TY - JOUR
T1 - Identification of proliferative progenitors associated with prominent postnatal growth of the pons
AU - Lindquist, Robert A.
AU - Guinto, Cristina D.
AU - Rodas-Rodriguez, Jose L.
AU - Fuentealba, Luis C.
AU - Tate, Matthew C.
AU - Rowitch, David H.
AU - Alvarez-Buylla, Arturo
PY - 2016/5/18
Y1 - 2016/5/18
N2 - The pons controls crucial sensorimotor and autonomic functions. In humans, it grows sixfold postnatally and is a site of paediatric gliomas; however, the mechanisms of pontine growth remain poorly understood. We show that the murine pons quadruples in volume postnatally; growth is fastest during postnatal days 0-4 (P0-P4), preceding most myelination. We identify three postnatal proliferative compartments: ventricular, midline and parenchymal. We find no evidence of postnatal neurogenesis in the pons, but each progenitor compartment produces new astroglia and oligodendroglia; the latter expand 10- to 18-fold postnatally, and are derived mostly from the parenchyma. Nearly all parenchymal progenitors at P4 are Sox2 + Olig2 +, but by P8 a Sox2 a' subpopulation emerges, suggesting a lineage progression from Sox2 + aearlya to Sox2 a' alatea oligodendrocyte progenitor. Fate mapping reveals that >90% of adult oligodendrocytes derive from P2-P3 Sox2 + progenitors. These results demonstrate the importance of postnatal Sox2 + Olig2 + progenitors in pontine growth and oligodendrogenesis.
AB - The pons controls crucial sensorimotor and autonomic functions. In humans, it grows sixfold postnatally and is a site of paediatric gliomas; however, the mechanisms of pontine growth remain poorly understood. We show that the murine pons quadruples in volume postnatally; growth is fastest during postnatal days 0-4 (P0-P4), preceding most myelination. We identify three postnatal proliferative compartments: ventricular, midline and parenchymal. We find no evidence of postnatal neurogenesis in the pons, but each progenitor compartment produces new astroglia and oligodendroglia; the latter expand 10- to 18-fold postnatally, and are derived mostly from the parenchyma. Nearly all parenchymal progenitors at P4 are Sox2 + Olig2 +, but by P8 a Sox2 a' subpopulation emerges, suggesting a lineage progression from Sox2 + aearlya to Sox2 a' alatea oligodendrocyte progenitor. Fate mapping reveals that >90% of adult oligodendrocytes derive from P2-P3 Sox2 + progenitors. These results demonstrate the importance of postnatal Sox2 + Olig2 + progenitors in pontine growth and oligodendrogenesis.
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U2 - 10.1038/ncomms11628
DO - 10.1038/ncomms11628
M3 - Article
C2 - 27188978
AN - SCOPUS:84969961310
SN - 2041-1723
VL - 7
JO - Nature Communications
JF - Nature Communications
M1 - 11628
ER -