TY - JOUR
T1 - AMPA glutamate receptors are required for sensory-organ formation and morphogenesis in the basal chordate
AU - Hirai, Shinobu
AU - Hotta, Kohji
AU - Kubo, Yoshihiro
AU - Nishino, Atsuo
AU - Okabe, Shigeo
AU - Okamura, Yasushi
AU - Okado, Haruo
N1 - Funding Information:
ACKNOWLEDGMENTS. We give special thanks to Dr. Takeo Horie (University of Tsukuba, Shimoda, Japan), who gave us the pSP eGFP plasmid and critical advice. The anti-arrestin antibody was a kind gift from Dr. Masashi Nakagawa (University of Hyogo, Kamigori, Japan) and Dr. Horie (University of Tsukuba, Shimoda, Japan). We thank Dr. Hiroki Takahashi (National Institute for Basic Biology, Okazaki, Japan) for providing the ascidian samples for the real-time PCR and in situ hybridization. We also thank Dr. Yoshimichi Murata (Tohoku University) for the pGEMHE plasmid. Rat GluA2 cDNA plasmid was kindly gifted by Dr. James Boulter (University of California, Los Angeles). Dr. Kotaro Oka (Keio University) and Dr. Junjiro Horiuch (Tokyo Metropolitan Institute of Medical Science, Tokyo) kindly gave us helpful discussion. This work was supported by Japan Society for the Promotion of Science KAKENHI Grants 26830033 (to S.H.), 16K07426 and 16H01451 (to K.H.), 25117006 and 26250014 (to S.O.), and 16K14569 and 26290016 (to H.O.) and also by Japan Science and Technology Agency CREST Grant 14529570 (to S.O.).
Funding Information:
We give special thanks to Dr. Takeo Horie (University of Tsukuba, Shimoda, Japan), who gave us the pSP eGFP plasmid and critical advice. The anti-arrestin antibody was a kind gift from Dr. Masashi Nakagawa (University of Hyogo, Kamigori, Japan) and Dr. Horie (University of Tsukuba, Shimoda, Japan). We thank Dr. Hiroki Takahashi (National Institute for Basic Biology, Okazaki, Japan) for providing the ascidian samples for the real-time PCR and in situ hybridization. We also thank Dr. Yoshimichi Murata (Tohoku University) for the pGEMHE plasmid. Rat GluA2 cDNA plasmid was kindly gifted by Dr. James Boulter (University of California, Los Angeles). Dr. Kotaro Oka (Keio University) and Dr. Junjiro Horiuch (Tokyo Metropolitan Institute of Medical Science, Tokyo) kindly gave us helpful discussion. This work was supported by Japan Society for the Promotion of Science KAKENHI Grants 26830033 (to S.H.), 16K07426 and 16H01451 (to K.H.), 25117006 and 26250014 (to S.O.), and 16K14569 and 26290016 (to H.O.) and also by Japan Science and Technology Agency CREST Grant 14529570 (to S.O.).
Publisher Copyright:
© 2017, National Academy of Sciences. All rights reserved.
PY - 2017/4/11
Y1 - 2017/4/11
N2 - AMPA-type glutamate receptors (GluAs) mediate fast excitatory transmission in the vertebrate central nervous system (CNS), and their function has been extensively studied in the mature mammalian brain. However, GluA expression begins very early in developing embryos, suggesting that they may also have unidentified developmental roles. Here, we identify developmental roles for GluAs in the ascidian Ciona intestinalis. Mammals express Ca2+-permeable GluAs (Ca-P GluAs) and Ca2+-impermeable GluAs (Ca-I GluAs) by combining subunits derived from four genes. In contrast, ascidians have a single gluA gene. Taking advantage of the simple genomic GluA organization in ascidians, we knocked down (KD) GluAs in Ciona and observed severe impairments in formation of the ocellus, a photoreceptive organ used during the swimming stage, and in resorption of the tail and body axis rotation during metamorphosis to the adult stage. These defects could be rescued by injection of KD-resistant GluAs. GluA KD phenotypes could also be reproduced by expressing a GluA mutant that dominantly inhibits glutamate-evoked currents. These results suggest that, in addition to their role in synaptic communication in mature animals, GluAs also have critical developmental functions.
AB - AMPA-type glutamate receptors (GluAs) mediate fast excitatory transmission in the vertebrate central nervous system (CNS), and their function has been extensively studied in the mature mammalian brain. However, GluA expression begins very early in developing embryos, suggesting that they may also have unidentified developmental roles. Here, we identify developmental roles for GluAs in the ascidian Ciona intestinalis. Mammals express Ca2+-permeable GluAs (Ca-P GluAs) and Ca2+-impermeable GluAs (Ca-I GluAs) by combining subunits derived from four genes. In contrast, ascidians have a single gluA gene. Taking advantage of the simple genomic GluA organization in ascidians, we knocked down (KD) GluAs in Ciona and observed severe impairments in formation of the ocellus, a photoreceptive organ used during the swimming stage, and in resorption of the tail and body axis rotation during metamorphosis to the adult stage. These defects could be rescued by injection of KD-resistant GluAs. GluA KD phenotypes could also be reproduced by expressing a GluA mutant that dominantly inhibits glutamate-evoked currents. These results suggest that, in addition to their role in synaptic communication in mature animals, GluAs also have critical developmental functions.
KW - AMPA-type glutamate receptor
KW - Ascidian
KW - Development
KW - Morphogeneis
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U2 - 10.1073/pnas.1612943114
DO - 10.1073/pnas.1612943114
M3 - Article
C2 - 28348228
AN - SCOPUS:85035213356
SN - 0027-8424
VL - 114
SP - 3939
EP - 3944
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 15
ER -