Identification of programmed cell death in situ via specific labeling of nuclear DNA fragmentation.

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  • Y Gavrieli
    Department of Experimental Medicine, Hebrew University-Hadassah Medical School, Jerusalem, Israel.
  • Y Sherman
    Department of Experimental Medicine, Hebrew University-Hadassah Medical School, Jerusalem, Israel.
  • S A Ben-Sasson
    Department of Experimental Medicine, Hebrew University-Hadassah Medical School, Jerusalem, Israel.

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<jats:p>Programmed cell death (PCD) plays a key role in developmental biology and in maintenance of the steady state in continuously renewing tissues. Currently, its existence is inferred mainly from gel electrophoresis of a pooled DNA extract as PCD was shown to be associated with DNA fragmentation. Based on this observation, we describe here the development of a method for the in situ visualization of PCD at the single-cell level, while preserving tissue architecture. Conventional histological sections, pretreated with protease, were nick end labeled with biotinylated poly dU, introduced by terminal deoxy-transferase, and then stained using avidin-conjugated peroxidase. The reaction is specific, only nuclei located at positions where PCD is expected are stained. The initial screening includes: small and large intestine, epidermis, lymphoid tissues, ovary, and other organs. A detailed analysis revealed that the process is initiated at the nuclear periphery, it is relatively short (1-3 h from initiation to cell elimination) and that PCD appears in tissues in clusters. The extent of tissue-PCD revealed by this method is considerably greater than apoptosis detected by nuclear morphology, and thus opens the way for a variety of studies.</jats:p>

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