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Multifunctional roles of γ-enolase in the central nervous system: more than a neuronal marker.
Horvat, Selena; Kos, Janko; Pislar, Anja.
Affiliation
  • Horvat S; Department of Pharmaceutical Biology, Faculty of Pharmacy, University of Ljubljana, Askerceva 7, 1000, Ljubljana, Slovenia.
  • Kos J; Department of Pharmaceutical Biology, Faculty of Pharmacy, University of Ljubljana, Askerceva 7, 1000, Ljubljana, Slovenia.
  • Pislar A; Department of Biotechnology, Jozef Stefan Institute, Jamova Cesta 39, 1000, Ljubljana, Slovenia.
Cell Biosci ; 14(1): 61, 2024 May 12.
Article in En | MEDLINE | ID: mdl-38735971
ABSTRACT
Enolase, a multifunctional protein with diverse isoforms, has generally been recognized for its primary roles in glycolysis and gluconeogenesis. The shift in isoform expression from α-enolase to neuron-specific γ-enolase extends beyond its enzymatic role. Enolase is essential for neuronal survival, differentiation, and the maturation of neurons and glial cells in the central nervous system. Neuron-specific γ-enolase is a critical biomarker for neurodegenerative pathologies and neurological conditions, not only indicating disease but also participating in nerve cell formation and neuroprotection and exhibiting neurotrophic-like properties. These properties are precisely regulated by cysteine peptidase cathepsin X and scaffold protein γ1-syntrophin. Our findings suggest that γ-enolase, specifically its C-terminal part, may offer neuroprotective benefits against neurotoxicity seen in Alzheimer's and Parkinson's disease. Furthermore, although the therapeutic potential of γ-enolase seems promising, the effectiveness of enolase inhibitors is under debate. This paper reviews the research on the roles of γ-enolase in the central nervous system, especially in pathophysiological events and the regulation of neurodegenerative diseases.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Cell Biosci Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Cell Biosci Year: 2024 Document type: Article