Serum-starved apoptotic fibroblasts reduce blastocyst production but enable development to term after SCNT in cattle

Cloning Stem Cells. 2009 Dec;11(4):565-73. doi: 10.1089/clo.2009.0028.

Abstract

Cell cycle synchronization by serum starvation (SS) induces apoptosis in somatic cells. This side effect of SS is hypothesized to negatively affect the outcome of somatic cell nuclear transfer (SCNT). We determined whether apoptotic fibroblasts affect SCNT yields. Serum-starved, adult, bovine fibroblasts were stained with annexin V-FITC/propidium iodide to allow apoptosis detection by flow cytometry. Positive and negative cells sorted by fluorescence activated cell sorting (FACS) and an unsorted control group were used as nuclear donors for SCNT. Reconstructed embryos were cultured in vitro and transferred to synchronized recipients. Apoptosis had no effect on fusion and cleavage rates; however, it resulted in reductions in blastocyst production and quality measured by apoptotic index. However, reconstructed embryos with apoptotic cells resulted in pregnancy rates similar to that of the control on day 30, and generated one live female calf. In conclusion, we showed that apoptotic cells present in serum-starved cultures negatively affect embryo production after SCNT without compromising full-term development. Further studies will evaluate the ability of the oocyte to reprogram cells in specific phases of apoptosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / physiology*
  • Blastocyst / cytology*
  • Cattle
  • Cell Cycle
  • Cell Nucleus / genetics
  • Cell Proliferation
  • Cellular Reprogramming
  • Cloning, Organism / methods*
  • Culture Media, Serum-Free
  • Embryonic Development*
  • Female
  • Fetal Development*
  • Fibroblasts / pathology*
  • Nuclear Transfer Techniques
  • Oocytes / cytology*
  • Oocytes / physiology
  • Parthenogenesis
  • Pregnancy
  • Pregnancy Rate

Substances

  • Culture Media, Serum-Free