Chromatin condensation in hamster sperm: A flow cytometric investigation

Sara Yossefi, Yitzchak Oschry, Lawrence M. Lewin

Research output: Contribution to journalArticlepeer-review

37 Scopus citations

Abstract

In this study we have used acridine orange staining, as described by Evenson (1990), to follow changes in DNA packaging as they occur in hamster spermatozoa which have left the testis and are undergoing maturation in the epididymis. Measurement of the green and red fluorescent intensities of hamster sperm nuclei by flow cytometry demonstrated a decrease in acridine orange binding to DNA as sperm made their way from proximal corpus epididymis to the vas deferens. Using sperm from the cauda epididymis of the mature hamster as the standard, a method was developed for estimating the % of cells in a given sample that have matured with regard to DNA packaging. Staining with bromobimane was used to determine the extent of sulfhydryl oxidation in the nuclei. It was seen that sulfhydryl oxidation occurred mainly in the cauda epididymis whereas another process in chromatin condensation occurred earlier, during sperm passage through the caput epididymis. This earlier process could be mimicked by incubating sperm nuclei with alkaline phosphatase, suggesting that it consists of removal of phosphate in protamine. © 1994 Wiley‐Liss, Inc.

Original languageEnglish
Pages (from-to)93-98
Number of pages6
JournalMolecular Reproduction and Development
Volume37
Issue number1
DOIs
StatePublished - Jan 1994

Keywords

  • Acridine orange
  • Bromobimane
  • Chromatin condensation
  • DNA packaging
  • Flow cytometry
  • Hamster
  • Spermatozoa

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