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Immune cell membrane-coated nanoparticles for targeted myocardial ischemia/reperfusion injury therapy

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  • Corresponding author: darcy_pann@hotmail.com
    1. Immune cell membrane coating can endow nanoparticles with targeting ability.

      Cell membrane coating opens up a new field for myocardial ischemia therapy.

      The therapeutic effect of nanoparticles can be enhanced by cell membrane coating.

  • Acute myocardial infarction (MI) remains a serious disease causing lots of death and disability worldwide. Early and effective application of thrombolytic therapy or primary percutaneous coronary intervention (PCI) for myocardial reperfusion can reduce the size of MI. However, the process of recovering blood flow to the ischemic myocardium can lead to myocardial cell death, known as myocardial reperfusion injury. Due largely to the lack of therapeutic targeting and the complexity of cytokine interactions, there is still no effective treatment to protect the heart from myocardial ischemia/reperfusion injury (MIRI). Nanomedicine has always been at the forefront of medicine. However, nanoparticles (NPs) possess several limitations, such as poor targeting, biological stability, and ease of clearance by the immune system in vivo. Therefore, a method of immune cell membrane-coated NPs is proposed to solve these problems. Recently, the targeted treatment of diseases by cell membrane-encapsulated drugs has received increasing attention. The technical progress of immune cell membrane-coated NPs can realize the benefits of high targeting, high specificity, and low side effects on lesions and has great potential for treating MIRI. Herein, cell-derived membrane-coated nanosystems, their preparation process, and the applicability of these biomimetic systems in reducing MIRI injury are discussed. Finally, the prospects and challenges for their clinical translation are also introduced.
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  • [1] Yellon, D.M., and Hausenloy, D.J. (2007). Myocardial reperfusion injury. N. Engl. J. Med. 357: 1121-1135. DOI: 10.1056/NEJMra071667.

    View in Article Google Scholar

    [2] Hausenloy, D.J., and Yellon, D.M. (2013). Myocardial ischemia-reperfusion injury: A neglected therapeutic target. J. Clin. Invest. 123: 92−100. DOI: 10.1172/JCI62874.

    View in Article CrossRef Google Scholar

    [3] Heusch, G. (2015). Treatment of myocardial ischemia/reperfusion injury by ischemic and pharmacological postconditioning. Compr. Physiol. 5: 1123−1145. DOI: 10.1002/cphy.c140075.

    View in Article CrossRef Google Scholar

    [4] Zhang, H., Kim, H., Park, B.W., et al. (2022). CU06-1004 enhances vascular integrity and improves cardiac remodeling by suppressing edema and inflammation in myocardial ischemia-reperfusion injury. Exp. Mol. Med. 54: 23−34. DOI: 10.1038/s12276-021-00720-w.

    View in Article CrossRef Google Scholar

    [5] Marchant, D.J., Boyd, J.H., Lin, D.C., et al. (2012). Inflammation in myocardial diseases. Circ. Res. 110: 126−144. DOI: 10.1161/CIRCRESAHA.111.243170.

    View in Article CrossRef Google Scholar

    [6] Davidson, S.M., Ferdinandy, P., Andreadou, I., et al. (2019). Multitarget strategies to reduce myocardial ischemia/reperfusion injury: JACC review topic of the week. J. Am. Coll. Cardiol. 73: 89−99. DOI: 10.1016/j.jacc.2018.09.086.

    View in Article CrossRef Google Scholar

    [7] Yu, Y., Yan, Y., Niu, F., et al. (2021). Ferroptosis: A cell death connecting oxidative stress, inflammation and cardiovascular diseases. Cell Death Discov. 7: 193. DOI: 10.1038/s41420-021-00579-w.

    View in Article CrossRef Google Scholar

    [8] Cadenas, S. (2018). ROS and redox signaling in myocardial ischemia-reperfusion injury and cardioprotection. Free Radic. Biol. Med. 117: 76−89. DOI: 10.1016/j.freeradbiomed.2018.01.024.

    View in Article CrossRef Google Scholar

    [9] Kurian, G.A., Rajagopal, R., Vedantham, S., et al. (2016). The role of oxidative stress in myocardial ischemia and reperfusion injury and remodeling: Revisited. Oxid. Med. Cell. Longev. 2016: 1656450. DOI: 10.1155/2016/1656450.

    View in Article CrossRef Google Scholar

    [10] Liu, Y., Ai, K., Ji, X., et al. (2017). Comprehensive insights into the multi-antioxidative mechanisms of melanin nanoparticles and their application to protect brain from injury in ischemic stroke. J. Am. Chem. Soc. 139: 856−862. DOI: 10.1021/jacs.6b11013.

    View in Article CrossRef Google Scholar

    [11] Paradies, G., Paradies, V., Ruggiero, F.M., et al. (2018). Mitochondrial bioenergetics and cardiolipin alterations in myocardial ischemia-reperfusion injury: Implications for pharmacological cardioprotection. Am. J. Physiol. Heart Circ. Physiol. 315: H1341−H1352. DOI: 10.1152/ajpheart.00028.2018.

    View in Article CrossRef Google Scholar

    [12] Walters, A.M., Porter, G.A., Jr., and Brookes, P.S. (2012). Mitochondria as a drug target in ischemic heart disease and cardiomyopathy. Circ. Res. 111: 1222−1236. DOI: 10.1161/CIRCRESAHA.112.265660.

    View in Article CrossRef Google Scholar

    [13] Wang, R., Wang, M., He, S., et al. (2020). Targeting calcium homeostasis in myocardial ischemia/reperfusion injury: An overview of regulatory mechanisms and therapeutic reagents. Front. Pharmacol. 11: 872. DOI: 10.3389/fphar.2020.00872.

    View in Article CrossRef Google Scholar

    [14] Li, Y., Li, Q., and Fan, G.C. (2021). Macrophage efferocytosis in cardiac pathophysiology and repair. Shock 55: 177−188. DOI: 10.1097/SHK.0000000000001625.

    View in Article CrossRef Google Scholar

    [15] Doran, A.C., Yurdagul, A., Jr., and Tabas, I. (2020). Efferocytosis in health and disease. Nat. Rev. Immunol. 20: 254−267. DOI: 10.1038/s41577-019-0240-6.

    View in Article CrossRef Google Scholar

    [16] Prabhu, S.D., and Frangogiannis, N.G. (2016). The biological basis for cardiac repair after myocardial infarction: From inflammation to fibrosis. Circ. Res. 119: 91−112. DOI: 10.1161/CIRCRESAHA.116.303577.

    View in Article CrossRef Google Scholar

    [17] Hu, C.M., Fang, R.H., Copp, J., et al. (2013). A biomimetic nanosponge that absorbs pore-forming toxins. Nat. Nanotechnol. 8: 336−340. DOI: 10.1038/nnano.2013.54.

    View in Article CrossRef Google Scholar

    [18] Kechagia, J.Z., Ivaska, J., and Roca-Cusachs, P. (2019). Integrins as biomechanical sensors of the microenvironment. Nat. Rev. Mol. Cell Biol. 20: 457−473. DOI: 10.1038/s41580-019-0134-2.

    View in Article CrossRef Google Scholar

    [19] Hartman, N.C., and Groves, J.T. (2011). Signaling clusters in the cell membrane. Curr. Opin. Cell Biol. 23: 370−376. DOI: 10.1016/j.ceb.2011.05.003.

    View in Article CrossRef Google Scholar

    [20] Yu, J., Duong, V.H.H., Westphal, K., et al. (2018). Surface receptor Toso controls B cell-mediated regulation of T cell immunity. J. Clin. Invest. 128: 1820−1836. DOI: 10.1172/JCI97280.

    View in Article CrossRef Google Scholar

    [21] Park, J.H., Mohapatra, A., Zhou, J., et al. (2022). Virus-mimicking cell membrane-coated nanoparticles for cytosolic delivery of mRNA. Angew. Chem. Int. Ed. Engl. 61: e202113671. DOI: 10.1002/anie.202113671.

    View in Article CrossRef Google Scholar

    [22] Uchida, S., Perche, F., Pichon, C., et al. (2020). Nanomedicine-based approaches for mRNA delivery. Mol. Pharm. 17: 3654−3684. DOI: 10.1021/acs.molpharmaceut.0c00618.

    View in Article CrossRef Google Scholar

    [23] Weingart, J., Vabbilisetty, P., and Sun, X.L. (2013). Membrane mimetic surface functionalization of nanoparticles: Methods and applications. Adv. Colloid. Interface. Sci. 197-198: 68-84. DOI: 10.1016/j.cis.2013.04.003.

    View in Article Google Scholar

    [24] Kostina, N.Y., Rahimi, K., Xiao, Q., et al. (2019). Membrane-mimetic dendrimersomes engulf living bacteria via endocytosis. Nano. Lett. 19: 5732−5738. DOI: 10.1021/acs.nanolett.9b02349.

    View in Article CrossRef Google Scholar

    [25] Thamphiwatana, S., Angsantikul, P., Escajadillo, T., et al. (2017). Macrophage-like nanoparticles concurrently absorbing endotoxins and proinflammatory cytokines for sepsis management. Proc. Natl. Acad. Sci. U. S. A. 114: 11488−11493. DOI: 10.1073/pnas.1714267114.

    View in Article CrossRef Google Scholar

    [26] Kou, L., Bhutia, Y.D., Yao, Q., et al. (2018). Transporter-guided delivery of nanoparticles to improve drug permeation across cellular barriers and drug exposure to selective cell types. Front. Pharmacol. 9: 27. DOI: 10.3389/fphar.2018.00027.

    View in Article CrossRef Google Scholar

    [27] Blanco, E., Shen, H., and Ferrari, M. (2015). Principles of nanoparticle design for overcoming biological barriers to drug delivery. Nat. Biotechnol. 33: 941−951. DOI: 10.1038/nbt.3330.

    View in Article CrossRef Google Scholar

    [28] Li, M., Jin, X., Liu, T., et al. (2022). Nanoparticle elasticity affects systemic circulation lifetime by modulating adsorption of apolipoprotein A-I in corona formation. Nat. Commun. 13: 4137. DOI: 10.1038/s41467-022-31882-4.

    View in Article CrossRef Google Scholar

    [29] Mu, L., and Feng, S.S. (2003). A novel controlled release formulation for the anticancer drug paclitaxel (Taxol ): PLGA nanoparticles containing vitamin E TPGS. J. Control. Release 1: 33−48. DOI: 10.1016/s0168-3659(02)00320-6.

    View in Article CrossRef Google Scholar

    [30] Wang, Q., Song, Y., Chen, J., et al. (2021). Direct in vivo reprogramming with non-viral sequential targeting nanoparticles promotes cardiac regeneration. Biomaterials 276: 121028. DOI: 10.1016/j.biomaterials.2021.121028.

    View in Article CrossRef Google Scholar

    [31] Zhou, T., Yang, X., Wang, T., et al. (2022). Platelet-membrane-encapsulated carvedilol with improved targeting ability for relieving myocardial ischemia-reperfusion injury. Membranes (Basel) 12: 605. DOI: 10.3390/membranes12060605.

    View in Article CrossRef Google Scholar

    [32] Xu, H., Li, S., and Liu, Y.S. (2022). Nanoparticles in the diagnosis and treatment of vascular aging and related diseases. Signal Transduct. Target. Ther. 7: 231. DOI: 10.1038/s41392-022-01082-z.

    View in Article CrossRef Google Scholar

    [33] Reda, M., Ngamcherdtrakul, W., Nelson, M.A., et al. (2022). Development of a nanoparticle-based immunotherapy targeting PD-L1 and PLK1 for lung cancer treatment. Nat. Commun. 13: 4261. DOI: 10.1038/s41467-022-31926-9.

    View in Article CrossRef Google Scholar

    [34] Furtado, D., Björnmalm, M., Ayton, S., et al. (2018). Overcoming the blood-brain barrier: The role of nanomaterials in treating neurological diseases. Adv. Mater. 30: e1801362. DOI: 10.1002/adma.201801362.

    View in Article CrossRef Google Scholar

    [35] Kasina, V., Mownn, R.J., Bahal, R., et al. (2022). Nanoparticle delivery systems for substance use disorder. Neuropsychopharmacology 47: 1431−1439. DOI: 10.1038/s41386-022-01311-7.

    View in Article CrossRef Google Scholar

    [36] Foged, C., Brodin, B., Frokjaer, S., et al. (2005). Particle size and surface charge affect particle uptake by human dendritic cells in an in vitro model. Int. J. Pharm. 298: 315−322. DOI: 10.1016/j.ijpharm.2005.03.035.

    View in Article CrossRef Google Scholar

    [37] Kumari, A., Yadav, S.K., and Yadav, S.C. (2010). Biodegradable polymeric nanoparticles based drug delivery systems. Colloids Surf. B Biointerfaces 75: 1−18. DOI: 10.1016/j.colsurfb.2009.09.001.

    View in Article CrossRef Google Scholar

    [38] Tokatlian, T., and Segura, T. (2010). siRNA applications in nanomedicine. Wiley interdisciplinary reviews. Nanomed. Nanobiotechnol. 2: 305−315. DOI: 10.1002/wnan.81.

    View in Article CrossRef Google Scholar

    [39] Tang, J., Baxter, S., Menon, A., et al. (2016). Immune cell screening of a nanoparticle library improves atherosclerosis therapy. Proc. Natl. Acad. Sci. U. S. A. 113: E6731−e6740. DOI: 10.1073/pnas.1601537113.

    View in Article CrossRef Google Scholar

    [40] Chen, W., Schilperoort, M., Cao, Y., et al. (2022). Macrophage-targeted nanomedicine for the diagnosis and treatment of atherosclerosis. Nat.Rev. Cardiol. 19: 228−249. DOI: 10.1038/s41569-021-00629-x.

    View in Article CrossRef Google Scholar

    [41] Dos Santos Rodrigues, B., Oue, H., Banerjee, A., et al. (2018). Dual functionalized liposome-mediated gene delivery across triple co-culture blood brain barrier model and specific in vivo neuronal transfection. J. Control Release 286: 264−278. DOI: 10.1016/j.jconrel.2018.07.043.

    View in Article CrossRef Google Scholar

    [42] Ouyang, C., Choice, E., Holland, J., et al. (1995). Liposomal cyclosporine. Characterization of drug incorporation and interbilayer exchange. Transplantation 60: 999−1006.

    View in Article Google Scholar

    [43] Fonseca-Santos, B., Gremião, M.P., and Chorilli, M. (2015). Nanotechnology-based drug delivery systems for the treatment of Alzheimer's disease. Int. J. Nanomedicine 10: 4981−5003. DOI: 10.2147/IJN.S87148.

    View in Article CrossRef Google Scholar

    [44] Sercombe, L., Veerati, T., Moheimani, F., et al. (2015). Advances and challenges of liposome assisted drug delivery. Front. Pharmacol. 6: 286. DOI: 10.3389/fphar.2015.00286.

    View in Article CrossRef Google Scholar

    [45] Allen, C., and Evans, J.C. (2020). ‘Hip to be square’: Designing PLGA formulations for the future. J. Control. Release 319: 487−488. DOI: 10.1016/j.jconrel.2020.01.050.

    View in Article CrossRef Google Scholar

    [46] Fonseca, C., Simões, S., and Gaspar, R. (2002). Paclitaxel-loaded PLGA nanoparticles preparation,physicochemical characterization and in vitro anti-tumoral activity. J. Control. Release 83: 273−286. DOI: 10.1016/S0168-3659(02)00212-2.

    View in Article CrossRef Google Scholar

    [47] Budhian, A., Siegel, S.J., and Winey, K.I. (2008). Controlling the in vitro release profiles for a system of haloperidol-loaded PLGA nanoparticles. Int. J. Pharm. 346: 151−159. DOI: 10.1016/j.ijpharm.2007.06.011.

    View in Article CrossRef Google Scholar

    [48] Iwasaki, Y., Maie, H., and Akiyoshi, K. (2007). Cell-specific delivery of polymeric nanoparticles to carbohydrate-tagging cells. Biomacromolecules 8: 3162−3168. DOI: 10.1021/bm700606z.

    View in Article CrossRef Google Scholar

    [49] Park, K., Skidmore, S., Hadar, J., et al. (2019). Injectable, long-acting PLGA formulations: Analyzing PLGA and understanding microparticle formation. J. Control. Release 304: 125−134. DOI: 10.1016/j.jconrel.2019.05.003.

    View in Article CrossRef Google Scholar

    [50] Tamada, J.A., and Langer, R. (1993). Erosion kinetics of hydrolytically degradable polymers. Proc. Natl. Acad. Sci. U. S. A. 90: 552−556. DOI: 10.1073/pnas.90.2.552.

    View in Article CrossRef Google Scholar

    [51] von Burkersroda, F., Schedl, L., and Gopferich, A. (2002). Why degradable polymers undergo surface erosion or bulk erosion. Biomaterials 23: 4221−4231. DOI: 10.1016/S0142-9612(02)00170-9.

    View in Article CrossRef Google Scholar

    [52] Kashi, T.S., Eskandarion, S., Esfandyari-Manesh, M., et al. (2012). Improved drug loading and antibacterial activity of minocycline-loaded PLGA nanoparticles prepared by solid/oil/water ion pairing method. Int. J. Nanomedicine 7: 221−234. DOI: 10.2147/IJN.S27709.

    View in Article CrossRef Google Scholar

    [53] Tosi, G., Costantino, L., Rivasi, F., et al. (2007). Targeting the central nervous system: in vivo experiments with peptide-derivatized nanoparticles loaded with Loperamide and Rhodamine-123. J. Control. Release 122: 1−9. DOI: 10.1016/j.jconrel.2007.05.022.

    View in Article CrossRef Google Scholar

    [54] Panyam, J., and Labhasetwar, V. (2003). Biodegradable nanoparticles for drug and gene delivery to cells and tissue. Adv. Drug Deliv. Rev. 55: 329−347. DOI: 10.1016/S0169-409X(02)00228-4.

    View in Article CrossRef Google Scholar

    [55] Fu, K., Pack, D.W., Klibanov, A.M., et al. (2000). Visual evidence of acidic environment within degrading poly(lactic-co-glycolic acid) (PLGA) microspheres. Pharm. Res. 17: 100−106. DOI: 10.1023/A:1007582911958.

    View in Article CrossRef Google Scholar

    [56] Pandita, D., Kumar, S., and Lather, V. (2015). Hybrid poly(lactic-co-glycolic acid) nanoparticles: design and delivery prospectives. Drug Discov. Today 20: 95−104. DOI: 10.1016/j.drudis.2014.09.018.

    View in Article CrossRef Google Scholar

    [57] Riffault, M., Six, J.L., Netter, P., et al. (2015). PLGA-based nanoparticles: A safe and suitable delivery platform for osteoarticular pathologies. Pharm. Res. 32: 3886−3898. DOI: 10.1007/s11095-015-1748-5.

    View in Article CrossRef Google Scholar

    [58] Zhang, C.X., Cheng, Y., Liu, D.Z., et al. (2019). Mitochondria-targeted cyclosporin A delivery system to treat myocardial ischemia reperfusion injury of rats. J. Nanobiotechnology 17: 18. DOI: 10.1186/s12951-019-0451-9.

    View in Article CrossRef Google Scholar

    [59] Millstone, J.E., Hurst, S.J., Metraux, G.S., et al. (2009). Colloidal gold and silver triangular nanoprisms. Small 5: 646−664. DOI: 10.1002/smll.200801480.

    View in Article CrossRef Google Scholar

    [60] Lee, S.H., Rho, W.Y., Park, S.J., et al. (2018). Multifunctional self-assembled monolayers via microcontact printing and degas-driven flow guided patterning. Sci. Rep. 8: 16763. DOI: 10.1038/s41598-018-35195-9.

    View in Article CrossRef Google Scholar

    [61] Lee, S.H., Sung, J.H., and Park, T.H. (2012). Nanomaterial-based biosensor as an emerging tool for biomedical applications. Ann. Biomed. Eng. 40: 1384−1397. DOI: 10.1007/s10439-011-0457-4.

    View in Article CrossRef Google Scholar

    [62] Cao, Y.C., Jin, R., and Mirkin, C.A. (2002). Nanoparticles with Raman spectroscopic fingerprints for DNA and RNA detection. Science 297: 1536−1540. DOI: 10.1126/science.297.5586.1536.

    View in Article CrossRef Google Scholar

    [63] Haes, A.J., Chang, L., Klein, W.L., et al. (2005). Detection of a biomarker for Alzheimer’s disease from synthetic and clinical samples using a nanoscale optical biosensor. J. Am. Chem. Soc. 1: 2264−2271. DOI: 10.1021/ja044087q.

    View in Article CrossRef Google Scholar

    [64] Georganopoulou, D.G., Chang, L., Nam, J.M., et al. (2005). Nanoparticle-based detection in cerebral spinal fluid of a soluble pathogenic biomarker for Alzheimer’s disease. Proc. Natl. Acad. Sci. U. S. A. 102: 2273−2276. DOI: 10.1073/pnas.0409336102.

    View in Article CrossRef Google Scholar

    [65] Taton, T.A., Mirkin, C.A., and Letsinger, R.L. (2000). Scanometric DNA array detection with nanoparticle probes. Science 289: 1757−1760. DOI: 10.1126/science.289.5485.1757.

    View in Article CrossRef Google Scholar

    [66] Park, S.J., Taton, T.A., and Mirkin, C.A. (2002). Array-based electrical detection of DNA with nanoparticle probes. Science 295: 1503−1506. DOI: 10.1126/science.1067003.

    View in Article CrossRef Google Scholar

    [67] Astruc, D., Lu, F., and Aranzaes, J.R. (2005). Nanoparticles as recyclable catalysts: The frontier between homogeneous and heterogeneous catalysis. Angew. Chem. Int. Ed. Engl. 44: 7852−7872. DOI: 10.1002/anie.200500766.

    View in Article CrossRef Google Scholar

    [68] Rosi, N.L., Giljohann, D.A., Thaxton, C.S., et al. (2006). Oligonucleotide-modified gold nanoparticles for intracellular gene regulation. Science 312: 1027−1030. DOI: 10.1126/science.1125559.

    View in Article CrossRef Google Scholar

    [69] Hood, J.D., Bednarski, M., Frausto, R., et al. (2002). Tumor regression by targeted gene delivery to the neovasculature. Science 296: 2404−2407. DOI: 10.1126/science.1070200.

    View in Article CrossRef Google Scholar

    [70] Brannon-Peppas, L., and Blanchette, J.O. (2004). Nanoparticle and targeted systems for cancer therapy. Adv. Drug Deliv. Rev. 56: 1649−1659. DOI: 10.1016/j.addr.2004.02.014.

    View in Article CrossRef Google Scholar

    [71] Arias, L.S., Pessan, J.P., Vieira, A.P.M., et al. (2018). Iron oxide nanoparticles for biomedical applications: A perspective on synthesis, drugs, antimicrobial activity, and toxicity. Antibiotics (Basel) 7: 46. DOI: 10.3390/antibiotics7020046.

    View in Article CrossRef Google Scholar

    [72] Manshian, B.B., Jimenez, J., Himmelreich, U., et al. (2017). Personalized medicine and follow-up of therapeutic delivery through exploitation of quantum dot toxicity. Biomaterials 127: 1−12. DOI: 10.1016/j.biomaterials.2017.02.039.

    View in Article CrossRef Google Scholar

    [73] Duncan, B., Kim, C., and Rotello, V.M. (2010). Gold nanoparticle platforms as drug and biomacromolecule delivery systems. J. Control. Release 148: 122−127. DOI: 10.1016/j.jconrel.2010.06.004.

    View in Article CrossRef Google Scholar

    [74] Gibson, J.D., Khanal, B.P., and Zubarev, E.R. (2007). Paclitaxel-functionalized gold nanoparticles. J. Am. Che. Soc. 129: 11653-11661. DOI: 10.1021/ja075181k.

    View in Article Google Scholar

    [75] Wu, R., Peng, H., Zhu, J.J., et al. (2020). Attaching DNA to gold nanoparticles with a protein corona. Front. Chem. 8: 121. DOI: 10.3389/fchem.2020.00121.

    View in Article CrossRef Google Scholar

    [76] Kumar, A., Vemula, P.K., Ajayan, P.M., et al. (2008). Silver-nanoparticle-embedded antimicrobial paints based on vegetable oil. Nat. Mater. 7: 236−241. DOI: 10.1038/nmat2099.

    View in Article CrossRef Google Scholar

    [77] Desireddy, A., Conn, B.E., Guo, J., et al. (2013). Ultrastable silver nanoparticles. Nature 501: 399−402. DOI: 10.1038/nature12523.

    View in Article CrossRef Google Scholar

    [78] Atwater, H.A., and Polman, A. (2010). Plasmonics for improved photovoltaic devices. Nat. Mater. 9: 205−213. DOI: 10.1038/nmat2629.

    View in Article CrossRef Google Scholar

    [79] Yan, Y., Yang, C., Dai, G., et al. (2021). Folic acid-conjugated CuFeSe2 nanoparticles for targeted T2-weighted magnetic resonance imaging and computed tomography of tumors in vivo. Int. J. Nanomedicine 16: 6429−6440. DOI: 10.2147/IJN.S320277.

    View in Article CrossRef Google Scholar

    [80] Blakney, A.K., Zhu, Y., McKay, P.F., et al. (2020). Big is beautiful: Enhanced saRNA delivery and immunogenicity by a higher molecular weight, bioreducible, cationic polymer. ACS Nano 14: 5711−5727. DOI: 10.1021/acsnano.0c00326.

    View in Article CrossRef Google Scholar

    [81] Li, Y., Che, J., Chang, L., et al. (2022). CD47- and integrin alpha4/beta1-comodified-macrophage-membrane-coated nanoparticles enable delivery of colchicine to atherosclerotic plaque. Adv. Healthc. Mater. 11: e2101788. DOI: 10.1002/adhm.202101788.

    View in Article CrossRef Google Scholar

    [82] Wang, Y., Zhang, K., Li, T., et al. (2021). Macrophage membrane functionalized biomimetic nanoparticles for targeted anti-atherosclerosis applications. Theranostics 11: 164−180. DOI: 10.7150/thno.47841.

    View in Article CrossRef Google Scholar

    [83] Shin, M.J., Park, J.Y., Lee, D.H., et al. (2021). Stem cell mimicking nanoencapsulation for targeting arthritis. Int. J. Nanomedicine 16: 8485−8507. DOI: 10.2147/IJN.S334298.

    View in Article CrossRef Google Scholar

    [84] Furtado, D., Bjornmalm, M., Ayton, S., et al. (2018). Overcoming the blood-brain barrier: The role of nanomaterials in treating neurological diseases. Adv. Mater. 30: e1801362. DOI: 10.1002/adma.201801362.

    View in Article CrossRef Google Scholar

    [85] Jiang, Q., Liu, Y., Guo, R., et al. (2019). Erythrocyte-cancer hybrid membrane-camouflaged melanin nanoparticles for enhancing photothermal therapy efficacy in tumors. Biomaterials 192: 292−308. DOI: 10.1016/j.biomaterials.2018.11.021.

    View in Article CrossRef Google Scholar

    [86] Song, Y., Huang, Z., Liu, X., et al. (2019). Platelet membrane-coated nanoparticle-mediated targeting delivery of Rapamycin blocks atherosclerotic plaque development and stabilizes plaque in apolipoprotein E-deficient (ApoE(-/-)) mice. Nanomedicine 15: 13−24. DOI: 10.1016/j.nano.2018.08.002.

    View in Article CrossRef Google Scholar

    [87] Ross, K.A., Brenza, T.M., Binnebose, A.M., et al. (2015). Nano-enabled delivery of diverse payloads across complex biological barriers. J. Control. Release 219: 548−559. DOI: 10.1016/j.jconrel.2015.08.039.

    View in Article CrossRef Google Scholar

    [88] Parodi, A., Quattrocchi, N., van de Ven, A.L., et al. (2013). Synthetic nanoparticles functionalized with biomimetic leukocyte membranes possess cell-like functions. Nat. Nanotechnol. 8: 61−68. DOI: 10.1038/nnano.2012.212.

    View in Article CrossRef Google Scholar

    [89] Hu, C.M., Zhang, L., Aryal, S., et al. (2011). Erythrocyte membrane-camouflaged polymeric nanoparticles as a biomimetic delivery platform. Proc. Natl. Acad. Sci. U. S. A. 108: 10980−10985. DOI: 10.1073/pnas.1106634108.

    View in Article CrossRef Google Scholar

    [90] Oroojalian, F., Beygi, M., Baradaran, B., et al. (2021). Immune cell membrane-coated biomimetic nanoparticles for targeted cancer therapy. Small 17: e2006484. DOI: 10.1002/smll.202006484.

    View in Article CrossRef Google Scholar

    [91] Choi, B., Park, W., Park, S.B., et al. (2020). Recent trends in cell membrane-cloaked nanoparticles for therapeutic applications. Methods 177: 2−14. DOI: 10.1016/j.ymeth.2019.12.004.

    View in Article CrossRef Google Scholar

    [92] Hu, C.M., Fang, R.H., Wang, K.C., et al. (2015). Nanoparticle biointerfacing by platelet membrane cloaking. Nature 526: 118−121. DOI: 10.1038/nature15373.

    View in Article CrossRef Google Scholar

    [93] Wei, X., Gao, J., Wang, F., et al. (2017). In situ capture of bacterial toxins for antivirulence vaccination. Adv. Mater. 29: 1701644. DOI: 10.1002/adma.201701644.

    View in Article CrossRef Google Scholar

    [94] Dehaini, D., Wei, X., Fang, R.H., et al. (2017). Erythrocyte-platelet hybrid membrane coating for enhanced nanoparticle functionalization. Adv. Mater. 29: 1606209. DOI: 10.1002/adma.201606209.

    View in Article CrossRef Google Scholar

    [95] Rao, L., Cai, B., Bu, L.L., et al. (2017). Microfluidic electroporation-facilitated synthesis of erythrocyte membrane-coated magnetic nanoparticles for enhanced imaging-guided cancer therapy. ACS Nano 11: 3496−3505. DOI: 10.1021/acsnano.7b00133.

    View in Article CrossRef Google Scholar

    [96] Hasler, P., Giaglis, S., and Hahn, S. (2016). Neutrophil extracellular traps in health and disease. Swiss Med. Wkly. 146: w14352. DOI: 10.4414/smw.2016.14352.

    View in Article CrossRef Google Scholar

    [97] Molinaro, R., Corbo, C., Martinez, J.O., et al. (2016). Biomimetic proteolipid vesicles for targeting inflamed tissues. Nat. Mater. 15: 1037−1046. DOI: 10.1038/nmat4644.

    View in Article CrossRef Google Scholar

    [98] Dunlay, S.M., Weston, S.A., Redfield, M.M., et al. (2008). Tumor necrosis factor-alpha and mortality in heart failure: A community study. Circulation 118: 625−631. DOI: 10.1161/CIRCULATIONAHA.107.759191.

    View in Article CrossRef Google Scholar

    [99] Frangogiannis, N.G., Smith, C.W., and Entman, M.L. (2002). The inflammatory response in myocardial infarction. Cardiovasc. Res. 53: 31−47. DOI: 10.1016/S0008-6363(01)00434-5.

    View in Article CrossRef Google Scholar

    [100] Beekhuizen, H., and van Furth, R. (1993). Monocyte adherence to human vascular endothelium. J. Leukoc. Biol. 54: 363−378. DOI: 10.1002/jlb.54.4.363.

    View in Article CrossRef Google Scholar

    [101] Imhof, B.A., and Aurrand-Lions, M. (2004). Adhesion mechanisms regulating the migration of monocytes. Nat. Rev. Immunol. 4: 432−444. DOI: 10.1038/nri1375.

    View in Article CrossRef Google Scholar

    [102] Sarma, J., Laan, C.A., Alam, S., et al. (2002). Increased platelet binding to circulating monocytes in acute coronary syndromes. Circulation 105: 2166−2171. DOI: 10.1161/01.CIR.0000015700.27754.6F.

    View in Article CrossRef Google Scholar

    [103] An, G., Wang, H., Tang, R., et al. (2008). P-selectin glycoprotein ligand-1 is highly expressed on Ly-6Chi monocytes and a major determinant for Ly-6Chi monocyte recruitment to sites of atherosclerosis in mice. Circulation 117: 3227−3237. DOI: 10.1161/CIRCULATIONAHA.108.771048.

    View in Article CrossRef Google Scholar

    [104] Huo, Y., Schober, A., Forlow, S.B., et al. (2003). Circulating activated platelets exacerbate atherosclerosis in mice deficient in apolipoprotein E. Nat. Med. 9: 61−67. DOI: 10.1038/nm810.

    View in Article CrossRef Google Scholar

    [105] Nahrendorf, M., Swirski, F.K., Aikawa, E., et al. (2007). The healing myocardium sequentially mobilizes two monocyte subsets with divergent and complementary functions. J. Exp. Med. 204: 3037−3047. DOI: 10.1084/jem.20070885.

    View in Article CrossRef Google Scholar

    [106] van der Laan, A.M., Ter Horst, E.N., Delewi, R., et al. (2014). Monocyte subset accumulation in the human heart following acute myocardial infarction and the role of the spleen as monocyte reservoir. Eur. Heart J. 35: 376−385. DOI: 10.1093/eurheartj/eht331.

    View in Article CrossRef Google Scholar

    [107] Honold, L., and Nahrendorf, M. (2018). Resident and monocyte-derived macrophages in cardiovascular disease. Circ. Res. 122: 113−127. DOI: 10.1161/CIRCRESAHA.117.311071.

    View in Article CrossRef Google Scholar

    [108] Dick, S.A., Macklin, J.A., Nejat, S., et al. (2019). Self-renewing resident cardiac macrophages limit adverse remodeling following myocardial infarction. Nat. Immunol. 20: 29−39. DOI: 10.1038/s41590-018-0272-2.

    View in Article CrossRef Google Scholar

    [109] Yan, X., Anzai, A., Katsumata, Y., et al. (2013). Temporal dynamics of cardiac immune cell accumulation following acute myocardial infarction. J. Mol. Cell. Cardiol. 62: 24−35. DOI: 10.1016/j.yjmcc.2013.04.023.

    View in Article CrossRef Google Scholar

    [110] Cao, D.J., Schiattarella, G.G., Villalobos, E., et al. (2018). Cytosolic DNA sensing promotes macrophage transformation and governs myocardial ischemic injury. Circulation 137: 2613−2634. DOI: 10.1161/CIRCULATIONAHA.117.031046.

    View in Article CrossRef Google Scholar

    [111] Yan, X., Zhang, H., Fan, Q., et al. (2017). Dectin-2 deficiency modulates Th1 differentiation and improves wound healing after myocardial infarction. Circ. Res. 120: 1116−1129. DOI: 10.1161/CIRCRESAHA.116.310260.

    View in Article CrossRef Google Scholar

    [112] Fan, Q., Tao, R., Zhang, H., et al. (2019). Dectin-1 contributes to myocardial ischemia/reperfusion injury by regulating macrophage polarization and neutrophil infiltration. Circulation 139: 663−678. DOI: 10.1161/CIRCULATIONAHA.118.036044.

    View in Article CrossRef Google Scholar

    [113] Zhang, N., Song, Y., Huang, Z., et al. (2020). Monocyte mimics improve mesenchymal stem cell-derived extracellular vesicle homing in a mouse MI/RI model. Biomaterials 255: 120168. DOI: 10.1016/j.biomaterials.2020.120168.

    View in Article CrossRef Google Scholar

    [114] Ong, S.G., and Wu, J.C. (2015). Exosomes as potential alternatives to stem cell therapy in mediating cardiac regeneration. Circ. Res. 117: 7−9. DOI: 10.1161/CIRCRESAHA.115.306593.

    View in Article CrossRef Google Scholar

    [115] Kishore, R., and Khan, M. (2016). More than tiny sacks: Stem cell exosomes as cell-free modality for cardiac repair. Circ. Res. 118: 330−343. DOI: 10.1161/CIRCRESAHA.115.307654.

    View in Article CrossRef Google Scholar

    [116] Zhao, J., Li, X., Hu, J., et al. (2019). Mesenchymal stromal cell-derived exosomes attenuate myocardial ischaemia-reperfusion injury through miR-182-regulated macrophage polarization. Cardiovasc. Res. 115: 1205−1216. DOI: 10.1093/cvr/cvz040.

    View in Article CrossRef Google Scholar

    [117] Xue, Y., Zeng, G., Cheng, J., et al. (2021). Engineered macrophage membrane-enveloped nanomedicine for ameliorating myocardial infarction in a mouse model. Bioeng. Transl. Med. 6: e10197. DOI: 10.1002/btm2.10197.

    View in Article CrossRef Google Scholar

    [118] Lesizza, P., Prosdocimo, G., Martinelli, V., et al. (2017). Single-dose intracardiac injection of pro-regenerative microRNAs improves cardiac function after myocardial infarction. Circ. Res. 120: 1298−1304. DOI: 10.1161/CIRCRESAHA.116.309589.

    View in Article CrossRef Google Scholar

    [119] Yang, H., Qin, X., Wang, H., et al. (2019). An in vivo miRNA delivery system for restoring infarcted myocardium. ACS Nano 13: 9880−9894. DOI: 10.1021/acsnano.9b03343.

    View in Article CrossRef Google Scholar

    [120] Summers, C., Rankin, S.M., Condliffe, A.M., et al. (2010). Neutrophil kinetics in health and disease. Trends. Immunol. 31: 318−324. DOI: 10.1016/j.it.2010.05.006.

    View in Article CrossRef Google Scholar

    [121] Horckmans, M., Ring, L., Duchene, J., et al. (2017). Neutrophils orchestrate post-myocardial infarction healing by polarizing macrophages towards a reparative phenotype. Eur. Heart J. 38: 187−197. DOI: 10.1093/eurheartj/ehw002.

    View in Article CrossRef Google Scholar

    [122] Han, D., Wang, F., Qiao, Z., et al. (2023). Neutrophil membrane-camouflaged nanoparticles alleviate inflammation and promote angiogenesis in ischemic myocardial injury. Bioact. Mater. 23: 369−382. DOI: 10.1016/j.bioactmat.2022.11.016.

    View in Article CrossRef Google Scholar

    [123] Melo, R.C., Liu, L., Xenakis, J.J., et al. (2013). Eosinophil-derived cytokines in health and disease: Unraveling novel mechanisms of selective secretion. Allergy 68: 274−284. DOI: 10.1111/all.12103.

    View in Article CrossRef Google Scholar

    [124] Gieseck, R.L., 3rd, Wilson, M.S., and Wynn, T.A. (2018). Type 2 immunity in tissue repair and fibrosis. Nat. Rev. Immunol. 18: 62−76. DOI: 10.1038/nri.2017.90.

    View in Article CrossRef Google Scholar

    [125] Liu, J., Yang, C., Liu, T., et al. (2020). Eosinophils improve cardiac function after myocardial infarction. Nat. Commun. 11: 6396. DOI: 10.1038/s41467-020-19297-5.

    View in Article CrossRef Google Scholar

    [126] Kandikattu, H.K., Upparahalli Venkateshaiah, S., and Mishra, A. (2019). Synergy of Interleukin (IL)-5 and IL-18 in eosinophil mediated pathogenesis of allergic diseases. Cytokine Growth Factor Rev. 47: 83−98. DOI: 10.1016/j.cytogfr.2019.05.003.

    View in Article CrossRef Google Scholar

    [127] Bird., L. (2004). Linking arms key role for IL-5. Nat. Rev. Immunol. 114: 427−437. DOI: 10.1038/nri1454.

    View in Article CrossRef Google Scholar

    [128] Chen, J., Song, Y., Wang, Q., et al. (2022). Targeted neutrophil-mimetic liposomes promote cardiac repair by adsorbing proinflammatory cytokines and regulating the immune microenvironment. J. Nanobiotechnology 20: 218. DOI: 10.1186/s12951-022-01433-6.

    View in Article CrossRef Google Scholar

    [129] Quach, M.E., Chen, W., and Li, R. (2018). Mechanisms of platelet clearance and translation to improve platelet storage. Blood 131: 1512−1521. DOI: 10.1182/blood-2017-08-743229.

    View in Article CrossRef Google Scholar

    [130] van der Meijden, P.E.J., and Heemskerk, J.W.M. (2019). Platelet biology and functions: new concepts and clinical perspectives. Nat. Rev. Cardiol. 16: 166−179. DOI: 10.1038/s41569-018-0110-0.

    View in Article CrossRef Google Scholar

    [131] Benkel, T., Zimmermann, M., Zeiner, J., et al. (2022). How Carvedilol activates beta(2)-adrenoceptors. Nat. Commun. 13: 7109. DOI: 10.1038/s41467-022-34765-w.

    View in Article CrossRef Google Scholar

    [132] Chen, Z., Wu, Y., Duan, J., et al. (2019). Carvedilol exerts myocardial protection via regulation of AMPK-mTOR-dependent autophagy. Biomed. Pharmacother. 118: 109283. DOI: 10.1016/j.biopha.2019.109283.

    View in Article CrossRef Google Scholar

    [133] Hayashi, T., De Velasco, M.A., Saitou, Y., et al. (2010). Carvedilol protects tubular epithelial cells from ischemia-reperfusion injury by inhibiting oxidative stress. Int. J. Urol. 17: 989−995. DOI: 10.1111/j.1442-2042.2010.02644.x.

    View in Article CrossRef Google Scholar

    [134] Park, K.M., Teoh, J.P., Wang, Y., et al. (2016). Carvedilol-responsive microRNAs, miR-199a-3p and -214 protect cardiomyocytes from simulated ischemia-reperfusion injury. Am. J. Physiol. Heart Circ. Physiol. 311: H371−383. DOI: 10.1152/ajpheart.00807.2015.

    View in Article CrossRef Google Scholar

    [135] Harima, M., Arumugam, S., Wen, J., et al. (2015). Effect of carvedilol against myocardial injury due to ischemia-reperfusion of the brain in rats. Exp. Mol. Pathol. 98: 558−562. DOI: 10.1016/j.yexmp.2015.04.001.

    View in Article CrossRef Google Scholar

    [136] Weng, X., Tan, H., Huang, Z., et al. (2022). Targeted delivery and ROS-responsive release of Resolvin D1 by platelet chimeric liposome ameliorates myocardial ischemia-reperfusion injury. J. Nanobiotechnology 20: 454. DOI: 10.1186/s12951-022-01652-x.

    View in Article CrossRef Google Scholar

    [137] Tan, H., Song, Y., Chen, J., et al. (2021). Platelet-like fusogenic liposome-mediated targeting delivery of miR-21 improves myocardial remodeling by reprogramming macrophages post myocardial ischemia-reperfusion injury. Adv. Sci. (Weinh). 8: e2100787. DOI: 10.1002/advs.202100787.

    View in Article CrossRef Google Scholar

    [138] Serhan, C.N. (2014). Pro-resolving lipid mediators are leads for resolution physiology. Nature 510: 92−101. DOI: 10.1038/nature13479.

    View in Article CrossRef Google Scholar

    [139] Sun, Y.P., Oh, S.F., Uddin, J., et al. (2007). Resolvin D1 and its aspirin-triggered 17R epimer. Stereochemical assignments, anti-inflammatory properties, and enzymatic inactivation. J. Biol. Chem. 282: 9323−9334. DOI: 10.1074/jbc.M609212200.

    View in Article CrossRef Google Scholar

    [140] Krishnamoorthy, S., Recchiuti, A., Chiang, N., et al. (2010). Resolvin D1 binds human phagocytes with evidence for proresolving receptors. Proc. Natl. Acad. Sci. U. S. A. 107: 1660−1665. DOI: 10.1073/pnas.0907342107.

    View in Article CrossRef Google Scholar

    [141] Gerlach, B.D., Marinello, M., Heinz, J., et al. (2020). Resolvin D1 promotes the targeting and clearance of necroptotic cells. Cell Death Differ. 27: 525−539. DOI: 10.1038/s41418-019-0370-1.

    View in Article CrossRef Google Scholar

    [142] Sansbury, B.E., and Spite, M. (2016). Resolution of acute inflammation and the role of resolvins in immunity, thrombosis, and vascular biology. Circ. Res. 119: 113−130. DOI: 10.1161/CIRCRESAHA.116.307308.

    View in Article CrossRef Google Scholar

    [143] Fredman, G., Ozcan, L., Spolitu, S., et al. (2014). Resolvin D1 limits 5-lipoxygenase nuclear localization and leukotriene B4 synthesis by inhibiting a calcium-activated kinase pathway. Proc. Natl. Acad. Sci. U. S. A. 111: 14530−14535. DOI: 10.1073/pnas.1410851111.

    View in Article CrossRef Google Scholar

    [144] Wang, T., Zhou, T., Xu, M., et al. (2022). Platelet membrane-camouflaged nanoparticles carry microRNA inhibitor against myocardial ischaemia‒reperfusion injury. J. Nanobiotechnol. 20: 434. DOI: 10.1186/s12951-022-01639-8.

    View in Article CrossRef Google Scholar

    [145] Narasimhan, M., and Rajasekaran, N.S. (2016). Exercise, Nrf2 and antioxidant signaling in cardiac aging. Front. Physiol. 7: 241. DOI: 10.3389/fphys.2016.00241.

    View in Article CrossRef Google Scholar

    [146] Dinkova-Kostova, A.T., and Abramov, A.Y. (2015). The emerging role of Nrf2 in mitochondrial function. Free Radic. Biol. Med. 88: 179−188. DOI: 10.1016/j.freeradbiomed.2015.04.036.

    View in Article CrossRef Google Scholar

    [147] Chen, X.J., Ren, S.M., Dong, J.Z., et al. (2019). Ginkgo biloba extract-761 protects myocardium by regulating Akt/Nrf2 signal pathway. Drug Des. Devel. Ther. 13: 647−655. DOI: 10.2147/DDDT.S191537.

    View in Article CrossRef Google Scholar

    [148] Dehaini, D., Wei, X., Fang, R.H., et al. (2017). Erythrocyte-platelet hybrid membrane coating for enhanced nanoparticle functionalization. Adv. Mater. 29: 1606209. DOI: 10.1002/adma.201606209.

    View in Article CrossRef Google Scholar

  • Cite this article:

    Lu H., Wang Y., and Yu R. (2023). Immune cell membrane-coated nanoparticles for targeted myocardial ischemia/reperfusion injury therapy. The Innovation Medicine 1(1), 100015. https://doi.org/10.59717/j.xinn-med.2023.100015
    Lu H., Wang Y., and Yu R. (2023). Immune cell membrane-coated nanoparticles for targeted myocardial ischemia/reperfusion injury therapy. The Innovation Medicine 1(1), 100015. https://doi.org/10.59717/j.xinn-med.2023.100015

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