The average background was then subtracted from the above-mentioned average of each experimental treatment group. Spectral analysis of images All images of the spinal cord dorsal horn and DRGs were captured by a Zeiss Axioscope Microscope at 20× magnification with a Nuance

Spectral Camera (Cambridge Research & Instrumentation, Woburn, MA). Utilizing the Nuance computer software, the fluorescent wavelength emission spectra was initially determined for each fluorophore utilized in the detection of the primary antibody of Alvespimycin interest (DAPI, 488 ± 10 nm; FITC, 575 ± 5 nm; Rhodamine Red 600 ± 5 nm) by using a control slide with only a drop of the pure fluorophore. This Inhibitors,research,lifescience,medical was performed in the absence of a tissue specimen that may potentially obscure the measurement of the fluorophore’s emission spectra. Two sets of additional control slides with tissue sections, one with only PBS without primary but with secondary antibody treatment,

and the other, with primary but Inhibitors,research,lifescience,medical without secondary antibody treatment, were then used to objectively eliminate low-intensity fluorescence and autofluorescence background “noise” from our measurements (Fig. 1C). Using control slides, the Nuance software allows the user to set an acceptable threshold of low-level emission Inhibitors,research,lifescience,medical fluorescent intensity (as opposed to the software’s “autothreshold” option) within and outside the defined wavelength of interest between tissue samples. The experimenter determined low-level emission intensity by closely replicating the

composite computer image with that observed through the eyepiece. Emission values that fall below this acceptable threshold of low-level emission, within and outside the defined wavelength Inhibitors,research,lifescience,medical of interest, were eliminated from our measurements (Fig. 1D). This level of fluorescent threshold for each protein Inhibitors,research,lifescience,medical marker was determined by the user, finding the most appropriate wavelength of interest that captures the specific FITC or Rhodamine Red staining for each protein marker within a tissue (e.g., dorsal horn spinal cord or DRG). Once the optimal level of fluorescent threshold was determined for a particular protein marker, this level Thymidine kinase was held consistent throughout all of the treatment groups for the image analysis (Fig. 1D). These steps were followed by software conversion of fluorescent wavelength intensity for each fluorophore to a numerical value. Autofluorescence was defined as the emission outside the defined wavelength of interest (e.g., DAPI, 488 ± 10 nm; FITC, 575 ± 5 nm; Rhodamine Red 600 ± 5 nm). These specific autofluorescent and low-level background emission values were subtracted from the image (Fig. 1E and 1F), yielding a numerical value of true fluorescent emission intensity for each fluorophore (Mansfield et al. 2008; Mahad et al. 2009).