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The Stimulation of Thalamic Neurite Outgrowth by Cortex-derived Growth Factors In Vitro: The Influence of Cortical Age and Activity


Correspondence to: D. J. Price, as above


Recent in vitro experiments have provided useful insights into the development of connections between the thalamus and the cortex. While most of these previous studies focused on neurite guidance and target recognition, our experiments used a serum-free culture system to examine the possible roles of unidentified diffusible cortex-derived growth factors. We demonstrated that occipital cortical explants release diffusible growth factors that enhance neurite outgrowth from explants of the posterior thalamus (the region around the developing lateral geniculate nucleus). The amount of thalamic outgrowth was dependent on the age of the cocultured cortical slices. Our results suggest that there is an overall increase in the release of cortex-derived growth factors during the first three postnatal weeks in mice; this parallels known postnatal increases in the production of several identified growth factors. We found evidence for two peaks in the release of cortex-derived growth factors during the general upward trend, the first at around postnatal day 6 (shortly after thalamocortical innervation of layer 4) and a second between postnatal days 14 and 18 (just after eye-opening). The increased release of cortex-derived growth factors was not found when cortical slices were from mice that had been dark-reared from birth, suggesting that neural activity may be important for enhancing release. Other regions of the central nervous system, including the cerebellum and medulla, were also capable of stimulating some thalamic outgrowth; neither additional explants of the thalamus nor hepatic explants enhanced outgrowth. Fibroblast growth factor is one substance that is distributed preferentially among those tissues that were stimulatory in our experiments. Its level of transcription is known to increase in the brain during the first three postnatal weeks and to be influenced by neural activity. At low doses, fibroblast growth factor greatly increased outgrowth from isolated posterior thalamic explants. Nerve growth factor, another candidate molecule, was less effective. Overall, our results complement the in vivo observations of others on the synthesis of identified growth factors in the cortex and the factors that influence their production. They suggest that growth factors may influence thalamic neurons, and indicate that fibroblast growth factor, and possibly nerve growth factor, are two candidates for molecules mediating the in vitro effects.