TY - JOUR
T1 - Generation of cerebellar neuron precursors from embryonic stem cells
AU - Su, Hong Lin
AU - Muguruma, Keiko
AU - Matsuo-Takasaki, Mami
AU - Kengaku, Mineko
AU - Watanabe, Kiichi
AU - Sasai, Yoshiki
N1 - Funding Information:
We are grateful to members of the Sasai laboratory for discussion, to A. Miyawaki, J. Miyazaki, J. Johnson, and R. Segal for the Venus plasmid, the CAGGS vector, and the control antibodies for Math1 and Zic1, to Y. Takahashi for advice on Purkinje cell markers, to H. Nakamura for discussion on the role of Fgf8, and to N. Sasai, T. Haraguchi, Y. Nakazawa, M. Matsumura, A. Nishiyama, T. Katayama, and M. Kawada for technical advice and assistance in preparation of antisera. This work was supported by grants-in-aid from MEXT (Y.S., M.K.), the Kobe Cluster Project (Y.S.), and the Leading Project (Y.S.).
PY - 2006/2/15
Y1 - 2006/2/15
N2 - Here, we report in vitro generation of Math1+ cerebellar granule cell precursors and Purkinje cells from ES cells by using soluble patterning signals. When neural progenitors induced from ES cells in a serum-free suspension culture are subsequently treated with BMP4 and Wnt3a, a significant proportion of these neural cells become Math1+. The induced Math1+ cells are mitotically active and express markers characteristic of granule cell precursors (Pax6, Zic1, and Zipro1). After purification by FACS and coculture with postnatal cerebellar neurons, ES cell-derived Math1+ cells exhibit typical features of neurons of the external granule cell layer, including extensive motility and a T-shaped morphology. Interestingly, differentiation of L7+/Calbindin-D28K + neurons (characteristic of Purkinje cells) is induced under similar culture conditions but exhibits a higher degree of enhancement by Fgf8 rather than by Wnt3a. This is the first report of in vitro recapitulation of early differentiation of cerebellar neurons by using the ES cell system.
AB - Here, we report in vitro generation of Math1+ cerebellar granule cell precursors and Purkinje cells from ES cells by using soluble patterning signals. When neural progenitors induced from ES cells in a serum-free suspension culture are subsequently treated with BMP4 and Wnt3a, a significant proportion of these neural cells become Math1+. The induced Math1+ cells are mitotically active and express markers characteristic of granule cell precursors (Pax6, Zic1, and Zipro1). After purification by FACS and coculture with postnatal cerebellar neurons, ES cell-derived Math1+ cells exhibit typical features of neurons of the external granule cell layer, including extensive motility and a T-shaped morphology. Interestingly, differentiation of L7+/Calbindin-D28K + neurons (characteristic of Purkinje cells) is induced under similar culture conditions but exhibits a higher degree of enhancement by Fgf8 rather than by Wnt3a. This is the first report of in vitro recapitulation of early differentiation of cerebellar neurons by using the ES cell system.
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U2 - 10.1016/j.ydbio.2005.11.010
DO - 10.1016/j.ydbio.2005.11.010
M3 - Article
C2 - 16406324
AN - SCOPUS:31544468914
SN - 0012-1606
VL - 290
SP - 287
EP - 296
JO - Developmental Biology
JF - Developmental Biology
IS - 2
ER -