Visual deprivation effects on the s100beta positive astrocytic population in the developing rat visual cortex: a quantitative study.

After birth, exposure to visual inputs modulates cortical development, inducing numerous changes of all components of the visual cortex. Most of the cortical changes thus induced occur during what is called the critical period. Astrocytes play an important role in the development, maintenance and plasticity of the cortex, as well as in the structure and function of the vascular network. Dark-reared Sprague-Dawley rats and age-matched controls sampled at 14, 21, 28, 35, 42, 49, 56 and 63 days postnatal (dpn) were studied in order to elucidate quantitative differences in the number of positive cells in the striate cortex. The astrocytic population was estimated by immunohistochemistry for S-100beta protein. The same quantification was also performed in a nonsensory area, the retrosplenial granular cortex. S-100beta positive cells had adult morphology in the visual cortex at 14 dpn and their numbers were not significantly different in light-exposed and nonexposed rats up to 35 dpn, and were even higher in dark-reared rats at 21 dpn. However, significant quantitative changes were recorded after the beginning of the critical period. The main finding of the present study was the significantly lower astroglial density estimated in the visual cortex of dark-reared rats over 35 dpn as well as the lack of difference at previous ages. Our results also showed that there were no differences when comparing the measurements from a nonsensory area between both groups. This led us to postulate that the astrocytic population in the visual cortex is downregulated by the lack of visual experience.

[1]  L. Maffei,et al.  Functional postnatal development of the rat primary visual cortex and the role of visual experience: Dark rearing and monocular deprivation , 1994, Vision Research.

[2]  S. Sherman,et al.  Organization of visual pathways in normal and visually deprived cats. , 1982, Physiological reviews.

[3]  The Human Brain Circulation , 1994, Vascular Biomedicine.

[4]  G. Paxinos The Rat nervous system , 1985 .

[5]  M. Marín‐padilla Prenatal development of fibrous (white matter), protoplasmic (gray matter), and layer I astrocytes in the human cerebral cortex: A Golgi study , 1995, The Journal of comparative neurology.

[6]  W. Greenough,et al.  Glial hypertrophy is associated with synaptogenesis following motor‐skill learning, but not with angiogenesis following exercise , 1994, Glia.

[7]  M. Salami,et al.  Differential effect of dark rearing on long-term potentiation induced by layer IV and white matter stimulation in rat visual cortex , 2000, Neuroscience Research.

[8]  A. Bignami,et al.  IMMUNOLOGICAL MARKERS IN ASTROCYTES , 1986 .

[9]  M. Stewart,et al.  Decreased levels of an astrocytic marker, glial fibrillary acidic protein, in the visual cortex of dark-reared rats: Measurement by enzyme-linked immunosorbent assay , 1986, Neuroscience Letters.

[10]  M. Stewart,et al.  Quantitative morphological effects of dark-rearing and light exposure on the synaptic connectivity of layer 4 in the rat visual cortex (area 17) , 2004, Experimental Brain Research.

[11]  A W Toga,et al.  The metabolic consequence of visual deprivation in the rat. , 1987, Brain research.

[12]  Priz.-Doz. Dr. Thomas Bär The Vascular System of the Cerebral Cortex , 1980, Advances in Anatomy, Embryology and Cell Biology.

[13]  J. Goldman,et al.  Interactions between glial progenitors and blood vessels during early postnatal corticogenesis: Blood vessel contact represents an early stage of astrocyte differentiation , 1997, The Journal of comparative neurology.

[14]  C. Müller Dark‐rearing retards the maturation of astrocytes in restricted layers of cat visual cortex , 1990, Glia.

[15]  L. Benevento,et al.  Effects of light/dark‐ and dark‐rearing on synaptic morphology in the superior colliculus and visual cortex of the postnatal and adult rat , 1991, Journal of neuroscience research.

[16]  E. Argandoña,et al.  Influence of visual experience deprivation on the postnatal development of the microvascular bed in layer IV of the rat visual cortex , 2000, Brain Research.

[17]  A. Nehlig,et al.  Postnatal Changes in Local Cerebral Blood Flow Measured by the Quantitative Autoradiographic [14C]Iodoantipyrine Technique in Freely Moving Rats , 1989, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[18]  P. Wahle,et al.  Visual activity is required to maintain the phenotype of supragranular NPY neurons in rat area 17 , 1998, The European journal of neuroscience.

[19]  Y. Frégnac,et al.  Early development of visual cortical cells in normal and dark‐reared kittens: relationship between orientation selectivity and ocular dominance. , 1978, The Journal of physiology.

[20]  F. Hajós,et al.  Distribution of glial fibrillary acidic protein (GFAP)-immunoreactive astrocytes in the rat brain , 2004, Experimental Brain Research.

[21]  K. Zilles,et al.  Distribution of glial fibrillary acidic protein and vimentin immunoreactivity during rat visual cortex development , 1991, Journal of neurocytology.

[22]  L. Maffei,et al.  BDNF Regulates the Maturation of Inhibition and the Critical Period of Plasticity in Mouse Visual Cortex , 1999, Cell.

[23]  E. Tongiorgi,et al.  Dark rearing blocks the developmental down-regulation of brain-derived neurotrophic factor messenger RNA expression in layers IV and V of the rat visual cortex , 1999, Neuroscience.

[24]  R. Janzer,et al.  Astrocytes induce blood–brain barrier properties in endothelial cells , 1987, Nature.

[25]  D. Busija Cerebral Circulation of the Fetus and Newborn , 1994 .

[26]  Michel Imbert,et al.  Vascularization in the primate visual cortex during development. , 2002, Cerebral cortex.

[27]  S. Rose,et al.  The quantitative effects of dark-rearing and light exposure on the laminar composition and depth distribution of neurons and glia in the visual cortex (area 17) of the rat , 2004, Experimental Brain Research.

[28]  C. Müller,et al.  Astrocytes in cat visual cortex studied by GFAP and S‐100 immunocytochemistry during postnatal development , 1992, The Journal of comparative neurology.

[29]  G. Paxinos,et al.  The Rat Brain in Stereotaxic Coordinates , 1983 .

[30]  M. Stewart,et al.  Distribution of neurons and glia in the visual cortex (area 17) of the adult albino rat: A quantitative description , 1987, Neuroscience.

[31]  W. Greenough,et al.  Monocular deprivation alters the morphology of glial fibrillary acidic protein-immunoreactive astrocytes in the rat visual cortex , 1995, Brain Research.

[32]  Sergey Fedoroff,et al.  Cell biology and pathology of astrocytes , 1986 .

[33]  R. Herndon,et al.  Astrocytes play a role in regulation of synaptic density , 1987, Brain Research.

[34]  K. Selmaj Pathophysiology of the blood-brain barrier , 2004, Springer Seminars in Immunopathology.

[35]  J. Wolff,et al.  Postnatal development of glial fibrillary acidic protein, vimentin and S100 protein in monkey visual cortex: evidence for a transient reduction of GFAP immunoreactivity. , 1994, Brain research. Developmental brain research.

[36]  D. Mitchell,et al.  Gene expression patterns during enhanced periods of visual cortex plasticity , 2002, Neuroscience.

[37]  E. Argandoña,et al.  Effects of dark-rearing on the vascularization of the developmental rat visual cortex , 1996, Brain Research.

[38]  F. Duffy,et al.  Dark rearing prolongs physiological but not anatomical plasticity of the cat visual cortex , 1985, The Journal of comparative neurology.

[39]  W. Greenough,et al.  Learning causes synaptogenesis, whereas motor activity causes angiogenesis, in cerebellar cortex of adult rats. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[40]  M. Cynader,et al.  Immunohistochemical localization of the S-100 beta protein in postnatal cat visual cortex: spatial and temporal patterns of expression in cortical and subcortical glia. , 1993, Brain research. Developmental brain research.

[41]  D. Tropea,et al.  Long term depression is expressed during postnatal development in rat visual cortex: a role for visual experience. , 1999, Brain research. Developmental brain research.

[42]  C. P. Leblond,et al.  Response of the three main types of glial cells of cortex nad corpus callosum in rats handled during suckling or exposed to enriched, control and impoverished environments following weaning , 1977, The Journal of comparative neurology.