Downregulation of activating transcription factor 5 is required for differentiation of neural progenitor cells into astrocytes

被引:72
作者
Angelastro, JM
Mason, JL
Ignatova, TN
Kukekov, VG
Stengren, GB
Goldman, JE
Greene, LA
机构
[1] Columbia Univ Coll Phys & Surg, Dept Pathol, New York, NY 10032 USA
[2] Columbia Univ Coll Phys & Surg, Ctr Neurobiol & Behav, New York, NY 10032 USA
[3] Thomas Jefferson Univ, Farber Inst Neurosci, Philadelphia, PA 19107 USA
[4] Univ Florida, Shands Canc Ctr, McKnight Brain Inst, Dept Neurosci, Gainesville, FL 32610 USA
[5] Univ Florida, Shands Canc Ctr, McKnight Brain Inst, Dept Neurosurg, Gainesville, FL 32610 USA
关键词
ATF5; neural progenitor cells; CNTF; astrocyte; ventricular zone; neuron;
D O I
10.1523/JNEUROSCI.3447-04.2005
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The mechanisms that regulate neural progenitor cell differentiation are primarily unknown. The transcription factor activating transcription factor 5 (ATF5) is expressed in neural progenitors of developing brain but is absent from mature astrocytes and neurons. Here, we demonstrate that ATF5 regulates the conversion of ventricular zone (VZ) and subventricular zone (SVZ) neural progenitors into astrocytes. Constitutive ATF5 expression maintains neural progenitor cell proliferation and blocks their in vitro and in vivo differentiation into astrocytes. Conversely, loss of ATF5 function promotes cell-cycle exit and allows astrocytic differentiation in vitro and in vivo. CNTF, a promoter of astrocytic differentiation, downregulates endogenous ATF5, whereas constitutively expressed ATF5 suppresses CNTF-promoted astrocyte genesis. Unexpectedly, constitutive ATF5 expression in neonatal SVZ cells both in vitro and in vivo causes them to acquire properties and anatomic distributions of VZ cells. These findings identify ATF5 as a key regulator of astrocyte formation and potentially of the VZ to SVZ transition.
引用
收藏
页码:3889 / 3899
页数:11
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