Promotion of Cortical Neurogenesis from the Neural Stem Cells in the Adult Mouse Subcallosal Zone

Author:

Kim Joo Yeon1,Choi Kyuhyun2,Shaker Mohammed R.1,Lee Ju-Hyun1,Lee Boram1,Lee Eunsoo1,Park Jae-Yong3,Lim Mi-Sun45,Park Chang-Hwan456,Shin Ki Soon2,Kim Hyun1,Geum Dongho7,Sun Woong1

Affiliation:

1. Department of Anatomy and Division of Brain Korea 21 Plus Biomedical Science, Korea University College of Medicine, Seoul, Korea

2. Department of Biology, Department of Life and Nanopharmaceutical Sciences, Kyung Hee University, Seoul, Republic of Korea

3. School of Biosystem and Biomedical Science, College of Health Science, Korea University, Seoul, Republic of Korea

4. Graduate School of Biomedical Science and Engineering, Seoul, Korea

5. Hanyang Biomedical Research Institute, Seoul, Korea

6. Department of Microbiology, College of Medicine, Hanyang University, Seoul, Korea

7. Department of Biomedical Sciences, Korea University College of Medicine, Seoul, Korea

Abstract

Abstract Neurogenesis occurs spontaneously in the subventricular zone (SVZ) of the lateral ventricle in adult rodent brain, but it has long been debated whether there is sufficient adult neurogenesis in human SVZ. Subcallosal zone (SCZ), a posterior continuum of SVZ closely associated with posterior regions of cortical white matter, has also been reported to contain adult neural stem cells (aNSCs) in both rodents and humans. However, little is known whether SCZ-derived aNSC (SCZ-aNSCs) can produce cortical neurons following brain injury. We found that SCZ-aNSCs exhibited limited neuronal differentiation potential in culture and after transplantation in mice. Neuroblasts derived from SCZ initially migrated toward injured cortex regions following brain injury, but later exhibited apoptosis. Overexpression of anti-apoptotic bcl-xL in the SCZ by retroviral infection rescued neuroblasts from cell death in the injured cortex, but neuronal maturation was still limited, resulting in atrophy. In combination with Bcl-xL, infusion of brain-derived neurotropic factor rescued atrophy, and importantly, a subset of such SCZ-aNSCs differentiated and attained morphological and physiological characteristics of mature, excitatory neurons. These results suggest that the combination of anti-apoptotic and neurotrophic factors might enable the use of aNSCs derived from the SCZ in cortical neurogenesis for neural replacement therapy.

Funder

National Research Foundation

Korean Ministry of Science, ICT, and Future Planning

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,Molecular Medicine

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