Cloning, expression and pharmacology of the mouse 5-HT(4L) receptor

• Published in: FEBS letters 1996-11, Vol.398 (1), p.19-25
• Main Authors: Claeysen, S, Sebben, M, Journot, L, Bockaert, J, Dumuis, A
• Format: Article
• Language: English
• Subjects: Age Factors; Amino Acid Sequence; Animals; Animals, Newborn; Base Sequence; Binding Sites; Brain - anatomy & histology; Brain - growth & development; Brain - metabolism; Brain Chemistry; Cloning, Molecular; Inferior Colliculi - chemistry; Mice; Molecular Sequence Data; Rats; Rats, Inbred Strains; Receptors, Serotonin - drug effects; Receptors, Serotonin - genetics; Receptors, Serotonin - metabolism; Receptors, Serotonin, 5-HT4; Serotonin Antagonists - pharmacology; Serotonin Receptor Agonists - pharmacology; Species Specificity; Transfection
• ISSN: 0014-5793
• DOI: 10.1016/s0014-5793(96)01132-5

Since most of our knowledge on pharmacological properties of brain 5-HT4 receptors have been discussed for mouse colliculi neurons, we cloned the corresponding receptor using the RT-PCR approach. As expected, the homology with the already cloned rat 5-HT(4L) receptor was high, revealing only 16 differences at the amino-acid level. One of the differences, proline75 in mouse, alanine75 in the already published rat sequences was not confirmed. Therefore this proline is part of the consensus sequence present in all 5-HT receptor transmembrane domain II (LVMP). Comparing the affinities of 11 agonists and five antagonists for the cloned mouse receptor (5-HT(4L))expressed in LLCPK1 and the corresponding receptor in mouse colliculi shows an excellent correlation. The transfected mouse 5-HT(4L) receptor stimulated cAMP production. When expressed at high density, it exhibited intrinsic activity. In contrast to the previously described distribution, we found that mRNA encoding for both the short (5-HT(4S))and the long form (5-HT(4L)) of 5-HT4 receptors are expressed in all mouse and rat brain areas.