The DOI matches its Crossref record; 34 of the 34 references it cites were found in a registry or an index.
Quantitative Reflection Interference Contrast Microscopy (RICM) in Soft Matter and Cell Adhesion
Abstract
Adhesion can be quantified by measuring the distance between the interacting surfaces. Reflection interference contrast microscopy (RICM), with its ability to measure inter‐surface distances under water with nanometric precision and milliseconds time resolution, is ideally suited to studying the dynamics of adhesion in soft systems. Recent technical developments, which include innovative image analysis and the use of multi‐coloured illumination, have led to renewed interest in this technique. Unambiguous quantitative measurements have been achieved for colloidal beads and model membranes, thus revealing new insights and applications. Quantification of data from cells shows exciting prospects. Herein, we review the basic principles and recent developments of RICM applied to studies of dynamical adhesion processes in soft matter and cell biology and provide practical hints to potential users.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Principles of Optics: 60th Anniversary Edition
Born, M., & Wolf, E. (2019) · Cambridge University Press eBooks · doi:10.1017/9781108769914 · Cited by 26,251
Elastic Properties of Lipid Bilayers: Theory and Possible Experiments
Helfrich, W. (1973) · Zeitschrift für Naturforschung C · doi:10.1515/znc-1973-11-1209 · Cited by 6,141
Single-molecule force spectroscopy: optical tweezers, magnetic tweezers and atomic force microscopy
Neuman, K. C., & Nagy, A. (2008) · Nature Methods · doi:10.1038/nmeth.1218 · Cited by 2,406
Focal Contacts as Mechanosensors
Riveline, D., Zamir, E., Balaban, N. Q., Schwarz, U. S., Ishizaki, T., Narumiya, S., Kam, Z., Geiger, B., & Bershadsky, A. D. (2001) · The Journal of Cell Biology · doi:10.1083/jcb.153.6.1175 · Cited by 1,419
THE MECHANISM OF ADHESION OF CELLS TO GLASS
Curtis, A. S. G. (1964) · The Journal of Cell Biology · doi:10.1083/jcb.20.2.199 · Cited by 592
Seifert, U., & Lipowsky, R. (1990) · Physical Review A · doi:10.1103/physreva.42.4768 · Cited by 511
Microscopic measurement of the pair interaction potential of charge-stabilized colloid
Crocker, J. C., & Grier, D. G. (1994) · Physical Review Letters · doi:10.1103/physrevlett.73.352 · Cited by 506
The Dynamics and Mechanics of Endothelial Cell Spreading
Reinhart-King, C. A., Dembo, M., & Hammer, D. A. (2005) · Biophysical Journal · doi:10.1529/biophysj.104.054320 · Cited by 366
The Universal Dynamics of Cell Spreading
Cuvelier, D., Théry, M., Chu, Y., Dufour, S., Thiery, J. P., Bornens, M., Nassoy, P., & Mahadevan, L. (2007) · Current Biology · doi:10.1016/j.cub.2007.02.058 · Cited by 280
Interference reflection microscopy in cell biology: methodology and applications
Verschueren, H. (1985) · Journal of Cell Science · doi:10.1242/jcs.75.1.279 · Cited by 232
Dubin-Thaler, B. J., Giannone, G., Döbereiner, H.-G., & Sheetz, M. P. (2004) · Biophysical Journal · doi:10.1016/s0006-3495(04)74246-0 · Cited by 219
MECHANISM AND DYNAMICS OF CADHERIN ADHESION
Leckband, D., & Prakasam, A. (2006) · Annual Review of Biomedical Engineering · doi:10.1146/annurev.bioeng.8.061505.095753 · Cited by 207
Quantitative reflection contrast microscopy of living cells.
Bereiter-Hahn, J., Fox, C. H., & Thorell, B. (1979) · The Journal of cell biology · doi:10.1083/jcb.82.3.767 · Cited by 195
Cell Adhesion as Wetting Transition?
Sackmann, E., & Bruinsma, R. F. (2002) · ChemPhysChem · doi:10.1002/1439-7641(20020315)3:3<262::aid-cphc262>3.0.co;2-u · Cited by 186
Role of vinculin in regulating focal adhesion turnover
Saunders, R. M., Holt, M. R., Jennings, L., Sutton, D. H., Barsukov, I. L., Bobkov, A., Liddington, R. C., Adamson, E. A., Dunn, G. A., & Critchley, D. R. (2006) · European Journal of Cell Biology · doi:10.1016/j.ejcb.2006.01.014 · Cited by 182
Dynamic Phase Transitions in Cell Spreading
Döbereiner, J., Dubin‐Thaler, B. J., Giannone, G., Xenias, H. S., & Sheetz, M. P. (2004) · Physical Review Letters · doi:10.1103/physrevlett.93.108105 · Cited by 149
Force-induced growth of adhesion domains is controlled by receptor mobility
Smith, A., Sengupta, K., Goennenwein, S., et al. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0801706105 · Cited by 146
Self-citationCell Force Microscopy on Elastic Layers of Finite Thickness
Merkel, R., Kirchgeßner, N., Cesa, C. M., & Hoffmann, B. (2007) · Biophysical Journal · doi:10.1529/biophysj.107.111328 · Cited by 138
Adhesion-Induced Receptor Segregation and Adhesion Plaque Formation: A Model Membrane Study
Kloboucek, A., Behrisch, A., Faix, J., & Sackmann, E. (1999) · Biophysical Journal · doi:10.1016/s0006-3495(99)77070-0 · Cited by 137
How Cells Tiptoe on Adhesive Surfaces before Sticking
Pierrès, A., Benoliel, A., Touchard, D., & Bongrand, P. (2008) · Biophysical Journal · doi:10.1529/biophysj.107.125278 · Cited by 136
The composition and dynamics of cell-substratum adhesions in locomoting fish keratocytes
Lee, J., & Jacobson, K. (1997) · Journal of Cell Science · doi:10.1242/jcs.110.22.2833 · Cited by 127
Micropatterned silicone elastomer substrates for high resolution analysis of cellular force patterns
Cesa, C. M., Kirchgeßner, N., Mayer, D., Schwarz, U. S., Hoffmann, B., & Merkel, R. (2007) · Review of Scientific Instruments · doi:10.1063/1.2712870 · Cited by 100
Rädler, J. O., & Sackmann, E. (1992) · Langmuir · doi:10.1021/la00039a019 · Cited by 90
Bunnell, S. C., Barr, V. A., Fuller, C. L., et al. (2003) · Science s STKE · doi:10.1126/stke.2003.177.pl8 · Cited by 72
Membrane-Grafted Hyaluronan Films: A Well-Defined Model System of Glycoconjugate Cell Coats
Richter, R. P., Hock, K. K., Burkhartsmeyer, J. M., Boehm, H., Bingen, P., Wang, G., Steinmetz, N. F., Evans, D. J., & Spatz, J. P. (2007) · Journal of the American Chemical Society · doi:10.1021/ja068768s · Cited by 69
Real-Time Measurement of Exocytosis and Endocytosis Using Interference of Light
Llobet, A., Beaumont, V., & Lagnado, L. (2003) · Neuron · doi:10.1016/s0896-6273(03)00765-7 · Cited by 68
Cell Membrane Alignment along Adhesive Surfaces: Contribution of Active and Passive Cell Processes
Pierrès, A., Eymeric, P., Baloche, E., Touchard, D., Benoliel, A., & Bongrand, P. (2003) · Biophysical Journal · doi:10.1016/s0006-3495(03)75013-9 · Cited by 65
Periasamy, A. (2014) · Methods · doi:10.1016/j.ymeth.2014.03.011 · Cited by 58
Modulation of Vesicle Adhesion and Spreading Kinetics by Hyaluronan Cushions
Limozin, L., & Sengupta, K. (2007) · Biophysical Journal · doi:10.1529/biophysj.107.105544 · Cited by 57
Self-citationKühner, M., & Sackmann, E. (1996) · Langmuir · doi:10.1021/la960282+ · Cited by 50
Microviscoelastic Moduli of Biomimetic Cell Envelopes
Limozin, L., Roth, A., & Sackmann, E. (2005) · Physical Review Letters · doi:10.1103/physrevlett.95.178101 · Cited by 49
Self-citationTuning the Formation and Rupture of Single Ligand-Receptor Bonds by Hyaluronan-Induced Repulsion
Robert, P., Sengupta, K., Puech, P., Bongrand, P., & Limozin, L. (2008) · Biophysical Journal · doi:10.1529/biophysj.108.135947 · Cited by 35
Self-citationHeinrich, V., Wong, W. P., Halvorsen, K., & Evans, E. A. (2008) · Langmuir · doi:10.1021/la7027059 · Cited by 31
Drazba, J. A., Liljelund, P., Smith, C., Payne, R., & Lemmon, V. (1997) · Developmental Brain Research · doi:10.1016/s0165-3806(97)00041-2 · Cited by 18
Cited by
Amyloid Precursor Protein Is an Autonomous Growth Cone Adhesion Molecule Engaged in Contact Guidance
Sosa, L. J., Bergman, J., Estrada-Bernal, A., Glorioso, T. J., Kittelson, J. M., & Pfenninger, K. H. (2013) · PLoS ONE · doi:10.1371/journal.pone.0064521 · Cited by 53
Biomimetic niches reveal the minimal cues to trigger apical lumen formation in single hepatocytes
Zhang, Y., De Mets, R., Monzel, C., Acharya, V., Toh, P., Chin, J. F. L., Van Hul, N., Ng, I. C., Yu, H., Ng, S. S., et al. (2020) · Nature Materials · doi:10.1038/s41563-020-0662-3 · Cited by 37
Metadata
- Authors
- Limozin, L., & Sengupta, K.
- Venue
- ChemPhysChem
- Publisher
- Wiley
- Published
- 2009-11-03
- Volume
- 10
- Issue
- 16
- Pages
- 2752-2768
- ISSN
- 1439-4235 (ISSN-L)
- 1439-7641
- OpenAlex
- W2160581130
- Cited by
- 286
- References
- 34
- FWCI
- 5.02
- Type
- journal article
- Language
- en
- Open access
- closed
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.