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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>The α- to γ-enolase switch</dc:title><dc:creator>Horvat,	Selena	(Avtor)
	</dc:creator><dc:creator>Pečar Fonović,	Urša	(Avtor)
	</dc:creator><dc:creator>Mitrović,	Ana	(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>oligodendrocytes</dc:subject><dc:subject>differentiation</dc:subject><dc:subject>γ-enolase</dc:subject><dc:subject>α-enolase</dc:subject><dc:subject>cathepsin X</dc:subject><dc:description>The glycolytic enzyme γ-enolase is a highly specific neuronal marker that is known to replace ubiquitously expressed α-enolase in the brain. Moreover, γ-enolase has been shown to exert neurotrophic activity, which is regulated by cathepsin X, a lysosomal peptidase. This study investigates the role of γ-enolase and its regulation by cathepsin X during the differentiation of oligodendrocytes, which are essential for normal brain function. We established a differentiation protocol for the human oligodendroglioma (HOG) cell line and demonstrated for the first time that an α- to γ-enolase switch occurs during HOG cell differentiation. This switch was confirmed by the expression of specific markers underscoring the role of γ-enolase in oligodendrocyte differentiation. Moreover, γ-enolase overexpression enhanced oligodendrocyte differentiation, while silencing of γ-enolase by siRNA significantly decreased maturation marker. Further, the regulatory role of cysteine peptidase cathepsin X on γ-enolase function was found. Silencing cathepsin X significantly changed cell morphology, enhanced oligodendrocyte differentiation, altered the expression of oligodendrocyte markers, and increased levels of the active form of γ-enolase. Inhibiting cathepsin X similarly changed cell morphology and enhanced oligodendrocyte differentiation. These findings suggest that cathepsin X modulates γ-enolase activity and thereby influences oligodendrocyte differentiation and thus neuronal function.</dc:description><dc:date>2025</dc:date><dc:date>2025-02-03 14:54:40</dc:date><dc:type>Članek v reviji</dc:type><dc:identifier>167011</dc:identifier><dc:identifier>UDK: 579</dc:identifier><dc:identifier>ISSN pri članku: 1879-0003</dc:identifier><dc:identifier>DOI: 10.1016/j.ijbiomac.2025.140464</dc:identifier><dc:identifier>COBISS_ID: 224856579</dc:identifier><dc:language>sl</dc:language></metadata>
