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The Journal of Neuroscience, January 1, 2003, 23(1):260-268
Signaling by Bone Morphogenetic Proteins and Smad1 Modulates the
Postnatal Differentiation of Cerebellar Cells
Catherine
Angley1,
Mallika
Kumar1,
Kyl J.
Dinsio2,
Alison K.
Hall2, and
Ruth E.
Siegel1
Departments of 1 Pharmacology and
2 Neurosciences, Case Western Reserve University, School of
Medicine, Cleveland, Ohio 44106
Previous studies have demonstrated that bone morphogenetic proteins
(BMPs) activate the Smad1 signaling pathway to regulate cell
determination and differentiation in the embryonic nervous system.
Studies examining gene and protein expression in the rat cerebellum
suggest that this pathway also regulates postnatal differentiation.
Using microarrays, we found that Smad1 mRNA expression in the
cerebellum increases transiently at postnatal day 6 (P6). Immunohistochemistry and Western blots showed that Smad1 and BMP4 proteins are present in the cerebellum, and that their expression also
changes postnatally. The proteins are detectable at P4-P6, a stage at
which most cerebellar cells reside in the external germinal layer
(EGL), where they extensively differentiate. The levels become maximal
at P8-P10, when neurons begin to migrate from the EGL into their
mature positions in the internal granule layer. In cerebellar cultures
prepared at P6 or P10, BMP4 activates Smad1 signaling to modulate cell
differentiation. Brief BMP4 application caused Smad1 translocation from
the neuronal cytoplasm into the nucleus, where it is known to regulate
transcription in association with Smad4. Longer BMP4 treatment promoted
the differentiation of both neuronal and non-neuronal cells. By 3 d, neuronal processes appeared more fasciculated, and the level of
synaptotagmin, a protein found in synaptic vesicles, increased. In
addition, many astroglial cells became more branched and stellate in
morphology. The BMP-induced changes were reduced by treatment with
antisense oligonucleotides to Smad1 or Smad4. These findings in
vivo and in culture suggest that BMP4 and Smad1 signaling
participate in regulating postnatal cerebellar differentiation.
Key words:
Smad1; BMP; granule neurons; cerebellum; differentiation; microarrays
Copyright © 2003 Society for Neuroscience 0270-6474/03/231260-09$05.00/0
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