Adrenomedullin 2 and 5 activate the calcitonin receptor-like receptor (clr) – Receptor activity-modifying protein 3 (ramp3) receptor complex in Xenopus tropicalis
•Amphibian receptors for adrenomedullin have similar structure with those in mammals.•Adrenomedullin 2 is the dominant ligand of clr-ramp3 receptor complex in amphibians.•The expression level of ramp3 transcript was the highest in the blood. The adrenomedullin (AM) family is involved in diverse biol...
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Veröffentlicht in: | General and comparative endocrinology 2021-05, Vol.306, p.113752-113752, Article 113752 |
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Zusammenfassung: | •Amphibian receptors for adrenomedullin have similar structure with those in mammals.•Adrenomedullin 2 is the dominant ligand of clr-ramp3 receptor complex in amphibians.•The expression level of ramp3 transcript was the highest in the blood.
The adrenomedullin (AM) family is involved in diverse biological functions, including cardiovascular regulation and body fluid homeostasis, in multiple vertebrate lineages. The AM family consists of AM1, AM2, and AM5 in tetrapods, and the receptor for mammalian AMs has been identified as the complex of calcitonin receptor-like receptor (CLR) and receptor activity-modifying protein 2 (RAMP2) or RAMP3. However, the receptors for AM in amphibians have not been identified. In this study, we identified the cDNAs encoding calcrl (clr), ramp2, and ramp3 receptor components from the western clawed frog (Xenopus tropicalis). Messenger RNAs of amphibian clr and ramp2 were highly expressed in the heart, whereas that of ramp3 was highly expressed in the whole blood. In HEK293T cells expressing clr-ramp2, cAMP response element luciferase (CRE-Luc) reporter activity was activated by am1. In HEK293T cells expressing clr-ramp3, CRE-Luc reporter activity was increased by the treatment with am2 at the lowest dose, but with am5 and am1 at higher dose. Our results provided new insights into the roles of AM family peptides through CLR-RAMP receptor complexes in the tetrapods. |
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ISSN: | 0016-6480 1095-6840 |
DOI: | 10.1016/j.ygcen.2021.113752 |