Giessener Elektronische Bibliothek

GEB - Giessener Elektronische Bibliothek

Detection of DNA Double Strand Breaks by gammaH2AX Does Not Result in 53bp1 Recruitment in Mouse Retinal Tissues

Müller, Brigitte ; Ellinwood, N. M. ; Lorenz, Birgit ; Stieger, Knut

Originalveröffentlichung: (2018) Frontiers in Neuroscience 12(286) doi: 10.3389/fnins.2018.00286
Zum Volltext im pdf-Format: Dokument 1.pdf (9.261 KB)

Bitte beziehen Sie sich beim Zitieren dieses Dokumentes immer auf folgende
URN: urn:nbn:de:hebis:26-opus-146408

Freie Schlagwörter (Englisch): DNA repair , DNA DSB , mouse retina , mouse models , photoreceptor cells
Sammlung: Open Access - Publikationsfonds
Universität Justus-Liebig-Universität Gießen
Institut: Department of Ophthalmology
Fachgebiet: Medizin
DDC-Sachgruppe: Medizin
Dokumentart: Aufsatz
Sprache: Englisch
Erstellungsjahr: 2018
Publikationsdatum: 22.05.2019
Kurzfassung auf Englisch: Gene editing is an attractive potential treatment of inherited retinopathies. However, it often relies on endogenous DNA repair. Retinal DNA repair is incompletely characterized in humans and animal models. We investigated recruitment of the double stranded break (DSB) repair complex of gammaH2AX and 53bp1 in both developing and mature mouse neuroretinas. We evaluated the immunofluorescent retinal expression of these proteins during development (P07-P30) in normal and retinal degeneration models, as well as in potassium bromate induced DSB repair in normal adult (3 months) retinal explants. The two murine retinopathy models used had different mutations in Pde6b: the severe rd1 and the milder rd10 models. Compared to normal adult retina, we found increased numbers of gammaH2AX positive foci in all retinal neurons of the developing retina in both model and control retinas, as well as in wild type untreated retinal explant cultures. In contrast, the 53Bp1 staining of the retina differed both in amount and character between cell types at all ages and in all model systems. There was strong pan-nuclear staining in ganglion, amacrine, and horizontal cells, and cone photoreceptors, which was attenuated. Rod photoreceptors did not stain unequivocally. In all samples, 53Bp1 stained foci only rarely occurred. There was negligible cCo-localization of 53Bp1 and gammaH2AX staining was a very rare event (< 1% of gammaH2AX foci in the ONL and < 3% in the INL), suggesting the potential for alternate DSB sensing and repair proteins in the murine retina. At a minimum, murine retinal DSB repair does not appear to follow canonical pathways, and our findings suggests further investigation is warranted.
Lizenz: Lizenz-Logo  Creative Commons - Namensnennung 4.0