Retention of labelled DNA precursor by murine cells after a single administration of tritium labelled thymidine

Cell Tissue Kinet. 1986 Sep;19(5):519-25. doi: 10.1111/j.1365-2184.1986.tb00751.x.

Abstract

The central zone of the rat lens epithelium, extending half way from the centre to the periphery of a whole mount preparation, normally has less than 1% of the cells in the cell cycle at any given time. Mechanical wounding initiates a burst of proliferation in the central zone. DNA synthesis begins 14 hr after wounding followed by mitosis 10 hr later. When [3H]TdR was applied at 2 hr prior to S phase, some moderately heavy and some light labelling was observed after the onset of S phase. When [3H]TdR was applied 5 hr before S phase (9 hr after wounding), all the cells were lightly labelled. Only small amounts of the label were available to these cells 5 hr after application. It is significant that there was labelling in this group because it indicates the persistence of relatively small intracellular pools of [3H]TdR for several hours after the initial 'pulse' labelling of cells. Determinations of the duration of S phase were based on the assumption that pulse labelling may be affected by the persistence of the pools of [3H]TdR and consequent light labelling of the cells.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Autoradiography
  • Cell Division*
  • Culture Techniques
  • DNA / biosynthesis*
  • Epithelial Cells
  • Lens, Crystalline / cytology
  • Mitosis
  • Rats
  • Thymidine / metabolism*
  • Time Factors
  • Wound Healing

Substances

  • DNA
  • Thymidine