Table 2.
Time after BrdU injection and naris reopening | OB |
RMS | SVZ | ||
---|---|---|---|---|---|
GL | EPL | GCL | |||
1 h | |||||
Control | 130 ± 19 | 94 ± 8 | 366 ± 30 | 1844 ± 45 | 6920 ± 355 |
Occlusion | 96 ± 12 | 64 ± 13 | 322 ± 11 | 1838 ± 191 | 6830 ± 237 |
1 week | |||||
Occlusion | 644 ± 132 | 228 ± 28 | 5624 ± 567 | 7226 ± 187 | 2174 ± 132 |
Reopening | 586 ± 88 | 212 ± 7 | 7228 ± 575 | 7870 ± 375 | 2230 ± 245 |
4 weeks | |||||
Occlusion | 624 ± 76 | 120 ± 30 | 5558 ± 400 | 50 ± 12 | 77 ± 17 |
Reopening | 931 ± 53* | 89 ± 8 | 7376 ± 473 * | 45 ± 10 | 84 ± 11 |
After 4 week naris occlusion, mice were injected with BrdU and the nasal plug was removed. Number of BrdU+ cells in the SVZ, RMS, and three OB layers (GL, EPL, and GCL) was counted 1 h, 1 week, and 4 weeks after BrdU injection. There was no significant difference in the number of BrdU+ proliferating cells in each region between the naris-occluded and control hemispheres (1 h). One week after BrdU injection, neuronal progenitors in the SVZ and RMS that had incorporated BrdU migrated toward the OB, resulting in a wide distribution of BrdU + cells along the SVZ–OB pathway. Naris reopening did not affect the distribution of BrdU + cells in the SVZ–OB (1 week). Four weeks after BrdU injection, we quantified the surviving BrdU+ cells in the GCL and GL layers of the OB. Naris reopening increased the number of BrdU+ cells in these layers (4 weeks, n = 4 animals in each condition;
*p < 0.05, unpaired t test).