Impaired Integrated Stress Response and Mitochondrial Integrity Modulate Genotoxic Stress Impact and Lower the Threshold for Immune Signalling

dc.cclicenceCC BYen
dc.contributor.authorMoisoi, Nicoleta
dc.contributor.authorTemelie, Mihaela
dc.contributor.authorTalpur, Rubab
dc.contributor.authorDominguez-Prieto, Marta
dc.contributor.authorSilva, Ayanda Dantas
dc.contributor.authorCenusa, Constantin
dc.contributor.authorCraciun, Liviu
dc.contributor.authorSavu, Diana Iulia
dc.date.acceptance2023-03-14
dc.date.accessioned2023-04-03T14:09:20Z
dc.date.available2023-04-03T14:09:20Z
dc.date.issued2023-03-20
dc.descriptionopen access articleen
dc.description.abstractMitochondria–nucleus communication during stress dictates cellular fate with consequences on the etiopathology of multiple age-related diseases. Impaired mitochondrial quality control through loss of function of the mitochondrial protease HtrA2 associates with accumulation of damaged mitochondria and triggers the integrated stress response, implicating the transcription factor CHOP. Here we have employed a combined model of impaired mitochondria quality control, namely HtrA2 loss of function, and/or integrated stress response, namely CHOP loss of function, and genotoxicity to address the distinctive roles of these cellular components in modulating intracellular and intercellular responses. The genotoxic agents employed were cancer therapeutic agents such as irradiation with X-ray and protons or treatment with the radiomimetic bleomycin. The irradiation had an enhanced effect in inducing DNA damage in cells with CHOP loss of function, while the bleomycin treatment induced more DNA damage in all the transgenic cells as compared to the control. The genetic modifications impaired the transmission of DNA damage signalling intercellularly. Furthermore, we have dissected the signalling pathways modulated by irradiation in selected genotypes with RNA sequencing analysis. We identified that loss of HtrA2 and CHOP function, respectively, lowers the threshold where irradiation may induce the activation of innate immune responses via cGAS-STING; this may have a significant impact on decisions for combined therapeutic approaches for various diseases.en
dc.funderNo external funderen
dc.identifier.citationTemelie, M., Talpur, R., Dominguez-Prieto, M., Dantas Silva, A., Cenusa, C., Craciun, L., Savu, D.I. and Moisoi, N. (2023) Impaired Integrated Stress Response and Mitochondrial Integrity Modulate Genotoxic Stress Impact and Lower the Threshold for Immune Signalling. International Journal of Molecular. Sciences, 24 (6), 5891en
dc.identifier.doihttps://doi.org/10.3390/ijms24065891
dc.identifier.urihttps://hdl.handle.net/2086/22661
dc.language.isoenen
dc.peerreviewedYesen
dc.publisherMDPIen
dc.titleImpaired Integrated Stress Response and Mitochondrial Integrity Modulate Genotoxic Stress Impact and Lower the Threshold for Immune Signallingen
dc.typeArticleen

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