Cell imaging and manipulation by nonlinear optical microscopy

被引:0
作者
L. Sacconi
I. M. Tolic-Nørrelykke
M. D'Amico
F. Vanzi
M. Olivotto
R. Antolini
F. S. Pavone
机构
[1] European Laboratory for Non-Linear Spectroscopy,Department of Physics
[2] University of Trento,Department of Experimental Pathology and Oncology
[3] Max Planck Institute of Molecular Cell Biology and Genetics,Department of Biology and Genetics
[4] University of Florence,Department of Physics
[5] University of Florence,undefined
[6] University of Florence,undefined
来源
Cell Biochemistry and Biophysics | 2006年 / 45卷
关键词
Nonlinear microscopy; optical manipulation;
D O I
暂无
中图分类号
学科分类号
摘要
Advances in the technologies for labeling and imaging biological samples drive a constant progress in our capability of studying structures and their dynamics within cells and tissues. In the last decade, the development of numerous nonlinear optical microscopies has led to a new prospective both in basic research and in the potential development of very powerful noninvasive diagnostic tools. These techniques offer large advantages over conventional linear microscopy with regard to penetration depth, spatial resolution, three-dimensional optical sectioning, and lower photobleaching. Additionally, some of these techniques offer the opportunity for optically probing biological functions directly in living cells, as highlighted, for example, by the application of second-harmonic generation to the optical measurement of electrical potential and activity in excitable cells. In parallel with imaging techniques, nonlinear microscopy has been developed into a new area for the selective disruption and manipulation of intracellular structures, providing an extremely useful tool of investigation in cell biology. In this review we present some basic features of nonlinear microscopy with regard both to imaging and manipulation, and show some examples to illustrate the advantages offered by these novel methodologies.
引用
收藏
页码:289 / 302
页数:13
相关论文
共 254 条
  • [1] Shimomura O.(1962)Extraction, purification and properties of aequorin, a bioluminescent protein from the luminous hydromedusan. Aequorea J. Cell Comp. Physiol. 59 223-239
  • [2] Johnson F. H.(1994)Green fluorescent protein as a marker for gene expression Science 263 802-805
  • [3] Saiga Y.(1976)Cell surgery by laser micro-dissection: a preparative method J. Microsc. 107 19-24
  • [4] Chalfie M.(2000)Single-molecule studies of DNA mechanics Curr. Opin. Struct. Biol. 10 279-285
  • [5] Tu Y.(2004)Exploring molecular motor and switches at the single-molecule level Microsc. Res. Tech. 65 194-204
  • [6] Euskirchen G.(1987)Optical trapping and manipulation of single cells using infrared laser beams Nature 330 769-771
  • [7] Ward W. W.(1987)Optical trapping and manipulation of viruses and bacteria Science 235 1517-1520
  • [8] Prasher D. C.(2003)Nonlinear magic: multiphoton microscopy in the bioscience Nat. Biotech. 21 1369-1377
  • [9] Isenberg G.(2003)Live tissue intrinsic emission microscopy using multiphoton-excited native fluorescence and second harmonic generation Proc. Natl. Acad. Sci. USA 100 7075-7780
  • [10] Bielser W.(2002)Two-photon imaging of lymphocyte motility and antigen response in intact lymph node Science 296 1869-1873