Kinetics of in vitro ageing of mouse embryo fibroblasts

1984 ◽  
Vol 65 (1) ◽  
pp. 163-175
Author(s):  
C. Karatza ◽  
W.D. Stein ◽  
S. Shall

The kinetics of ageing of normal mouse embryo fibroblast cells in culture have been determined. The growth pattern during every passage was established. It was observed that the growth pattern was not exponential, but that the growth rate declined progressively both within and with every passage. We also estimated the cell cycle parameters using the Fraction of Labelled Mitoses method at every passage. We found that the cell cycle duration was constant throughout the lifespan of this cell strain; the median value of the cell cycle duration was found to be 15.5 +/− 0.5 h (S.D., n = 8). From these two sets of observations we infer that the fraction of dividing cells declines smoothly from the beginning of the culture. Our data exclude quite positively any description of ageing of the fibroblast population in terms of a catastrophe or any abrupt change in the population. Our data are also inconsistent with a linear decline in growth fraction. On the contrary, we observed that there was a gradual and smooth decline in the growth rate of the strain, due to a smoothly declining growth fraction. This smooth change in the growth behaviour of this cell strain is accurately described by the mortalization theory of Shall & Stein in which the single parameter gamma (gamma), describes the change in reproductive potential over the entire lifespan. The parameter gamma describes the rate at which the doubling time of the culture increases. It is the number of generations at which half of the newborn cells are themselves reproductively sterile. Our present data provided an estimate of gamma for this cell strain, which was consistent during the entire lifespan of the strain; the best estimate of gamma for this cell strain was 20.3 +/− 0.6 generations (S.D., n = 19).

2018 ◽  
Vol 9 (1) ◽  
Author(s):  
Clotilde Cadart ◽  
Sylvain Monnier ◽  
Jacopo Grilli ◽  
Pablo J. Sáez ◽  
Nishit Srivastava ◽  
...  

1984 ◽  
Vol 66 (1) ◽  
pp. 401-409
Author(s):  
C. Karatza ◽  
S. Shall

A direct estimate of the reproductive potential of mouse embryo fibroblasts through their entire lifespan has been made using the mini-clone technique, which permits the direct observation of the growth fraction in a bulk population by inspection of the growth behaviour of individual cells. We have measured the colony size on each island that contained one or two cells at the beginning and the fraction of islands which, starting from one or two cells failed to divide even once. We observed that even in a young culture there are individual cells that can only reproduce two or three times. With each succeeding passage the distribution of colony sizes shifts to a greater proportion of small colonies. The median colony size decreases with each passage. Furthermore, the fraction of non-dividers directly observed increases smoothly with time; the fraction of non-dividers is quite small at the first passage but increases steadily to reach 0.6 at the last passage, after about 30 generations. These smooth changes in the growth behaviour of this cell strain are accurately described by the mortalization theory of Shall and Stein, in which the single parameter gamma, describes the change in reproductive potential over the entire lifespan. The parameter gamma describes the rate at which the doubling time of the culture increases; it is the number of generations at which half of the newborn cells are themselves reproductively sterile. Our present data provide an estimate of gamma for this cell strain equal to 21.2 generations, which compares well with a previous estimate of 20.3 generations.


1982 ◽  
Vol 47 (3) ◽  
pp. 445-450 ◽  
Author(s):  
P. Balakrishna Murthy ◽  
M. Abdul Rahiman ◽  
P. G. Tulpule

1. Utilizing the bromodeoxyuridine differential-chromatid labelling technique the in vitro proliferation of lymphocytes from children with kwashiorkor was followed in phytohaemagglutinin-stimulated cultures and compared with controls.2. Analyses of first, second and third or subsequent division cells as a function of culture time between 40 and 96 h showed that cell-cycle duration was prolonged in kwashiorkor cultures. The extent of this increase was approximately 4.5 h for the first-division cells and 1.5 h for third-division cells.3. The peak for second-division cells was depressed in kwashiorkor cultures.4. A decreased number of third or subsequent-division cells was observed in kwashiorkor cultures at all time points studied.5. These findings suggest that the loss in lymphocyte activity to PHA in malnourished children in general could be due to an increase in cell-cycle duration of responding lymphocytes.


2018 ◽  
Author(s):  
Clotilde Cadart ◽  
Sylvain Monnier ◽  
Jacopo Grilli ◽  
Rafaele Attia ◽  
Emmanuel Terriac ◽  
...  

2012 ◽  
Vol 24 (1) ◽  
pp. 191
Author(s):  
S. Sugimura ◽  
Y. Hashiyada ◽  
Y. Aikawa ◽  
M. Ohtake ◽  
H. Matsuda ◽  
...  

In cattle, the prediction of embryonic viability after embryo transfer is an important research target. A previous study has indicated that the duration of the fourth cell cycle at the time of maternal-zygotic transition, which is involved in in vitro embryonic development, may be an indicator of blastocyst formation; this study showed that embryos with a short fourth cell cycle have a better potential of developing into blastocysts than those with a long fourth cell cycle (Lequarre et al. 2003 Biol. Reprod. 69, 1707–1713). However, the relationship between the fourth cell cycle duration and post-transfer viability of embryos is unclear. The aim of the present study was to examine the effect of the fourth cell cycle duration on embryo development after embryo transfer. Twenty-five IVF bovine embryos were cultured in well-of-the-well culture dishes contained 125 μ of CR1aa supplemented with 5% calf serum at 38.5°C in 5% O2 and 5% CO2 for 168 h after insemination. In vitro development of the embryos was monitored using time-lapse cinematography (Sugimura et al. 2010 Biol. Reprod. 83, 970–978). We found that 61% of the blastocysts had a long fourth cell cycle (41.5 ± 5.9 h), which is commonly referred to as the lag phase, whereas the remaining embryos had a short fourth cell cycle (7.4 ± 4.5 h). All the embryos with a short fourth cell cycle exhibited a lag phase in the next cell cycle (32.9 ± 6.6 h). Moreover, embryos with a short fourth cell cycle were found to have a higher blastocyst rate (75.8%) than those with a long fourth cell cycle (48.1%; Student's t-test, P < 0.01). However, embryonic cell number, apoptosis incidence, chromosomal abnormality and O2 consumption were found to be identical between the 2 groups (Student's t-test, P > 0.05). Real-time reverse-transcription PCR results of the individual blastocysts showed that the relative expression of 5 genes related to pregnancy reorganization, placentation and fetal growth—namely, CDX2, IFN-τ, PLAC8, AKR1B1 and IGF2R—did not differ between the 2 groups (Student's t-test, P > 0.05). Furthermore, blastocysts derived from embryos with long (n = 30) and short (n = 19) fourth cell cycles were transferred into 49 recipient cows; we did not observe any difference between the long and short fourth cell cycles on the rates of pregnancy (long vs short fourth cell cycle, 30.0 vs 52.6%) and delivery (long vs short fourth cell cycle, 30.0 vs 47.4%; Yates' corrected chi-square test, P > 0.10). These results show that blastocysts derived from embryos with either long or short fourth cell cycles have identical developmental competence after embryo transfer. Therefore, the fourth cell cycle duration during maternal-zygotic transition appears to be unavailable as the indicator of post-transfer viability of IVF bovine embryos. This work was supported by the Research and Developmental Program for New Bio-Industry Initiatives.


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