Ghrelin regulates expression of the transcription factor Pax6 in hypoxic brain progenitor cells and neurons

dc.contributor.authorStoyanova, Irina I.
dc.contributor.authorKlymenko, Andrii
dc.contributor.authorWillms, Jeannette
dc.contributor.authorDöppner, Thorsten R.
dc.contributor.authorTonchev, Anton B.
dc.contributor.authorLutz, David
dc.date.accessioned2022-03-04T05:52:28Z
dc.date.available2022-03-04T05:52:28Z
dc.date.issued2022
dc.departmentİstanbul Medipol Üniversitesi, Rektörlük, Sağlık Bilim ve Teknolojileri Araştırma Enstitüsü
dc.description.abstractThe nature of brain impairment after hypoxia is complex and recovery harnesses different mechanisms, including neuroprotection and neurogenesis. Experimental evidence suggests that hypoxia may trigger neurogenesis postnatally by influencing the expression of a variety of transcription factors. However, the existing data are controversial. As a proof-of-principle, we subjected cultured cerebral cortex neurons, cerebellar granule neurons and organotypic cerebral cortex slices from rat brains to hypoxia and treated these cultures with the hormone ghrelin, which is well-known for its neuroprotective functions. We found that hypoxia elevated the expression levels and stimulated nuclear translocation of ghrelin’s receptor GHSR1 in the cultured neurons and the acute organotypic slices, whereas ghrelin treatment reduced the receptor expression to normoxic levels. GHSR1 expression was also increased in cerebral cortex neurons of mice with induced experimental stroke. Additional quantitative analyses of immunostainings for neuronal proliferation and differentiation markers revealed that hypoxia stimulated the proliferation of neuronal progenitors, whereas ghrelin application during the phase of recovery from hypoxia counteracted these effects. At the mechanistic level, we provide a link between the described post-ischemic phenomena and the expression of the transcription factor Pax6, an important regulator of neural progenitor cell fate. In contrast to the neurogenic niches in the brain where hypoxia is known to increase Pax6 expression, the levels of the transcription factor in cultured hypoxic cerebral cortex cells were downregulated. Moreover, the application of ghrelin to hypoxic neurons normalised the expression levels of these factors. Our findings suggest that ghrelin stimulates neurogenic factors for the protection of neurons in a GHSR1-dependent manner in non-neurogenic brain areas such as the cerebral cortex after exposure to hypoxia.
dc.identifier.citationStoyanova, I. I., Klymenko, A., Willms, J., Döppner, T. R., Tonchev, A. B. ve Lutz, D. (2022). Ghrelin regulates expression of the transcription factor Pax6 in hypoxic brain progenitor cells and neurons. Cells, 11(5). https://doi.org/10.3390/cells11050782
dc.identifier.doi10.3390/cells11050782
dc.identifier.issn2073-4409
dc.identifier.issue5
dc.identifier.pmid35269403
dc.identifier.scopus2-s2.0-85125285995
dc.identifier.scopusqualityQ1
dc.identifier.urihttps://doi.org/10.3390/cells11050782
dc.identifier.urihttps://hdl.handle.net/20.500.12511/9092
dc.identifier.volume11
dc.identifier.wos000768109500001en_US
dc.identifier.wosqualityQ2
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.institutionauthorDöppner, Thorsten R.
dc.language.isoen
dc.publisherMDPI
dc.relation.ispartofCellsen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsAttribution 4.0 International*
dc.rightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/*
dc.subjectGhrelin
dc.subjectGHSR1
dc.subjectHypoxia
dc.subjectNeurogenesis
dc.subjectProgenitor Cells
dc.subjectTranscription Factors
dc.titleGhrelin regulates expression of the transcription factor Pax6 in hypoxic brain progenitor cells and neurons
dc.typeArticle

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