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The Journal of Neuroscience, January 1, 2000, 20(1):294-305
Serotonin and the 5-HT2B Receptor in the Development
of Enteric Neurons
Elena
Fiorica-Howells1,
Luc
Maroteaux2, and
Michael
D.
Gershon1
1 Department of Anatomy and Cell Biology, Columbia University,
College of Physicians and Surgeons, New York, New York 10032, and
2 Institut de Génétique et de Biologie
Moléculaire et Cellulaire, Université Louis Pasteur de
Strasbourg, Centre National de la Recherche Scientifique, Institut
National de la Santé et de la Recherche Médicale, BP
163-67404, Illkirch Cedex-France
We tested the hypothesis that 5-HT promotes the
differentiation of enteric neurons by stimulating a developmentally
regulated receptor expressed by crest-derived neuronal progenitors.
5-HT and the 5-HT2 agonist
(±)-2,5-dimethoxy-4-iodoamphetamine.HCl
(DOI) enhanced in vitro differentiation of
enteric neurons, both in dissociated cultures of mixed cells and in
cultures of crest-derived cells isolated from the gut by
immunoselection with antibodies to p75NTR. The
promotion of in vitro neuronal differentiation by 5-HT
and DOI was blocked by the 5-HT1/2 antagonist methysergide,
the pan-5-HT2 antagonist ritanserin, and the
5-HT2B/2C-selective antagonist SB206553. The
5-HT2A-selective antagonist ketanserin did not completely block the developmental effects of 5-HT. 5-HT induced the nuclear translocation of mitogen-activated protein kinase. This effect was
blocked by ritanserin. mRNA encoding 5-HT2A and
5-HT2B receptors was detected in the fetal bowel (stomach
and small and large intestine), but that encoding the
5-HT2C receptor was not. mRNA encoding the 5-HT2B receptor and 5-HT2B immunoreactivity
were found to be abundant in primordial [embryonic day 15 (E15)-E16]
but not in mature myenteric ganglia. 5-HT2B-immunoreactive
cells were found to be a subset of cells that expressed the neuronal
marker PGP9.5. These data demonstrate for the first time that the
5-HT2B receptor is expressed in the small intestine as well
as the stomach and that it is expressed by enteric neurons as well as
by muscle. It is possible that by stimulating 5-HT2B
receptors, 5-HT affects the fate of the large subset of enteric neurons
that arises after the development of endogenous sources of 5-HT.
Key words:
enteric nervous system; bowel; gut; neuronal development; serotonin receptors; 5-HT
Copyright © 2000 Society for Neuroscience 0270-6474/0/201294-12$05.00/0
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