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. 2016 Jun 28;2016:2371893. doi: 10.1155/2016/2371893

Figure 2.

Figure 2

(a) Two motoneurons in a single optical section in lamina IX of the ventral horn of the lumbar spinal cord of a tamoxifen treated SLICK::trkBf/f mouse are shown. Both neurons are marked by the presence of a red fluorescent retrograde tracer, cholera toxin B-Alexa Fluor 546, that had been injected into the gastrocnemius muscles three days prior to tissue harvesting, identifying these cells as motoneurons. One of the cells also expresses yellow fluorescent protein (YFP) and was assumed to be null for the gene for trkB. Cyan structures are immunoreactive for glutamic acid decarboxylase 67 (GAD67). (b) Profile plots are shown for GAD67 immunoreactivity along the perimeters of these cells. In each plot, the average fluorescence intensity + one standard deviation is shown as a threshold by the horizontal dashed line. Fluorescence intensity values greater than this threshold are assumed to represent contacts between the perimeter of the cell and structures immunoreactive for GAD67. The numbers next to each plot indicate the percent of the perimeter of the cell in such contact.