scholarly journals Brain Area-Specific Effect of TGF-β Signaling on Wnt-Dependent Neural Stem Cell Expansion

2008 ◽  
Vol 2 (5) ◽  
pp. 472-483 ◽  
Author(s):  
Sven Falk ◽  
Heiko Wurdak ◽  
Lars M. Ittner ◽  
Fabian Ille ◽  
Grzegorz Sumara ◽  
...  
2013 ◽  
Vol 12 (1) ◽  
pp. 88-100 ◽  
Author(s):  
M. Ángeles Marqués-Torrejón ◽  
Eva Porlan ◽  
Ana Banito ◽  
Esther Gómez-Ibarlucea ◽  
Andrés J. Lopez-Contreras ◽  
...  

Cell Reports ◽  
2013 ◽  
Vol 3 (5) ◽  
pp. 1398-1406 ◽  
Author(s):  
Shan Bian ◽  
Janet Hong ◽  
Qingsong Li ◽  
Laura Schebelle ◽  
Andrew Pollock ◽  
...  

2014 ◽  
Vol 289 (8) ◽  
pp. 4626-4633 ◽  
Author(s):  
Amber N. Ziegler ◽  
Shravanthi Chidambaram ◽  
Briony E. Forbes ◽  
Teresa L. Wood ◽  
Steven W. Levison

2021 ◽  
Author(s):  
Nannan Guo ◽  
Kelsey McDermott ◽  
Yu-Tzu Shih ◽  
Haley Zanga ◽  
Debolina Ghosh ◽  
...  

Experience governs neurogenesis from radial-glial neural stem cells (RGLs) in the adult hippocampus to support memory. Transcription factors in RGLs integrate physiological signals to dictate self-renewal division mode. Whereas asymmetric RGL divisions drive neurogenesis during favorable conditions, symmetric divisions prevent premature neurogenesis while amplifying RGLs to anticipate future neurogenic demands. The identities of transcription factors regulating RGL symmetric self-renewal, unlike those that regulate RGL asymmetric self-renewal, are not known. Here, we show that the transcription factor Kruppel-like factor 9 (Klf9) is elevated in quiescent RGLs and inducible, deletion of Klf9 promotes RGL activation state. Clonal analysis and longitudinal intravital 2-photon imaging directly demonstrate that Klf9 functions as a brake on RGL symmetric self-renewal. In vivo translational profiling of RGLs lacking Klf9 generated a blueprint of RGL symmetric self-renewal for stem cell community. Together, these observations identify Klf9 as a transcriptional regulator of neural stem cell expansion in the adult hippocampus.


2018 ◽  
Vol 8 (1) ◽  
Author(s):  
Chan-Il Choi ◽  
Hyesook Yoon ◽  
Kristen L. Drucker ◽  
Monica R. Langley ◽  
Laurel Kleppe ◽  
...  

eLife ◽  
2022 ◽  
Vol 11 ◽  
Author(s):  
Nannan Guo ◽  
Kelsey D McDermott ◽  
Yu-Tzu Shih ◽  
Haley Zanga ◽  
Debolina Ghosh ◽  
...  

Experience governs neurogenesis from radial-glial neural stem cells (RGLs) in the adult hippocampus to support memory. Transcription factors in RGLs integrate physiological signals to dictate self-renewal division mode. Whereas asymmetric RGL divisions drive neurogenesis during favorable conditions, symmetric divisions prevent premature neurogenesis while amplifying RGLs to anticipate future neurogenic demands. The identities of transcription factors regulating RGL symmetric self-renewal, unlike those that regulate RGL asymmetric self-renewal, are not known. Here, we show in mice that the transcription factor Kruppel-like factor 9 (Klf9) is elevated in quiescent RGLs and inducible, deletion of Klf9 promotes RGL activation state. Clonal analysis and longitudinal intravital 2-photon imaging directly demonstrate that Klf9 functions as a brake on RGL symmetric self-renewal. In vivo translational profiling of RGLs lacking Klf9 generated a molecular blueprint for RGL symmetric self-renewal that was characterized by upregulation of genetic programs underlying Notch and mitogen signaling, cell-cycle, fatty acid oxidation and lipogenesis. Together, these observations identify Klf9 as a transcriptional regulator of neural stem cell expansion in the adult hippocampus.


2010 ◽  
Vol 24 (7) ◽  
pp. 683-695 ◽  
Author(s):  
H. K. Liu ◽  
Y. Wang ◽  
T. Belz ◽  
D. Bock ◽  
A. Takacs ◽  
...  

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