The vesicular acetylcholine transporter is required for neuromuscular development and function.

Published

Journal Article

The vesicular acetylcholine (ACh) transporter (VAChT) mediates ACh storage by synaptic vesicles. However, the VAChT-independent release of ACh is believed to be important during development. Here we generated VAChT knockout mice and tested the physiological relevance of the VAChT-independent release of ACh. Homozygous VAChT knockout mice died shortly after birth, indicating that VAChT-mediated storage of ACh is essential for life. Indeed, synaptosomes obtained from brains of homozygous knockouts were incapable of releasing ACh in response to depolarization. Surprisingly, electrophysiological recordings at the skeletal-neuromuscular junction show that VAChT knockout mice present spontaneous miniature end-plate potentials with reduced amplitude and frequency, which are likely the result of a passive transport of ACh into synaptic vesicles. Interestingly, VAChT knockouts exhibit substantial increases in amounts of choline acetyltransferase, high-affinity choline transporter, and ACh. However, the development of the neuromuscular junction in these mice is severely affected. Mutant VAChT mice show increases in motoneuron and nerve terminal numbers. End plates are large, nerves exhibit abnormal sprouting, and muscle is necrotic. The abnormalities are similar to those of mice that cannot synthesize ACh due to a lack of choline acetyltransferase. Our results indicate that VAChT is essential to the normal development of motor neurons and the release of ACh.

Full Text

Duke Authors

Cited Authors

  • de Castro, BM; De Jaeger, X; Martins-Silva, C; Lima, RDF; Amaral, E; Menezes, C; Lima, P; Neves, CML; Pires, RG; Gould, TW; Welch, I; Kushmerick, C; Guatimosim, C; Izquierdo, I; Cammarota, M; Rylett, RJ; Gomez, MV; Caron, MG; Oppenheim, RW; Prado, MAM; Prado, VF

Published Date

  • October 2009

Published In

Volume / Issue

  • 29 / 19

Start / End Page

  • 5238 - 5250

PubMed ID

  • 19635813

Pubmed Central ID

  • 19635813

Electronic International Standard Serial Number (EISSN)

  • 1098-5549

Digital Object Identifier (DOI)

  • 10.1128/MCB.00245-09

Language

  • eng

Conference Location

  • United States