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The Vesicular Acetylcholine Transporter Is Required for Neuromuscular Development and Function

delete2023-03-21
delete124
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OA
AI
B
Braulio M. de Castro
X
Xavier De Jaeger
C
Cristina Martins-Silva
R
Ricardo Lima
E
Ernani Aloysio Amaral
C
Cristiane A. S. Menezes
P
Patrícia Lima
C
Cintia M. L. Neves
R
Rita Gomes Wanderley Pires
T
Thomas W. Gould
I
Ian Welch
C
Christopher Kushmerick
C
Cristina Guatimosim
I
Iván Izquierdo
M
Martı́n Cammarota
R
R. Jane Rylett
M
Marcus V. Gomez
M
Marc G. Caron
R
Ronald W. Oppenheim
M
Marco A. M. Prado *
V
Vânia F. Prado
DOI:10.1128/MCB.00245-09delete
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Abstract

Abstract

En 中文
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.
Keywords:
AFFINITY CHOLINE TRANSPORTER
QUANTAL TRANSMITTER SECRETION
CRE TRANSGENE EXPRESSION
PROGRAMMED CELL-DEATH
PROTEIN-KINASE-C
SYMPATHETIC-GANGLION
SYNAPTIC VESICLES
VESAMICOL AH5183
RELEASE
ACETYLTRANSFERASE
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Journal

Molecular and Cellular Biology cover
Molecular and Cellular Biology
IF:
2.7
Papers:
1.3W
Citations:
3.8W

Organization

W
wake forest university
Scholars:
1.7W
Papers: 1.4W
Citations: 15
W
western university (university of western ontario)
Scholars:
2.9W
Papers: 2.7W
Citations: 33
U
Universidade Federal de Minas Gerais
Scholars:
2.5W
Papers: 1.5W
Citations: 1.4W
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