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Proceedings Paper

Mitotic spindle studied using picosecond laser scissors
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Paper Abstract

In previous studies we have shown that the second harmonic 532 nm, from a picosecond frequency doubled Nd:YAG laser, can cleanly and selectively disrupt spindle fiber microtubules in live cells (Botvinick et al 2004, Biophys. J. 87:4303-4212). In the present study we have ablated different locations and amounts of the metaphase mitotic spindle, and followed the cells in order to observe the fate of the irradiated spindle and the ability of the cell to continue through mitosis. Cells of the rat kangaroo line (PTK2) were stably transfected by ECFP-tubulin and, using fluorescent microscopy and the automated RoboLase microscope, (Botvinick and Berns, 2005, Micros. Res. Tech. 68:65-74) brightly fluorescent individual cells in metaphase were irradiated with 0.2447 nJ/micropulse corresponding to an irradiance of 1.4496*10^7 J/(ps*cm^2) . Upon irradiation the exposed part of the mitotic spindle immediately lost fluorescence and the following events were observed in the cells over time: (1) immediate contraction of the spindle pole towards the cut, (2) recovery of connection between pole and cut microtubule, (3) completion of mitosis. This system should be very useful in studying internal cellular dynamics of the mitotic spindle.

Paper Details

Date Published: 11 September 2006
PDF: 5 pages
Proc. SPIE 6326, Optical Trapping and Optical Micromanipulation III, 63262C (11 September 2006); doi: 10.1117/12.680965
Show Author Affiliations
N. M. Baker, Univ. of California, San Diego (United States)
E. L. Botvinick, Univ. of California, Irvine (United States)
Linda Shi, Univ. of California, San Diego (United States)
M. B. Berns, Univ. of California, San Diego (United States)
Univ. of California, Irvine (United States)
George Wu, Univ. of California, San Diego (United States)


Published in SPIE Proceedings Vol. 6326:
Optical Trapping and Optical Micromanipulation III
Kishan Dholakia; Gabriel C. Spalding, Editor(s)

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