A pivotal issue for patients with multiple sclerosis (MS) is the long-term survival and integrity of neurons and oligodendrocytes, and maintenance of the myelin sheath. Over time, the progressive nature of MS results in a chronic disease course with permanent axonal damage, neuronal and oligodendrocyte loss, demyelination, and diminished re-myelination. Studies in animal models have proved useful in exploring disease mechanisms and in testing therapeutic paradigms, however model systems using cells of human origin are clearly essential for the identification of proteins required to maintain and enhance myelination in humans. In this proposal, our goal is to use our human co-culture system of dorsal root ganglia and oligodendrocyte precursor cells (OPC) to determine the extent to which factors proposed to enhance myelination in rodents function similarly in the human system. We will expand upon our preliminary data that show that growth-arrest specific protein 6 (gas6) enhances OPC maturation and axon ensheathment, and test whether in combination with gas6, the activation of cannabinoid receptors, or the retinoid X receptor (RXR) can promote further the maturation and myelinating activity of human OPC in vitro.
In Specific Aim 1, we will continue to examine the ability of gas6 to enhance axonal ensheathment, and examine by immunofluorescent microscopy and electron microscopy the extent to which myelin proteins are expressed in the developing myelin sheath, whether compact myelin is achieved over time, and the correlation between axonal diameter and myelin sheath formation.
In Specific Aim 2 A, we will examine the contribution of agonists and antagonists of cannabinoid (CB) receptors plus and minus gas6 to determine whether CB2 agonists enhance myelination and aid in myelin compaction.
In Specific Aim 2 B, we will determine whether 9-cis-retinoic acid signaling through the RXR? receptor enhances myelination. These studies will help to define factors required for human myelination. Analysis of growth factors, receptor agonists and signaling molecules will determine the potential role of these factors in enhancing human myelination with a focus on the factors required for compact myelin formation in a human model system.

Public Health Relevance

We propose to use a novel human neuronal/oligodendrocyte co-culture model to study factors required by human OLs to form myelin. A particular focus of these studies will be to examine the contribution of growth-arrest specific protein 6 (gas6) to oligodendrocyte maturation and myelin protein expression. In addition, we will examine the role of cannabinoid receptors and retinoid X receptors on myelin protein expression and the role of specific agonists and antagonists in enhancing myelination. To our knowledge, our system is the only completely human co-culture model in which mature myelin synthesizing proteins are expressed, and in which OLs are shown to wrap axons by electron microscopy.

National Institute of Health (NIH)
National Institute of Neurological Disorders and Stroke (NINDS)
Exploratory/Developmental Grants (R21)
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Cellular and Molecular Biology of Glia Study Section (CMBG)
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Utz, Ursula
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Albert Einstein College of Medicine
Schools of Medicine
United States
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Gruber, Ross C; Ray, Alex K; Johndrow, Christopher T et al. (2014) Targeted GAS6 delivery to the CNS protects axons from damage during experimental autoimmune encephalomyelitis. J Neurosci 34:16320-35
O'Guin, Kathleen N; Gruber, Ross C; Raine, Cedric S et al. (2014) Gas6 enhances axonal ensheathment by MBP+ membranous processes in human DRG/OL promyelinating co-cultures. ASN Neuro 6:e00135
Tsiperson, Vladislav; Gruber, Ross C; Goldberg, Michael F et al. (2013) Suppression of inflammatory responses during myelin oligodendrocyte glycoprotein-induced experimental autoimmune encephalomyelitis is regulated by AKT3 signaling. J Immunol 190:1528-39