Connecting neurodevelopment to neurodegeneration: A spotlight on the role of kinesin superfamily protein 2A (KIF2A)

  • Nuria Ruiz-Reig
  • , Janne Hakanen
  • , Fadel Tissir*
  • *Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

8 Citations (Scopus)

Abstract

Microtubules play a central role in cytoskeletal changes during neuronal development and maintenance. Microtubule dynamics is essential to polarity and shape transitions underlying neural cell division, differentiation, motility, and maturation. Kinesin superfamily protein 2A is a member of human kinesin 13 gene family of proteins that depolymerize and destabilize microtubules. In dividing cells, kinesin superfamily protein 2A is involved in mitotic progression, spindle assembly, and chromosome segregation. In postmitotic neurons, it is required for axon/dendrite specification and extension, neuronal migration, connectivity, and survival. Humans with kinesin superfamily protein 2A mutations suffer from a variety of malformations of cortical development, epilepsy, autism spectrum disorder, and neurodegeneration. In this review, we discuss how kinesin superfamily protein 2A regulates neuronal development and function, and how its deregulation causes neurodevelopmental and neurological disorders.

Original languageEnglish
Pages (from-to)375-379
Number of pages5
JournalNeural Regeneration Research
Volume19
Issue number2
DOIs
Publication statusPublished - Feb 2024

Keywords

  • brain disorders
  • cortical malformations
  • kinesin
  • microtubules
  • neurodegeneration
  • neurodevelopment

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