ACS Nano 2020, 14, 3, 2827–2846
Pervasive Genomic Damage in Experimental Intracerebral Hemorrhage: Therapeutic Potential of a Mechanistic Based Carbon Nanoparticle.
Dharmalingam, Prakash; Tal-akatta, Girish; Mitra, Joy; Wang, Haibo; Derry, Paul; Nilewski, Li-zanne; McHugh, Emily; Fabian, Roderic; Mendoza, Kimberly; Vasquez, Velmarini; Hegde, Pavana; Kakadiaris, Eugenia; Roy, Trenton; Boldogh, Istvan; Hegde, Venkatesh; Mitra, San-kar; Tour, James; Kent, Thomas; Hegde, Muralidhar.
Therapy for intracerebral hemorrhage (ICH) remains elusive, in part dependent on the severity of the hemorrhage itself as well as multiple deleterious effects of blood and its breakdown products such as hemin and free iron. While oxi-dative injury and genomic damage have been seen following ICH, the details of this injury and implications remain unclear. Here, we discovered that, while free iron produced mostly reactive oxygen species (ROS)-related single-strand DNA breaks, hemin unexpectedly induced rapid and persistent nuclear and mitochondrial double-strand breaks (DSBs) in neuronal and endothelial cell genomes and in mouse brains following experimental ICH comparable to that seen with γ radiation and DNA-complexing chemotherapies. Potentially as a result of persistent DSBs and the DNA damage response, hemin also resulted in senescence phenotype in cultured neurons and endothelial cells. Subse-quent resistance to ferroptosis reported in other senescent cell types was also observed here in neurons. While antioxidant therapy prevented senescence, cells became sensitized to ferroptosis. To address both senescence and resistance to ferroptosis, we synthesized a modified, catalytic, and rapidly in-ternalized carbon nanomaterial, poly(ethylene glycol)-conjugated hydrophilic carbon clusters (PEG-HCC) by covalently bonding the iron chelator, deferox-amine (DEF). This multifunctional nanoparticle, DEF-HCC-PEG, protected cells from both senescence and ferroptosis and restored nuclear and mitochondrial genome integrity in vitro and in vivo. We thus describe a potential molecular mechanism of hemin/iron-induced toxicity in ICH that involves a rapid induc-tion of DSBs, senescence, and the consequent resistance to ferroptosis and provide a mechanistic-based combinatorial therapeutic strategy.
Tel: (507) 5170700 - Fax: (507) 5070020 - EFax: (507) 5170701 | INDICASAT - AIP | Edificio 219, Ciudad del Saber | Clayton, Apartado 0843-01103 | Panamá 5 Panamá, Rep. de Panamá.
© Copyright 2014. INDICASAT AIP. Todos los derechos reservados.