TY - JOUR
T1 - Current understanding of adult neurogenesis in the mammalian brain
T2 - How does adult neurogenesis decrease with age?
AU - Kase, Yoshitaka
AU - Kase, Yoshitaka
AU - Shimazaki, Takuya
AU - Okano, Hideyuki
N1 - Publisher Copyright:
© 2020 The Author(s).
PY - 2020/6/18
Y1 - 2020/6/18
N2 - Adult neurogenesis occurs throughout life in restricted brain regions in mammals. However, the number of neural stem cells (NSCs) that generate new neurons steadily decreases with age, resulting in a decrease in neurogenesis. Transplantation of mesenchymal cells or cultured NSCs has been studied as a promising treatment in models of several brain injuries including cerebral infarction and cerebral contusion. Considering the problems of host-versus-graft reactions and the tumorigenicity of transplanted cells, the mobilization of endogenous adult NSCs should be more feasible for the treatment of these brain injuries. However, the number of adult NSCs in the adult brain is limited, and their mitotic potential is low. Here, we outline what we know to date about why the number of NSCs and adult neurogenesis decrease with age. We also discuss issues applicable to regenerative medicine.
AB - Adult neurogenesis occurs throughout life in restricted brain regions in mammals. However, the number of neural stem cells (NSCs) that generate new neurons steadily decreases with age, resulting in a decrease in neurogenesis. Transplantation of mesenchymal cells or cultured NSCs has been studied as a promising treatment in models of several brain injuries including cerebral infarction and cerebral contusion. Considering the problems of host-versus-graft reactions and the tumorigenicity of transplanted cells, the mobilization of endogenous adult NSCs should be more feasible for the treatment of these brain injuries. However, the number of adult NSCs in the adult brain is limited, and their mitotic potential is low. Here, we outline what we know to date about why the number of NSCs and adult neurogenesis decrease with age. We also discuss issues applicable to regenerative medicine.
KW - Adult neurogenesis
KW - Aging
KW - Neural stem cell
KW - Subgranular zone
KW - Transit amplifying progenitor cell
KW - Ventricular-subventricular zone
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U2 - 10.1186/s41232-020-00122-x
DO - 10.1186/s41232-020-00122-x
M3 - Review article
AN - SCOPUS:85087058643
SN - 1880-9693
VL - 40
JO - Inflammation and Regeneration
JF - Inflammation and Regeneration
IS - 1
M1 - 10
ER -