Completed Genetics & Molecular Biology Brain & Nervous System

The TNF superfamily in neuronal development.

In plain English

AI plain-English summary

A developing mouse neuron’s growth cone—the tip of a growing nerve fibre—must decide whether to extend or retract, and a family of immune-signalling molecules called the TNF superfamily helps make that call. This project asks how these same molecules, already known to guide axon growth, also shape dendrites and steer growth cones, and whether they act locally or globally within a single neuron. The researchers will use compartment cultures, pharmacological inhibitors, and transgenic mice to map the signalling pathways and identify the genes switched on by the master regulator NF-κB. They will also test whether selected TNF cytokines influence neuronal survival and early neuroblast development, guided by a comprehensive map of receptor expression across development. This is fundamental science. It does not aim to produce a therapy or diagnostic. But understanding how the TNF superfamily wires the nervous system in mice could eventually illuminate why wiring goes wrong in neurodevelopmental disorders such as autism or schizophrenia. Similar curiosity-driven work on axon guidance molecules has already informed strategies for repairing spinal cord injury. A clearer picture of these molecular signals may one day help researchers design interventions that coax damaged nerves to reconnect.

View original technical description
We will use a multidisciplinary approach to investigate the functions and mechanism of action of the TNFSF in the developing mouse nervous system. We will use well-characterized primary neuron culture systems to investigate whether the TNFSF cytokines we have already shown to promote or inhibit axon growth also affect dendrite growth and whether they are capable of influencing growth cone direction as either diffusible or cell surface ligands. We will use compartment cultures to determine wheth er localized receptor activation by individual cytokines has purely localized or generalized effects on neurite growth. We will use pharmacological inhibitors, expression of mutated signalling proteins and biochemical methods to delineate the signalling mechanisms by which these cytokines affect neurite growth and will use microarrays to identify NF-kB regulated genes required for promoting and/or inhibiting neurite growth. We will investigate appropriate phenotypic changes in neural processes and tissue innervation in transgenic mice to ascertain the physiological and developmental relevance of our in vitro observations. We will also investigate the roles of selected cytokines in neuronal survival and neuroblast development based on pilot data. Finally, will explore the roles of additional TNFSF cytokines selected on the basis of our comprehensive developmental profiling of TNFSF receptors.

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Researchers

Alun Davies (EPMC Awardee)

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Original classification

Programme Grant

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