PMID- 29182610 OWN - NLM STAT- MEDLINE DCOM- 20180706 LR - 20240229 IS - 1689-0035 (Electronic) IS - 0065-1400 (Linking) VI - 77 IP - 3 DP - 2017 TI - BDNF expression in cat striate cortex is regulated by binocular pattern deprivation. PG - 199-204 LID - 10.21307/ane-2017-053 [doi] AB - Deprivation of patterned visual information, as in early onset congenital cataract patients, results in a severe impairment in global motion perception. Previously we reported a delayed maturation of the peripheral visual field representation in primary visual area 17, based on a 2-D DIGE screen for protein expression changes and in situ hybridization for the activity reporter gene ZIF268. To corroborate these findings we here explore the binocular pattern deprivation (BD)-regulated expression of brain-derived neurotrophic factor (BDNF), a well-described neurotrophin precipitously regulated by early visual experience. To assess the timing of maturation-related BDNF expression we compared the central and the peripheral visual field representations of area 17 of 1, 2, 4 and 6-month-old and adult cats reared under normal visual conditions. To scrutinize the outcome of BD, four different deprivation strategies were compared, including early onset BD from birth and lasting for 2, 4 or 6 months (2BD, 4BD, 6BD), and late onset BD for 2 months upon 2 months of normal vision (2N2BD), as animal models of congenital and delayed onset cataract. During normal cortical development the BDNF transcript levels, measured by quantitative RT-PCR, remained stable. Higher BDNF mRNA levels were found in central area 17 of 2BD and 6BD animals compared to age-matched controls. In central area 17, the high BDNF mRNA levels at the end of the BD period may activate a mechanism by which plastic processes, halted by deprivation, may begin. We here confirm that the peripheral visual field representation of area 17 matures slower than its central counterpart. Only in central area 17 normal visual input upon BD could upregulate BDNF mRNA which may lead to a fast activation of local plastic adaptations. FAU - Laskowska-Macios, Karolina AU - Laskowska-Macios K AD - Laboratory of Neuroplasticity, Department of Molecular and Cellular Neurobiology, Nencki Institute of Experimental Biology, Polish Academy of Sciences, Warsaw, Poland; Laboratory of Neuroplasticity and Neuroproteomics, KU Leuven, Leuven, Belgium. FAU - Arckens, Lutgarde AU - Arckens L AD - Laboratory of Neuroplasticity and Neuroproteomics, KU Leuven, Leuven, Belgium. FAU - Kossut, Malgorzata AU - Kossut M AD - Laboratory of Neuroplasticity, Department of Molecular and Cellular Neurobiology, Nencki Institute of Experimental Biology, Polish Academy of Sciences, Warsaw, Poland; Department of Psychology, SWPS University of Social Sciences and Humanities, Warsaw, Poland. FAU - Burnat, Kalina AU - Burnat K AD - Laboratory of Neuroplasticity, Department of Molecular and Cellular Neurobiology, Nencki Institute of Experimental Biology, Polish Academy of Sciences, Warsaw, Poland; k.burnat@nencki.gov.pl. LA - eng PT - Journal Article PL - Poland TA - Acta Neurobiol Exp (Wars) JT - Acta neurobiologiae experimentalis JID - 1246675 RN - 0 (Brain-Derived Neurotrophic Factor) RN - 0 (Early Growth Response Protein 1) RN - 0 (RNA, Messenger) SB - IM MH - Age Factors MH - Animals MH - Brain-Derived Neurotrophic Factor/*metabolism MH - Cats MH - Early Growth Response Protein 1/genetics/*metabolism MH - Gene Expression Regulation/*physiology MH - RNA, Messenger/metabolism MH - Sensory Deprivation/*physiology MH - Visual Cortex/*metabolism MH - Visual Fields/physiology EDAT- 2017/11/29 06:00 MHDA- 2018/07/07 06:00 CRDT- 2017/11/29 06:00 PHST- 2017/11/29 06:00 [entrez] PHST- 2017/11/29 06:00 [pubmed] PHST- 2018/07/07 06:00 [medline] AID - 7723 [pii] AID - 10.21307/ane-2017-053 [doi] PST - ppublish SO - Acta Neurobiol Exp (Wars). 2017;77(3):199-204. doi: 10.21307/ane-2017-053.