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Development and plasticity‐related changes in protein expression patterns in cat visual cortex: A fluorescent two‐dimensional difference gel electrophoresis approach
Author(s) -
Van den Bergh Gert,
Clerens Stefan,
Firestein Bonnie L.,
Burnat Kalina,
Arckens Lutgarde
Publication year - 2006
Publication title -
proteomics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.26
H-Index - 167
eISSN - 1615-9861
pISSN - 1615-9853
DOI - 10.1002/pmic.200500570
Subject(s) - visual cortex , neuroplasticity , biology , period (music) , cortex (anatomy) , protein expression , plasticity , neuroscience , microbiology and biotechnology , biochemistry , gene , physics , acoustics , thermodynamics
During early postnatal brain development, changes in visual input can lead to specific alteration of function and connectivity in mammalian visual cortex. In cat, this so‐called critical period exhibits maximal sensory‐driven adaptations around postnatal day 30 (P30), and ceases toward adulthood. We examined the molecular framework that directs age‐ and experience‐dependent plasticity in cat visual cortex, by comparing protein expression profiles at eye opening (postnatal day 10 (P10), when experience‐dependent plasticity starts), the peak of the critical period (P30), and in adulthood. Using 2‐D DIGE, we performed comparisons of P10–P30 and P30‐adult brain protein samples. Sixty protein spots showed statistically significant intensity changes in at least one comparison. Fifty‐one spots were identified using quadrupole‐TOF MS/MS or LC‐MS/MS, containing 37 different proteins. The progressive increase or decrease in protein expression levels could be correlated to age‐dependent postnatal brain development. Four spots containing transferrin, 14–3‐3 alpha/beta and cypin, showed maximal protein expression levels at P30, thereby showing a positive correlation to critical period plasticity. Western analysis indeed revealed a clear effect of visual deprivation on cypin expression in cat visual cortex. Our results therefore demonstrate the power of 2‐D DIGE as a tool toward understanding the molecular basis of nervous system development and plasticity.