Distinct Cerebellar Contributions to Intrinsic Connectivity Networks

Convergent data from various scientific approaches strongly implicate cerebellar systems in nonmotor functions. The functional anatomy of these systems has been pieced together from disparate sources, such as animal studies, lesion studies in humans, and structural and functional imaging studies in...

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Published inThe Journal of neuroscience Vol. 29; no. 26; pp. 8586 - 8594
Main Authors Habas, Christophe, Kamdar, Nirav, Nguyen, Daniel, Prater, Katherine, Beckmann, Christian F, Menon, Vinod, Greicius, Michael D
Format Journal Article
LanguageEnglish
Published United States Soc Neuroscience 01.07.2009
Society for Neuroscience
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Abstract Convergent data from various scientific approaches strongly implicate cerebellar systems in nonmotor functions. The functional anatomy of these systems has been pieced together from disparate sources, such as animal studies, lesion studies in humans, and structural and functional imaging studies in humans. To better define this distinct functional anatomy, in the current study we delineate the role of the cerebellum in several nonmotor systems simultaneously and in the same subjects using resting state functional connectivity MRI. Independent component analysis was applied to resting state data from two independent datasets to identify common cerebellar contributions to several previously identified intrinsic connectivity networks (ICNs) involved in executive control, episodic memory/self-reflection, salience detection, and sensorimotor function. We found distinct cerebellar contributions to each of these ICNs. The neocerebellum participates in (1) the right and left executive control networks (especially crus I and II), (2) the salience network (lobule VI), and (3) the default-mode network (lobule IX). Little to no overlap was detected between these cerebellar regions and the sensorimotor cerebellum (lobules V-VI). Clusters were also located in pontine and dentate nuclei, prominent points of convergence for cerebellar input and output, respectively. The results suggest that the most phylogenetically recent part of the cerebellum, particularly crus I and II, make contributions to parallel cortico-cerebellar loops involved in executive control, salience detection, and episodic memory/self-reflection. The largest portions of the neocerebellum take part in the executive control network implicated in higher cognitive functions such as working memory.
AbstractList Convergent data from various scientific approaches strongly implicate cerebellar systems in nonmotor functions. The functional anatomy of these systems has been pieced together from disparate sources, such as animal studies, lesion studies in humans, and structural and functional imaging studies in humans. To better define this distinct functional anatomy, in the current study we delineate the role of the cerebellum in several nonmotor systems simultaneously and in the same subjects using resting state functional connectivity MRI. Independent component analysis was applied to resting state data from two independent datasets to identify common cerebellar contributions to several previously identified intrinsic connectivity networks (ICNs) involved in executive control, episodic memory/self-reflection, salience detection, and sensorimotor function. We found distinct cerebellar contributions to each of these ICNs. The neocerebellum participates in (1) the right and left executive control networks (especially crus I and II), (2) the salience network (lobule VI), and (3) the default-mode network (lobule IX). Little to no overlap was detected between these cerebellar regions and the sensorimotor cerebellum (lobules V-VI). Clusters were also located in pontine and dentate nuclei, prominent points of convergence for cerebellar input and output, respectively. The results suggest that the most phylogenetically recent part of the cerebellum, particularly crus I and II, make contributions to parallel cortico-cerebellar loops involved in executive control, salience detection, and episodic memory/self-reflection. The largest portions of the neocerebellum take part in the executive control network implicated in higher cognitive functions such as working memory.
Author Greicius, Michael D
Habas, Christophe
Prater, Katherine
Menon, Vinod
Kamdar, Nirav
Beckmann, Christian F
Nguyen, Daniel
Author_xml – sequence: 1
  fullname: Habas, Christophe
– sequence: 2
  fullname: Kamdar, Nirav
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  fullname: Nguyen, Daniel
– sequence: 4
  fullname: Prater, Katherine
– sequence: 5
  fullname: Beckmann, Christian F
– sequence: 6
  fullname: Menon, Vinod
– sequence: 7
  fullname: Greicius, Michael D
BackLink https://www.ncbi.nlm.nih.gov/pubmed/19571149$$D View this record in MEDLINE/PubMed
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Snippet Convergent data from various scientific approaches strongly implicate cerebellar systems in nonmotor functions. The functional anatomy of these systems has...
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StartPage 8586
SubjectTerms Adult
Brain Mapping
Cerebellum - anatomy & histology
Cerebellum - blood supply
Cerebellum - physiology
Cerebral Cortex - blood supply
Cerebral Cortex - physiology
Female
Functional Laterality
Humans
Image Processing, Computer-Assisted - methods
Magnetic Resonance Imaging - methods
Male
Models, Neurological
Nerve Net - blood supply
Nerve Net - physiology
Neural Pathways - blood supply
Neural Pathways - physiology
Oxygen - blood
Principal Component Analysis
Problem Solving - physiology
Psychomotor Performance - physiology
Rest - physiology
Young Adult
Title Distinct Cerebellar Contributions to Intrinsic Connectivity Networks
URI http://www.jneurosci.org/cgi/content/abstract/29/26/8586
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