
03-6403T1 10xBP
First turn of a mouse cochlea labeled to show all cell nuclei (green)
and calretinin (red) which occurs in neurons and in Inner Hair Cells
(IHC). The single row of Inner Hair Cells arcs across the middle
of the image. The 3 rows of Outer Hair Cell nuclei are observed
in their characteristic arrangement paralleling the arc of IHC.
Whole mount label embedded in epoxy resin, imaged with Bio-Rad MRC-1024
confocal microscope, 10x objective (Nikon). Glen MacDonald. |

311T2MLEproj
High resolution imaging of 3 inner hair cells (IHC) innervated by
dendrites of the neurons in the spiral ganglion. Calretinin (red)
labels the IHC while nerve fibers were labeled for neurofilaments
(green). Afferent fibers may be seen extending to the left of the
IHC, en route to the outer hair cells and support cells. Nuclei
appear blue. Whole mount label embedded in epoxy resin, imaged with
widefield microscope, 63x objective (Zeiss) and deconvolved (Huygens
software). Glen MacDonald. |

NL_Synaptophysin
Single neuron in avian N. lamaris filled with rhodamine-conjugated
dextran (red) surrounded by fluorescent label for the pre-synaptic
protein, synaptophysin (green). The blue dots represent putative
colocalization of synaptophysin along the dendrites. 100X/1.4 (Nikon)
on a Bio-Rad MRC-1024, deconvolved by Huygens, masking and projection
by Slidebook. Staci Sorensen and Rachael Nehmer. |

NM
phalloidin TOPRO PIC
This is a picture of zebrafish neuromasts stained with flourescent
dyes, Phalloidin (green) and Topro-3 (blue). Keri O'Connell. |

mtgmtrtp3BP
adj
Raw images of live neuromast hair cells from a zebrafish. Cells
appear outlined in yellow as mitochondria are labeled for a fluorescent
indicators of all mitochondria (green) and mitochondria with a high
electropotential gradient (red). The raw images appear blurred from
out of focus light and optical effects of the sample. Some mitochondria
appear of one color due to organelle motion during the image acquisition.
Brightest point projection of 72 images collected by widefield fluorescence
with a 63X water immersion objective (Zeiss). Glen MacDonald. |

MTRMTGTP3ci
bp
The same optical volume displayed above, but processed by deconvolution
using Slidebook. Removal of blur restores the resolution of the
image. Mitochondria are distinctly visible. Glen MacDonald. |

P75cochlea3D
This volumetric projection of the apical turn of a P5 mouse cochlea
labeled for p75 (red) and nuclei (green). The characteristic arch
formed by the union of the inner (left) and outer (right) pillar
cells (red) is seen to the left. The large green nuclei to the left
of the pillars are of inner hair cells. The red nerve fibers may
be seen below the outer hair cells (OHC), partly obscured by the
the OHC nuclei, and extending upwards around the OHC. The Claudius
cells at far right are intensely labeled for p75. Dr. Elizabeth
Oesterle. |

P75cochleaBP
A brightest point projection from a confocal image volume of the
apical turn of a mouse cochlea, aged P5. This shows the Organ of
Corti stained for p75 receptors (red) and nuclei (green). The U-shaped
structures are the feet of inner and outer pillar cells, while cicumferential
nerve fibers run between the 3 rows of outer hair cells. Dr. Elizabeth
Oesterle. |

05-6809_6p_fitc
GFP-expressing auditory brainstem cell of a five day old animal
after 7 days in culture. The GFP plasmid was electroporated after
3 days in vitro. |