Person

Hibi, Masahiko

Person ID
ZDB-PERS-960805-246
Email
hibi.masahiko.s7@f.mail.nagoya-u.ac.jp
URL
Affiliation
Hibi Lab
Address
Graduate School of Science Nagoya University Furo, Chikusa Nagoya, Aichi, 464-8601 Japan
Country
Japan
Phone
81-52-789-5198
Fax
81-52-789-5053
ORCID ID
Biography and Research Interest
In vertebrates, the process by which a fertilized egg forms organs with complex structures and functions is precisely regulated. In our laboratory, using zebrafish and medaka, we are analyzing the molecular mechanisms that regulate the formation and function of vertebrate organs through two major research themes.

The first theme pertains to the study of neural circuits that control complex animal behaviors. During the developmental process, individual neural domains are determined along the anterior-posterior axis within the neural tissue, where neural stem cells or neural progenitor cells are generated. Neurons are produced from these cells and, as they move, they extend their neural processes to form neural circuits. In our research, we focus on the cerebellum as a model for studying neural circuits. We aim to understand the molecular mechanisms of cerebellar neural circuit formation and to elucidate the role of the cerebellar neural circuit in higher functions such as motor learning, fear response learning, and social behaviors.

The second theme involves analyzing the differentiation mechanism of neural crest cells. Neural crest cells are stem cells formed on the dorsal side of the early vertebrate embryo. These cells migrate and differentiate into various cell types, including pigment cells, while exerting their functions. We are deciphering the gene cascade that controls the differentiation process from neural crest cells to diverse cell types.
Publications
Non-Zebrafish Publications
Ikenaga T, Shimomai R, Hagio H, Kimura S, Matsumoto K, Kato DI, Uesugi K, Takeuchi A, Yamamoto N, Hibi M. Morphological analysis of the cerebellum and its efferent system in a basal actinopterygian fish, Polypterus senegalus. J Comp Neurol. 2022 Jun;530(8):1231-1246. doi: 10.1002/cne.25271. Epub 2021 Nov 24. PMID: 34729771.

Wu D, Arakawa H, Fujita A, Hashimoto H, Hibi M, Naruse K, Kamei Y, Sato C, Kitajima K. A point-mutation in the C-domain of CMP-sialic acid synthetase leads to lethality of medaka due to protein insolubility. Sci Rep. 2021 Dec 1;11(1):23211. doi: 10.1038/s41598-021-01715-3. PMID: 34853329; PMCID: PMC8636478.