Diverse cellular and molecular modes of axon degeneration

Lukas J. Neukomm, Marc Freeman

Research output: Contribution to journalReview article

51 Citations (Scopus)

Abstract

The elimination of large portions of axons is a widespread event in the developing and diseased nervous system. Subsets of axons are selectively destroyed to help fine-tune neural circuit connectivity during development. Axonal degeneration is also an early feature of nearly all neurodegenerative diseases, occurs after most neural injuries, and is a primary driver of functional impairment in patients. In this review we discuss the diversity of cellular mechanisms by which axons degenerate. Initial molecular characterization highlights some similarities in their execution but also argues that unique genetic programs modulate each mode of degeneration. Defining these pathways rigorously will provide new targets for therapeutic intervention after neural injury or in neurodegenerative disease.

Original languageEnglish (US)
Pages (from-to)515-523
Number of pages9
JournalTrends in Cell Biology
Volume24
Issue number9
DOIs
StatePublished - 2014
Externally publishedYes

Fingerprint

Axons
Neurodegenerative Diseases
Wounds and Injuries
Nervous System Diseases
Therapeutics

Keywords

  • Axon degeneration
  • Axon retraction
  • Axosome shedding
  • Glia
  • Pruning
  • Wallerian degeneration

ASJC Scopus subject areas

  • Cell Biology
  • Medicine(all)

Cite this

Diverse cellular and molecular modes of axon degeneration. / Neukomm, Lukas J.; Freeman, Marc.

In: Trends in Cell Biology, Vol. 24, No. 9, 2014, p. 515-523.

Research output: Contribution to journalReview article

Neukomm, Lukas J. ; Freeman, Marc. / Diverse cellular and molecular modes of axon degeneration. In: Trends in Cell Biology. 2014 ; Vol. 24, No. 9. pp. 515-523.
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