Studies Of The Effect Of Temperature Shocks On Preparation For Cell Division In Mouse Fibroblast Cells (L Cells)

1973 ◽  
Vol 13 (3) ◽  
pp. 889-900
Author(s):  
HIROSHI MIYAMOTO ◽  
L. RASMUSSEN ◽  
E. ZEUTHEN

As L cells go through their growth-division cycle they acquire the capacity to respond progressively more strongly to certain standard changes in the temperature of the environment. Using techniques described earlier, we found that chilling to 1, 6 or 10 °C for 1 h had little effect on the timing of the forthcoming division. Conversely, heating for 1 h to temperatures between 41 and 42 °C had a strong effect. Generally, the older the cell when heated, the more extended is its generation time; in other words, the longer is the forthcoming division postponed. We found evidence that late in the cycle the cells undergo transition from a state in which they are maximally delayed with respect to the performance of a division to one in which they are less delayed. We attempted to synchronize cell divisions with single and with series of heat shocks (41.6 °C for 1 h). Like our predecessors in the field, we obtained only partial synchrony. However, because L cells appear to prepare for division between shocks, and because heat shocks tend to reverse such preparations for division, we find reason to continue these experiments, using previous experience with Tetrahymena and Schizosaccharomyces as a guide. Both the latter cells respond to proper temperature treatment with synchronous cell division.

1970 ◽  
Vol 1 (3) ◽  
pp. 259-262
Author(s):  
Joyce Banks ◽  
B. Eddie ◽  
Julius Schachter ◽  
K. F. Meyer

Chlamydiae were found capable of producing plaques in several cell lines. Mouse fibroblast cells, L-929, proved the most sensitive to infection and yielded plaques of the highest clarity. Assay of chlamydial infectivity by plaque titration was at least as sensitive as egg ld 50 determination. Among chlamydial isolates of avian, mammalian, and human origin, only slow-growing trachoma-inclusion-conjunctivitis agents did not produce plaques. The plaque assay is highly sensitive, reproducible, and offers a potential tool for investigations requiring accurate measurement of small changes in chlamydial infectivity.


1986 ◽  
Vol 96 (3) ◽  
pp. 453-458 ◽  
Author(s):  
B. J. Bevan ◽  
C. D. Bracewell

SUMMARYA total of 1531 diagnostic submissions from birds were examined by culture for the presence of Chlamydia psittaci between June 1976 and December 1984 by growth in NCTC 929 clone L mouse fibroblast cells, pretreated with an inhibitor of cell division, followed by direct immunofluorescence microscopy. Of these, 196 were found positive. The continued importance of psittacine birds as potential sources of infection was shown by the high number of positives (139) obtained from birds of that order. The percentage of submissions found positive was highest in parakeets (30·1) and was fairly high in psittacines as a group (16·6), but the latter figure was exceeded by the group ofcollared doves (Streptopelia decaocto) and wood pigeons (Columba palumbus) (25·0). Domestic poultry generally gave low rates, turkeys being the highest.Both the numbers of submissions and their rates of positives increased between 1980 and 1984.Comparing the isolation rates from the various organs sampled, the intestines gave the highest rate (20·4 per cent positive), closely followed by the other internal sites. The superficial swabbed sites (eye, nasal cavity, cloaca) gave lower rates.


1969 ◽  
Vol 130 (3) ◽  
pp. 543-556 ◽  
Author(s):  
George C. Saunders

Investigations of the induction period of an in vitro hemolysin response to sheep erythrocyte antigen revealed the following: 1. After antigen stimulation precursors of plaque-forming cells rapidly maturate to the point of hemolysin production. 2. Initial maturation probably occurs in the absence of cell division. 3. After initial maturation, a latent period of about 12 hr occurs before the first doubling of PFC. 4. At least the first three cell doublings are synchronous, with a generation time of 7–8 hr. 5. Synchronous cell division implies that all precursor cells are at the same point in the cell cyde when they are initially stimulated.


1972 ◽  
Vol 20 (3) ◽  
pp. 203-217
Author(s):  
A. Kleinendorst ◽  
R. Brouwer

In maize cv. Pioneer 395 grown in controlled environment in Hoagland solution at 20 deg C with 18-h photoperiods, low-temperature treatment of localized parts of the plant inhibited leaf elongation to an extent dependent on the site of cooling. Root temperatures of 5 deg C decreased leaf elongation as a result of water shortage and consequent retardation of cell extension. Plant osmotic potential increased and leaf elongation then resumed. When roots were cooled rapidly to 2-2.5 deg C the lower leaves died as a result of irreversible wilting, but with slow cooling the leaves survived. The response to these low temperatures was considerably less in older than in younger plants. Low temperatures at leaf meristem level directly reduced leaf elongation by acting on cell division and cell extension; the effect tended to increase with time. Local cooling above the meristem temporarily retarded growth by inhibiting carbohydrate translocation (demonstrated using 14CO2), but resulted in an increased concentration gradient which partly offset the effect of temperature. Cell extension was considerably inhibited, cell division probably only slightly. (Abstract retrieved from CAB Abstracts by CABI’s permission)


2013 ◽  
Vol 21 (2) ◽  
pp. 115-123 ◽  
Author(s):  
Nathan Unsworth ◽  
Raymond Dawson ◽  
John Wade ◽  
Chun-Qiang Liu

1992 ◽  
Vol 115 (1) ◽  
pp. 183-204 ◽  
Author(s):  
JORGE M. OLIVARES ◽  
NIKOLAOS A. PEPPAS

2001 ◽  
Vol 75 (21) ◽  
pp. 10015-10023 ◽  
Author(s):  
Shouting Zhang ◽  
Göran Magnusson

ABSTRACT The Kilham strain of polyomavirus (KV) infects vascular endothelial cells in vivo (J. E. Greenlee, Infect. Immun. 26:705–713, 1979), but no permissive cell type for growth of the virus in vitro has been identified. The failure of KV DNA to replicate in mouse fibroblast cells after transfection suggested that viral gene expression had narrow cell specificity. A KV substitution mutant having a part of the regulatory region of KV DNA replaced with a segment of the polyomavirus transcriptional enhancer was constructed. The substitution mutant was able to replicate in transfected 3T3 cells, and the newly replicated viral DNA associated with protein to form particles with the density of virions in CsCl equilibrium gradients. However, these particles were noninfectious when tested on 3T3 cells, suggesting that absorption or uptake of virus particles was defective for these cells. Analysis of early and late promoter activities by luciferase reporter gene expression showed that the enhancer substitution had a moderate positive effect on early gene expression and a large effect on the expression of the late genes. KV large T antigen inhibited the activities of both the wild-type and the substitution mutant early promoter, whereas only the mutant late promoter was activated under the same conditions. A comparison of the KV and polyomavirus large T antigens showed that they were not interchangeable in the initiation of KV and polyomavirus DNA synthesis. Furthermore, the wild-type KV origin of DNA replication was less active than the mutant structure in the presence of saturating amounts of KV large T antigen. Together, our data demonstrate several differences between the two types of large T antigen in their interactions with cellular proteins.


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