Macrophages morphology and cytokine reeducation by ex situ copper thiol complexes

References

• Orekhov AN, Orekhova VA, Nikiforov NG, et al. Monocyte differentiation and macrophage polarization. Vessel Plus. 2019;2019:10. doi: 10.20517/2574-1209.2019.04.
   Google Scholar
• Tufet M. Re-educating macrophages. Nat Rev Immunol. 2008;8(7):488–488. doi: 10.1038/nri2365.
   Web of Science ®Google Scholar
• Hagemann T, Lawrence T, McNeish I, et al. Re-educating tumor-associated macrophages by targeting NF-kappaB. J Exp Med. 2008;205(6):1261–1268. doi: 10.1084/jem.20080108.
   PubMed Web of Science ®Google Scholar
• Kowal J, Kornete M, Joyce JA. Re-education of macrophages as a therapeutic strategy in cancer. Immunotherapy. 2019;11(8):677–689. doi: 10.2217/imt-2018-0156.
   PubMed Web of Science ®Google Scholar
• Chistiakov DA, Myasoedova VA, Revin VV, et al. The impact of interferon-regulatory factors to macrophage differentiation and polarization into M1 and M2. Immunobiology. 2018;223(1):101–111. doi: 10.1016/j.imbio.2017.10.005.
   PubMed Web of Science ®Google Scholar
• Huang X, Li Y, Fu M, et al. Polarizing macrophages in vitro. Methods Mol Biol. 2018;1784:119–126.
   PubMedGoogle Scholar
• Chen W, Sandoval H, Kubiak JZ, et al. The phenotype of peritoneal mouse macrophages depends on the mitochondria and ATP/ADP homeostasis. Cell Immunol. 2018;324:1–7. doi: 10.1016/j.cellimm.2017.11.003.
   PubMed Web of Science ®Google Scholar
• Boutilier AJ, Elsawa SF. Macrophage polarization states in the tumor microenvironment. Int J Mol Sci. 2021;22(13):6995. doi: 10.3390/ijms22136995.
   PubMed Web of Science ®Google Scholar
• Li C, Levin M, Kaplan DL. Bioelectric modulation of macrophage polarization. Sci Rep. 2016;6:21044. doi: 10.1038/srep21044.
   PubMed Web of Science ®Google Scholar
• Ferraro B, Leoni G, Hinkel R, et al. Pro-angiogenic macrophage phenotype to promote myocardial repair. J Am Coll Cardiol. 2019;73(23):2990–3002. doi: 10.1016/j.jacc.2019.03.503.
   PubMed Web of Science ®Google Scholar
• Bevan L, Lim ZW, Venkatesh B, et al. Specific macrophage populations promote both cardiac scar deposition and subsequent resolution in adult zebrafish. Cardiovasc Res. 2020;116(7):1357–1371. doi: 10.1093/cvr/cvz221.
   PubMed Web of Science ®Google Scholar
• Sarkar B, Lingertat-Walsh K, Clarke JT. Copper-histidine therapy for menkes disease. J Pediatr. 1993;123(5):828–830. doi: 10.1016/S0022-3476(05)80870-4.
   PubMed Web of Science ®Google Scholar
• Guthrie LM, Soma S, Yuan S, et al. Elesclomol alleviates menkes pathology and mortality by escorting Cu to cuproenzymes in mice. Science. 2020;368(6491):620–625. doi: 10.1126/science.aaz8899.
   PubMed Web of Science ®Google Scholar
• Stremmel W, Weiskirchen R. Therapeutic strategies in wilson disease: pathophysiology and mode of action. Ann Transl Med. 2021;9(8):732. doi: 10.21037/atm-20-3090.
   PubMed Web of Science ®Google Scholar
• Zapata-Catzin GA, Zumbardo-Bacelis GA, Vargas-Coronado R, et al. Novel copper complexes-polyurethane composites that mimics anti-inflammatory response. J Biomater Sci Polym Ed. 2023;34(8):1067–1089. doi: 10.1080/09205063.2022.2155783.
   PubMed Web of Science ®Google Scholar
• Climova A, Pivovarova E, Szczesio M, et al. Anticancer and antimicrobial activity of new copper (II) complexes. J Inorg Biochem. 2023;240:112108. doi: 10.1016/j.jinorgbio.2022.112108.
   PubMed Web of Science ®Google Scholar
• Patteson JB, Putz AT, Tao L, et al. Biosynthesis of fluopsin C, a copper-containing antibiotic from. Science. 2021;374(6570):1005–1009. doi: 10.1126/science.abj6749.
   PubMed Web of Science ®Google Scholar
• Ji P, Wang P, Chen H, et al. Potential of copper and copper compounds for anticancer applications. Pharmaceuticals. 2023;16(2):234. doi: 10.3390/ph16020234.
   Web of Science ®Google Scholar
• Xiong C, Ling H, Hao Q, et al. Cuproptosis: p53-regulated metabolic cell death? Cell Death Differ. 2023;30(4):876–884. doi: 10.1038/s41418-023-01125-0.
   PubMed Web of Science ®Google Scholar
• Xool-Tamayo J, Castillo-Cruz O, Vargas-Coronado RF, et al. Non inflammatory properties of ex situ thiol-based copper chelates. Mater Lett. 2021;282:128657. doi: 10.1016/j.matlet.2020.128657.
   Web of Science ®Google Scholar
• Xool-Tamayo J, Chan-Zapata I, Arana-Argaez VE, et al. In vitro and in vivo anti-inflammatory properties of mayan propolis. Eur J Inflamm. 2020;18:205873922093528. 2058739220935280. doi: 10.1177/2058739220935280.
   Web of Science ®Google Scholar
• Davies JQ, Gordon S. Isolation and culture of human macrophages. Methods Mol Biol. 2005;290:105–116. doi: 10.1385/1-59259-838-2:105.
   PubMedGoogle Scholar
• Ray A, Dittel BN. Isolation of mouse peritoneal cavity cells. J Vis Exp. 2010;28(35):1488.
   Google Scholar
• Pineda-Torra I, Gage M, de Juan A, et al. Isolation, culture, and polarization of murine bone marrow-derived and peritoneal macrophages. Methods Mol Biol. 2015;1339:101–109.
   PubMedGoogle Scholar
• Arana-Argáez VE, Chan-Zapata I, Canul-Canche J, et al. Immunosuppresive effects of the methanolic extract of chrysophyllum cainito leaves on macrophage functions. Afr J Tradit Complement Altern Med. 2017;14(1):179–186.
   PubMedGoogle Scholar
• Spiller KL, Koh TJ. Macrophage-based therapeutic strategies in regenerative medicine. Adv Drug Deliv Rev. 2017;122:74–83. doi: 10.1016/j.addr.2017.05.010.
   PubMed Web of Science ®Google Scholar
• Ma Y, Yang H, Zong X, et al. Artificial M2 macrophages for disease-modifying osteoarthritis therapeutics. Biomaterials. 2021;274:120865. doi: 10.1016/j.biomaterials.2021.120865.
   PubMed Web of Science ®Google Scholar
• Villar-Fincheira P, Sanhueza-Olivares F, Norambuena-Soto I, et al. Role of interleukin-6 in vascular health and disease. Front Mol Biosci. 2021;8:641734. doi: 10.3389/fmolb.2021.641734.
   PubMed Web of Science ®Google Scholar
• Casella G, Garzetti L, Gatta AT, et al. IL4 induces IL6-producing M2 macrophages associated to inhibition of neuroinflammation in vitro and in vivo. J Neuroinflammation. 2016;13(1):139. doi: 10.1186/s12974-016-0596-5.
   PubMedGoogle Scholar
• Malyshev I, Malyshev Y. Current concept and update of the macrophage plasticity concept: intracellular mechanisms of reprogramming and m3 macrophage “switch” phenotype. Biomed Res Int. 2015;2015:341308. doi: 10.1155/2015/341308.
   PubMed Web of Science ®Google Scholar
• Kalish S, Lyamina S, Manukhina E, et al. M3 macrophages stop division of tumor cells in vitro and extend survival of mice with ehrlich ascites carcinoma. Med Sci Monit Basic Res. 2017;23:8–19. doi: 10.12659/msmbr.902285.
   PubMedGoogle Scholar
• Pérez S, Rius-Pérez S. Macrophage polarization and reprogramming in acute inflammation: a redox perspective. Antioxidants. 2022;11(7):1394. doi: 10.3390/antiox11071394.
   Web of Science ®Google Scholar
• Solier S, Müller S, Cañeque T, et al. A druggable copper-signalling pathway that drives inflammation. Nature. 2023;617(7960):386–394. doi: 10.1038/s41586-023-06017-4.
   PubMed Web of Science ®Google Scholar
• Chen W, Zhang F, Ju Y, et al. Gold nanomaterial engineering for macrophage-mediated inflammation and tumor treatment. Adv Healthc Mater. 2021;10(5):e2000818. doi: 10.1002/adhm.202000818.
   PubMed Web of Science ®Google Scholar
• Ni C, Zhou J, Kong N, et al. Gold nanoparticles modulate the crosstalk between macrophages and periodontal ligament cells for periodontitis treatment. Biomaterials. 2019;206:115–132. doi: 10.1016/j.biomaterials.2019.03.039.
   PubMed Web of Science ®Google Scholar
• Smith TD, Tse MJ, Read EL, et al. Regulation of macrophage polarization and plasticity by complex activation signals. Integr Biol. 2016;8(9):946–955. doi: 10.1039/c6ib00105j.
   Google Scholar