scholarly journals DIBUTYRYL CYCLIC ADENOSINE 3' 5' MONOPHOSPHATE, SUGAR TRANSPORT, AND REGULATORY CONTROL OF CELL DIVISION IN NORMAL AND TRANSFORMED CELLS

1973 ◽  
Vol 56 (2) ◽  
pp. 487-491 ◽  
Author(s):  
William J. Grimes ◽  
Judith L. Schroeder

Swiss 3T3 cells exhibit contact-regulated cell growth and have a lower ability to transport 2-deoxyglucose than polyoma (Py)-transformed 3T3 cells. Py3T3 cells treated with dibutyryl cyclic adenosine 3'5' monophosphate (dBcAMP) and theophylline have reduced cell growth and transport 2-deoxyglucose at the same rate as normal 3T3 cells. Evidence that the cessation of cell growth and reduced transport abilities in Py3T3 cells does not represent a return to contact-regulated growth comes from the following observations. First, treating high density Py3T3 cells with dBcAMP allows more than two doublings of cell number, even though ability to transport 2-deoxyglucose is returned to levels equal to those of normal 3T3 cells. Second, dBcAMP prevents serum-stimulated increases in 2-deoxyglucose transport in Py3T3 but not in 3T3 cells.

1985 ◽  
Vol 156 (1) ◽  
pp. 1-6 ◽  
Author(s):  
Robert F. Brooks ◽  
Robert Shields

1970 ◽  
Vol 7 (2) ◽  
pp. 337-355
Author(s):  
K. ONODERA ◽  
ROSE SHEININ

It has been demonstrated that a glucosamine-containing macromolecular component of the cell surface of 3T3 mouse cells, and SV40-transformed cells, is released from cells by treatment with trypsin under conditions in which the plasma membrane remains functionally intact. This was shown by the fact that the treated cells could be cloned with high plating efficiency and remained impermeable to the vital stain, erythrocin. A method for specifically marking this surface component has been devised based on the finding that in 3T3 cells growing synchronously after subculture by trypsin maximum incorporation of glucosamine into this material occurs 12-13 h thereafter. Of the total radioactive glucosamine incorporated into macro-molecular cell constituents, over 80% was recovered in surface component. Studies on the biosynthesis of surface component revealed that this was periodic during a cycle of cell duplication, with an increased rate of formation immediately after cell division. It was found that the surface component of 3T3 cells differed from that of SV40-transformed cells.


1985 ◽  
Vol 248 (3) ◽  
pp. C288-C295 ◽  
Author(s):  
N. E. Owen ◽  
M. L. Villereal

Previous studies in human foreskin fibroblasts suggested that the mechanism by which serum stimulates Na+ influx is via a Ca2+-calmodulin-mediated event. In the present experiments in normal WI-38 cells (human lung fibroblasts), both the intracellular Ca2+ antagonist 8-(N,N-diethylamino)-octyl-3,4,5-trimethoxybenzoate (TMB-8) and the potent calmodulin antagonist trifluoperazine (TFP) blocked serum-stimulated Na+ influx [TMB-8 concentration causing half-maximal inhibition (Ki) = 15 microM and TFP Ki = 10 microM]. Similar results were obtained in Swiss 3T3 cells. In contrast, in transformed WI-38 or Swiss 3T3 cells neither TMB-8 nor TFP had any effect on serum-stimulated Na+ influx (TMB-8 Ki greater than 100 microM and TFP Ki greater than 100 microM). In addition, when 45Ca2+ efflux measurements were made on normal and transformed cells, serum stimulated significant 45Ca2+ efflux (P less than 0.05) from WI-38 and Swiss 3T3 cells, while having no effect on 45Ca2+ efflux from simian virus 40 (SV40)-WI-38 or SV40-Swiss 3T3 cells. However, an elevation of intracellular Ca2+ can stimulate Na+ influx, since it was found that A23187 mimicked the effects of serum in both normal and transformed cells. These results suggest that the Ca2+-calmodulin-mediated event, which is thought to be involved in serum-stimulated Na+ influx in normal cells, may be bypassed or overridden in transformed cells.


1976 ◽  
Vol 68 (2) ◽  
pp. 276-286 ◽  
Author(s):  
H Gershman ◽  
J Drumm ◽  
L Culp

The sorting-out behavior (self-segregation of two cell types from mixtures of the two) of five different established cell lines was studied. Eight of the ten possible binary combinations of these lines, cultured as cellular aggregates, were examined. Mouse BALB/c 3T3 cells sorted out internally to the corresponding malignant SV40 virus-transformed 3T3 cells. The transformed 3T3 line (SVT-2) did not sort out from a revertant line selected from SVT-2 cells by resistance to concanavalin A (con A). The revertant cells sorted out externally to the parent BALB/c 3T3 cells, although segregation was generally incomplete. BALB/c 3T3 cells did not sort out from another contact-inhibited line of 3T3 cells derived from Swiss albino mice (Swiss 3T3). Both BALB/c 3T3 and Swiss 3T3 cells sorted out from cells of the contact-inhibited hamster line, NIL B. Instead of a two-layered sphere, however, a three-layered structure was observed with most of the NIL B cells external to the 3T3 cells, and a few NIL B cells comprising the center of the sphere. On the other hand, NIL B cells did not consistently sort out from either the SVT-2 or con A cells. In general, sorting out between pairs of these five lines are slower and less complete than is generally observed between the more extensively studied chick embryonic tissue cells, suggesting that the cultured cells may be more closely related in their adhesive properties. The internal segregation of BALB/c 3T3 cells relative to SVT-2 cells is consistent with the hypothesis that transformed cells are less adhesive than their nontransformed counterparts.


Author(s):  
W. Mark Saltzman

The expansion in size of a region of tissue, often called growth, is critical to embryonic development and tissue repair. Growth of a tissue most often occurs by an increase in cell number. In fact, sequential cell division—and a resulting increase in total cell number—is the most important change of early development. As development proceeds, however, the rate of increase in cell number slows but the overall size of the organism continues to increase steadily. Growth throughout life can occur by a variety of mechanisms in addition to increased cell number; for example, increases in cell volume or extracellular volume also produce growth. The overall growth of an organ or tissue can involve multiple mechanisms. For example, in the nervous system, neurons increase in size, but not number, as a juvenile grows to adulthood. By contrast, glial cells within the nervous system divide and proliferate throughout life. Overall, however, cell proliferation (which occurs by the process of sequential cell division) is the most important feature of tissue growth. Growth is only one of the changes that occurs with development. As a child grows to adulthood, her increase in size is probably less astonishing than her overall change in behavior and ability. Underlying this overall change are dramatic alterations in function and operation of individual cells; this observation is related to the discussion in Chapter 3, in which the processes of cellular differentiation and specialization were introduced. The child develops by reference to a fixed instructional program, the genome, which somehow encodes all of the molecular signals that lead to increases in size, changes in shape, and inexorable dynamics of aging. But the child is also influenced by her environment and the opportunities for change that her environment presents. One child becomes a doctor and another a cellist; the factors and forces that nudge each down her path are not programmed by the genes alone. Similarly, differentiation of a cell is influenced by its genetic composition and the environment that surrounds it. This chapter begins with a discussion of mechanisms and kinetics of cell division. Later parts of the chapter consider some of the factors that influence cell differentiation. The relationship of cell growth during development of a normal organism and cell growth in culture is introduced in the final sections.


1993 ◽  
Vol 45 (1-2) ◽  
pp. 231-236 ◽  
Author(s):  
Ian Zachary ◽  
James Sinnett-Smith ◽  
Enrique Rozengurt
Keyword(s):  

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