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\n \n\n \n \n Krasovec, G., Renaud, C., Quéinnec, É., Sasakura, Y., & Chambon, J.\n\n\n \n \n \n \n \n Extrinsic apoptosis participates to tail regression during the metamorphosis of the chordate Ciona.\n \n \n \n \n\n\n \n\n\n\n Scientific Reports, 14(1): 5729. March 2024.\n \n\n\n\n
\n\n\n\n \n \n \"ExtrinsicPaper\n  \n \n\n \n \n doi\n  \n \n\n \n link\n  \n \n\n bibtex\n \n\n \n  \n \n abstract \n \n\n \n\n \n \n \n \n \n \n \n\n  \n \n \n\n\n\n
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@article{krasovec_extrinsic_2024,\n\ttitle = {Extrinsic apoptosis participates to tail regression during the metamorphosis of the chordate \\textit{{Ciona}}},\n\tvolume = {14},\n\tissn = {2045-2322},\n\turl = {https://www.nature.com/articles/s41598-023-48411-y},\n\tdoi = {10.1038/s41598-023-48411-y},\n\tabstract = {Abstract\n            \n              Apoptosis is a regulated cell death ubiquitous in animals defined by morphological features depending on caspases. Two regulation pathways are described, currently named the intrinsic and the extrinsic apoptosis. While intrinsic apoptosis is well studied and considered ancestral among metazoans, extrinsic apoptosis is poorly studied outside mammals. Here, we address extrinsic apoptosis in the urochordates\n              Ciona\n              , belonging to the sister group of vertebrates. During metamorphosis,\n              Ciona\n              larvae undergo a tail regression depending on tissue contraction, migration and apoptosis. Apoptosis begin at the tail tip and propagates towards the trunk as a polarized wave. We identified\n              Ci-caspase 8/10\n              by phylogenetic analysis as homolog to vertebrate caspases 8 and 10 that are the specific initiator of extrinsic apoptosis. We detected\n              Ci-caspase 8/10\n              expression in\n              Ciona\n              larvae, especially at the tail tip. We showed that chemical inhibition of\n              Ci-caspase 8/10\n              leads to a delay of tail regression, and\n              Ci-caspase 8/10\n              loss of function induced an incomplete tail regression. The specificity between apoptotic pathways and initiator caspase suggests that extrinsic apoptosis regulates cell death during the tail regression. Our study presents rare in vivo work on extrinsic apoptosis outside mammals, and contribute to the discussion on its evolutionary history in animals.},\n\tlanguage = {en},\n\tnumber = {1},\n\turldate = {2024-04-04},\n\tjournal = {Scientific Reports},\n\tauthor = {Krasovec, Gabriel and Renaud, Cécile and Quéinnec, Éric and Sasakura, Yasunori and Chambon, Jean-Philippe},\n\tmonth = mar,\n\tyear = {2024},\n\tpages = {5729},\n}\n
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\n Abstract Apoptosis is a regulated cell death ubiquitous in animals defined by morphological features depending on caspases. Two regulation pathways are described, currently named the intrinsic and the extrinsic apoptosis. While intrinsic apoptosis is well studied and considered ancestral among metazoans, extrinsic apoptosis is poorly studied outside mammals. Here, we address extrinsic apoptosis in the urochordates Ciona , belonging to the sister group of vertebrates. During metamorphosis, Ciona larvae undergo a tail regression depending on tissue contraction, migration and apoptosis. Apoptosis begin at the tail tip and propagates towards the trunk as a polarized wave. We identified Ci-caspase 8/10 by phylogenetic analysis as homolog to vertebrate caspases 8 and 10 that are the specific initiator of extrinsic apoptosis. We detected Ci-caspase 8/10 expression in Ciona larvae, especially at the tail tip. We showed that chemical inhibition of Ci-caspase 8/10 leads to a delay of tail regression, and Ci-caspase 8/10 loss of function induced an incomplete tail regression. The specificity between apoptotic pathways and initiator caspase suggests that extrinsic apoptosis regulates cell death during the tail regression. Our study presents rare in vivo work on extrinsic apoptosis outside mammals, and contribute to the discussion on its evolutionary history in animals.\n
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\n \n\n \n \n Satake, H., & Sasakura, Y.\n\n\n \n \n \n \n \n The neuroendocrine system of Ciona intestinalis Type A, a deuterostome invertebrate and the closest relative of vertebrates.\n \n \n \n \n\n\n \n\n\n\n Molecular and Cellular Endocrinology, 582: 112122. March 2024.\n \n\n\n\n
\n\n\n\n \n \n \"ThePaper\n  \n \n\n \n \n doi\n  \n \n\n \n link\n  \n \n\n bibtex\n \n\n \n\n \n\n \n \n \n \n \n \n \n\n  \n \n \n\n\n\n
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@article{satake_neuroendocrine_2024,\n\ttitle = {The neuroendocrine system of \\textit{{Ciona} intestinalis} {Type} {A}, a deuterostome invertebrate and the closest relative of vertebrates},\n\tvolume = {582},\n\tissn = {03037207},\n\turl = {https://linkinghub.elsevier.com/retrieve/pii/S0303720723002733},\n\tdoi = {10.1016/j.mce.2023.112122},\n\tlanguage = {en},\n\turldate = {2024-04-04},\n\tjournal = {Molecular and Cellular Endocrinology},\n\tauthor = {Satake, Honoo and Sasakura, Yasunori},\n\tmonth = mar,\n\tyear = {2024},\n\tpages = {112122},\n}\n\n
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\n \n\n \n \n Taniguchi, S., Nakayama, S., Iguchi, R., Sasakura, Y., Satake, H., Wada, S., Suzuki, N., Ogasawara, M., & Sekiguchi, T.\n\n\n \n \n \n \n \n Distribution of cionin, a cholecystokinin/gastrin family peptide, and its receptor in the central nervous system of Ciona intestinalis type A.\n \n \n \n \n\n\n \n\n\n\n Scientific Reports, 14(1): 6277. March 2024.\n \n\n\n\n
\n\n\n\n \n \n \"DistributionPaper\n  \n \n\n \n \n doi\n  \n \n\n \n link\n  \n \n\n bibtex\n \n\n \n  \n \n abstract \n \n\n \n\n \n \n \n \n \n \n \n\n  \n \n \n \n \n\n\n\n
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@article{taniguchi_distribution_2024,\n\ttitle = {Distribution of cionin, a cholecystokinin/gastrin family peptide, and its receptor in the central nervous system of \\textit{{Ciona} intestinalis} type {A}},\n\tvolume = {14},\n\tissn = {2045-2322},\n\turl = {https://www.nature.com/articles/s41598-024-55908-7},\n\tdoi = {10.1038/s41598-024-55908-7},\n\tabstract = {Abstract\n            \n              The cholecystokinin (CCK)/gastrin family peptides are involved in regulation of feeding and digestion in vertebrates. In the ascidian\n              Ciona intestinalis\n              type A (\n              Ciona robusta\n              ), cionin, a CCK/gastrin family peptide, has been identified. Cionin is expressed exclusively in the central nervous system (CNS). In contrast, cionin receptor expression has been detected in the CNS, digestive tract, and ovary. Although cionin has been reported to be involved in ovulation, its physiological function in the CNS remains to be investigated. To elucidate its neural function, in the present study, we analyzed the expression of cionin and cionin receptors in the CNS. Cionin was expressed mainly in neurons residing in the anterior region of the cerebral ganglion. In contrast, the gene expressin of the cionin receptor gene\n              CioR1\n              , was detected in the middle part of the cerebral ganglion and showed a similar expression pattern to that of\n              VACHT\n              , a cholinergic neuron marker gene. Moreover,\n              CioR1\n              was found to be expressed in cholinergic neurons. Consequently, these results suggest that cionin interacts with cholinergic neurons as a neurotransmitter or neuromodulator via CioR1. This study provides insights into a biological role of a CCK/gastrin family peptide in the CNS of ascidians.},\n\tlanguage = {en},\n\tnumber = {1},\n\turldate = {2024-04-04},\n\tjournal = {Scientific Reports},\n\tauthor = {Taniguchi, Shiho and Nakayama, Satoshi and Iguchi, Rin and Sasakura, Yasunori and Satake, Honoo and Wada, Shuichi and Suzuki, Nobuo and Ogasawara, Michio and Sekiguchi, Toshio},\n\tmonth = mar,\n\tyear = {2024},\n\tkeywords = {wrongWada},\n\tpages = {6277},\n}\n\n
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\n Abstract The cholecystokinin (CCK)/gastrin family peptides are involved in regulation of feeding and digestion in vertebrates. In the ascidian Ciona intestinalis type A ( Ciona robusta ), cionin, a CCK/gastrin family peptide, has been identified. Cionin is expressed exclusively in the central nervous system (CNS). In contrast, cionin receptor expression has been detected in the CNS, digestive tract, and ovary. Although cionin has been reported to be involved in ovulation, its physiological function in the CNS remains to be investigated. To elucidate its neural function, in the present study, we analyzed the expression of cionin and cionin receptors in the CNS. Cionin was expressed mainly in neurons residing in the anterior region of the cerebral ganglion. In contrast, the gene expressin of the cionin receptor gene CioR1 , was detected in the middle part of the cerebral ganglion and showed a similar expression pattern to that of VACHT , a cholinergic neuron marker gene. Moreover, CioR1 was found to be expressed in cholinergic neurons. Consequently, these results suggest that cionin interacts with cholinergic neurons as a neurotransmitter or neuromodulator via CioR1. This study provides insights into a biological role of a CCK/gastrin family peptide in the CNS of ascidians.\n
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