Differential expression of neurodegeneration-related genes in SH-SY5Y neuroblastoma cells under the influence of Cyclophilin A: could the enzyme be a likely trigger and therapeutic target for Alzheimer's disease? Show others and affiliations
2025 (English) In: Neurochemical Research, ISSN 0364-3190, E-ISSN 1573-6903, Vol. 50, no 1, article id 47Article in journal (Refereed) Published
Abstract [en]
The function and mechanism of Cyclophilin A (CypA) in modulating gene expression associated with Alzheimer’s disease (AD) remain unclear. This multifunctional protein is found to be elevated in the cerebrospinal fluid (CSF) of individuals at risk for AD. The cytotoxic effects of CypA, including both wild-type and the mutant R55A, were assessed using the MTT assay. Prior to this evaluation, the purified recombinant protein was validated through enzymatic activity assays and western blot analysis. Following treatment with CypA and transient transfection using the CypA construct, real-time PCR (qRT-PCR) and western blotting were conducted to analyze the expression of factors involved in various signaling pathways, with an emphasis on inflammation, cell death, and intercellular communication. The findings indicate that CypA has a significant impact on the gene expression of factors associated with inflammation and the progression of AD in SH-SY5Y cells. It can be concluded that CypA is capable of regulating gene expression in SH-SY5Y cells, either in a manner dependent on or independent of its enzymatic activity. Additionally, the influence of this multifunctional protein on gene expression is contingent upon the specific site of action, as well as the dosage and duration of exposure to the cells.
Place, publisher, year, edition, pages Springer Nature, 2025. Vol. 50, no 1, article id 47
Keywords [en]
Alzheimer’s disease, Cyclophilin A, Gene expression, Inflammation, Post translational modifications
National Category
Neurosciences Medical Biotechnology (with a focus on Cell Biology (including Stem Cell Biology), Molecular Biology, Microbiology, Biochemistry or Biopharmacy)
Identifiers URN: urn:nbn:se:umu:diva-233334 DOI: 10.1007/s11064-024-04253-2 ISI: 001371017900002 PubMedID: 39636462 Scopus ID: 2-s2.0-85211328280 OAI: oai:DiVA.org:umu-233334 DiVA, id: diva2:1923978
2025-01-022025-01-022025-01-02 Bibliographically approved