Selective introduction of antisense oligonucleotides into single adult CNS progenitor cells using electroporation demonstrates the requirement of STAT3 activation for CNTF-induced gliogenesis

被引:48
作者
Åberg, MAI [1 ]
Ryttsén, F
Hellgren, G
Lindell, K
Rosengren, LE
MacLennan, AJ
Carlsson, B
Orwar, O
Eriksson, PS
机构
[1] Univ Gothenburg, Sahlgrens Hosp, Inst Clin Neurosci, SE-41345 Gothenburg, Sweden
[2] Univ Gothenburg, Dept Chem, SE-41296 Gothenburg, Sweden
[3] Sahlgrens Univ Hosp, Res Ctr Endocrinol & Metab, SE-41345 Gothenburg, Sweden
[4] Univ Cincinnati, Cincinnati, OH 45267 USA
关键词
D O I
10.1006/mcne.2000.0947
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
We have developed a novel method in which antisense DNA is selectively electroporated into individual adult neural progenitor cells. By electropopation of antisense oligonucleotides against signal transducer and activator of transcription 3 (STAT3) we demonstrate that ciliary neurotrophic factor (CNTF) is an instructive signal for astroglial type 2 cell fate specifically mediated via activation of STAT3. Activation of the mitogen-activated protein kinase (MAPK) signaling pathway induced only a transient increase in glial fibrillary acidic protein (GFAP) expression, and inhibition of this signaling pathway did not block the induction by CNTF of glial differentiation in progenitor cells. In addition we show that microelectroporation is a new powerful method for introducing antisense agents into single cells in complex cellular networks.
引用
收藏
页码:426 / 443
页数:18
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