2003
DOI: 10.1073/pnas.1030502100
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Dynamic assembly of surface structures in living cells

Abstract: Although the dynamics of cell membranes and associated structures is vital for cell function, little is known due to lack of suitable methods. We found, using scanning ion conductance microscopy, that microvilli, membrane projections supported by internal actin bundles, undergo a life cycle: fast height-dependent growth, relatively short steady state, and slow height-independent retraction. The microvilli can aggregate into relatively stable structures where the steady state is extended. We suggest that the in… Show more

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Cited by 167 publications
(169 citation statements)
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References 28 publications
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“…Typical SICM experiments are performed in moderate 19 to high ionic strengths (>100 mM), 3,31,32,45,67,68 as are many nanopipette measurements. 14,15,18,19 Under these conditions, the diffuse double layer is expected to be compressed to a sub-nanometer scale, and therefore undetectable, level according to: 50…”
Section: Characterization Of Nanopipettes In High Ionic Strength Mediamentioning
confidence: 99%
“…Typical SICM experiments are performed in moderate 19 to high ionic strengths (>100 mM), 3,31,32,45,67,68 as are many nanopipette measurements. 14,15,18,19 Under these conditions, the diffuse double layer is expected to be compressed to a sub-nanometer scale, and therefore undetectable, level according to: 50…”
Section: Characterization Of Nanopipettes In High Ionic Strength Mediamentioning
confidence: 99%
“…As the nanopipette-surface distance decreases, the solution resistance in the probe-surface gap increases which, in turn, reduces the ion current. This decrease in ion current is used as a non-contact signal to sense the nanopipette-surface distance and ultimately for topographical imaging, [14][15][16] proving particularly effective for soft samples. 10,12 SICM is typically operated in aqueous solutions with relatively high ionic strength.…”
Section: Introductionmentioning
confidence: 99%
“…Some studies have considered the fluctuation of the cell volume as a function of time via the acquisition of multiple topographical maps [48,61,62], while others improved the scan rate (image time) to study the dynamics of subcellular structures [50] such as microvilli [63] or processes including exocytosis [64] and the cell cycle [3]. Phenotypic changes in cell morphology [65,66] have also been used as a diagnostic tool for a variety of conditions including heart disorders [67] and Alzheimer's disease [68].…”
Section: (C) Topographical Imaging Of Living Cellsmentioning
confidence: 99%