annexin V/PI staining. Statistical significance was determined by two-tailed Student’s t test (B and E). ns, not significant; **P < 0.01; ***P < 0.001.
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irradiation of dual NIR light was 2.1fold higher relative to those with 980nm irradiation only (fig. S6B). As a control, cells incubated with inactive nPTUN plus dual NIR light irradiation exhibited negligible change of intracellular ROS signal in comparison to that irradiated with 980nm light only (fig. S6, A and B). Next, the photodynamic efficacy of PTUN was examined by Cell Counting Kit8 (CCK8) assay. As shown in Fig. 3D, PTUN successively treated with 808 and 980nm NIR light showed stronger cytotoxicity than that irradiated by 980nm NIR light only, indicating phototargetingmediated enhancement of therapeutic efficiency. After sequential irradiation of the dual NIR light, viability of PTUN–treated cells (32.3%) was comparable to that of cells exposed to TUN (28.4%) and was 2.0fold lower than that of cells incubated with PTUN plus 980nm light irradiation (63.2%) (Fig. 3E). For cells incubated with TUN or
nPTUN, dual NIR light irradiation could not decrease cell viability in comparison to that irradiated with only 980nm light (Fig. 3E). These results were further supported by calcein AM/propidium iodide (PI) costaining assay and annexin V and PI double staining analysis. PTUN exposed to dual NIR light irradiation evoked the highest levels of dead cells represented by red fluorescence (Fig. 3F and fig. S6C) and the lowest level of healthy cells indicated by annexin V–APC/PI apoptosis assay (Fig. 3G and fig. S6D).
Orthogonally regulated tumor targeting and therapy in vivoTo investigate the NIR light–mediated regulation of the nanodevice in vivo, BALB/c mice bearing subcutaneous tumors were administered intravenously with TUN, PTUN, or nPTUN followed by 808nm NIR light irradiation at the tumor region. The wholebody
Fig. 4. Photoregulated tumor targeting in vivo. (A) Representative whole-body fluorescence images of 4T1 tumor–bearing mice injected intravenously with different samples without or with subsequent 808-nm NIR light irradiation at the tumor site. Tumors are indicated by red circles. (B) Intratumoral fluorescence in (A) as a function of time. Data are means ± SD (n = 5). (C) Intratumoral fluorescence in (A) 4 hours after injection. Data are means ± SD (n = 5). (D) Representative fluorescence images of ex vivo organs and tumors at 24 hours after injection. (E) The ratio of fluorescence intensity in tumors to that in livers for mice in (D). Data are means ± SD (n = 5). Statisti-cal significance was determined by two-tailed Student’s t test (C and E). ns, not significant; **P < 0.01.
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fluorescence imaging was then performed at indicated time points. The fluorescence intensity at the tumor sites showed a timedependent increase before reaching a maximum at 8 hours after injection in all groups (Fig. 4, A and B). Mice treated with PTUN displayed relatively weak intratumoral fluorescence compared with those receiving TUN. Irradiation of the tumor site in the PTUN group with 808nm NIR light led to enhanced intratumoral fluorescence (Fig. 4, A and B), which was 1.7fold higher than the nonirradiated PTUN group at 4 hours after injection (Fig. 4C). As a control, the phototriggering did not enhance the intratumoral accumulation of nPTUN (Fig. 4, A to C). These results indicated that enhanced accumulation of PTUN upon NIR triggering was due to photoactivation of the aptamer modules on their surface. Biodistribution of NPs was evaluated by ex vivo imaging of harvested organs and tumors 24 hours after administration (Fig. 4D). In the liver, the PTUN + 808 nm group showed fluorescence intensity similar to that in the nonirradiated PTUN group, but lower than that in the TUN group. These data suggest that PTUN could be locally activated to specifically recognize its target in tumor, while the offtarget binding in liver was reduced, resulting in a higher specificity to tumor compared with the “always on” targeting system (TUN). The fluorescence ratio of tumor to liver in the PTUN + 808 nm group was 2.0fold higher than that in the TUN group (Fig. 4E), confirming that NIR
irradiation enhanced accumulation of PTUN in tumor relative to the level in liver.
We then assessed the PDT potency of the nanodevice. 4T1 tumor– bearing mice were intravenously injected with PTUN or nPTUN, followed by dual NIR light activation. The 980nm laser irradiation was applied with an interval between shorttime irradiation cycles to alleviate potential overheating effect (fig. S7). As shown in Fig. 5A, tumors in mice treated with phosphatebuffered saline (PBS) followed by sequential irradiation with two NIR light grew rapidly with the average volume similar to that in the PBS group, excluding the effect of irradiation on tumor regression. Treatment with PTUN or nPTUN had no antitumor effect. After irradiation with the 980nm laser only, moderate tumor inhibition was observed in mice treated with PTUN (48.6%) or nPTUN (51.2%) compared with the PBS group. PTUN with sequential irradiation of 808 and 980nm NIR light exhibited enhanced tumor eradication (77.8%) compared with that irradiated with 980nm NIR light alone, whereas tumor growth in mice treated with nPTUN plus dual NIR light irradiation was similar to that irradiated by 980nm laser alone, confirming that the 808nm NIR light–mediated targeting enhanced the anticancer efficiency of PTUN. As expected, PTUN plus dual NIR light irradiation resulted in the least average tumor weight among all groups (Fig. 5B). The hematoxylin and eosin (H&E) and terminal deoxynucleotidyl
Fig. 5. Orthogonally regulated tumor treatment. (A) Tumor growth curves of mice with different treatments. Group 1, phosphate-buffered saline (PBS); group 2, PBS + 808 nm + 980 nm; group 3, nPT-UN; group 4, PT-UN; group 5, nPT-UN + 980 nm; group 6, PT-UN + 980 nm; group 7, nPT-UN + 808 nm + 980 nm; and group 8, PT-UN + 808 nm + 980 nm. Data are means ± SD (n = 5). Statistical significance was determined by one-way analysis of variance (ANOVA). **P < 0.01. (B) Final weight of tumors collected from mice after various treatments. Data are means ± SD (n = 5). Statistical significance was determined by two-tailed Student’s t test. ns, not significant; **P < 0.01. (C and D) Hematoxylin and eosin (H&E) (C) and terminal deoxynucleotidyl transferase–mediated deoxyuridine triphosphate nick end labeling (TUNEL) (D) staining of tumor sections collected from mice with indicated treatments. Scale bars, 100 (C) and 50 m (D).
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transferase–mediated deoxyuridine triphosphate nick end labeling (TUNEL) staining showed that the group treated with PTUN plus dual NIR light activation had the highest level of necrosis in tumor tissues in comparison with the other groups (Fig. 5, C and D, and fig. S8). No abnormal change in body weight was observed in all groups (fig. S9A). In addition, PTUN induced neither serum biochemistry defects nor organ damage (fig. S9, B to D), demonstrating that the platform is devoid of systemic toxicity.
Combinational therapy with immune checkpoint blockadeWe further examined whether antitumor immunity triggered by the nanodevice could be combined with checkpoint blockade therapy to realize systemic cancer management. It has been reported that PDT could cause calreticulin (CRT) exposure, thus inducing immunogenic cell death (ICD) and activating the engulfment of apoptotic tumor cells by antigen presenting cells (dendritic cells and macrophages) (44). Therefore, we first evaluated the ability of the nanodevice to stimulate ICD by detecting cellsurface CRT expression. As expected, PTUN incubation followed by dual NIR light irradiation induced membrane CRT expression in vitro (fig. S10, A and B), suggesting phototriggered
immunogenicity. The analysis of CRT expression in tumor tissues verified the immunogenic property of the platform in vivo (fig. S10C). A bilateral tumor model of breast cancer was then established with the left tumors defined as primary tumors for NIR light irradiation and the right tumors designated as distant tumors without direct irradiation. When the primary tumors reached ~100 mm3, mice were randomly divided into four groups for the treatment with (i) PBS, (ii) programmed deathligand 1 (PDL1), (iii) PTUN with dual NIR light irradiation [donated PTUN(+)], and (iv) PTUN(+) plus PDL1. PTUN was intravenously injected every 4 days for a total of two injections followed by sequential irradiation with dual NIR light, while PDL1 was intravenously injected at indicated time after the irradiation (Fig. 6A). As shown in Fig. 6 (B to D), PDL1 alone exhibited slight inhibition effect on growth of the primary and the distant tumors. PTUN(+) led to extraordinary primary tumor inhibition but exhibited slight inhibition on the distant tumors. In contrast, the combination of PTUN(+) with checkpoint blockade resulted in obvious growth inhibition of primary tumors (synergistic effect) and distant tumors (abscopal effect).
The antitumor performance on distant tumors implied a successful activation of systemic immune response. As anticipated, the
Fig. 6. Orthogonally regulated PT-UN for immunotherapy. (A) Schematic illustration of combining PT-UN(+) with -PD-L1 therapy to inhibit tumor growth at both primary and distant sites. (B and C) Tumor growth curves of primary tumors (B) and distant tumors (C) of bilateral tumor-bearing mice with different treatments. Data are means ± SD (n = 5). (D) Weight of primary and distant tumors at the endpoint of the experiment. Data are means ± SD (n = 5). (E to G) The percentages of CD45+ leukocytes (CD45+PI−) (E), CD8+ T cells (CD45+CD3e+CD8+PI−) (F), and CD4+ T cells (CD45+CD3e+CD4+PI−) (G) in total tumor cells in distant tumors. (H) Cytokine levels in sera of mice isolated 20 days after different treatments. Data are means ± SD (n = 5). Statistical significance was determined by two-tailed Student’s t test (B to H). *P < 0.05; **P < 0.01; ***P < 0.001.
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percentage of infiltrating CD45+ leukocytes in distant tumors increased significantly in the group of PTUN(+) plus PDL1 (35.80 ± 9.07%), compared with the PBS group (21.82 ± 6.61%) (Fig. 6E). Specifically, the proportion of CD8+ T cells (1.46 ± 0.75%) and CD4+ T cells (0.94 ± 0.40%) significantly increased in the PTUN(+) plus PDL1 group compared with the PBS group (CD8+ T cells, 0.52 ± 0.32%; CD4+ T cells, 0.34 ± 0.18%) (Fig. 6, F and G). Meanwhile, these positive responses led to the robust generation of immunoactivated cytokines including interferon (IFN) and tumor necrosis factor– (TNF), which play important roles in cytotoxic activities of cytotoxic T lymphocytes (Fig. 6H) (45). Together, PTUN–mediated PDT coupled with PDL1 treatment elicited potent systemic antitumor immune responses by promoting the infiltration of effector T cells.
DISCUSSIONAlthough nanotechnology holds great promise for controlled drug delivery since its demonstration for passive and active targeting, smarter systems with precise control over the anticancer response are urgently needed. In this work, we present a DNAbased nanodevice that permits tumor recognition and treatment with high spatialtemporal selectivity under the control of NIR light. UCNPs used here act as transducers to generate orthogonal UCL for the controlled operation of the nanodevice in the deep tissue–penetrable NIR window. We demonstrated that orthogonal regulation endows the nanodevice with spatiotemporalcontrolled biorecognition, enhanced tumor specificity, and robust antitumor efficacy. Furthermore, the nanodevice generated an immunogenic tumor microenvironment and significantly improved the efficacy of immune checkpoint blockade therapy. We envision that the design illustrated here would open up an avenue for cancer precision diagnosis and therapy.
On the other hand, UCNPs have recently been used for NIR light–induced, deeperpenetrating PDT, in which the UCL is absorbed by a PS that then converts tissue oxygen into ROS to eradicate cancer cells (32, 33). Despite the progress made, the lack of precise spatial control over such nanophotosensitizers is accompanied with offtumor phototoxicity. Our design allows conferring NIR light sensitivity to the biorecognition of the UCNPbased nanophotosensitizer to enable remote control of tumor targeting with high spatiotemporal precision and is, therefore, amenable to triggering of ROS generation at the right time and place. The present study highlights the potential of the integration of UCNPs with DNA nanotechnology for precision PDT.
MATERIALS AND METHODSPreparation of PT-UNOleatecapped UCNPs were synthesized with a thermal decomposition approach (32, 43). The assynthesized coremultishell UCNPs were first coated with mesoporous silica layer. Typically, 400 l of the asprepared UCNPs (25 nM) was slowly added to 20 ml of cetyltriethylammnonium bromide (CTAB) aqueous solution (5 mg ml−1), and the solution was stirred overnight. After adding ethanol (6 ml) and NaOH solution (2 M, 100 l), the mixture was heated to 60°C under stirring. Then, 80 l of TEOS (tetraethyl orthosilicate) was added to the mixture, and the resultant solution was stirred for 1 hour. One milliliter of ethanol solution containing 20 l of 3aminopropyltriethoxysilane was added dropwise. The mixture was stirred for 30 min, and the resulting particles were collected by centrifugation and washed three times with ethanol. The CTAB within the particles was removed by refluxing in am
monium chloride alcohol solution (2 mg ml−1) at 60°C for 2 hours. Next, the obtained UCNP@mSiO2 (0.05 nmol) was dispersed in the mixture of HEPES buffer (20 mM and 150 mM NaCl, pH 7.2) and dimethylformamide (DMF; v/v, 7:3) containing sulfosuccinimidyl 4(Nmaleimidomethyl) cyclohexane1carboxylate (sulfoSMCC) (4 mg). After shaking for 6 hours, the maleimideactivated UCNP@mSiO2 was collected by centrifugation and washed with DMF and the HEPES buffer. Subsequently, thiolmodified aptamer strands (10 nmol) activated by 1.5 equivalents of Tris (2carboxyethyl) phosphine (TCEP) were added to the HEPES buffer containing the maleimide modified UCNP@mSiO2. After shaking for 24 hours, the aptamer modified UCNPs were collected by centrifugation, washed, and redispersed in 1 ml of HEPES buffer containing RB (1 mg ml−1) for loading of RB in the mesopores. After shaking for 24 hours, the RBloaded particles were collected by centrifugation, washed, and added in 0.5 ml of hybridization buffer (20 mM HEPES, 150 mM NaCl, and 5 mM MgCl2) containing LHD (6 nmol). After incubation for 4 hours, the resulting PTUN was centrifuged, washed with the buffer three times, and redispersed in the buffer.
Singlet oxygen detectionTypically, PTUN (2 × 10−4 nmol) was added to a cuvette containing water solution of DPBF (1 ml, 10 M). The mixture was then irradiated with 808nm (0.5 W cm−2) or 980nm (1.0 W cm−2) NIR laser for different times, and the corresponding absorption spectra were measured immediately. The change in absorbance of DPBF at 415 nm as a function of irradiation time was used to evaluate the 1O2 generation ability.
Cell culture4T1 cells were purchased from the American Type Culture Collection (Manassas, VA) and cultured in RPMI 1640 supplemented with 10% fetal bovine serum (FBS), penicillin (100 U), and streptomycin (0.1 mg ml−1) in a 37°C humidified incubator containing 5% CO2.
Cellular uptake analysisFor CLSM imaging, 4T1 cells were seeded in 35mm confocal dishes at a density of ~1 × 105 cells per well overnight. Afterward, cells were washed twice with PBS and supplemented fresh Opti–minimum essential medium (MEM) containing 0.2 nM Cy5loaded PTUN, TUN, or nPTUN, followed with or without 808nm laser irradiation (0.5 W cm−2, 10 min). After incubation for another 1 hour, the cells were washed with PBS twice, stained with Hoechst 33342, and subjected for CLSM imaging. For flow cytometry analysis, cells were cultured in a sixwell plate at a density of ~2 × 105 cells per well, followed by the treatments with materials and irradiation as the same with those for CLSM imaging. The cells were washed with PBS twice, detached with 200 l of 0.25% trypsinEDTA solution, and resuspended in 300 l of PBS containing 1% FBS for flow cytometry assay.
Intracellular 1O2 detectionIntracellular 1O2 was detected by both CLSM imaging and flow cytometry analysis. 4T1 cells were plated onto 35mm confocal dishes (~1 × 105 cells per well, for CLSM imaging) or sixwell plates (~2 × 105 cells per well, for flow cytometry analysis) 24 hours in advance. Then, the growth medium was replaced with OptiMEM containing PTUN, TUN, or nPTUN (0.2 nM). For sequential irradiation, the cells were first irradiated by 808nm laser (0.5 W cm−2,
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10 min). After incubation for 2 hours in the dark, cells were washed with PBS twice to remove uninternalized materials. Fresh OptiMEM containing H2DCFDA (10 M) was added for another 30min incubation. Then, cells were irradiated with 980nm laser (1.0 W cm−2, 3min break after 1min irradiation) for 20 min. The treated cells were washed with PBS twice and collected for CLSM imaging or flow cytometry analysis.
Cell viability test4T1 cells (~2 × 104 cells per well, 100 l) were seeded in a 96well plate beforehand. When the confluence reached 70 to 80%, cells were exposed to PTUN, TUN, or nPTUN (0.2 nM), followed by the irradiation of 808nm laser (0.5 W cm−2, 10 min). After incubation for 2 hours, the cells were washed with PBS twice to remove uninternalized materials and then irradiated with 980nm laser (1.0 W cm−2, 3min break after 1min irradiation) for 20 min. Thereafter, cells were maintained at 37°C for another 24 hours. Last, cells were supplemented with 100 l of FBSfree RPMI 1640 containing 10% CCK8 1 hour after incubation, and absorbance at 450 nm was measured with the microplate reader.
Cell apoptosis assay4T1 cells were grown in a sixwell plate at a density of ~4 × 105 cells per well. After 24hour incubation, the growth medium was replaced with OptiMEM containing PTUN, TUN, or nPTUN (0.2 nM), followed by 808nm laser irradiation (0.5 W cm−2, 10 min). After incubation for 2 hours, cells were washed with PBS twice to remove uninternalized materials and then irradiated with 980nm laser (1.0 W cm−2, 3min break after 1min irradiation) for 20 min. The cells after treatment were stained with annexin V and PI using annexin V–APC/PI apoptosis detection kit according to the manufacturer’s instructions for flow cytometry analysis.
Live/dead cell costainingCells were plated on 35mm confocal dishes at a density of ~1 × 105 cells per well and treated with materials and irradiation as the same with that for cell apoptosis assay. Then, the cells were stained with calcein AM/PI doublestain kit under the instructions of the manufacturer for CLSM imaging.
Mice and tumor modelsAll the experiments were in accordance with the regulations of the Institutional Animal Care and Use Committee at the Chinese Academy of Sciences. BALB/c mice (female, ~20 g) were obtained from Beijing Vital River Laboratory Animal Technology Co. Ltd. 4T1 cells [~2 × 106 cells/100 l in 1:1 (v/v) PBS and Matrigel, BD bioscience] were inoculated subcutaneously for the establishment of tumor model. Imaging was performed when the tumors grew to 200 to 300 mm3, while the treatment started when the volume of tumors reached about 100 mm3. For the examination of the combination of PTUN and immune checkpoint blockade therapy, ~4 × 105 and ~ 1 × 105 4T1 cells were inoculated onto the left and the right flanks of BALB/c mice for the establishment of primary and secondary tumors, respectively.
In vivo imagingThe tumorbearing mice were intravenously injected with Cy5loaded PTUN, TUN, or nPTUN (1.5 nmol kg−1). Then, the tumor regions were irradiated by 808nm laser (0.5 W cm−2, 10 min) at 0, 1, and 2 hours after injection. Wholebody fluorescence images were
collected on an IVIS imaging system. At 24 hours after injection, main organs and tumors were excised and subjected for imaging.
Antitumor activity analysisMice bearing 4T1 tumors were randomly divided into eight groups (n = 5) for different treatments. PTUN or nPTUN was intravenously injected into mice at a dose of 1.25 nmol kg−1. For sequential irradiation with dual NIR light, tumor regions were irradiated with 808nm laser (0.5 W cm−2, 10 min) at 0, 1, and 2 hours after injection. At 4 hours after the last irradiation, tumor sites were further irradiated with 980nm laser (1.0 W cm−2, 3min break after 1min irradiation) for 20 min. Treatment was performed every 4 days for a total of two times. Body weight and tumor volume were recorded every other day. At the end of the experiment, mice were euthanized with tumors excised, weighed, and subjected for H&E and TUNEL staining.
Abscopal effect on bilateral tumor modelsBilateral 4T1 tumor–bearing mice were intravenously injected with PTUN (1.25 nmol kg−1) on days 8 and 12 after tumor inoculation. Sequential irradiation after each injection was performed, as described above. Anti–PDL1 (10 g per mouse) was intravenously administered on days 9, 13, 15, and 17. At the end of the experiment, mice were euthanized, with primary and distant tumors harvested and weighed. For the analysis of tumorinfiltrating T cells, distant tumors collected from different groups were cut into small pieces, disaggregated with collagenase I and DNase I at 37°C for 1 hour, and filtered through 75m mesh filters to obtain singlecell suspension. Cells were stained with fluorochromeconjugated antibodies to differentiate different T cells. For the evaluation of serum cytokines, mice serum was collected 20 days after the first treatment and was subjected for IFN and TNF measurement using corresponding enzymelinked immunosorbent assay kit according to the manufacturer’s instruction.
Statistical analysisData were expressed as means ± SD. Student’s t test was used for the comparison of difference between two groups, while oneway analysis of variance (ANOVA) was applied to evaluate the statistically significant difference of multiple groups. A P value of <0.05 was regarded statistically different. Both tests were carried out by SPSS 19.0 (SPSS Inc., Chicago, IL).
SUPPLEMENTARY MATERIALSSupplementary material for this article is available at http://advances.sciencemag.org/cgi/content/full/6/25/eaba9381/DC1
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Acknowledgments Funding: This work was supported financially by NSFC (grant nos. 21822401, 21805060, and 21771044) and the Young Thousand Talented Program. Author contributions: Z.D., Y.Z., and L.L. conceived and designed the experiments, Z.D., B.L., and J.Z. performed the experiments. Z.D., B.L., J.Z., Z.G., Y.Z., and L.L. analyzed the results. Z.D., Y.Z., and L.L wrote the paper. Y.Z. and L.L. supervised the entire project. Competing interests: The authors declare that they have no competing interests. Data and materials availability: All data needed to evaluate the conclusions in the paper are present in the paper and/or the Supplementary Materials. Additional data related to this paper may be requested from the authors.
Submitted 17 January 2020Accepted 4 May 2020Published 17 June 202010.1126/sciadv.aba9381
Citation: Z. Di, B. Liu, J. Zhao, Z. Gu, Y. Zhao, L. Li, An orthogonally regulatable DNA nanodevice for spatiotemporally controlled biorecognition and tumor treatment. Sci. Adv. 6, eaba9381 (2020).
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and tumor treatmentAn orthogonally regulatable DNA nanodevice for spatiotemporally controlled biorecognition
Zhenghan Di, Bei Liu, Jian Zhao, Zhanjun Gu, Yuliang Zhao and Lele Li
DOI: 10.1126/sciadv.aba9381 (25), eaba9381.6Sci Adv
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MATERIALSSUPPLEMENTARY http://advances.sciencemag.org/content/suppl/2020/06/15/6.25.eaba9381.DC1
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