TY - JOUR
T1 - Optically Resolving Individual Microtubules in Live Axons
AU - Mudrakola, Harsha V.
AU - Zhang, Kai
AU - Cui, Bianxiao
N1 - We thank Drs. Chengbiao Wu, Wei Wang, and Janice S. Valletta for their assistance in carrying out the experiments and helpful discussions. B.C. wishes to express her gratitude to Prof. William W. Mobley and Prof. Yanmin Yang for their generosity in sharing resources and knowledge that significantly accelerated the research. This work was supported by National Institutes of Health grant NS057906, Bio-X interdisciplinary initiatives program, Dreyfus new faculty award, and Searle Scholar Award (to B.C.).
PY - 2009/11/11
Y1 - 2009/11/11
N2 - Microtubules are essential cytoskeletal tracks for cargo transportation in axons and also serve as the primary structural scaffold of neurons. Structural assembly, stability, and dynamics of axonal microtubules are of great interest for understanding neuronal functions and pathologies. However, microtubules are so densely packed in axons that their separations are well below the diffraction limit of light, which precludes using optical microscopy for live-cell studies. Here, we present a single-molecule imaging method capable of resolving individual microtubules in live axons. In our method, unlabeled microtubules are revealed by following individual axonal cargos that travel along them. We resolved more than six microtubules in a 1 μm diameter axon by real-time tracking of endosomes containing quantum dots. Our live-cell study also provided direct evidence that endosomes switch between microtubules while traveling along axons, which has been proposed to be the primary means for axonal cargos to effectively navigate through the crowded axoplasmic environment.
AB - Microtubules are essential cytoskeletal tracks for cargo transportation in axons and also serve as the primary structural scaffold of neurons. Structural assembly, stability, and dynamics of axonal microtubules are of great interest for understanding neuronal functions and pathologies. However, microtubules are so densely packed in axons that their separations are well below the diffraction limit of light, which precludes using optical microscopy for live-cell studies. Here, we present a single-molecule imaging method capable of resolving individual microtubules in live axons. In our method, unlabeled microtubules are revealed by following individual axonal cargos that travel along them. We resolved more than six microtubules in a 1 μm diameter axon by real-time tracking of endosomes containing quantum dots. Our live-cell study also provided direct evidence that endosomes switch between microtubules while traveling along axons, which has been proposed to be the primary means for axonal cargos to effectively navigate through the crowded axoplasmic environment.
KW - CELLBIO
KW - PROTEINS
UR - http://www.scopus.com/inward/record.url?scp=70350716183&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=70350716183&partnerID=8YFLogxK
U2 - 10.1016/j.str.2009.09.008
DO - 10.1016/j.str.2009.09.008
M3 - Article
C2 - 19913478
AN - SCOPUS:70350716183
SN - 0969-2126
VL - 17
SP - 1433
EP - 1441
JO - Structure
JF - Structure
IS - 11
ER -