Ratio imaging instrumentation

Methods in Cell Biology

Volumn , Issue 56, 1998, Pages 217-236

  Dunn, Kenneth ^a   Maxfield, Frederick R ^b  

^a INDIANA UNIVERSITY MEDICAL CENTER   (United States)

^b WEILL CORNELL MEDICAL COLLEGE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL; FLUORESCENCE MICROSCOPY; IMAGE PROCESSING; INSTRUMENTATION; METHODOLOGY; REVIEW;

ANIMALS; IMAGE PROCESSING, COMPUTER-ASSISTED; MICROSCOPY, FLUORESCENCE;

EID: 34548055271     PISSN: 0091679X     EISSN: None     Source Type: Book Series    
DOI: 10.1016/s0091-679x(08)60428-8     Document Type: Article

References (43)

1. Adams, S. R., Harootunian, A. T., Buechler, Y. J., Taylor, S. S., and Tsien, R. Y. (1991). Fluorescence ratio imaging of cyclic AMP in single cells. Nature 349, 694-697.
2. Adams, C. L., Nelson, W. J., and Smith, S. J. (1996). Quantitative analysis of cadherin-catenin-actin reorganization during development of cell-cell adhesion. J. Cell Biol. 135, 1899-1912.
3. Benson, D. M., Bryan, J., Plant, A. L., Gotto, A. M., and Smith, L. C. (1985). Digital imaging fluorescence microscopy: Spatial heterogeneity of photobleaching rate constants in individual cells. J. Cell Biol. 100, 1309-1323.
4. Bliton, A. C, and Lechleitner, J. D. (1995). Optical considerations at ultraviolet wavelengths in confocal microscopy. In "Handbook of Biological Confocal Microscopy" (J. B. Pawley, ed.), 2nd edition, pp. 431-444. Plenum, New York.
5. Boyde, A. (1987). Colour-coded stereo image from the tandem scanning reflected light microscope (TSRLM). J. Microsc. 146, 137-142.
6. Bright, G. R., Fisher, G. W., Rogowska, J., and Taylor, D. L. (1989). Fluorescence ratio imaging microscopy. In "Methods in Cell Biology: Fluorescence Microscopy of Living Cells in Culture" (Y.-L. Wang and D. L. Taylor, Eds.), Vol. 29, Part B, pp. 157-192. Academic Press, New York.
7. Carlsson, K., and Mossberg, K. (1992). Reduction of cross-talk between fluorescent labels in scanning laser microscopy. J. Microsc. 167, 23-37.
8. Carlsson, K., Aslund, N., Mossberg, K., and Philip, J. (1994). Simultaneous confocal recording of multiple fluorescent labels withimproved channel separation. J. Microsc. 176, 287-299.
9. Chen, C.-S., Martin, O. C., and Pagano, R. E. (1997). Changes in spectral properties of a plasma membrane lipid analog during the first seconds of endocytosis in living cells. Biophys. J. 72, 37-50.
10. de Lange, J. H., Schipper, N. W., Schuurhuis, G. J., ten Kate, T. K., van Heijningen, T. H., Pinedo, H. M., Lankelma, J., and Baak J. P. (1992). Quantification by laser scan microscopy of intracellular doxorubicin distribution. Cytometry 13, 571-576.
11. Denk, W., Piston, D. W., and Webb, W. W. (1995). Two-photon molecular excitation in laser-scanning microscopy. In "Handbook of Biological Confocal Microscopy" (J. B. Pawley, Ed.), 2nd edition, pp. 445-458. Plenum, New York.
12. Dunn, K. W., and Maxfield, F. R. (1992). Delivery of ligands from sorting endosomes to late endosomes occurs by maturation of sorting endosomes. J. Cell Biol. 117, 301-310.
13. Dunn, K., Maxfield, F., Whitaker, J., Haugland, R., and Haugland, R. (1991). Fluorescence excitation ratio measurements of lysosomal pH using laser scanning confocal microscopy. Biophys. J. 59, 345a.
14. Dunn, K., Mayor, S., Meyer, J., and Maxfield, F. R. (1994a). Applications of ratio fluorescence microscopy in the study of cell physiology. FASEB J. 8, 573-582.
15. Dunn, K., Park, J., Semrad, C, Gelman, D., Shevell, T., and McGraw, T. E. (1994b). Regulation of endocytic trafficking and acidification are independent of the cystic fibrosis transmembrane regulator. J. Biol. Chem. 269, 5336-5345.
16. Fagotto, F., and Maxfield, F. R. (1994). Changes in yolk platelet pH during Xenopus laevis development correlate with yolk utilization: A quantitative confocal study. J. Cell Sci. 107, 3325-3337.
17. Ghosh, R. N., Gelman, D. L., and Maxfield, F. R. (1994). Quantification of low density lipoprotein and transferrin endocytic sorting in HEp2 cells using confocal microscopy. J. Cell Sci. 107, 2177-2189.
18. Giuliano, K. A., and Taylor, D. L. (1994). Fluorescent actin analogs with a high affinity for profilin in vitro exhibit an enhanced gradient of assembly in living cells. J. Cell Biol. 124, 971-983.
19. Gonzalez, J. E., and Tsien, R. Y. (1995). Voltage sensing by fluorescence resonance energy transfer in single cells. Biophys. J. 69, 1272-1280.
20. Hell, S. W., and Stelzer, E. H. K. (1995). Lens aberrations in confocal fluorescence microscopy. In "Handbook of Biological Confocal Microscopy" (J. B. Pawley, Ed.), 2nd edition, pp. 347-354. Plenum, New York.
21. Inoue, S. (1995). Foundations of confocal scanned imaging in light microscopy. In "Handbook of Biological Confocal Microscopy" (J. B. Pawley, Ed.), 2nd edition, pp. 1-17. Plenum, New York.
22. Jericevic, Z., Wiese, B., Bryan, J., and Smith, L. C. (1989). Validation of an imaging system: Steps to evaluate and validate a microscope imaging system for quantitative studies. In "Methods in Cell Biology: Fluorescence Microscopy of Living Cells in Culture" (Y.-L. Wang and D. L. Taylor, Eds.), Vol. 29, Part B, pp. 47-83. Academic Press, New York.
23. Kallioniemi, A., Kallioniemi, O.-P., Sudar, D., Rutowitz, D., Gray, J. W., Waldman, R, and Pinkel, D. (1992). Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors. Science 258, 818-821.
24. Kam, Z., Jones, M. O., Chen, H., Agard, D. A., and Sedat, J. W. (1993). Design and construction of an optimal illumination system for quantitative wide-field multi-dimensional microscopy. Bioimaging 1, 71-81.
25. Keller, H. E. (1995). Objective lenses for confocal microscopy. In "Handbook of Biological Confocal Microscopy" (J. B. Pawley, Ed.), 2nd edition, pp. 111-126. Plenum, New York.
26. Kurtz, I., and Emmons, C. (1993). Measurement of intracellular pH with a laser scanning confocal microscope. In "Methods in Cell Biology: Cell Biological Applications of Confocal Microscopy" (B. Matsumoto, Ed.), Vol. 28 pp. 183-193. Academic Press, New York.
27. Loew, L. M. (1993). Confocal microscopy of potentiometric fluorescent dyes. In "Methods in Cell Biology: Cell Biological Applications of Confocal Microscopy" (B. Matsumoto, Ed.), Vol. 28, pp. 195-209. Academic Press, New York.
28. Luby-Phelps, K., and Taylor, D. L. (1988). Subcellular compartmentalization by local differentiation of cytoplasmic structure. Cell Motil. Cytoskeleton 10, 28-37.
29. Majlof, L., and Forsgren, P.-O. (1993). Confocal microscopy: Important considerations for accurate imaging. In "Methods in Cell Biology: Cell Biological Applications of Confocal Microscopy" (B. Matsumoto, Ed.), Vol. 28, pp. 79-95. Academic Press, New York.
30. Marks, P. W., and Maxfield, F. R. (1990). Ratio imaging of cytosolic free calcium in neutrophils undergoing chemotaxis and phagocytosis. Cell Calcium 11, 181-190.
31. Maxfield, F. R., Bush, A., Marks, P., and Shelanski, M. L. (1989). Measurement of cytoplasmic free calcium in single motile cells. Methodol. Surveys Biochem. Analysis 19, 257-272.
32. Mayor, S., Presley, J., and Maxfield, F. R. (1993). Sorting of membrane components from endosomes and subsequent recycling to the cell surface occurs by a bulk flow process. J. Cell Biol. 121, 1257-1269.
33. Myers, J. N., Tabas, I., Jones, N. L., and Maxfield, F. R. (1993). β-VLDL is sequestered in surface-connected tubules in mouse peritoneal macrophages. J. Cell Biol. 123, 1389-1403.
34. Oida, T., Sako, Y., and Kusumi, A. (1993). Fluorescence lifetime imaging microscopy (flimscopy): Methodology development and application to studies of endosome fusion in single cells. Biophys. J. 64, 676-685.
35. O'Malley, D. M. (1994). Calcium permeability of the neuronal nuclear envelope: Evaluation using confocal volumes and intracellular perfusion. J. Neurosc. 14, 5741-5758.
36. Reid, T., Baldini, A., Rand, T. C, and Ward, D. C. (1992). Simultaneous visualization of seven different DNA probes by in situ hybridization using combinatorial fluorescence and digital imaging microscopy. Proc. Natl. Acad. Sci. USA 89, 1388-1392.
37. Salzman, N. H., and Maxfield, F. R. (1989). Fusion accessibility of endocytic compartments along the recycling and lysosomal endocytic pathways in intact cells. J. Cell Biol. 109, 2097-2104.
38. Sanders, R., Draaijer, A., Gerritsen, H. C., Houpt, P. M., and Levine, Y. K. (1995). Quantitative pH imaging in cells using confocal fluorescence lifetime imaging microscopy. Anal. Biochem. 227, 302-308.
39. Sandison, D. R., Williams, R. M., Wells, K. S., Strickler, J., and Webb, W. W. (1995). Quantitative fluorescence confocal laser scanning microscopy. In "Handbook of Biological Confocal Microscopy" (J. B. Pawley, Ed.), 2nd edition, pp. 39-53. Plenum, New York.
40. Terzaghi, A., Tettamanti, G., Palestini, P., Acquotti, D., Bottiroli, G., and Masserini, M. (1994). Fluorescence excimer formation imaging: A new technique to investigate association to cells and membrane behavior of glycolipids. Eur. J. Cell Biol. 65, 172-177.
41. Tsien, R. Y., and Harootunian, A. T. (1990). Practical design criteria for a dynamic ratio imaging system. Cell Calcium 11, 93-109.
42. Uster, S., and Pagano, R. E. (1986). Resonance energy transfer microscopy: Observations of membrane-bound fluorescent probes in model membranes and in living cells. J. Cell Biol. 102,1221-1234.
43. Yamashiro, D. J., and Maxfield, F. R. (1987). Acidification of morphologically distinct endocytic compartments in mutant and wild type Chinese hamster ovary cells. J. Cell Biol. 105, 2723-2733.