Biochemical, Anatomical, and Pharmacological Characterization of Calcitonin-Type Neuropeptides in Starfish: Discovery of an Ancient Role as Muscle Relaxants
Calcitonin (CT) is a peptide hormone released by the thyroid gland that regulates blood Ca2+ levels in mammals. The CT gene is alternatively spliced, with one transcript encoding CT and another transcript encoding the CT-like neuropeptide calcitonin-gene related peptide (α-CGRP), which is a powerful...
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doaj-699d6dbb9d1b4cda9571adf6081b70452020-11-24T23:11:19ZengFrontiers Media S.A.Frontiers in Neuroscience1662-453X2018-06-011210.3389/fnins.2018.00382371559Biochemical, Anatomical, and Pharmacological Characterization of Calcitonin-Type Neuropeptides in Starfish: Discovery of an Ancient Role as Muscle RelaxantsWeigang Cai0Chan-Hee Kim1Hye-Jin Go2Michaela Egertová3Cleidiane G. Zampronio4Alexandra M. Jones5Nam Gyu Park6Maurice R. Elphick7School of Biological & Chemical SciencesQueen Mary University of London, London, United KingdomDepartment of Biotechnology, College of Fisheries SciencesPukyong National University, Busan, South KoreaDepartment of Biotechnology, College of Fisheries SciencesPukyong National University, Busan, South KoreaSchool of Biological & Chemical SciencesQueen Mary University of London, London, United KingdomSchool of Life Sciences and Proteomics Research Technology PlatformUniversity of Warwick, Coventry, United KingdomSchool of Life Sciences and Proteomics Research Technology PlatformUniversity of Warwick, Coventry, United KingdomDepartment of Biotechnology, College of Fisheries SciencesPukyong National University, Busan, South KoreaSchool of Biological & Chemical SciencesQueen Mary University of London, London, United KingdomCalcitonin (CT) is a peptide hormone released by the thyroid gland that regulates blood Ca2+ levels in mammals. The CT gene is alternatively spliced, with one transcript encoding CT and another transcript encoding the CT-like neuropeptide calcitonin-gene related peptide (α-CGRP), which is a powerful vasodilator. Other CT-related peptides in vertebrates include adrenomedullin, amylin, and intermedin, which also act as smooth muscle relaxants. The evolutionary origin of CT-type peptides has been traced to the bilaterian common ancestor of protostomes and deuterostomes and a CT-like peptide (DH31) has been identified as a diuretic hormone in some insect species. However, little is known about the physiological roles of CT-type peptides in other invertebrates. Here we characterized a CT-type neuropeptide in a deuterostomian invertebrate—the starfish Asterias rubens (Phylum Echinodermata). A CT-type precursor cDNA (ArCTP) was sequenced and the predicted structure of the peptide (ArCT) derived from ArCTP was confirmed using mass spectrometry. The distribution of ArCTP mRNA and the ArCT peptide was investigated using in situ hybridization and immunohistochemistry, respectively, revealing stained cells/processes in the nervous system, digestive system, and muscular organs, including the apical muscle and tube feet. Investigation of the effects of synthetic ArCT on in vitro preparations of the apical muscle and tube feet revealed that it acts as a relaxant, causing dose-dependent reversal of acetylcholine-induced contraction. Furthermore, a muscle relaxant present in whole-animal extracts of another starfish species, Patiria pectinifera, was identified as an ortholog of ArCT and named PpCT. Consistent with the expression pattern of ArCTP in A. rubens, RT-qPCR revealed that in P. pectinifera the PpCT precursor transcript is more abundant in the radial nerve cords than in other tissues/organs analyzed. In conclusion, our findings indicate that the physiological action of CT-related peptides as muscle relaxants in vertebrates may reflect an evolutionarily ancient role of CT-type neuropeptides that can be traced back to the common ancestor of deuterostomes.https://www.frontiersin.org/article/10.3389/fnins.2018.00382/fullcalcitoninechinodermAsterias rubensstarfishevolutionneuropeptide |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Weigang Cai Chan-Hee Kim Hye-Jin Go Michaela Egertová Cleidiane G. Zampronio Alexandra M. Jones Nam Gyu Park Maurice R. Elphick |
spellingShingle |
Weigang Cai Chan-Hee Kim Hye-Jin Go Michaela Egertová Cleidiane G. Zampronio Alexandra M. Jones Nam Gyu Park Maurice R. Elphick Biochemical, Anatomical, and Pharmacological Characterization of Calcitonin-Type Neuropeptides in Starfish: Discovery of an Ancient Role as Muscle Relaxants Frontiers in Neuroscience calcitonin echinoderm Asterias rubens starfish evolution neuropeptide |
author_facet |
Weigang Cai Chan-Hee Kim Hye-Jin Go Michaela Egertová Cleidiane G. Zampronio Alexandra M. Jones Nam Gyu Park Maurice R. Elphick |
author_sort |
Weigang Cai |
title |
Biochemical, Anatomical, and Pharmacological Characterization of Calcitonin-Type Neuropeptides in Starfish: Discovery of an Ancient Role as Muscle Relaxants |
title_short |
Biochemical, Anatomical, and Pharmacological Characterization of Calcitonin-Type Neuropeptides in Starfish: Discovery of an Ancient Role as Muscle Relaxants |
title_full |
Biochemical, Anatomical, and Pharmacological Characterization of Calcitonin-Type Neuropeptides in Starfish: Discovery of an Ancient Role as Muscle Relaxants |
title_fullStr |
Biochemical, Anatomical, and Pharmacological Characterization of Calcitonin-Type Neuropeptides in Starfish: Discovery of an Ancient Role as Muscle Relaxants |
title_full_unstemmed |
Biochemical, Anatomical, and Pharmacological Characterization of Calcitonin-Type Neuropeptides in Starfish: Discovery of an Ancient Role as Muscle Relaxants |
title_sort |
biochemical, anatomical, and pharmacological characterization of calcitonin-type neuropeptides in starfish: discovery of an ancient role as muscle relaxants |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Neuroscience |
issn |
1662-453X |
publishDate |
2018-06-01 |
description |
Calcitonin (CT) is a peptide hormone released by the thyroid gland that regulates blood Ca2+ levels in mammals. The CT gene is alternatively spliced, with one transcript encoding CT and another transcript encoding the CT-like neuropeptide calcitonin-gene related peptide (α-CGRP), which is a powerful vasodilator. Other CT-related peptides in vertebrates include adrenomedullin, amylin, and intermedin, which also act as smooth muscle relaxants. The evolutionary origin of CT-type peptides has been traced to the bilaterian common ancestor of protostomes and deuterostomes and a CT-like peptide (DH31) has been identified as a diuretic hormone in some insect species. However, little is known about the physiological roles of CT-type peptides in other invertebrates. Here we characterized a CT-type neuropeptide in a deuterostomian invertebrate—the starfish Asterias rubens (Phylum Echinodermata). A CT-type precursor cDNA (ArCTP) was sequenced and the predicted structure of the peptide (ArCT) derived from ArCTP was confirmed using mass spectrometry. The distribution of ArCTP mRNA and the ArCT peptide was investigated using in situ hybridization and immunohistochemistry, respectively, revealing stained cells/processes in the nervous system, digestive system, and muscular organs, including the apical muscle and tube feet. Investigation of the effects of synthetic ArCT on in vitro preparations of the apical muscle and tube feet revealed that it acts as a relaxant, causing dose-dependent reversal of acetylcholine-induced contraction. Furthermore, a muscle relaxant present in whole-animal extracts of another starfish species, Patiria pectinifera, was identified as an ortholog of ArCT and named PpCT. Consistent with the expression pattern of ArCTP in A. rubens, RT-qPCR revealed that in P. pectinifera the PpCT precursor transcript is more abundant in the radial nerve cords than in other tissues/organs analyzed. In conclusion, our findings indicate that the physiological action of CT-related peptides as muscle relaxants in vertebrates may reflect an evolutionarily ancient role of CT-type neuropeptides that can be traced back to the common ancestor of deuterostomes. |
topic |
calcitonin echinoderm Asterias rubens starfish evolution neuropeptide |
url |
https://www.frontiersin.org/article/10.3389/fnins.2018.00382/full |
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