Neurogenesis and brain injury: managing a renewable resource for repair
J. Clin. Invest. Anna F. Hallbergson, et al. 112:1128 doi:10.1172/JCI20098 [
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Figure 1Germinal centers in the adult brain. Neurogenesis in the adult brain is largely confined to two germinal centers: the dentate gyrus and the subventricular zone, shown schematically (
a) and in a corresponding sagittal section of the rodent brain (
b). Insets in
b show the position of high-resolution micrographs in
c–
f. In the dentate gyrus (
c), newly generated cells are detected through incorporation of the thymidine analog BrdU and labeled with a green fluorophore (Cy2). These cells differentiate into mature neurons, as seen by their coexpression of the marker NeuN (red) but not S100β (blue), a marker for mature astrocytes. In contrast, cells generated in the subventricular zone (
d) do not differentiate into mature neurons (red) but migrate away through the rostral migratory stream (RMS). Within the RMS (
e), newly generated cells are surrounded by astrocytes (glial fibrillary acidic protein [GFAP], blue) and begin to express immature neuronal markers (polysialylated neural cell adhesion molecule [PSA-NCAM], red) as they migrate to the olfactory bulb. Upon arrival in the olfactory bulb (
f), newly generated cells differentiate into mature neurons (NeuN, red), but not astrocytes (S100β, blue).