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               542                                                                                Cell Death (Apoptosis)


               APOPTOSIS, or programed cell death, plays an impor-  and Kerr in 1972. In the necrotic process, swelling of cells
               tant role in the development of organisms and in the main-  precedes their explosion and results in the release of in-
               tenance of homeostasis. The failure of apoptotic programs  tracellular components that may be toxic to other cells.
               causes various diseases. So far, many genes regulating  In apoptosis, the dying cells exhibit nuclear and cytoplas-
               apoptosis have been identified and the molecular mecha-  mic condensation, fragmentation of cell bodies, chromo-
               nism of apoptosis is being clarified. In this article, I will  somal DNA fragmentation into nucleosomal units, loss
               discuss cell death elicited through death receptors.  of mitochondrial function, and alterations of cell mem-
                                                                 brane composition (Fig. 1). Subsequently, apoptotic cells
                                                                 are engulfed by phagocytes and neighboring cells, and are
               I. OVERVIEW                                       recycled. Most cells suffering physiological cell death un-
                                                                 dergo the apoptotic process and the superfluous or harmful
               Homeostasis in multicellular organisms is based on a bal-  cells generated during the developmental process are re-
               ance between life and death of cells. Apoptosis was recog-  moved by apoptosis. For example, apoptosis occurs in tail
               nized as a phenomenon distinct from necrosis by Wyllie  resorption, neuronal network formation, clonal deletion of



















































                      FIGURE 1 (a) Fas-induced apoptosis in lymphoid cells (WR19L cells overexpressing Fas). The cells were incubated
                      with 0.5 µg/ml of an agonistic anti-Fas antibody at 37 C for 120 min and their ultrastructure was examined under
                                                             ◦
                      a transmission electron microscope. The electron micrograph of untreated cells is shown in the upper panel. Bars,
                      1 µm. (b) Chromosomal DNA of growing cells (lane 1) or dying cells (lane 2) was run through a 1.5% agarose gel. M
                      indicates molecular weight markers.
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