N-METHYL-4-PHENYLPYRİDİNİUM IODİDE (MPP+) ARACILI PARKİNSON HÜCRE MODELİNDE OTOFAJİ AKTİVATÖRÜ FLUSPİRİLENİN ENDOPLAZMA RETİKULUMU STRESİNDEKİ IRE1 YOLAĞINA ETKİSİNİN ARAŞTIRILMASI
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Tarih
2024Yazar
Ayan Türeli, Merve
Ambargo Süresi
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Tureli Ayan Merve, Investigation of the Effect of the Autophagy Activator
Fluspirylene on the Ire1 Pathway in Endoplasmic Reticulum Stress in N-Methyl-
4-Phenylpyridinium Iodide (Mpp+) Mediated Parkinson's Cell Model, Hacettepe
University Faculty of Medicine Department of Histology and Embryology
Residency Thesis, Ankara, 2024. Parkinson's disease, the second most common
neurodegenerative disease worldwide, has many underlying molecular mechanisms.
One of these mechanisms is endoplasmic reticulum stress. Endoplasmic reticulum
stress is detected by three proteins acting as sensors, activating pathways associated
with synthesis or degradation in the endoplasmic reticulum. Another molecular
mechanism observed in Parkinson's disease is impaired autophagy. Autophagy not
only serves as a cellular death mechanism but also plays a salvaging role by clearing
damaged organelles and misfolded proteins in the cell. In this study, we aimed to
observe and describe the effect of Fluspirilene, which induces ATG5-mediated
autophagy, on IRE1, one of the endoplasmic reticulum stress sensors, in a Parkinson's
disease model created with MPP+ toxin on H4 human neuroglioma cells. We
determined the effect of autophagy on cell viability in the Parkinson's disease model
by using the MTT assay. The reversal of impaired autophagy with ATG5-mediated
autophagy activation is detected by LC3B immunocytochemistry. By the pIRE1
immunocytochemistry used to detect the endoplasmic reticulum stress, after the
standardization of pIRE1 immunoreactivity with the total IRE1 levels measured using
the ELISA method, endoplasmic reticulum stress was found to be increased. With the
ER-Tracker staining it is seen that the morphology of the endoplasmic reticulum was
destroyed in the Parkinson's disease model, but restored with autophagy. With this
study, in the MPP+ toxin-mediated Parkinson's disease model the relationship between
ATG5-mediated autophagy and IRE1 mediated endoplasmic reticulum stress was
shown for the first time