TY - JOUR
T1 - Astrocyte differentiation of fetal neuroepithelial cells involving cardiotrophin-1-induced activation of STAT3
AU - Ochiai, Wataru
AU - Yanagisawa, Makoto
AU - Takizawa, Takumi
AU - Nakashima, Kinichi
AU - Taga, Tetsuya
N1 - Funding Information:
We are very grateful to Ms Yuko Nakamura and Ms Yuki Noguchi for their excellent secretarial assistance. We also thank Mr Ryotaro Watabe and Ms Kaori Kaneko for technical help. This work was supported by Grant-in-Aid from the Ministry of Education, Science, Sports and Culture, Human Frontier Science Program, Ichiro Kanehara Foundation, Inamori Foundation, Kato Memorial Bioscience Foundation, and Naito Foundation.
PY - 2001/6/7
Y1 - 2001/6/7
N2 - Cardiotrophin-1 (CT-1) belongs to the interleukin (IL-)6 family of cytokines that share membrane glycoprotein 130 (gp130) as a receptor component critical for signal transduction. We here observed that CT-1 was expressed in mouse fetal neuroepithelial cells, and was capable of inducing astrocyte differentiation from these cells in a synergistic manner with bone morphogenetic protein (BMP)-2, whose expression was also found in the fetal brain. CT-1-induced astrocyte differentiation was solely gp130-dependent. CT-1-stimulation led to promoter activation of the gene for an astrocyte marker, glial fibrillary acidic protein (GFAP), which was clearly inhibited by expression of a dominant negative form of a gp130-downstream transcription factor, signal transducer and activator of transcription 3(STAT3), or by introduction of a mutation in a single STAT3-binding site in the promoter, suggesting a critical role of STAT3 in the CT-1-induced GFAP transcription. These results suggest that astrocyte differentiation in the developing brain involves CT-1-signaling which cooperates with BMP2.
AB - Cardiotrophin-1 (CT-1) belongs to the interleukin (IL-)6 family of cytokines that share membrane glycoprotein 130 (gp130) as a receptor component critical for signal transduction. We here observed that CT-1 was expressed in mouse fetal neuroepithelial cells, and was capable of inducing astrocyte differentiation from these cells in a synergistic manner with bone morphogenetic protein (BMP)-2, whose expression was also found in the fetal brain. CT-1-induced astrocyte differentiation was solely gp130-dependent. CT-1-stimulation led to promoter activation of the gene for an astrocyte marker, glial fibrillary acidic protein (GFAP), which was clearly inhibited by expression of a dominant negative form of a gp130-downstream transcription factor, signal transducer and activator of transcription 3(STAT3), or by introduction of a mutation in a single STAT3-binding site in the promoter, suggesting a critical role of STAT3 in the CT-1-induced GFAP transcription. These results suggest that astrocyte differentiation in the developing brain involves CT-1-signaling which cooperates with BMP2.
UR - http://www.scopus.com/inward/record.url?scp=0035821609&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0035821609&partnerID=8YFLogxK
U2 - 10.1006/cyto.2001.0883
DO - 10.1006/cyto.2001.0883
M3 - Article
C2 - 11444906
AN - SCOPUS:0035821609
SN - 1043-4666
VL - 14
SP - 264
EP - 271
JO - Cytokine
JF - Cytokine
IS - 5
ER -