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Impacts of brain serotonin deficiency following Tph2 inactivation on development and raphe neuron serotonergic specification
- Source :
- PLoS ONE, Vol 7, Iss 8, p e43157 (2012), PLoS ONE, PLoS ONE; Vol 7
- Publication Year :
- 2012
- Publisher :
- Public Library of Science (PLoS), 2012.
-
Abstract
- Brain serotonin (5-HT) is implicated in a wide range of functions from basic physiological mechanisms to complex behaviors, including neuropsychiatric conditions, as well as in developmental processes. Increasing evidence links 5-HT signaling alterations during development to emotional dysregulation and psychopathology in adult age. To further analyze the importance of brain 5-HT in somatic and brain development and function, and more specifically differentiation and specification of the serotonergic system itself, we generated a mouse model with brain-specific 5-HT deficiency resulting from a genetically driven constitutive inactivation of neuronal tryptophan hydroxylase-2 (Tph2). Tph2 inactivation (Tph2-/-) resulted in brain 5-HT deficiency leading to growth retardation and persistent leanness, whereas a sex- and age-dependent increase in body weight was observed in Tph2+/- mice. The conserved expression pattern of the 5-HT neuron-specific markers (except Tph2 and 5-HT) demonstrates that brain 5-HT synthesis is not a prerequisite for the proliferation, differentiation and survival of raphe neurons subjected to the developmental program of serotonergic specification. Furthermore, although these neurons are unable to synthesize 5-HT from the precursor tryptophan, they still display electrophysiological properties characteristic of 5-HT neurons. Moreover, 5-HT deficiency induces an up-regulation of 5-HT\(_{1A}\) and 5-HT\(_{1B}\) receptors across brain regions as well as a reduction of norepinephrine concentrations accompanied by a reduced number of noradrenergic neurons. Together, our results characterize developmental, neurochemical, neurobiological and electrophysiological consequences of brain-specific 5-HT deficiency, reveal a dual dose-dependent role of 5-HT in body weight regulation and show that differentiation of serotonergic neuron phenotype is independent from endogenous 5-HT synthesis.
- Subjects :
- Mouse
Psychopharmacology
Eating Disorders
lcsh:Medicine
Tryptophan Hydroxylase
Biochemistry
Mice
Norepinephrine
0302 clinical medicine
Molecular Cell Biology
Neurobiology of Disease and Regeneration
Morphogenesis
lcsh:Science
Neurons
Psychiatry
0303 health sciences
Multidisciplinary
Neuronal Morphology
TPH2
Neuromodulation
Histological Techniques
Age Factors
Brain
Neurochemistry
Cell Differentiation
Animal Models
Neurotransmitters
Hydroxyindoleacetic Acid
Anxiety Disorders
Mental Health
medicine.anatomical_structure
Neurology
Medicine
Growth and Development
Cellular Types
Neurochemicals
Research Article
Serotonin
Drugs and Devices
medicine.medical_specialty
Histology
Neuropsychiatric Disorders
Biology
Serotonergic
03 medical and health sciences
Sex Factors
Model Organisms
Neuropharmacology
Neurochemical
Developmental Neuroscience
Internal medicine
Genetics
medicine
Animals
Gene Silencing
Obesity
ddc:610
Nutrition
030304 developmental biology
Growth Control
Raphe
Mood Disorders
Body Weight
lcsh:R
Molecular Development
Tryptophan hydroxylase
Neuroanatomy
tryptophan hydroxylase-2
brain development
5-HT receptors
raphe neurons
serotonergic differentiation
Endocrinology
Receptors, Serotonin
Cellular Neuroscience
Genetics of Disease
Autoradiography
Raphe Nuclei
lcsh:Q
Neural Circuit Formation
Neuron
Gene Function
Raphe nuclei
Neuroscience
030217 neurology & neurosurgery
Developmental Biology
Subjects
Details
- Language :
- English
- ISSN :
- 19326203
- Volume :
- 7
- Issue :
- 8
- Database :
- OpenAIRE
- Journal :
- PLoS ONE
- Accession number :
- edsair.doi.dedup.....374228f4eae02aa939e4616486225be6