X-ray tomography of cryopreserved human prostate cancer cells: mitochondrial targeting by an organoiridium photosensitiser.
Elizabeth M BolithoCarlos Sanchez-CanoHuaiyi HuangIan J Hands-PortmanMatthew SpinkPaul D QuinnMaria HarkiolakiPeter J SadlerPublished in: Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry (2020)
The organoiridium complex Ir[(C,N)2(O,O)] (1) where C, N = 1-phenylisoquinoline and O,O = 2,2,6,6-tetramethyl-3,5-heptanedionate is a promising photosensitiser for Photo-Dynamic Therapy (PDT). 1 is not toxic to cells in the dark. However, irradiation of the compound with one-photon blue or two-photon red light generates high levels of singlet oxygen (1O2) (in Zhang et al. Angew Chem Int Ed Engl 56 (47):14898-14902 https://doi.org/10.1002/anie.201709082,2017), both within cell monolayers and in tumour models. Moreover, photo-excited 1 oxidises key proteins, causing metabolic alterations in cancer cells with potent antiproliferative activity. Here, the tomograms obtained by cryo-Soft X-ray Tomography (cryo-SXT) of human PC3 prostate cancer cells treated with 1, irradiated with blue light, and cryopreserved to maintain them in their native state, reveal that irradiation causes extensive and specific alterations to mitochondria, but not other cellular components. Such new insights into the effect of 1O2 generation during PDT using iridium photosensitisers on cells contribute to a detailed understanding of their cellular mode of action.
Keyphrases
- electron microscopy
- high resolution
- induced apoptosis
- endothelial cells
- cell cycle arrest
- photodynamic therapy
- emergency department
- oxidative stress
- induced pluripotent stem cells
- endoplasmic reticulum stress
- genome wide
- magnetic resonance imaging
- gene expression
- signaling pathway
- umbilical cord
- dna methylation
- mesenchymal stem cells
- stem cells
- radiation induced
- cord blood
- dual energy