ERK2 Contributes to the Control of Social Behaviors in Mice
Open accessAbstract
Signaling through extracellular signal-regulated kinase (ERK) is important in multiple signal transduction networks in the CNS. However, the specific role of ERK2 in in vivo brain functions is not fully understood. Here we show that ERK2 play a critical role in regulating social behaviors as well as cognitive and emotional behaviors in mice. To study the brain function of ERK2, we used a conditional, region-specific, genetic approach to target Erk2 using the Cre/loxP strategy with a nestin promoter-driven cre transgenic mouse line to induce recombination in the CNS. The resulting Erk2 conditional knock-out (CKO) mice, in which Erk2 was abrogated specifically in the CNS, were viable and fertile with a normal appearance. These mice, however, exhibited marked anomalies in multiple aspects of social behaviors related to facets of autism-spectrum disorders: elevated aggressive behaviors, deficits in maternal nurturing, poor nest-building, and lower levels of social familiarity and social interaction.Erk2 CKO mice also exhibited decreased anxiety-related behaviors and impaired long-term memory. Pharmacological inhibition of ERK1 phosphorylation in Erk2 CKO mice did not affect the impairments in social behaviors and learning disabilities, indicating that ERK2, but not ERK1 plays a critical role in these behaviors. Our findings suggest that ERK2 has complex and multiple roles in the CNS, with important implications for human psychiatric disorders characterized by deficits in social behaviors.
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Mice deficient for Erk2 in the central nervous system exhibited learning impairment and social deficits similar to those seen in ASD.
“We previously reported that mice deficient for Erk2 in the central nervous system (CNS) exhibited learning impairment and social deficits similar to those seen in ASD10.”
From Transient blockade of ERK phosphorylation in the critical period causes autistic phenotypes as an adult in mice (2015) · cites this paper as [10]
SL327 at 50 mg/kg can cross the blood-brain barrier and effectively reduce the basal level of ERK activation in the CNS.
“It was previously reported that SL327 at this concentration can cross the blood-brain barrier and effectively reduce the basal level of ERK activation in the CNS101213.”
From Transient blockade of ERK phosphorylation in the critical period causes autistic phenotypes as an adult in mice (2015) · cites this paper as [10]
Many studies reporting that ERK1 and ERK2 play distinct roles in neuronal functioning.
“There are many studies reporting that ERK1 and ERK2 play distinct roles in neuronal functioning.”
From Transient blockade of ERK phosphorylation in the critical period causes autistic phenotypes as an adult in mice (2015) · cites this paper as [10]
Genetic abrogation of ERK2 has profound deleterious effects on neural functioning, whereas Erk1 KO mice do not exhibit significant impairment in neural functioning.
“For instance, genetic abrogation of ERK2 has profound deleterious effects on neural functioning, whereas Erk1 KO mice do not exhibit significant impairment in neural functioning10192021.”
From Transient blockade of ERK phosphorylation in the critical period causes autistic phenotypes as an adult in mice (2015) · cites this paper as [10]
Genetic abrogation of Erk2 gene in the CNS results in ASD-like behavior in mice.
“We previously reported that genetic abrogation of Erk2 gene in the CNS results in ASD-like behavior in mice10.”
From Transient blockade of ERK phosphorylation in the critical period causes autistic phenotypes as an adult in mice (2015) · cites this paper as [10]
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References 50 · Cited by 145
- Authors
- Satoh, Y., Endo, S., Nakata, T., Kobayashi, Y., Yamada, K., Ikeda, T., Takeuchi, A., Hiramoto, T., Watanabe, Y., & Kazama, T.
- Affiliations
- National Defense Medical College Hospital (JP)
- Tokyo Metropolitan Institute of Gerontology (JP)
- National Defense Medical College (JP)
- RIKEN Center for Brain Science (JP)
- National Center for Geriatrics and Gerontology (JP)
- Naito Foundation (JP)
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2011-08-17
- Volume
- 31
- Issue
- 33
- Pages
- 11953-11967
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC6623182
- OpenAlex
- W1971626420
- Cited by
- 145
- References
- 50
- Citations by year
- 2026: 6 · 2025: 5 · 2024: 9 · 2023: 5 · 2022: 10 · 2021: 14 · 2020: 9 · 2019: 11 · 2018: 8 · 2017: 9 · 2016: 12 · 2015: 13 · 2014: 12 · 2013: 9 · 2012: 11
- FWCI
- 6.78
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Japan Society for the Promotion of Science (22500304)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetics and Neurodevelopmental Disorders
- Social Sciences › Psychology › Social Psychology › Neuroendocrine regulation and behavior
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- ERK2, extracellular signal-regulated kinase, social behavior, autism spectrum disorder, aggression, nest building, social interaction, anxiety, long-term memory, conditional knockout mice, ERK1, cognitive impairment, emotional behavior
- MeSH terms
- Animals, Female, Male, Mice, Inbred C57BL, Mice, Transgenic, Motor Activity, Pregnancy, Social Behavior, Down-Regulation, Mice, Knockout, Mitogen-Activated Protein Kinase 1, Mice, Mice, 129 Strain
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