Two Types of Neurons in Cerebellum Influence Motor and Social Behaviors

Summary: Researchers reveal distinct roles for two types of neurons in the cerebellum. The study offers compelling in vivo evidence that a specific group of excitatory glutamatergic neurons plays a key role in acquiring motor and sensory/emotional behaviors.

Additionally, the study demonstrates that neurons located in different regions of the cerebellum differently contribute to motor and non-motor behaviors during development and adulthood. These findings offer new insights into the cerebellum’s complex circuitry and its implications for movement, language, and social behaviors.

Key Facts:

  1. The study shows that two different types of cerebellar neurons play distinct roles in regulating motor and non-motor behaviors during development and adulthood.
  2. Researchers found that silencing the excitatory lineages in the cerebellar cortex and cerebellar nuclei in early postnatal stages caused severe impairments in both motor and social vocalization behavior, however, natural molecular transitions later normalized social behaviors with only mild motor deficits persisting in adult mice.
  3. The study identified that the cerebellar cortex neurons control the acquisition of social skills whereas the cerebellar nuclei affect the establishment of motor behaviors, showing that the brain can compensate for some, but not all, perturbations occurring in the developing cerebellum.

Source: Texas Children’s Hospital

The cerebellum, a major part of the hindbrain in all vertebrates, is important for motor coordination, language acquisition, and regulating social and emotional behaviors.

A study led by Dr. Roy Sillitoe, professor of Pathology and Neuroscience at Baylor College of Medicine and investigator at the Jan and Dan Duncan Neurological Research Institute (Duncan NRI) at Texas Children’s Hospital, shows two distinct types of cerebellar neurons differentially regulate motor and non-motor behaviors during development and in adulthood.

The study, published in Nature Communications, provides the first in vivo evidence supporting the critical role of a specific subset of excitatory glutamatergic neurons in acquiring motor and sensory/emotional behaviors.

Further, it shows that neurons present in different regions of the cerebellum contribute differently to motor versus non-motor behaviors during development and in adulthood.

Cerebellar circuits are established by two major types of neurons

The cerebellar nuclei are present in the deepest layer of the cerebellum. These nuclei are encased by an outer highly convoluted sheet of tissue called the cerebellar cortex, which contains most of the other types of neurons in the cerebellum. 

This is a cartoon of two neurons.
During development, cerebellar injury in preterm infants is often associated with movement disorders, language impairments, and social deficits. Credit: Neuroscience News

The cerebellar cortex receives information from most parts of the body and other brain regions. These inputs are integrated by many types of cerebellar neurons and the deep-set cerebellar nuclei – the sole output structures in the cerebellum – then send those signals to the other parts of the brain.

During development, cerebellar injury in preterm infants is often associated with movement disorders, language impairments, and social deficits. However, growing evidence in patients and animal models suggests that the site of injury and its relative severity determines the type and extent of the resulting symptoms.

Unraveling the function of two types of cerebellar neurons

“Our goal in undertaking this study was to determine if excitatory neurons in the cerebellar cortex and cerebellar nuclei act differentially to establish and maintain motor and social behaviors during developmental stages and in adulthood,” lead author, Dr. Meike van der Heijden, a postdoctoral fellow in the Sillitoe lab at the time of the study, said.

“Several recent studies have hinted at discrete roles for various cerebellar neuronal types and these findings inspired us to conduct a deeper examination of how relatively few neuron types in the cerebellum contribute to a wide range of motor and non-motor functions.

“When we embarked on this study, very little was known about how circuit cerebellar-associated behaviors originate, and whether the same neuronal subtypes contribute equally to the acquisition of these diverse behaviors.”

Dr. van der Heijden and graduate student in the Sillitoe lab, Alejandro G. Rey Hipolito, focused on the excitatory glutamatergic neuronal lineages in the cerebellum because it is commonly believed that these neuronal lineages drive the majority of cerebellar behaviors.

Dissecting the functional contributions of these two neuronal lineages in the acquisition of different cerebellar-dependent behaviors requires the use of non-invasive and cell-type- specific manipulations during circuit development.

They employed a combination of intersectional genetics and behavioral paradigms which allowed them to address this question with unparalleled precision and specificity in mice models of various developmental ages.

Neurons of the cerebellar cortex control social behaviors whereas cerebellar nuclei neurons regulate motor function

The team found silencing the excitatory lineages in the cerebellar cortex and cerebellar nuclei in early postnatal stages by genetically removing the Vglut2 gene from Atoh1-expressing neurons caused severe impairments in both motor and social vocalization behavior in early prenatal stages.

However, by the time these Atoh1mutant mice reach adulthood, natural molecular transitions result in the normalization of the cerebellar cortex function, which to their surprise coincided with the restoration of social behaviors and only mild motor deficits in these mice.

This finding indicated that early social deficits and delayed acquisition of normal social behaviors in these mice were likely due to the progressive normalization of the function of cerebellar cortex neurons.

To test if this hypothesis was true, they eliminated neurotransmission from a subset of glutamatergic nuclei neurons using Ntsr1-cre driver. Upon repeating the same behavioral paradigms, they did not observe any social deficits but observed severe motor deficits in early postnatal mice that were fully resolved with age.

“Together, several major novel findings emerged from our experiments,” co-first author, Alejandro Rey Hipolito, said.

“First, we were surprised to find that silencing the excitatory neurons did not impair all the cerebellar functions.

“Second, we observed that glutamatergic neurotransmission from cerebellar cortical versus cerebellar nuclei neurons regulates the acquisition of motor and social behaviors differentially – the cerebellar cortex neurons control the acquisition of social skills whereas the cerebellar nuclei affect the establishment of motor behaviors.

“Finally, it appears that the brain is able to compensate for some, but not all, perturbations that occur in the developing cerebellum.

“This study has not only led to several important discoveries about the roles of different cerebellar neurons but has opened several interesting questions about the role of inhibitory GABAergic nuclei neurons in compensating for the loss of excitatory glutamatergic neurons and restoring the function, which we intend to explore in the future,” Dr. Sillitoe, added.

“Moreover, these findings offer several exciting and new possibilities to regulate specific cerebellar lineages to restore motor and non-motor functions after brain injury and disease.”

Others involved in the study are Linda H. Kim, Dominic J. Kizek, Ross M. Perez,and Tao Lin. They are affiliated with Baylor College of Medicine and the Jan and Dan Duncan Neurological Research Institute

Funding: This work was supported by Baylor College of Medicine, Texas Children’s Hospital, The Hamill Foundation, and the National Institutes of Neurological Disorders and Stroke (NINDS), a postdoctoral award from the Dystonia Medical Research Foundation (DMRF) and NINDS, and a postdoctoral award from the DMRF. Research reported in this publication was supported by the Eunice Kennedy Shriver National Institute of Child Health & Human Development of the National Institutes of Health for use of the Cell and Tissue Pathogenesis Core and In Situ Hybridization Core, a part of the BCM IDDRC.

About this neuroscience research news

Author: Rajalaxmi Natarajan
Source: Texas Children’s Hospital
Contact: Rajalaxmi Natarajan – Texas Children’s Hospital
Image: The image is credited to Neuroscience News

Original Research: Open access.
Glutamatergic cerebellar neurons differentially contribute to the acquisition of motor and social behaviors” by Roy Sillitoe et al. Nature Communications


Abstract

Glutamatergic cerebellar neurons differentially contribute to the acquisition of motor and social behaviors

Insults to the developing cerebellum can cause motor, language, and social deficits. Here, we investigate whether developmental insults to different cerebellar neurons constrain the ability to acquire cerebellar-dependent behaviors.

We perturb cerebellar cortical or nuclei neuron function by eliminating glutamatergic neurotransmission during development, and then we measure motor and social behaviors in early postnatal and adult mice. Altering cortical and nuclei neurons impacts postnatal motor control and social vocalizations.

Normalizing neurotransmission in cortical neurons but not nuclei neurons restores social behaviors while the motor deficits remain impaired in adults. In contrast, manipulating only a subset of nuclei neurons leaves social behaviors intact but leads to early motor deficits that are restored by adulthood.

Our data uncover that glutamatergic neurotransmission from cerebellar cortical and nuclei neurons differentially control the acquisition of motor and social behaviors, and that the brain can compensate for some but not all perturbations to the developing cerebellum.

Join our Newsletter
I agree to have my personal information transferred to AWeber for Neuroscience Newsletter ( more information )
Sign up to receive our recent neuroscience headlines and summaries sent to your email once a day, totally free.
We hate spam and only use your email to contact you about newsletters. You can cancel your subscription any time.