In vitro formation of fibrous septa by liver connective tissue cells

1987 ◽  
Vol 23 (1) ◽  
pp. 10-14 ◽  
Author(s):  
Alvaron A. Monteiro ◽  
Radovan Borojevic
1913 ◽  
Vol 18 (3) ◽  
pp. 287-298 ◽  
Author(s):  
Alexis Carrel

When connective tissue cells have been cultivated for a certain length of time in a medium which has been repeatedly changed, a definite relation arises between the rate of growth of the cells and the composition of the medium. It is possible, by adding to the culture medium a given quantity of certain substances, such as embryonic juices, to foresee the extent to which a fragment of tissue composed of a given strain of cells will increase in a given time. The rate of growth of a strain of cells can be accelerated or retarded by the addition to the medium of activating or retarding substances. The dynamic condition of a strain of connective tissue cells, which have been living in a given medium for some time, is not a definitely acquired characteristic, but a temporary state, and is the product or function of the medium in which the cells are living, and is readily modified merely by altering the composition of the medium. A knowledge of the characteristics of the growth of connective tissue described has led to a new result,—the indefinite proliferation of a strain of connective tissue cells outside of the organism. The strain of connective tissue originally obtained from a fragment of chick embryo heart, which had been pulsating in vitro for 104 days, was still actively alive after sixteen months of independent life and more than 190 passages. The rate of proliferation of the connective tissue sixteen months old equalled and even exceeded that of fresh connective tissue taken from an eight day old embryo. It appears, therefore, that time has no effect on the tissues isolated from the organism and preserved by means of the technique described above. During the sixteenth month of life in vitro the cells increased rapidly in number and were able in a short time to produce a large quantity of new tissue. This fact, therefore, definitely demonstrates that the tissues were not in a state of survival, as was the case in certain earlier experiments, but in a condition of real life, since the cells of which they were composed, like microorganisms, multiplied indefinitely in the culture medium.


1913 ◽  
Vol 18 (2) ◽  
pp. 183-186 ◽  
Author(s):  
Peyton Rous

Connective tissue cells of chick embryos and cells of a chicken sarcoma, proliferating in vitro, soon render acid the plasma about them, but they nevertheless continue to grow well. Evidently the tissue cell will withstand a considerably greater change in the reaction of the fluids about it than has usually been supposed. Under conditions of in vitro life in plasma, which do not provide for an artificial circulation, the acid produced by growing tissues diffuses only slowly and is subject to little dilution from this source. About tissues which grow very rapidly in vitro, as, for example, tumor tissues, there must be a marked concentration of metabolic products, and this may largely account for the poor results of attempts at the continuous propagation of such tissues in vitro.


1913 ◽  
Vol 17 (5) ◽  
pp. 499-510 ◽  
Author(s):  
Robert A. Lambert

1. In primary cultures sarcoma cells exhibit a much greater activity than do normal connective tissue cells grown from the adult blood vessel; there is a shorter latent period, ameboid phenomena are more marked, and cell multiplication proceeds more rapidly. 2. In secondary cultures sarcoma cells are less active than in primary cultures; connective tissue cells, on the other hand, show a markedly accelerated growth. 3. Connective tissue cells are more easily propagated over long periods in vitro than are sarcoma cells; they multiply actively in cultures more than three months old. 4. The method of tissue cultivation is well adapted to the study of normal and pathological cell division; the nuclear changes are easily discernible in the living cell as division proceeds, and staining methods may be applied to verify observations upon the unstained structures. 5. Atypical mitoses of several kinds are found in cultures of sarcoma cells but are not seen in growths of connective tissue. 6. The time required for division in rat connective tissue cells kept at body temperature (38° C.) varies within relatively narrow limits (twenty to fifty minutes); sarcoma cells, on the contrary, exhibit marked variations and several hours may be required. 7. In studies upon living cells amitotic division has not been observed in either normal or tumor tissue. Evidences of nuclear budding, however, with the formation of cells containing several nuclei of irregular size have been noted.3 The development of a cell with two nuclei from a mononuclear cell by mitotic division of the nucleus without division of the cytoplasm has also been observed.


1919 ◽  
Vol 30 (6) ◽  
pp. 531-537 ◽  
Author(s):  
Albert H. Ebeling

1. A strain of connective tissue is still very active after more than 7 years of life in vitro. 2. The rate of growth of the fragments of tissue can be measured accurately and used for testing the action of many different factors on the growth of connective tissue cells. 3. The rate of growth of the strain is at least as rapid as it was 5 years ago, and may be more active. 4. The connective tissue cells appear to have the power of multiplying indefinitely in a culture medium, as do microorganisms.


1974 ◽  
Vol 96 (2) ◽  
pp. 131-137
Author(s):  
K. D. Ansevin ◽  
H. G. Welgus ◽  
C. A. Homsy ◽  
B. V. Lipps

Disaggregated cells of kidney, lung and liver of 14-day-old chick embryos were cultivated in vitro on several open-pore, organic-polymer sponges and on one gelatin sponge; in some cases this was followed by short-term, subcutaneous implantation into rats. In order to study invasion of connective tissue cells into the porous matrix, the same organic-polymer materials were implanted into rats, and in one experimental series this was followed by in vitro cultivation after they had been retrieved from the animals. The results showed that: 1) epithelial cells have different requirements for invasion and histogenesis from those of connective tissue cells; 2) the type of porous substrate influences morphology of connective tissue that forms within it.


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