2015
DOI: 10.1002/sca.21200
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Long‐term, long‐distance recording of a living migrating neuron by scanning ion conductance microscopy

Abstract: Bias-free, three-dimensional imaging of entire living cellular specimen is required for investigating shape and volume changes that occur during cellular growth or migration. Here we present fifty consecutive recordings of a living cultured neuron from a mouse dorsal root ganglion obtained by Scanning ion conductance microscopy (SICM). We observed a saltatory migration of the neuron with a mean velocity of approximately 20 μm/h. These results demonstrate the non-invasiveness of SICM, which makes it unique amon… Show more

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Cited by 9 publications
(7 citation statements)
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“…The reason is that the imaging of AFM is realized by measuring the interaction force between probe and sample which will inevitably affect the cells. And the contactless imaging mechanism of SICM can avoid cell deformation 47,48 …”
Section: Application Of Sicm In Biomedical Researchmentioning
confidence: 99%
See 2 more Smart Citations
“…The reason is that the imaging of AFM is realized by measuring the interaction force between probe and sample which will inevitably affect the cells. And the contactless imaging mechanism of SICM can avoid cell deformation 47,48 …”
Section: Application Of Sicm In Biomedical Researchmentioning
confidence: 99%
“…SICM can also be used to record living cells for a long time. Gesper et al used SICM to record the migration of neurons for a long time and long distance, indicating that SICM has little effect on cells which makes it have an irreplaceable position in scanning probe microscopy 47 …”
Section: Application Of Sicm In Biomedical Researchmentioning
confidence: 99%
See 1 more Smart Citation
“…Scanning ion conductance microscopy (SICM) was first proposed by Hansma et al in 1989, then further improved by Korchev et al , in 1997, and has become a formidable high-resolution microimaging tool. It has been applied to a wide range of applications in the fields of biology, medicine, and electrochemistry. SICM uses a thin nanopipette filled with electrolyte solution as its scanning probe. By monitoring the change of ion current in the nanopipette, the distance between the nanopipette and sample can be controlled, which allows for reconstruction of the microscopic surface topography of the sample.…”
Section: Introductionmentioning
confidence: 99%
“…However, AFM has been found to bias cellular samples more than SICM . The nearly contact-free operating principle of SICM, operated in a mode where the scanning tip is advanced to the sample at every single pixel and subsequently withdrawn before lateral movement to avoid probe sample collisions (see also Figure E), allowed SICM to, for example, determine the volume changes during the migration of neural cells. Hitherto, no combined recordings of SICM and any fluorescence super-resolution technique have been reported, but direct stochastic optical reconstruction microscopy (dSTORM) has been used to quantify the number of fluorescent molecules deposited by a SICM tip onto a surface . However, SICM has been combined with conventional confocal fluorescence microscopy .…”
mentioning
confidence: 99%