Expression of 5-HT2A, 5-HT2B and 5-HT2C receptors in the mouse embryo

被引:78
作者
Lauder, JM
Wilkie, MB
Wu, C
Singh, S
机构
[1] Univ N Carolina, Sch Med, Dept Cell Biol & Anat, Chapel Hill, NC 27599 USA
[2] Univ Manchester, Dept Pathol Sci, Manchester M13 9PT, Lancs, England
[3] Imgenex, San Diego, CA 92121 USA
关键词
serotonin; craniofacial; cardiac; morphogenesis; malformations;
D O I
10.1016/S0736-5748(00)00032-0
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Expression patterns of 5-HT2A, 5-HT2B and 5-HT2C receptors during mouse embryogenesis were investigated using highly specific monoclonal antibodies. Differential and overlapping spatio-temporal patterns of 5-HT2A, 5-HT2B and 5-HT2C receptor immunoreactivity were observed during active phases of morphogenesis of a variety of embryonic tissues, including neuroepithelia of brain and spinal cord, notochord, somites, cranial neural crest, craniofacial mesenchyme and epithelia, heart myocardium and endocardial cushions, tooth germs, whisker follicles, cartilage and striated muscle. The functional significance of these receptors was tested by exposing headfold stage mouse embryos to different subtype-selective 5-HT2 receptor antagonists for 2 days in whole embryo culture. The most potent was the pan 5-HT2 receptor antagonist ritanserin, which has high affinity for the 5-HT2B receptor. Ritanserin caused 100% malformed embryos at a dose of 1 mu M. The 5-HT2A/2C receptor antagonist mianserin also caused a significant number of malformed embryos, but only when used at a 10 fold higher dose (10 mu M). Ketanserin, which primarily targets 5-HT2A receptors, did not cause a significant number of malformed embryos at any dose tested. Together with previous evidence that 5-HT acts as an important morphoregulatory signal during mouse embryogenesis, present evidence for the early and continued expression of functional 5-HT2 receptors throughout gestation raises the possibility that psychotropic drugs taken during pregnancy could interfere with developmental actions of 5-HT during prenatal development of neural and non-neural tissues. (C) 2000 ISDN. Published by Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:653 / 662
页数:10
相关论文
共 32 条
[1]  
Bhasin N., 1999, Society for Neuroscience Abstracts, V25, P525
[2]   Mouse 5-HT2B receptor-mediated serotonin trophic functions [J].
Choi, DS ;
Kellermann, O ;
Richard, S ;
Colas, JF ;
Bolaños-Jimenez, F ;
Tournois, C ;
Launay, JM ;
Maroteaux, L .
ADVANCES IN SEROTONIN RECEPTOR RESEARCH: MOLECULAR BIOLOGY, SIGNAL TRANSDUCTION, AND THERAPEUTICS, 1998, 861 :67-73
[3]  
Choi DS, 1997, DEVELOPMENT, V124, P1745
[4]   Serotonin and the 5-HT2B receptor in the development of enteric neurons [J].
Fiorica-Howells, E ;
Maroteaux, L ;
Gershon, MD .
JOURNAL OF NEUROSCIENCE, 2000, 20 (01) :294-305
[5]  
Fitzgerald LW, 2000, MOL PHARMACOL, V57, P75
[6]   Identification and localization of a skeletal muscle secrotonin 5-HT2A receptor coupled to the Jak/STAT pathway [J].
GuilletDeniau, I ;
Burnol, AF ;
Girard, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (23) :14825-14829
[7]   Serotonin transporter messenger RNA expression in neural crest-derived structures and sensory pathways of the developing rat embryo [J].
Hansson, SR ;
Mezey, É ;
Hoffman, BJ .
NEUROSCIENCE, 1999, 89 (01) :243-265
[8]   THE 5HT2 RECEPTOR DEFINES A FAMILY OF STRUCTURALLY DISTINCT BUT FUNCTIONALLY CONSERVED SEROTONIN RECEPTORS [J].
JULIUS, D ;
HUANG, KN ;
LIVELLI, TJ ;
AXEL, R ;
JESSELL, TM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (03) :928-932
[9]   ECTOPIC EXPRESSION OF THE SEROTONIN 1C RECEPTOR AND THE TRIGGERING OF MALIGNANT TRANSFORMATION [J].
JULIUS, D ;
LIVELLI, TJ ;
JESSELL, TM ;
AXEL, R .
SCIENCE, 1989, 244 (4908) :1057-1062
[10]   Signaling pathways and targets of the 5-HT2B receptor in the 1C11 serotonergic cell line [J].
Kellermann, O ;
Tournois, C ;
Richard, S ;
Manivet, P ;
Maroteaux, L ;
Launay, JM .
ADVANCES IN SEROTONIN RECEPTOR RESEARCH: MOLECULAR BIOLOGY, SIGNAL TRANSDUCTION, AND THERAPEUTICS, 1998, 861 :248-248