학술논문

Freeze-Fracture Studies of Frog Neuromuscular Junctions during Intense Release of Neurotransmitter: II. Effects of Electrical Stimulation and High Potassium
Document Type
research-article
Source
The Journal of Cell Biology, 1979 Apr 01. 81(1), 178-192.
Subject
Membrane fusion
Active zones
Potassium
Endocytosis
Vesicle retrieval
Synapses
Nerves
Exocytosis
Secretion
Endocytosis
Transmitters
Histograms
Transport vesicles
Muscle fibers
Mitochondria
Language
English
ISSN
00219525
Abstract
Frog cutaneous pectoris nerve muscle preparations were studied by the freeze-fracture technique under the following conditions: (a) during repetitive indirect stimulation for 20 min, 10/s; (b) during recovery from this stimulation; and (c) during treatment with 20 mM K + . Indirect stimulation causes numerous dimples or protuberances to appear on the presynaptic membrane of the nerve terminal, and most are located near the active zones. Deep infoldings of the axolemma often develop between the active zones. Neither the number nor the distribution of dimples, protuberances, or infoldings changes markedly during the first minute of recovery. The number of dimples, protuberances, and infoldings is greatly reduced after 10 min of recovery. Since endocytosis proceeds vigorously during the recovery periods, we conclude that endocytosis occurs mostly at the active zones, close to the sites of exocytosis. 20 mM K + also causes many dimples or protuberances to appear on the axolemma of the nerve terminal but they are distributed almost uniformly along the presynaptic membrane. Experiments with horseradish peroxidase (HRP) show that recycling of synaptic vesicles occurs in 20 mM K + . This recycling is not accompanied by changes in the number of coated vesicles. Since both exocytosis and endocytosis occur in 20 mM K + , it is difficult to account for this unique distribution. However, we suggest that K + causes dimples or protuberances to appear between the active zones because it activates latent sites of exocytosis specified by small numbers of large intramembrane particles located between active zones. The activation of latent release sites may be related to the complex effects that K + has on the quantal release of neurotransmitter.