“…A relatively high incidence of cellular autophagy is frequently exhibited by cells of tissues undergoing regeneration (Becker and Lane, 1965), atrophy (Helminen, 1976), differentiation (Scharrer, 1966) or embryological development (Locke and Collins, 1965;Locke and McMahon, 1971). The appearance of autophagic vacuoles in tissues can be drastically increased following exposure of animals to diverse chemical, physical, and biological agents, such as: glucagon (Ashford and Porter, 1962;Arstila and Trump, 1968;Deter, 1971Deter, , 1975a, chloroquine (Abraham et al, 1968), mitotic inhibitors (Arstila et al, 1974;Hirsimaki et al, 1975), cyclic AMP (Hirsimaki et al, 1975;Shelburne and Trump, 1968), actinomycin D (Arstila and Trump, 1968;Kovacs, 1972;Shelburne et al, 1973), DDT (Gray et al, 1970), hypoxia (Abraham et al, 1967;Cole et al, 1971), and ionizing irradiation (Hendlee and Alders, 1968;Rene et al, 1971;Jordan et al, 1972).…”