The balance of Id3 and E47 determines neural stem/precursor cell differentiation into astrocytes

被引:58
作者
Bohrer, Christian [1 ,2 ]
Pfurr, Sabrina [1 ,2 ]
Mammadzada, Koenuel [1 ,2 ]
Schildge, Sebastian [1 ,2 ]
Plappert, Leandra [1 ,2 ]
Hils, Miriam [2 ,3 ]
Pous, Lauriane [1 ,2 ]
Rauch, Katharina S. [2 ,3 ]
Dumit, Veronica I. [4 ]
Pfeifer, Dietmar [5 ]
Dengjel, Joern [4 ]
Kirsch, Matthias [1 ]
Schachtrup, Kristina [3 ]
Schachtrup, Christian [1 ]
机构
[1] Univ Freiburg, Inst Anat & Cell Biol, D-79106 Freiburg, Germany
[2] Univ Freiburg, Fac Biol, D-79106 Freiburg, Germany
[3] Univ Freiburg, Univ Med Ctr Freiburg, CCI, D-79106 Freiburg, Germany
[4] Univ Freiburg, Dept Dermatol, Med Ctr,BIOSS Ctr Biol Signalling Studies, Freiburg Inst Adv Studies FRIAS,ZBSA Ctr Biol Sys, D-79106 Freiburg, Germany
[5] Univ Freiburg, Univ Med Ctr Freiburg, Dept Hematol Oncol & Stem Cell Transplantat, D-79106 Freiburg, Germany
关键词
astrocyte-specific genes; basic helix-loop-helix transcription factor; bone morphogenetic protein; traumatic brain injury; vascular damage; TRANSCRIPTION FACTOR OLIG2; CENTRAL-NERVOUS-SYSTEM; STEM-CELLS; SUBVENTRICULAR ZONE; TGF-BETA; POSTNATAL NEUROGENESIS; ADULT NEUROGENESIS; BRAIN; PROTEINS; NICHE;
D O I
10.15252/embj.201591118
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Adult neural stem/precursor cells (NSPCs) of the subventricular zone (SVZ) are an endogenous source for neuronal replacement in CNS disease. However, adult neurogenesis is compromised after brain injury in favor of a glial cell fate, which is mainly attributed to changes in the NSPC environment. Yet, it is unknown how this unfavorable extracellular environment translates into a transcriptional program altering NSPC differentiation. Here, we show that genetic depletion of the transcriptional regulator Id3 decreased the number of astrocytes generated from SVZ-derived adult NSPCs in the cortical lesion area after traumatic brain injury. Cortical brain injury resulted in rapid BMP-2 and Id3 up-regulation in the SVZ stem cell niche. Id3(-/-) adult NSPCs failed to differentiate into BMP-2-induced astrocytes, while NSPCs deficient for the Id3-controlled transcription factor E47 readily differentiated into astrocytes in the absence of BMP-2. Mechanistically, E47 repressed the expression of several astrocyte-specific genes in adult NSPCs. These results identify Id3 as the BMP-2-induced transcriptional regulator, promoting adult NSPC differentiation into astrocytes upon CNS injury and reveal a molecular link between environmental changes and NSPC differentiation in the CNS after injury.
引用
收藏
页码:2804 / 2819
页数:16
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