Cell cycle phase dependent emergence of thymidylate synthase studied by monoclonal antibody (M-TS-4)

Cell Tissue Kinet. 1989 May;22(3):259-68. doi: 10.1111/j.1365-2184.1989.tb00211.x.

Abstract

A method of identifying thymidylate synthase (TS) at the cellular level was developed using anti-TS monoclonal antibody (M-TS-4), a monoclonal antibody created against purified TS from a HeLa cell line. In HeLa cells and four human glioma cell lines (U-251, U-87, 343-MGA, and SF-188), TS was identified primarily in the cytoplasm. Autoradiographic and flow cytometric studies showed that TS appeared mainly in the G1 phase and subsided early in the S phase; thus, the G1 phase can be divided into TS-positive and -negative fractions. Nuclear TS was not demonstrated unequivocally with M-TS-4, and the relationship between nuclear TS and DNA synthesis could not be determined. Although the percentage of TS-positive cells was larger than the S-phase fraction measured by autoradiography after a pulse of tritiated thymidine or by the immunoperoxidase method using BUdR, the ratios were within a similar range (1.2-1.4) in all cell lines studied. Therefore, the S-phase fraction can be estimated indirectly from the percentage of TS-positive cells measured by M-TS-4. Because the emergence of TS detected by our method is cell cycle dependent, M-TS-4 may be useful for biochemical studies of TS and for cytokinetic analysis.

Publication types

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

MeSH terms

  • Antibodies, Monoclonal*
  • Autoradiography
  • Bromodeoxyuridine
  • Cell Cycle / physiology*
  • Cell Line
  • DNA / biosynthesis
  • Flow Cytometry
  • Glioma
  • HeLa Cells
  • Humans
  • Immunoenzyme Techniques
  • Staining and Labeling
  • Thymidylate Synthase / analysis*
  • Thymidylate Synthase / immunology

Substances

  • Antibodies, Monoclonal
  • DNA
  • Thymidylate Synthase
  • Bromodeoxyuridine