Role of the centrosome in mitosis: UV micro-irradiation study

J Photochem Photobiol B. 1995 Aug;29(2-3):163-70. doi: 10.1016/1011-1344(95)07129-p.

Abstract

Ultraviolet micro-irradiation (UV-MI) of the PK (pig kidney embryo) cell centrosome (lambda max = 280 nm, spot diameter 1.6 mm, exposure time 5-15 s) at metaphase and anaphase resulted in functional damage of the centrosome. After UV-MI of the centrosome at early metaphase, chromosomes quickly (in 1-3 min) moved away from the irradiated pole and then encircled the non-irradiated pole. Within 10 min after UV-MI the spindle disassembled and chromosomes remained unseparated. The minimal dose inducing this effect in 90% of cells was accumulated in 5 s. After the same UV-MI at late metaphase, chromosomes shifted towards the non-irradiated pole; however, anaphase started and chromosome motion towards the non-irradiated pole continued normally. UV-MI of the centrosome at early anaphase for 5-15 s slowed down and then stopped chromosome motion towards the irradiated pole. This was a result of rapid (within 2-3 min) disorganization of the half-spindle. Chromosomes continued to move towards the opposite pole normally, while cytokinesis was significantly retarded. No visible lesion was revealed by electron microscopy after 5 s UV-MI, while 15 s irradiation resulted in the truncation of the microtubule bundles 1.5-2 microns from the centrosome. We concluded that UV-MI inactivates the centrosome and induces disaggregation of microtubule initiation sites. The critical point (checkpoint) in mitosis up to which this damage induces mitotic arrest is mid-metaphase.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anaphase
  • Animals
  • Centrosome / radiation effects
  • Centrosome / ultrastructure*
  • Chromosomes / radiation effects
  • Chromosomes / ultrastructure
  • Embryo, Mammalian
  • Fluorescent Antibody Technique
  • Kidney / pathology
  • Kidney / radiation effects
  • Microscopy, Electron
  • Microscopy, Fluorescence / instrumentation
  • Microscopy, Fluorescence / methods
  • Microscopy, Video / instrumentation
  • Microscopy, Video / methods
  • Mitosis / physiology
  • Mitosis / radiation effects
  • Swine
  • Ultraviolet Rays*