TY - JOUR
T1 - Transient, afferent input-dependent, postnatal niche for neural progenitor cells in the cochlear nucleus
AU - Volkenstein, Stefan
AU - Oshima, Kazuo
AU - Sinkkonen, Saku T.
AU - Eduardo Corrales, C.
AU - Most, Sam P.
AU - Chai, Renjie
AU - Jan, Taha A.
AU - Cheng, Alan G.
AU - Heller, Stefan
PY - 2013/8/27
Y1 - 2013/8/27
N2 - In the cochlear nucleus (CN), the first central relay of the auditory pathway, the survival of neurons during the first weeks after birth depends on afferent innervation from the cochlea. Although input-dependent neuron survival has been extensively studied in the CN, neurogenesis has not been evaluated as a possible mechanism of postnatal plasticity. Here we show that new neurons are born in the CN during the critical period of postnatal plasticity. Coincidently, we found a population of neural progenitor cells that are controlled by a complex interplay of Wnt, Notch, and TGFβ/BMP signaling, in which low levels of TGFβ/BMP signaling are permissive for progenitor proliferation that is promoted by Wnt and Notch activation. We further show that cells with activated Wnt signaling reside in the CN and that these cells have high propensity for neurosphere formation. Cochlear ablation resulted in diminishment of progenitors and Wnt/β-cateninactive cells, suggesting that the neonatal CN maintains an afferent innervation-dependent population of progenitor cells that display active canonical Wnt signaling.
AB - In the cochlear nucleus (CN), the first central relay of the auditory pathway, the survival of neurons during the first weeks after birth depends on afferent innervation from the cochlea. Although input-dependent neuron survival has been extensively studied in the CN, neurogenesis has not been evaluated as a possible mechanism of postnatal plasticity. Here we show that new neurons are born in the CN during the critical period of postnatal plasticity. Coincidently, we found a population of neural progenitor cells that are controlled by a complex interplay of Wnt, Notch, and TGFβ/BMP signaling, in which low levels of TGFβ/BMP signaling are permissive for progenitor proliferation that is promoted by Wnt and Notch activation. We further show that cells with activated Wnt signaling reside in the CN and that these cells have high propensity for neurosphere formation. Cochlear ablation resulted in diminishment of progenitors and Wnt/β-cateninactive cells, suggesting that the neonatal CN maintains an afferent innervation-dependent population of progenitor cells that display active canonical Wnt signaling.
UR - http://www.scopus.com/inward/record.url?scp=84883412187&partnerID=8YFLogxK
U2 - 10.1073/pnas.1307376110
DO - 10.1073/pnas.1307376110
M3 - Article
C2 - 23940359
AN - SCOPUS:84883412187
SN - 0027-8424
VL - 110
SP - 14456
EP - 14461
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 35
ER -