Videomicroscopy of acute brain slices from amygdala and hippocampus

Video-enhanced contrast, differential-interference contrast microscopy (VEC-DICM) was used to visualize the cytoarchitecture and subcellular neuronal structure of acute brain slices from rat hippocampus and amygdala. Even at low-power magnification, the VEC-DICM system vastly improved our ability to visualize and examine the gross organization of the tissue. With medium-power magnification, the neuronal somata and proximal dendrites were clearly visible. With high-power magnification, some of the subcellular details could be clearly discerned--including cell nuclei, cell nucleoli, fine dendritic processes, and varicosities that may be synaptic expansions. We conclude that improved optical techniques should be valuable to cellular neurobiologists interested in structure-function relationships in brain slices.

[1]  T. H. Brown,et al.  Voltage-clamp analysis of mossy fiber synaptic input to hippocampal neurons. , 1983, Journal of neurophysiology.

[2]  S. Kelso,et al.  Differential conditioning of associative synaptic enhancement in hippocampal brain slices. , 1986, Science.

[3]  S. Kater,et al.  The regulation of neurite outgrowth, growth cone motility, and electrical synaptogenesis by serotonin. , 1987, Journal of neurobiology.

[4]  B. Gähwiler Organotypic monolayer cultures of nervous tissue , 1981, Journal of Neuroscience Methods.

[5]  W. N. Ross,et al.  Regional properties of calcium entry in barnacle neurons determined with Arsenazo III and a photodiode array , 1986, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[6]  Hamlyn Lh The fine structure of the mossy fibre endings in the hippocampus of the rabbit. , 1962 .

[7]  B. MacVicar Infrared video microscopy to visualize neurons in the in vitro brain slice preparation , 1984, Journal of Neuroscience Methods.

[8]  D. Amaral,et al.  Development of the mossy fibers of the dentate gyrus: I. A light and electron microscopic study of the mossy fibers and their expansions , 1981, The Journal of comparative neurology.

[9]  S. Deadwyler,et al.  Long-term potentiation : from biophysics to behavior , 1988 .

[10]  T. H. Brown,et al.  Voltage-clamp analysis of synaptic inhibition during long-term potentiation in hippocampus. , 1986, Journal of neurophysiology.

[11]  Stephen J. Smith,et al.  NMDA-receptor activation increases cytoplasmic calcium concentration in cultured spinal cord neurones , 1986, Nature.

[12]  G. Blasdel,et al.  Voltage-sensitive dyes reveal a modular organization in monkey striate cortex , 1986, Nature.

[13]  S. Schacher,et al.  Absolute specificity for retrograde fast axonal transport displayed by lipid droplets originating in the axon of an identifiedAplysia neuron in vitro , 1987, Brain Research.

[14]  J. Connor Digital imaging of free calcium changes and of spatial gradients in growing processes in single, mammalian central nervous system cells. , 1986, Proceedings of the National Academy of Sciences of the United States of America.

[15]  S. Kelso,et al.  Hebbian synapses in hippocampus. , 1986, Proceedings of the National Academy of Sciences of the United States of America.

[16]  Daniel Johnston,et al.  Biophysics and Microphysiology of Synaptic Transmission in Hippocampus , 1984 .

[17]  J. L. Wang,et al.  Endogenous lectins from cultured cells: nuclear localization of carbohydrate-binding protein 35 in proliferating 3T3 fibroblasts. , 1987, Proceedings of the National Academy of Sciences of the United States of America.

[18]  R D Allen,et al.  Video-enhanced contrast, differential interference contrast (AVEC-DIC) microscopy: a new method capable of analyzing microtubule-related motility in the reticulopodial network of Allogromia laticollaris. , 1981, Cell motility.

[19]  T. Blackstad,et al.  Special axo‐dendritic synapses in the hippocampal cortex: Electron and light microscopic studies on the layer of mossy fibers , 1961, The Journal of comparative neurology.

[20]  Elizabeth Hall Some Aspects of the Structural Organization of the Amygdala , 1972 .

[21]  M. Schindler,et al.  Nuclear actin and myosin as control elements in nucleocytoplasmic transport , 1986, The Journal of cell biology.

[22]  D. Amaral,et al.  A light and electron microscopic analysis of the mossy fibers of the rat dentate gyrus , 1986, The Journal of comparative neurology.

[23]  M. Fordham,et al.  An evaluation of confocal versus conventional imaging of biological structures by fluorescence light microscopy , 1987, The Journal of cell biology.

[24]  E. W. Kairiss,et al.  Long-Term Potentiation in Two Synaptic Systems of the Hippocampal Brain Slice , 1989 .

[25]  T. Ry New tetracarboxylate chelators for fluorescence measurement and photochemical manipulation of cytosolic free calcium concentrations. , 1986 .

[26]  Allen Rd Video-enhanced microscopy. , 1986 .

[27]  L. Cohen,et al.  Optical monitoring of membrane potential: methods of multisite optical measurement. , 1986, Society of General Physiologists series.

[28]  L. Squire CHAPTER 7 – Memory and the Brain* , 1986 .

[29]  T. H. Brown,et al.  Conductance mechanism responsible for long-term potentiation in monosynaptic and isolated excitatory synaptic inputs to hippocampus. , 1986, Journal of neurophysiology.