Cited by 381Neurotransmitter Receptor Influence on BehaviorNeurogenesis and neuroplasticity mechanismsTryptophan and brain disorders

Maternal serotonin is crucial for murine embryonic development

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Côté, Francine, Fligny, Cécile, Bayard, Elisa, Launay, Jean-Marie, Gershon, Michael D., Mallet, Jacques, Vodjdani, Guilan·2007·Proceedings of the National Academy of Sciences

Abstract

The early appearance of serotonin and its receptors during prenatal development, together with the many effects serotonin exerts during CNS morphogenesis, strongly suggest that serotonin influences the development and maturation of the mammalian brain before it becomes a neuromodulator/neurotransmitter. Sites of early serotonin biosynthesis, however, have not been detected in mouse embryos or extraembryonic structures, suggesting that the main source of serotonin could be of maternal origin. This hypothesis was tested by using knockout mice lacking the tph1 gene, which is responsible for the synthesis of peripheral serotonin. Genetic crosses were performed to compare the phenotype of pups born from homozygous and heterozygous mothers. Observations provide the first clear evidence that ( i ) maternal serotonin is involved in the control of morphogenesis during developmental stages that precede the appearance of serotonergic neurons and ( ii ) serotonin is critical for normal murine development. Most strikingly, the phenotype of tph1 −/− embryos depends more on the maternal genotype than on that of the concepti. Consideration of the maternal genotype may thus help to clarify the influence of other genes in complex diseases, such as mental illness.

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  • Gut microbiota manufactures neuroactive chemicals and influences levels of circulating 5-HT and serotonin, thereby altering fetal neuronal cell synaptogenesis and neuronal morphogenesis.

    “Furthermore, gut microbiota manufactures neuroactive chemicals and influences levels of circulating 5-hydroxytryptamine (5-HT) and serotonin, thereby altering fetal neuronal cell synaptogenesis [89] and neuronal morphogenesis [90], respectively.”

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References 36 · Cited by 381

Research works printed but not linked: 1

  1. [10]Lauder JM, Zimmermann EF. J Craniofac Genet Dev Biol. 1988;8:265–276. [[PubMed](https://pubmed.ncbi.nlm.nih.gov/3209688/)] [[Google Scholar](https://scholar.google.com/scholar_lookup?journal=J%20Craniofac%20Genet%20Dev%20Biol&author=JM%20Lauder&author=EF%20Zimmermann&volume=8&publication_year=1988&pages=265-276&pmid=3209688&)]

Authors
Côté, F., Fligny, C., Bayard, E., Launay, J.-M., Gershon, M. D., Mallet, J., & Vodjdani, G.
Affiliations
  • Centre National de la Recherche Scientifique (FR)
  • Hôpital Lariboisière (FR)
  • Columbia University (US)
Venue
Proceedings of the National Academy of Sciences
Published
2007-01-02
Volume
104
Issue
1
Pages
329-334
ISSN
  • 0027-8424 (ISSN-L)
  • 1091-6490
OpenAlex
W2098331502
Cited by
381
References
36
Citations by year
2026: 13 · 2025: 9 · 2024: 16 · 2023: 16 · 2022: 19 · 2021: 23 · 2020: 28 · 2019: 18 · 2018: 31 · 2017: 11 · 2016: 14 · 2015: 20 · 2014: 20 · 2013: 23 · 2012: 21
FWCI
5.74
Type
journal article
Language
en
Open access
Locations
  • Proceedings of the National Academy of Sciences (publishedVersion)
  • Europe PMC (PubMed Central) (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
  • HAL (submittedVersion)
Topics
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
  • Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
  • Life Sciences › Neuroscience › Biological Psychiatry › Tryptophan and brain disorders
Keywords
embryonic development, serotonin synthesis, maternal genotype, serotonergic neurons, extraembryonic tissues, mouse embryo, psychiatric genetics
MeSH terms
Animals, Genotype, Mice, Inbred C57BL, Phenotype, Phenylketonurias, RNA, Messenger, Serotonin, Tryptophan Hydroxylase, Signal Transduction, Embryonic Development, Mice

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