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<metadata xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dc="http://purl.org/dc/elements/1.1/"><dc:title>α‑enolase and γ‑enolase expression in enriched S- and N-type SH-SY5Y cells</dc:title><dc:creator>Horvat,	Selena	(Avtor)
	</dc:creator><dc:creator>Zidar,	Nace	(Avtor)
	</dc:creator><dc:creator>Kos,	Janko	(Avtor)
	</dc:creator><dc:creator>Pišlar,	Anja	(Avtor)
	</dc:creator><dc:subject>neuron-like cells</dc:subject><dc:subject>neuronal diferentiation</dc:subject><dc:subject>SH-SY5Y cell phenotypes</dc:subject><dc:subject>enolase isoforms</dc:subject><dc:subject>cathepsin X inhibition</dc:subject><dc:description>Enolase is well-known for its role in glycolysis but also plays other roles in the central nervous system, including neuronal survival, differentiation, and axonal regeneration. Here, we investigated α- and γ-enolase expression patterns and their association with cathepsin X in distinct SH-SY5Y cell phenotypes. Enriched substrate-adherent S-type cells are characterized by large, flat morphology with extensive cytoplasm and higher expression of vimentin, while neuroblastic N-type are recognized by neurite extensions and higher expression of B-cell lymphoma 2 (Bcl-2) and growth-associated protein-43. We demonstrated that γ-enolase expression was specific to N-type cells, whereas α-enolase expression was not phenotype-specific. Moreover, a shift from ubiquitously expressed α-enolase to neuron-specific γ-enolase was observed during the enrichment and differentiation. Additionally, cathepsin X exhibited higher proteolytic activity in S-type cells. Inhibition of cathepsin X with AMS36 promoted differentiated cell morphology and increased expression of the active form of γ-enolase. Furthermore, AMS36 altered the expression of vimentin and Bcl-2, indicating a regulatory role in neuronal differentiation. Furthermore, AMS36 activated extracellular signal-regulated kinase 1/2 in N-type cells and enhanced the association between γ-enolase and tyrosine receptor kinase in both, suggesting a link between cathepsin X/γ-enolase and the key signaling pathways of differentiation. Our findings underscore the multifaceted role of enolase isoforms in SH-SY5Y cell differentiation, with α-enolase and γ-enolase showing distinct expression patterns in S- and N-type cells. The expression and activity of cathepsin X in S-type cells, along with its regulatory impact on γ-enolase in N-type cells, highlight the importance of these proteins in neuronal differentiation.</dc:description><dc:date>2025</dc:date><dc:date>2026-01-27 15:56:03</dc:date><dc:type>Članek v reviji</dc:type><dc:identifier>178431</dc:identifier><dc:identifier>UDK: 577.152.34</dc:identifier><dc:identifier>ISSN pri članku: 1559-1182</dc:identifier><dc:identifier>DOI: 10.1007/s12035-025-04898-2</dc:identifier><dc:identifier>COBISS_ID: 231412483</dc:identifier><dc:language>sl</dc:language></metadata>
