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Distribution of TrkB cells within the adult rat spinal cord: comparison with OPCs and mature OLs So as to ascertain whether or not TrkB nonneuronal cells have been from the OL lineage, TrkB cells were co-labeled with Olig2 (Fig. 1.C.), a transcription factor that is certainly expressed by cells in the OL cell lineage (Nishiyama et al., 2009). TrkB cells exhibited a thin rim of TrkB immunoreactivity surrounding a rounded nucleus (Fig. 1.B.; Skup et al., 2002) and all of the TrkB nonneuronal cells also expressed Olig2 (Fig. 1.C.). Frequent TrkB cells that did not express Olig2 exhibited traits of neurons and are denoted by asterisks in Figure 1.C. Some Olig2 cells did not express TrkB (Fig. 1.C.) and probably represented the NG2 or CC1 populations that did not express detectable levels of TrkB (see under). The density of TrkB nonneuronal cells within the spinal cord and their place all through the GM and WM of the spinal cord had been examined. The density of TrkB cells inside the cervical segment averaged 143 cells/mm2 within the WM and 204 cells/mm2 in GM (Fig. two.A.). No difference was observed when comparing the number of clusters amongst the two spinal segments. two.4. Perineuronal OL lineage cells inside the adult spinal cord As described in preceding studies (Skup et al., 2002; Macias et al., 2007; McCartney et al., 2008; Coulibaly and Isaacson, 2012), TrkB cells regularly had been observed in close proximity to neuronal cell bodies within the IML along with the ventral horn and hence have been categorized as perineuronal. In order to figure out the overlap of these cells with OL lineage cells markers, the expression of NG2, CC1 and/or TrkB by perineuronal cells and their association with ChAT immunoreactive (-ir) ventral horn neurons have been analyzed. Approximately 57 from the ChAT-ir neurons within the ventral horn on the cervical and thoracic cord was connected with at the very least one particular perineuronal cell (Fig. 6). CC1 and TrkB perineuronal cells both resided in close proximity for the neuronal cell body membrane (Fig. 6. A. B.) but perineuronal NG2 cells hardly ever had been observed (Fig. six.C.). About 12 with the CC1 population was perineuronal although the amount of TrkB perineuronal cells ranged from 15 -20 in the cervical and thoracic segments. Though some overlap existed amongst the CC1 and TrkB perineuronal populations, it was not comprehensive and approximately 65 and 75 on the TrkB perineuronal cells co-expressed CC1 inside the respective cervical and thoracic segments. Within the cervical segment, 5 in the NG2 population was perineuronal, though no perineuronal NG2 cells had been observed within the thoracic segment. Each segments showed fine NG2-ir processes in close proximity for the perimeter on the ventral horn motor neurons (Fig. six.C.).NIH-PA Author Manuscript NIH-PA Author Manuscript NIH-PA Author Manuscript3. Discussion3.1. Phenotype of TrkB nonneuronal cells within the intact spinal cord TrkB cells inside the rat spinal cord have been initially described by Skup et al. (2002), who noted their presence throughout the cord, and reported their co-localization with OL markers including GalC, RIP, and/or NG2. Subsequent research from our laboratory confirmed that the TrkB cells have been nonneuronal (McCartney et al., 2008), that lots of of the cells expressed CC1 (Coulibaly and Isaacson, 2012), and that they didn't express markers for astrocytes or microglia (Skup et al. 2002; Coulibaly, unpublished).