Abstract
AbstractNineteen cultures of human embryonic or adult‐tissue cells were exposed to SV40 as primary cultures or developed cell strains in Phase II of cultural life; 12 cultures were exposed to virus in Phase III, at the end of in vitro life. After the expected proliferative response, infected cultures exhibited morphological change, accelerated growth, and prolongation of propagability. After an average of 22.6 weeks for cultures infected as primary explants or in Phase II, the proliferative stage of transformation ended in a stage of “crisis.” Crisis was characterized by progressive decline in vigor of culture proliferation, increasingly abnormal cell division, and limitation in propagability of cells eventually resulting in diminution in cell number. Cytological features of crisis included detachment of cells and appearance of multinucleated and giant cells. Temporally and cytologically, crisis was similar for transformed cells whether of adult or embryonic origin, whether derived from skin, buccal mucosa or lung, whether in Phase II or III of culture life at the time of infection (the “older” cultures entering crisis sooner than the “younger”), and whether propagated continuously or with intervening periods of growth arrest or proliferation in vivo. After a variable time “recovery” of cultures from crisis occurred by repopulation from small groups of surviving but seemingly dormant cells. The new populations, always obtained with care of cultures in crisis, formed continuously propagable cell lines. Control uninfected cultures have always exhibited the finite life terminating in Phase III which is characteristic of human diploid cell strains. Passage of transformed cultures through crisis and recovery was accompanied by loss of capacity to release infectious SV40 and enhancement of production of SV40‐induced complement‐fixing antigen.
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