Cited by 47Histone Deacetylase Inhibitors ResearchNeuroendocrine regulation and behaviorNeurotransmitter Receptor Influence on Behavior

Monoaminergic and Neuropeptidergic Neurons Have Distinct Expression Profiles of Histone Deacetylases

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Takase, Kenkichi, Oda, Satoko, Kuroda, Masaru, Funato, Hiromasa·2013·PLoS ONE

Abstract

Monoaminergic and neuropeptidergic neurons regulate a wide variety of behaviors, such as feeding, sleep/wakefulness behavior, stress response, addiction, and social behavior. These neurons form neural circuits to integrate different modalities of behavioral and environmental factors, such as stress, maternal care, and feeding conditions. One possible mechanism for integrating environmental factors through the monoaminergic and neuropeptidergic neurons is through the epigenetic regulation of gene expression via altered acetylation of histones. Histone deacetylases (HDACs) play an important role in altering behavior in response to environmental factors. Despite increasing attention and the versatile roles of HDACs in a variety of brain functions and disorders, no reports have detailed the localization of the HDACs in the monoaminergic and neuropeptidergic neurons. Here, we examined the expression profile of the HDAC protein family from HDAC1 to HDAC11 in corticotropin-releasing hormone, oxytocin, vasopressin, agouti-related peptide (AgRP), pro-opiomelanocortin (POMC), orexin, histamine, dopamine, serotonin, and noradrenaline neurons. Immunoreactivities for HDAC1,-2,-3,-5,-6,-7,-9, and -11 were very similar among the monoaminergic and neuropeptidergic neurons, while the HDAC4, -8, and -10 immunoreactivities were clearly different among neuronal groups. HDAC10 expression was found in AgRP neurons, POMC neurons, dopamine neurons and noradrenaline neurons but not in other neuronal groups. HDAC8 immunoreactivity was detected in the cytoplasm of almost all histamine neurons with a pericellular pattern but not in other neuropeptidergic and monoaminergic neurons. Thus, the differential expression of HDACs in monoaminergic and neuropeptidergic neurons may be crucial for the maintenance of biological characteristics and may be altered in response to environmental factors.

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References 44 · Cited by 47

Authors
Takase, K., Oda, S., Kuroda, M., & Funato, H.
Affiliations
Toho University (JP)
Corresponding author
  • Takase, Kenkichi
  • Oda, Satoko
  • Kuroda, Masaru
  • Funato, Hiromasa
Venue
PLoS ONE
Published
2013-03-04
Volume
8
Issue
3
Pages
e58473
ISSN
1932-6203 (ISSN-L)
OpenAlex
W1970189693
Cited by
47
References
44
Citations by year
2025: 1 · 2024: 2 · 2023: 1 · 2022: 5 · 2021: 6 · 2020: 2 · 2019: 2 · 2018: 6 · 2017: 5 · 2016: 5 · 2015: 1 · 2014: 9 · 2013: 2
FWCI
2.54
Type
journal article
Language
en
Open access
Locations
  • PLoS ONE (publishedVersion, cc-by)
  • Europe PMC (PubMed Central) (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
Funders
  • Ministry of Education, Culture, Sports, Science and Technology (23126526)
  • Japan Society for the Promotion of Science (22590228, 25460318)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Histone Deacetylase Inhibitors Research
  • Social Sciences › Psychology › Social Psychology › Neuroendocrine regulation and behavior
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
Keywords
histone deacetylase, monoaminergic neurons, HDAC10, HDAC8, HDAC4, corticotropin-releasing hormone neurons, oxytocin neurons, vasopressin neurons, agouti-related peptide neurons, proopiomelanocortin neurons, orexin neurons, histamine neurons, dopaminergic neurons, serotonergic neurons, noradrenergic neurons, epigenetic regulation, histone acetylation
MeSH terms
Animals, Biological Transport, Brain, Cell Nucleus, Cytoplasm, Histone Deacetylases, Male, Mice, Inbred C57BL, Microtomy, Neurons, Neuropeptides, Biogenic Monoamines, Gene Expression, Microscopy, Confocal, Gene Expression Profiling, Epigenesis, Genetic, Mice

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