TY - JOUR
T1 - Differential Motion Dynamics of Synaptic Vesicles Undergoing Spontaneous and Activity-Evoked Endocytosis
AU - Peng, Amy
AU - Rotman, Ziv
AU - Deng, Pan Yue
AU - Klyachko, Vitaly A.
N1 - Funding Information:
This work was supported in part by grants to V.A.K. from the Esther A. & Joseph Klingenstein Foundation, the Edward Mallinckrodt, Jr. Foundation, the Whitehall Foundation, and the Alzheimer's Association. We thank Dr. G. Danuzer and Dr. K. Jaqaman for kindly sharing their uTrack particle tracking software. We also thank Dr. S. Mennerick, Dr. V. Cavalli, and Dr. D. Owyoung for their constructive comments on the manuscript.
PY - 2012/3/22
Y1 - 2012/3/22
N2 - Synaptic vesicle exo- and endocytosis are usually driven by neuronal activity but can also occur spontaneously. The identity and differences between vesicles supporting evoked and spontaneous neurotransmission remain highly debated. Here we combined nanometer-resolution imaging with a transient motion analysis approach to examine the dynamics of individual synaptic vesicles in hippocampal terminals under physiological conditions. We found that vesicles undergoing spontaneous and stimulated endocytosis differ in their dynamic behavior, particularly in the ability to engage in directed motion. Our data indicate that such motional differences depend on the myosin family of motor proteins, particularly myosin II. Analysis of synaptic transmission in the presence of myosin II inhibitor confirmed a specific role for myosin II in evoked, but not spontaneous, neurotransmission and also suggested a functional role of myosin II-mediated vesicle motion in supporting vesicle mobilization during neural activity. The properties of synaptic vesicles supporting activity-evoked and spontaneous neurotransmission remain highly debated. Here, Peng et al. use nanometer-resolution imaging to show that synaptic vesicle categories differ in dynamic behavior, particularly in the ability to engage in motor-mediated transport.
AB - Synaptic vesicle exo- and endocytosis are usually driven by neuronal activity but can also occur spontaneously. The identity and differences between vesicles supporting evoked and spontaneous neurotransmission remain highly debated. Here we combined nanometer-resolution imaging with a transient motion analysis approach to examine the dynamics of individual synaptic vesicles in hippocampal terminals under physiological conditions. We found that vesicles undergoing spontaneous and stimulated endocytosis differ in their dynamic behavior, particularly in the ability to engage in directed motion. Our data indicate that such motional differences depend on the myosin family of motor proteins, particularly myosin II. Analysis of synaptic transmission in the presence of myosin II inhibitor confirmed a specific role for myosin II in evoked, but not spontaneous, neurotransmission and also suggested a functional role of myosin II-mediated vesicle motion in supporting vesicle mobilization during neural activity. The properties of synaptic vesicles supporting activity-evoked and spontaneous neurotransmission remain highly debated. Here, Peng et al. use nanometer-resolution imaging to show that synaptic vesicle categories differ in dynamic behavior, particularly in the ability to engage in motor-mediated transport.
UR - http://www.scopus.com/inward/record.url?scp=84858667235&partnerID=8YFLogxK
U2 - 10.1016/j.neuron.2012.01.023
DO - 10.1016/j.neuron.2012.01.023
M3 - Article
C2 - 22445339
AN - SCOPUS:84858667235
SN - 0896-6273
VL - 73
SP - 1108
EP - 1115
JO - Neuron
JF - Neuron
IS - 6
ER -