Induction of Heat Shock Protein 70 in Mouse RPE as an In Vivo Model of Transpupillary Thermal Stimulation
Autor: | Amirkavei, Mooud, Pitkänen, Marja, Kaikkonen, Ossi, Kaarniranta, Kai, André, Helder, Koskelainen, Ari |
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Přispěvatelé: | Department of Neuroscience and Biomedical Engineering, University of Eastern Finland, Karolinska Institutet, Aalto-yliopisto, Aalto University |
Jazyk: | angličtina |
Rok vydání: | 2020 |
Předmět: |
Retinal pigment epithelium (RPE)
Mouse Cell Survival Gene Expression Apoptosis Retinal Pigment Epithelium Article lcsh:Chemistry Immunohistology Macular Degeneration Mice age-related macular degeneration (amd) Physical Stimulation Animals HSP70 Heat-Shock Proteins lcsh:QH301-705.5 mouse Lasers immunohistology retinal pigment epithelium (rpe) Hyperthermia Induced Immunohistochemistry heat shock protein 70 (hsp70) lcsh:Biology (General) lcsh:QD1-999 Age-related macular degeneration (AMD) Transpupillary laser-induced heating Heat shock protein 70 (HSP70) sense organs Biomarkers transpupillary laser-induced heating |
Zdroj: | International Journal of Molecular Sciences, Vol 21, Iss 6, p 2063 (2020) International Journal of Molecular Sciences Volume 21 Issue 6 |
ISSN: | 1422-0067 |
Popis: | The induction of heat shock response in the macula has been proposed as a useful therapeutic strategy for retinal neurodegenerative diseases by promoting proteostasis and enhancing protective chaperone mechanisms. We applied transpupillary 1064 nm long-duration laser heating to the mouse (C57Bl/6J) fundus to examine the heat shock response in vivo. The intensity and spatial distribution of heat shock protein (HSP) 70 expression along with the concomitant probability for damage were measured 24 h after laser irradiation in the mouse retinal pigment epithelium (RPE) as a function of laser power. Our results show that the range of heating powers for producing heat shock response while avoiding damage in the mouse RPE is narrow. At powers of 64 and 70 mW, HSP70 immunostaining indicates 90 and 100% probability for clearly elevated HSP expression while the corresponding probability for damage is 20 and 33%, respectively. Tunel staining identified the apoptotic regions, and the estimated 50% damaging threshold probability for the heating (ED50) was ~72 mW. The staining with Bestrophin1 (BEST1) demonstrated RPE cell atrophy with the most intense powers. Consequently, fundus heating with a long-duration laser provides an approachable method to develop heat shock-based therapies for the RPE of retinal disease model mice. |
Databáze: | OpenAIRE |
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