The Effect of the Variation in the Osmotic Tension and of the Dilution of Culture Media on the Cell Proliferation of Connective Tissue
نویسنده
چکیده
For the first few days of cultivation of connective tissue in hypertonic, hypotonic, and diluted medium, cell proliferation was stimulated. The first outgrowths of new cells in the modified media did not occur sooner than in normal medium. In hypertonic medium the density of the area of cell proliferation appeared to be greater than the control, but in hypotonic or diluted medium there seemed to be no increase in actual mass over the control. These observations confirm the conclusions of Carrel and Burrows, as well as those of Lambert. Subsequent to the first few days of cultivation in hypertonic medium the area of cell proliferation decreased and in a short time conditions developed which were unfavorable to growth, and finally resulted in death of the culture, unless it revived before this stage. Hypotonic medium after about ten days no longer caused more extensive areas of proliferating cells; but instead, the extent of new growth gradually decreased, and the culture merely remained alive unless revived. In diluted medium the extent of the area of cell proliferation remained greater with no actual increase in mass. The area of cell proliferation which is observed during the first few days in a culture of fresh tissue recently extirpated does not indicate the actual influence of modified media. It was only after continued cultivation of strains of connective tissue in these modified media that their influence on cell proliferation was determined.
منابع مشابه
Effect of Agar and Different Culture Media on the Micropropagation of Rosa hybrida cv.’Black Baccara’
In vitro propagation of plant has played a very important role in rapidmultiplication of cultivars with desirable traits and production of healthy and disease-free plants. In the present investigation, the objectives were to optimize the micropropagation of Rose hybrid ‘Black Baccarat’ cultivar. In proliferation step, the nodal segments (1.5 cm) was cultured on both liquid and solid media (MS, ...
متن کاملImprovement of shoot-tip culture proliferation in banana using PEG6000. Leila Saeedavi, Ali Soleimani* and Mohammad Esmaeil Amiri
In order to improve the shoot proliferation rate of ‘Dwarf Cavendish’ banana shoot tip cultures, polyethylene glycol (PEG6000) was employed at concentrations of 2, 4, and 6% (w/v). The medium without PEG was considered as negative control. An increasing of shoot proliferation was achieved in MS medium containing 2% PEG. Furthermore, application of 2% PEG significantly increased the shoot dry we...
متن کاملComparison of the effect of platelet lysate derived from umbilical cord blood and peripheral blood on the expansion and differentiation of MSCs
Abstract Background and Objectives Proliferation and differentiation of mesenchymal stem cells (MSCs) in culture media requires the presence of nutrient supplements such as bovine fetal serum (FBS), which increases the risk of prion/xenotic infections. Platelet lysates as a rich source of growth factors and cytokines can replace FBS in cell culture medium. This study aimed to compare the effe...
متن کاملP-116: The Catalase Effect on LDH Enzyme Leakage of Buffalo Epididymal Sperm During Culture in Human Tubal Fluid Mediaa
Background: Mammalian spermatozoa are highly susceptible to lipid peroxidation, which leads to structural damage to the sperm cell, the enzymatic leakage from spermatozoa accompanied by lowered motility and metabolism. Catalase, an enzyme that detoxify hydrogen peroxide and reduce the enzyme leakage from sperm cell Materials and Methods: For this study, buffalo bull testicles (20 pairs) were pi...
متن کاملEffect of Simulated Microgravity Conditions on Differentiation of Adipose Derived Stem Cells towards Fibroblasts Using Connective Tissue Growth Factor
Background: Mesenchymal stem cells (MSCs) are multipotent cells able to differentiating into a variety of mesenchymal tissues including osteoblasts, adipocytes and several other tissues. Objectives: Differentiation of MSCs into fibroblast cells in vitro is an attractive strategy to achieve fibroblast cell and use them for purposes such as regeneration medicine. The goal of this s...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید
ثبت ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
- The Journal of Experimental Medicine
دوره 20 شماره
صفحات -
تاریخ انتشار 2003