Elucidating the diverse identities of oligodendrocyte precursor cells

BBSRC · United Kingdom government procurement

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September 29, 2028
Response Due
Active
Status

Opportunity Overview

It has long been known that central nervous system (CNS) neurons are a diverse cell population, but in recent years it has also become clear that non-neuronal support cells of the CNS, summarised as ‘glia’, exhibit diverse properties and functions. One particular type of glia is called the oligodendrocyte precursor cell (OPC), which has established roles in giving rise to myelinating oligodendrocytes during long-term development, as a form of CNS plasticity, and in myelin regeneration. OPCs can do so because they exist throughout the CNS lifelong, comprising approximately 5% of all CNS cells. However, despite their abundance, it is also apparent that not all OPCs contribute to myelination with equal efficiency. Understanding how new myelin can be recruited from the OPC pool is an important question for both neurodevelopmental and regenerative myelination.
Work over the past decade has revealed that OPCs have diverse properties. However, we do not understand what this diversity reflects. One major reason for this lack of knowledge is that there is a notorious lack of markers to categorise different OPCs at any point in time, and lack of knowledge to predict their properties and functions. The other reason is that OPC properties can change over time, and we have only very limited understanding of the relationships between OPC subgroups with different properties.
Here, we propose to address these problems through newly generated zebrafish knock-in reporter lines for two identified markers of OPC subpopulations. In a first step, we will carry out clonal analysis of OPC dynamics across the entire CNS using in vivo imaging methods to monitor how OPCs transition between marker identities, and how this relates to the production of new myelinating oligodendrocytes. In a second step, we will manipulate the generation of new oligodendrocytes in experimental models of myelin regeneration and of myelin plasticity to test how OPC subpopulations with different marker identities...

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Solicitation Details

Issuing agencyBBSRC
CountryUnited Kingdom
CategoryResearch Development
PublishedSeptember 29, 2025
Procurement stageActive solicitation
Response dueSeptember 29, 2028
StatusOpen — accepting responses
Official sourceView original notice
Last verifiedAugust 10, 2026

Source: UK Research and Innovation (UKRI) — Open Government Licence v3.0.

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