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Cerebellar output neurons impair non-motor behaviors by altering development of extracerebellar connectivity.
Lee, Andrew S; Arefin, Tanzil M; Gubanova, Alina; Stephen, Daniel N; Liu, Yu; Lao, Zhimin; Krishnamurthy, Anjana; De Marco García, Natalia V; Heck, Detlef H; Zhang, Jiangyang; Rajadhyaksha, Anjali M; Joyner, Alexandra L.
Affiliation
  • Lee AS; Developmental Biology Program, Sloan Kettering Institute, New York 10065, NY, USA.
  • Arefin TM; Neuroscience Program, Weill Cornell Graduate School of Medical Sciences, New York 10021, NY, USA.
  • Gubanova A; Bernard and Irene Schwartz Center for Biomedical Imaging, Department of Radiology, New York University Grossman School of Medicine, New York 10016, NY, USA.
  • Stephen DN; Present Address: Center for Neurotechnology in Mental Health Research, Department of Biomedical Engineering, The Pennsylvania State University, University Park, PA 16801, USA.
  • Liu Y; Developmental Biology Program, Sloan Kettering Institute, New York 10065, NY, USA.
  • Lao Z; Developmental Biology Program, Sloan Kettering Institute, New York 10065, NY, USA.
  • Krishnamurthy A; Department of Biomedical Sciences, University of Minnesota Medical School, Duluth, MN 55812, USA.
  • De Marco García NV; Center for Cerebellar Network Structure and Function in Health and Disease, University of Minnesota, Duluth, MN 55812, USA.
  • Heck DH; Developmental Biology Program, Sloan Kettering Institute, New York 10065, NY, USA.
  • Zhang J; Developmental Biology Program, Sloan Kettering Institute, New York 10065, NY, USA.
  • Rajadhyaksha AM; Neuroscience Program, Weill Cornell Graduate School of Medical Sciences, New York 10021, NY, USA.
  • Joyner AL; Neuroscience Program, Weill Cornell Graduate School of Medical Sciences, New York 10021, NY, USA.
bioRxiv ; 2024 Jul 08.
Article in En | MEDLINE | ID: mdl-39026865
ABSTRACT
The capacity of the brain to compensate for insults during development depends on the type of cell loss, whereas the consequences of genetic mutations in the same neurons are difficult to predict. We reveal powerful compensation from outside the cerebellum when the excitatory cerebellar output neurons are ablated embryonically and demonstrate that the minimum requirement for these neurons is for motor coordination and not learning and social behaviors. In contrast, loss of the homeobox transcription factors Engrailed1/2 (EN1/2) in the cerebellar excitatory lineage leads to additional deficits in adult learning and spatial working memory, despite half of the excitatory output neurons being intact. Diffusion MRI indicates increased thalamo-cortico-striatal connectivity in En1/2 mutants, showing that the remaining excitatory neurons lacking En1/2 exert adverse effects on extracerebellar circuits regulating motor learning and select non-motor behaviors. Thus, an absence of cerebellar output neurons is less disruptive than having cerebellar genetic mutations.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: BioRxiv Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: BioRxiv Year: 2024 Document type: Article