Figure 6BrdU+/nestin+ cells exhibited the distribution, morphology, and staining specificity consistent with adult-derived bi- or tri-potential progenitor cells
(Horner et al., 2000; Shihabuddin et al., 2000). Confocal microscope images of ventrolateral white matter of an FES-treated rat in the cell birth group. Nestin immunoreactivity shown in blue, BrdU labeling shown in red. A, D, and G show overlays of nestin and BrdU; B, E, and H show overlays of BrdU and other markers; C, F, and I show triple overlays. (A-C) Nestin immunoreactivity (blue) was found predominantly in white matter (L5 shown). Less than 2% of nestin+/BrdU+ cells co-labeled with GFAP (green, arrowhead). (D-F) A few BrdU+/nestin+ cells also expressed NG2 (green, arrowhead). These triple-labeled cells were distinguished from other BrdU+/nestin+ cells by their pial location and their morphologies (L5 shown). (G-I) Macrophages, labeled with ED1 (green), were located within and surrounding the injury site (T11 shown). We did not identify a substantial number of NG2+/ED-1+, nestin+/ED1+ cells. (J-L) BrdU+ oligodendrocytes. Representative examples of the distribution pattern and cell morphology of BrdU+/APC-CC1+ cells (arrowheads) located at levels above (J, C2) and below (K, L5) the injury. These features are most consistent with oligodendrocytes, as is the fact that the number of BrdU+/APC-CC1+ cells increased substantially in the cell survival groups (see text). (L) Single confocal section of a BrdU+/APC-CC1+ cell. Scale bar (A-K) = 50 μm, (L) = 10 μm.