From BBB to PPP: Bioenergetic requirements and challenges for oligodendrocytes in health and disease.
Milton Guilherme Forestieri FernandesFlorian PerninJack P AntelTimothy E KennedyPublished in: Journal of neurochemistry (2024)
Mature myelinating oligodendrocytes, the cells that produce the myelin sheath that insulates axons in the central nervous system, have distinct energetic and metabolic requirements compared to neurons. Neurons require substantial energy to execute action potentials, while the energy needs of oligodendrocytes are directed toward building the lipid-rich components of myelin and supporting neuronal metabolism by transferring glycolytic products to axons as additional fuel. The utilization of energy metabolites in the brain parenchyma is tightly regulated to meet the needs of different cell types. Disruption of the supply of metabolites can lead to stress and oligodendrocyte injury, contributing to various neurological disorders, including some demyelinating diseases. Understanding the physiological properties, structures, and mechanisms involved in oligodendrocyte energy metabolism, as well as the relationship between oligodendrocytes and neighboring cells, is crucial to investigate the underlying pathophysiology caused by metabolic impairment in these disorders. In this review, we describe the particular physiological properties of oligodendrocyte energy metabolism and the response of oligodendrocytes to metabolic stress. We delineate the relationship between oligodendrocytes and other cells in the context of the neurovascular unit, and the regulation of metabolite supply according to energetic needs. We focus on the specific bioenergetic requirements of oligodendrocytes and address the disruption of metabolic energy in demyelinating diseases. We encourage further studies to increase understanding of the significance of metabolic stress on oligodendrocyte injury, to support the development of novel therapeutic approaches for the treatment of demyelinating diseases.
Keyphrases
- induced apoptosis
- cell cycle arrest
- healthcare
- endoplasmic reticulum stress
- white matter
- spinal cord
- ms ms
- mental health
- multiple sclerosis
- single cell
- signaling pathway
- stem cells
- risk assessment
- blood brain barrier
- stress induced
- spinal cord injury
- bone marrow
- cell proliferation
- fatty acid
- climate change
- pi k akt
- functional connectivity
- neural stem cells