Cats were raised from birth with one eye viewing horizontal lines and one eye viewing vertical lines. Elongated receptive fields of cells in the visual cortex were horizontally or vertically oriented-no oblique fields were found. Units with horizontal fields were activated only by the eye exposed to horizontal lines; units with vertical fields only by the eye exposed to vertical lines.

Early experience can affect nervous system development in both vertebrate and invertebrate animals. We have now demonstrated that visual stimulation modifies the size of the optic lobes in the laboratory fruitfly Drosophila melanogaster. Monocular deprivation (painting over one eye) decreases the aggregate volume of the lamina, medulla, and lobula plate by up to 6%. The laminae of control flies kept in complete darkness showed a more robust volume difference that could be as much as 30%. An electron microscopy study revealed that the changes in the lamina are largely attributable to an increase in the terminals of the photoreceptor cell axons. The volume of the lamina increases during the first 24 hr after emergence, and it grows more in the light than in darkness. When flies are kept in the dark for the first 12 hr of their adult life and are then brought back to light for the next 3.5 days, the lamina is almost as small as in flies raised for 4 d in constant darkness. Twelve hour dark shifts at a later time are less effective. This finding suggests a critical period for lamina development during day 1 of the adult. The lamina depends on visual stimulation to maintain its size during the first 5 d after emergence. Dark-rearing for 1 d or more at any stage during that period decreases its volume to the level of flies raised in constant darkness. A lamina that is once reduced in size seems not to recover.

1. The early visual experience of nine cats was restricted to viewing horizontal or vertical lines inside opaque goggles. 2. When the kittens were 3-4 mo old, extracellular recordings were made in the primary visual cortex. To obtain a representative sample of cortical cells, units were studied at regularly spaced intervals along the course of electrode penetrations traveling oblique to the cortical surface. An automated assessment of preferred orientation using a computer-driven optical display was employed, and during the recording session the experimenters did not know which orientation(s) each animal had viewed in early life. 3. In the cats that viewed horizontal lines with one eye and vertical lines with the other during rearing, two major findings of previous workers (14) were confirmed. First, a majority of units were not selective for orientation. Second, units with preferred orientations near vertical tended to be activated exclusively by the eye that had viewed vertical, and likewise for horizontal. 4. In cats that viewed lines of the same orientation with both eyes during rearing, a substantially smaller proportion of units were selective for orientation; the preferred orientations of these units also tended to match the orientation to which the cats had been exposed. 5. Portions of some electrode penetrations showed an orderly arrangement of cells according to preferred orientation similar to that seen in normal cats, but with regions over which only nonselective cells were found. Many penetrations appeared less orderly. 6. The results are consistent with a role for early visual experience in maintaining the responsiveness and innate selectivity of cortical neurons, although they cannot entirely rule out the possibility that experience may alter or determine the preferred orientation of some cells.

The epigenetic machinery plays a pivotal role in the control of many of the body's key cellular functions. It modulates an array of pliable mechanisms that are readily and durably modified by intracellular or extracellular factors. In the fast-moving field of neuroepigenetics, it is emerging that faulty epigenetic gene regulation can have dramatic consequences on the developing CNS that can last a lifetime and perhaps even affect future generations. Mounting evidence suggests that environmental factors can impact the developing brain through these epigenetic mechanisms and this report reviews and examines the epigenetic effects of one of the most common neurotoxic pollutants of our environment, which is believed to have no safe level of exposure during human development: lead.

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The genetics of gene expression in recombinant inbred lines (RILs) can be mapped as expression quantitative trait loci (eQTLs). So-called "genetical genomics" studies have identified locally-acting eQTLs (cis-eQTLs) for genes that show differences in steady state RNA levels. These studies have also identified distantly-acting master-modulatory trans-eQTLs that regulate tens or hundreds of transcripts (hotspots or transbands). We expand on these studies by performing genetical genomics experiments in two environments in order to identify trans-eQTL that might be regulated by developmental exposure to the neurotoxin lead. Flies from each of 75 RIL were raised from eggs to adults on either control food (made with 250 µM sodium acetate), or lead-treated food (made with 250 µM lead acetate, PbAc). RNA expression analyses of whole adult male flies (5-10 days old) were performed with Affymetrix DrosII whole genome arrays (18,952 probesets). Among the 1,389 genes with cis-eQTL, there were 405 genes unique to control flies and 544 genes unique to leadtreated ones (440 genes had the same cis-eQTLs in both samples). There are 2,396 genes with trans-eQTL which mapped to 12 major transbands with greater than 95 genes. Permutation analyses of the strain labels but not the expression data suggests that the total number of eQTL and the number of transbands are more important criteria for validation than the size of the transband. Two transbands, one located on the 2 nd chromosome and one on the 3 rd chromosome, co-regulate 33 lead-induced genes, many of which are involved in neurodevelopmental processes. For these 33 genes, rather than allelic variation at one locus exerting differential effects in two environments, we found that variation at two different loci are required for optimal effects on lead-induced expression.

The class of neurons within the visual cortex of normal adult cats that has the smallest receptive fields (<2.25 degrees2) and that responds only to low rates of stimulus motion (S5O0/sec) responds preferentially to lines oriented about either the horizontal axis (+22.50) or the vertical axis (±22.50). In animals reared without exposure to patterned visual stimulation, many of these cells display orientation preferences but are activated monocularly. In contrast, in normal animals, neurons that have larger receptive fields or that respond to higher rates of stimulus motion do not exhibit a similar bias in the distribution of their orientation preferences. Cells of this type, studied in animals reared without exposure to patterned visual stimuli, are activated binocularly but do not display orientation preferences.Three classes of cells have been identified in the retina and in the dorsal lateral geniculate nucleus (LGNd) of the cat: X cells, Y cells, and W cells. During postnatal development these three neuron types are not affected equally by visual stimulation-the populations of X cells and W cells in the cat's visual system appear to be less dependent than the population of Y cells upon sensory stimulation for the maintenance or for the development of normal function (1-5). The manner in which these differences in experience sensitivity in the retina and LGNd affect cortical development, however, remains unclear (6).To examine further the role that early visual experience plays in the development or maintenance of the response properties of cortical neurons, we have compared cells in the visual cortex of normal cats with those in cats reared from birth for prolonged periods without exposure to patterned visual stimuli. We now report that the class of cortical cells found in normal cats that has the smallest receptive fields and that responds only to relatively low rates of stimulus motion responds preferentially to horizontal and to vertical lines. These cells appear to be insensitive to early experience for the development or maintenance of orientation sensitivity but appear to be sensitive to such experience for the development or maintenance of binocularity.