TY - JOUR
T1 - A Unique “Reversed” Migration of Neurons in the Developing Claustrum
AU - Oshima, Kota
AU - Yoshinaga, Satoshi
AU - Kitazawa, Ayako
AU - Hirota, Yuki
AU - Nakajima, Kazunori
AU - Kubo, Ken Ichiro
N1 - Funding Information:
This work was supported by Ministry of Education, Culture, Sports, Science, and Technology/Japan Society for the Promotion of Science Grants-in-Aid for Scientific Research JP20H05688, JP16H06482, JP21H02853, JP20H03649, JP19H05227, and JP19H01152; Keio Gijuku Academic Development Funds; Keio Gijuku Fukuzawa Memorial Fund for the Advancement of Education and Research; Takeda Science Foundation; Uehara Memorial Foundation; PRIME; AMED JP19gm6310004, JP20gm6310004, and JP21gm6310004; SENSHIN Medical Research Foundation; and the Jikei University Exploratory Collaboration Research Fund. We thank the members of our laboratories for their valuable discussions; and Dr. J. Miyazaki (pCAGGS vector) for permission to use the CAG promoter. The authors declare no competing financial interests.
Publisher Copyright:
Copyright © 2023 the authors.
PY - 2023/2/1
Y1 - 2023/2/1
N2 - The claustrum (CLA) is a cluster of neurons located between the insular cortex and striatum. Many studies have shown that the CLA plays an important role in higher brain function. Additionally, growing evidence suggests that CLA dysfunction is associated with neuropsychological symptoms. However, how the CLA is formed during development is not fully understood. In the present study, we analyzed the development of the CLA, especially focusing on the migration profiles of CLA neurons in mice of both sexes. First, we showed that CLA neurons were generated between embryonic day (E) 10.5 and E12.5, but mostly at E11.5. Next, we labeled CLA neurons born at E11.5 using the FlashTag technology and revealed that most neurons reached the brain surface by E13.5 but were distributed deep in the CLA 1 d later at E14.5. Time-lapse imaging of GFP-labeled cells revealed that some CLA neurons first migrated radially outward and then changed their direction inward after reaching the surface. Moreover, we demonstrated that Reelin signal is necessary for the appropriate distribution of CLA neurons. The switch from outward to “reversed” migration of developing CLA neurons is distinct from other migration modes, in which neurons typically migrate in a certain direction, which is simply outward or inward. Future elucidation of the characteristics and precise molecular mechanisms of CLA development may provide insights into the unique cognitive functions of the CLA.
AB - The claustrum (CLA) is a cluster of neurons located between the insular cortex and striatum. Many studies have shown that the CLA plays an important role in higher brain function. Additionally, growing evidence suggests that CLA dysfunction is associated with neuropsychological symptoms. However, how the CLA is formed during development is not fully understood. In the present study, we analyzed the development of the CLA, especially focusing on the migration profiles of CLA neurons in mice of both sexes. First, we showed that CLA neurons were generated between embryonic day (E) 10.5 and E12.5, but mostly at E11.5. Next, we labeled CLA neurons born at E11.5 using the FlashTag technology and revealed that most neurons reached the brain surface by E13.5 but were distributed deep in the CLA 1 d later at E14.5. Time-lapse imaging of GFP-labeled cells revealed that some CLA neurons first migrated radially outward and then changed their direction inward after reaching the surface. Moreover, we demonstrated that Reelin signal is necessary for the appropriate distribution of CLA neurons. The switch from outward to “reversed” migration of developing CLA neurons is distinct from other migration modes, in which neurons typically migrate in a certain direction, which is simply outward or inward. Future elucidation of the characteristics and precise molecular mechanisms of CLA development may provide insights into the unique cognitive functions of the CLA.
KW - claustrum
KW - development
KW - migration
KW - neuron
UR - http://www.scopus.com/inward/record.url?scp=85147318348&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85147318348&partnerID=8YFLogxK
U2 - 10.1523/JNEUROSCI.0704-22.2022
DO - 10.1523/JNEUROSCI.0704-22.2022
M3 - Article
C2 - 36631266
AN - SCOPUS:85147318348
SN - 0270-6474
VL - 43
SP - 693
EP - 708
JO - Journal of Neuroscience
JF - Journal of Neuroscience
IS - 5
ER -