TY - JOUR
T1 - Cellular identity and Ca2+ signaling activity of the non-reproductive GnRH system in the Ciona intestinalis type A (Ciona robusta) larva
AU - Okawa, Nanako
AU - Shimai, Kotaro
AU - Ohnishi, Kohei
AU - Ohkura, Masamichi
AU - Nakai, Junichi
AU - Horie, Takeo
AU - Kuhara, Atsushi
AU - Kusakabe, Takehiro G.
N1 - Funding Information:
Biological materials. Mature adults of Ciona intestinalis type A were provided by the Maizuru Fisheries Research Station of Kyoto University and by the Misaki Marine Biological Station of the University of Tokyo through the National Bio-Resource Project of the Ministry of Education, Culture, Sports, Science and Technology of Japan (MEXT), and were maintained in indoor tanks of artificial seawater (ASW) (Marine Art BR; Tomita Pharmaceutical, Tokushima, Japan) at 18 °C. The adults were also collected from the pond on the Fukae campus of Kobe University, Kobe, Japan and from the fishing harbor in Murotsu, Hyogo, Japan. Eggs and sperm were obtained surgically from the gonoducts, and the eggs were fertilized in vitro. After insemination, the embryos were raised in ASW containing 50 µg/ml streptomycin sulfate (S6501; Sigma-Aldrich, St. Louis, MO, USA) at 18 °C.
Funding Information:
We thank the National BioResource Project of MEXT and all members of the Maizuru Fisheries Research Station and Yutaka Satou Lab of Kyoto University and the Misaki Marine Biological Station of the University of Tokyo for providing us with C. intestinalis adults. We also thank the Graduate School of Maritime Sciences, Kobe University for generously allowing us to collect C. intestinalis on the campus. This study was supported in part by Grants-in-Aid for Scientific Research from JSPS to T.G.K. (25650118, 25290067, 16H04724, 19H03213), A.K. (18H02484, 20H05074), J.N. (15H05723), and T.H. (16K07433, 19H03204). This study was also supported in part by research grants from the Takeda Science Foundation and the Hirao Taro Foundation of the Konan University Association for Academic Research.
Publisher Copyright:
© 2020, The Author(s).
PY - 2020/12/1
Y1 - 2020/12/1
N2 - Tunicate larvae have a non-reproductive gonadotropin-releasing hormone (GnRH) system with multiple ligands and receptor heterodimerization enabling complex regulation. In Ciona intestinalis type A larvae, one of the gnrh genes, gnrh2, is conspicuously expressed in the motor ganglion and nerve cord, which are homologous structures to the hindbrain and spinal cord, respectively, of vertebrates. The gnrh2 gene is also expressed in the proto-placodal sensory neurons, which are the proposed homologue of vertebrate olfactory neurons. Tunicate larvae occupy a non-reproductive dispersal stage, yet the role of their GnRH system remains elusive. In this study, we investigated neuronal types of gnrh2-expressing cells in Ciona larvae and visualized the activity of these cells by fluorescence imaging using a calcium sensor protein. Some cholinergic neurons and dopaminergic cells express gnrh2, suggesting that GnRH plays a role in controlling swimming behavior. However, none of the gnrh2-expressing cells overlap with glycinergic or GABAergic neurons. A role in motor control is also suggested by a relationship between the activity of gnrh2-expressing cells and tail movements. Interestingly, gnrh2-positive ependymal cells in the nerve cord, known as a kind of glia cells, actively produced Ca2+ transients, suggesting that active intercellular signaling occurs in the glia cells of the nerve cord.
AB - Tunicate larvae have a non-reproductive gonadotropin-releasing hormone (GnRH) system with multiple ligands and receptor heterodimerization enabling complex regulation. In Ciona intestinalis type A larvae, one of the gnrh genes, gnrh2, is conspicuously expressed in the motor ganglion and nerve cord, which are homologous structures to the hindbrain and spinal cord, respectively, of vertebrates. The gnrh2 gene is also expressed in the proto-placodal sensory neurons, which are the proposed homologue of vertebrate olfactory neurons. Tunicate larvae occupy a non-reproductive dispersal stage, yet the role of their GnRH system remains elusive. In this study, we investigated neuronal types of gnrh2-expressing cells in Ciona larvae and visualized the activity of these cells by fluorescence imaging using a calcium sensor protein. Some cholinergic neurons and dopaminergic cells express gnrh2, suggesting that GnRH plays a role in controlling swimming behavior. However, none of the gnrh2-expressing cells overlap with glycinergic or GABAergic neurons. A role in motor control is also suggested by a relationship between the activity of gnrh2-expressing cells and tail movements. Interestingly, gnrh2-positive ependymal cells in the nerve cord, known as a kind of glia cells, actively produced Ca2+ transients, suggesting that active intercellular signaling occurs in the glia cells of the nerve cord.
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U2 - 10.1038/s41598-020-75344-7
DO - 10.1038/s41598-020-75344-7
M3 - Article
C2 - 33122709
AN - SCOPUS:85094183631
SN - 2045-2322
VL - 10
JO - Scientific Reports
JF - Scientific Reports
IS - 1
M1 - 18590
ER -