Tropea D, Kreiman G, Lyckman A, Mukherjee S, Yu H, Horng S, Sur M.
Distinct gene systems mediating activity-dependent plasticity in visual cortex.
Nature Neuroscience (2006) 9:660-668 PDF
Two key paradigms for examining activity-dependent development of primary visual cortex (V1) involve either reduction of activity in both eyes via dark-rearing (DR) or imbalance of activity between the two eyes via monocular deprivation (MD). Combining DNA microarray analysis with computational approaches, RT-PCR, immunohistochemistry and physiological imaging, we find that DR leads to (i) upregulation of genes subserving synaptic transmission and electrical activity, consistent with a coordinated response of cortical neurons to reduction of visual drive, and (ii) downregulation of parvalbumin, implicating parvalbumin-expressing interneurons as underlying the delay in cortical maturation after DR. MD partially activates homeostatic mechanisms but differentially upregulates molecular pathways related to growth factors and neuronal degeneration, consistent with reorganization of connections after MD. A binding protein of Insulin-like Growth Factor 1 is highly upregulated after MD, and exogenous application of IGF1 prevents the physiological effects of MD on ocular dominance plasticity examined in vivo.
| Department of Ophthalmology | ![]() |
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| Program in Neurobiology | ||
| Children's Hospital Harvard Medical School | ||
| Center for Brain Science, Harvard University | ||
| Swartz Center for Theoretical Neuroscience |
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