Premium
Cell cycle control by Ca ++ ‐ions in mouse 3T3 cells and in transformed 3T3 cells
Author(s) -
Paul Dieter,
Ristow HansJ.
Publication year - 1979
Publication title -
journal of cellular physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.529
H-Index - 174
eISSN - 1097-4652
pISSN - 0021-9541
DOI - 10.1002/jcp.1040980105
Subject(s) - 3t3 cells , calcium , intracellular , stimulation , cell culture , calcium in biology , biophysics , cell cycle , chemistry , microbiology and biotechnology , cell , biology , biochemistry , endocrinology , transfection , genetics , organic chemistry
Total cellular calcium levels do not change when 3T3‐4a cells stop proliferating due to serum depletion, or when serum‐arrested quiescent cells are incubated for up to 44 hours in calcium‐deficient medium (∼10 μM Ca ++ ). Upon stimulation with dialyzed serum cells enter S and progress through at least one cycle even at extremely low calcium levels in the culture medium (≥10 μM). Cells divide until a final cell density is attained which is proportional to the calcium concentration in the medium and cells reversibly arrest in G 1 . Cells which arrested in G 1 in medium containing ≤26 μM Ca ++ in the presence of excess serum can be stimulated to enter S in response to added calcium after a prereplicative phase of 14 to 16 hours. Serum does not affect 45 Ca‐uptake in these cells. Benzo[a]pyrene transformed 3T3 (BP3T3) cells have a 100–200 times lower Ca ++ ‐requirement than 3T3 cells but arrest in G 1 at low Ca ++ levels. In contrast, SV40‐virus transformed 3T3 (SV3T3) cells that grow without restriction in monolayer cultures have even lower Ca ++ ‐requirements for growth than BP3T3 cells and have no Ca ++ ‐sensitive restriction point. Therefore, 3T3 and BP3T3 cells have retained the capacity to sense intracellular Ca ++ ‐pool sizes and to arrest in G 1 at subthreshold cellular Ca ++ ‐levels.