TY - JOUR
T1 - Comprehensive characterization of migration profiles of murine cerebral cortical neurons during development using FlashTag labeling
AU - Yoshinaga, Satoshi
AU - Shin, Minkyung
AU - Kitazawa, Ayako
AU - Ishii, Kazuhiro
AU - Tanuma, Masato
AU - Kasai, Atsushi
AU - Hashimoto, Hitoshi
AU - Kubo, Ken ichiro
AU - Nakajima, Kazunori
N1 - Funding Information:
This work was supported by Grants-in-Aid for Scientific Research of the Ministry of Education, Culture, Sports, Science, and Technology (MEXT), Japan/Japan Society for the Promotion of Science, Japan, Grants-in-Aid for Scientific Research (KAKENHI) ( JP17J05365 , JP18K19379 , JP19H05227 , JP18K07855 , JP19H01152 , JP19K08306 , JP20H03649 , JP20H05688 , JP16H06482 , JP20K21467 , JP20H00492 , JP19H05217 , JP18H05416 ), the Keio Gijuku Academic Development Funds , Keio Gijuku Fukuzawa Memorial Fund for the Advancement of Education and Research , Takeda Science Foundation, and, AMED , Japan ( JP20dm0207061 ), and PRIME, AMED, Japan ( JP19gm6310004 , JP20gm6310004 ). S.Y. was a Research Fellow of Japan Society for the Promotion of Science from fiscal year (FY) 2017 to FY 2019.
Funding Information:
This work was supported by Grants-in-Aid for Scientific Research of the Ministry of Education, Culture, Sports, Science, and Technology (MEXT), Japan/Japan Society for the Promotion of Science, Japan, Grants-in-Aid for Scientific Research (KAKENHI) (JP17J05365, JP18K19379, JP19H05227, JP18K07855, JP19H01152, JP19K08306, JP20H03649, JP20H05688, JP16H06482, JP20K21467, JP20H00492, JP19H05217, JP18H05416), the Keio Gijuku Academic Development Funds, Keio Gijuku Fukuzawa Memorial Fund for the Advancement of Education and Research, Takeda Science Foundation, and, AMED, Japan (JP20dm0207061), and PRIME, AMED, Japan (JP19gm6310004, JP20gm6310004). S.Y. was a Research Fellow of Japan Society for the Promotion of Science from fiscal year (FY) 2017 to FY 2019. We thank Drs. Ludovic Telley and Denis Jabaudon (University of Geneva) for technical advice and valuable discussions. We also thank Core Instrumentation Facility, Collaborative Research Resources, Keio University School of Medicine, Dr. Yoshifumi Takatsume, and distinguished technicians including Emiko Shimeno, Miki Sakota, Noriko Suzuki, Chisa Konno, and Maiko Saito for technical assistance. Greatest gratitude is expressed to all the members of Nakajima laboratory for the valuable advice, expertise, and encouragement. Conceptualization, S.Y. K.K. and K.N.; Methodology, S.Y. M.T. A. Kasai. and H.H.; Investigation, S.Y. M.K. A. Kitazawa, K.I. and M.T.; Writing – Original Draft, S.Y.; Writing – Review & Editing, K.K. and K.N.; Visualization, S.Y. M.T. and A. Kasai; Supervision, K.-i.K. and K.N.; Funding Acquisition, S.Y. A. Kasai, H.H. K.-i.K. and K.N. The authors declare no competing interests.
Publisher Copyright:
© 2021 The Author(s)
PY - 2021/4/23
Y1 - 2021/4/23
N2 - In the mammalian cerebral neocortex, different regions have different cytoarchitecture, neuronal birthdates, and functions. In most regions, neuronal migratory profiles are speculated similar based on observations using thymidine analogs. Few reports have investigated regional migratory differences from mitosis at the ventricular surface. In this study, we applied FlashTag technology, in which dyes are injected intraventricularly, to describe migratory profiles. We revealed a mediolateral regional difference in the migratory profiles of neurons that is dependent on developmental stage; for example, neurons labeled at embryonic day 12.5–15.5 reached their destination earlier dorsomedially than dorsolaterally, even where there were underlying ventricular surfaces, reflecting sojourning below the subplate. This difference was hardly recapitulated by thymidine analogs, which visualize neurogenic gradients, suggesting a biological significance different from the neurogenic gradient. These observations advance our understanding of cortical development and the power of FlashTag in studying migration and are thus resources for future neurodevelopmental studies.
AB - In the mammalian cerebral neocortex, different regions have different cytoarchitecture, neuronal birthdates, and functions. In most regions, neuronal migratory profiles are speculated similar based on observations using thymidine analogs. Few reports have investigated regional migratory differences from mitosis at the ventricular surface. In this study, we applied FlashTag technology, in which dyes are injected intraventricularly, to describe migratory profiles. We revealed a mediolateral regional difference in the migratory profiles of neurons that is dependent on developmental stage; for example, neurons labeled at embryonic day 12.5–15.5 reached their destination earlier dorsomedially than dorsolaterally, even where there were underlying ventricular surfaces, reflecting sojourning below the subplate. This difference was hardly recapitulated by thymidine analogs, which visualize neurogenic gradients, suggesting a biological significance different from the neurogenic gradient. These observations advance our understanding of cortical development and the power of FlashTag in studying migration and are thus resources for future neurodevelopmental studies.
KW - Biological Sciences
KW - Developmental Neuroscience
KW - Neuroanatomy
KW - Neuroscience
KW - Techniques in Neuroscience
UR - http://www.scopus.com/inward/record.url?scp=85103047676&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85103047676&partnerID=8YFLogxK
U2 - 10.1016/j.isci.2021.102277
DO - 10.1016/j.isci.2021.102277
M3 - Article
AN - SCOPUS:85103047676
SN - 2589-0042
VL - 24
JO - iScience
JF - iScience
IS - 4
M1 - 102277
ER -