Ultraviolet microbeam irradiations of spindle fibres in crane-fly spermatocytes and newt epithelial cells: Resolution of previously conflicting observations |
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Authors: | Arthur Forer T Spurck J D Pickett-Heaps |
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Institution: | (1) Biology Department, York University, M3J 1P3 Downsview, Ont, Canada;(2) School of Botany, University of Melbourne, Parkville, Victoria |
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Abstract: | Summary In order to resolve apparent differences in reported experiments, we directly compared the effects of ultraviolet (UV) microbeam irradiations on the behaviour of spindle fibres in newt epithelial cells and crane-fly spermatocytes, using the same apparatus for both cell types. This work represents the first time that irradiated crane-fly spermatocytes have been followed using a high-NA objective and video-enhancement of images. In both cell types, irradiation of a kinetochore fibre in metaphase produced an area of reduced birefringence (ARB), known to be devoid of spindle microtubules (MTs). Subsequently the kinetochore-ward edge of the ARB moved poleward with average velocities of 0.5 m/min (n=20) in spermatocytes and 1.1 m/min (n=6) in epithelial cells. The poleward edge of the ARB rapidly disappeared when viewed using a ×100, high-NA objective but generally remained visible when viewed with a ×32, low-NA objective; this difference suggests that MTs poleward from the ARB disperse vertically out of the narrow depth of field of the ×100 objective but that many remain encompassed by that of the ×32 objective. The primary difference in response between the two cell types was in the behaviour of the spindle poles after an ARB formed. In spermatocytes the spindle maintained its original length whereas in epithelial cells the pole on the irradiated side very soon moved towards the chromosomes, after which the other pole did the same and a much shortened functional metaphase spindle was formed. |
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Keywords: | Mitosis Ultraviolet microbeam Spindle fibres Microtubules Crane-fly spermatocytes Newt epithelial cells |
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