Muscle proteins in the chick myotome examined by the immunofluorescent method

Development ◽  
1968 ◽  
Vol 19 (2) ◽  
pp. 193-202
Author(s):  
Akira Ikeda ◽  
Rana L. Abbott ◽  
Jan Langman

In previous studies on the development of the somite (Langman & Nelson, 1968), the majority of the cells of the myotome appeared to arise from the dermatome and not, as previously suggested, from the cells of the so-called dorso-medial somite lip (Williams, 1910; Hamilton, 1952; Boyd, 1960). Once the myotome cells, characterized by a pale, round to irregular, nucleus and darkly stained nucleolus, are formed, they fail to synthesize DNA. During subsequent development, the myotome appears to extend in ventro-lateral direction by the addition of new cells originating primarily from the dermatome. After the dermatome has lost its epithelial structure, the myotome, in transverse section, consists of a tissue band with an abundance of cytoplasm and a large number of round to spindle-shaped nuclei. Though DNA synthesis was rarely observed among the cells of the extended myotome, considerable proliferative activity was observed in the adjacent tissues.

Blood ◽  
1965 ◽  
Vol 25 (3) ◽  
pp. 292-298 ◽  
Author(s):  
EFSTRATIOS S. KURTIDES ◽  
WALTER A. RAMBACH ◽  
HOWARD L. ALT

Abstract The proliferative activity of erythropoietic and other tissues has been studied in normal, nephrectomized and bilateral ureter ligated rats. Forty-eight hours after bilateral nephrectomy, rats showed a significant suppression of DNA synthesis and Fe59 incorporation in the bone marrow and spleen. The administration of erythropoietin prevented this suppression of Fe59 uptake, and produced an increase in splenic DNA synthesis comparable to that noted in the normal, similarly stimulated animal. Bilateral ureter ligation in animals, producing a blood urea nitrogen elevation equal to that induced by nephrectomy, caused no suppression of DNA synthesis in bone marrow or spleen. These latter animals exceeded the normal in their response to erythropoietin administration. Intestinal DNA synthesis was unaffected in uremia produced by nephrectomy or ureter ligation. Thymic proliferative activity was suppressed in uremia induced by either procedure. The observations indicate that acute, severe uremia of relatively short duration does not influence the DNA synthetic activity of all tissues in an adverse fashion. What factors may modify tissue responses are unknown. In the case of erythropoietic organs, such factors seem to originate in the kidney.


1983 ◽  
Vol 61 (11) ◽  
pp. 1197-1200 ◽  
Author(s):  
Hélène Larue ◽  
Elyse Bissonnette ◽  
Luc Bélanger

Histone Hl° appears in rat liver nuclei around the time of birth; it increases to near-adult levels by 30 days of age, in waves which correlate with distinct phases of liver developmental growth. Hl° emerges as the liver terminates the bulk of its proliferative activity, but it accumulates mainly during the terminal cytodifferentiation phases leading to polyploidization. Premature interruption of liver DNA synthesis in neonatal rats, with cytosine arabinoside or dexamethasone, induces some accumulation of Hl° in the liver. Our data suggest that DNA synthesis arrest conditions in part, but is not the main developmental event underlying Hl° expression during differentiation of rat liver.


Author(s):  
N. J. Unakar ◽  
J. R. Reddan ◽  
C. V. Harding ◽  
R. M. Bell

Mitosis in the adult lens is normally confined to a region of the epithelium referred to as the germinative zone. Cells of the central epithelium are normally devoid of proliferative activity but can be induced to undergo a parasynchronous burst of DNA synthesis and mitosis when cultured under suitable conditions. It would seem that the maintenance of the "blocked" mitotic state and the release of the cells from this state must have a basis in the overall organization of the tissue. If this is true, triggering of mitosis might be reflected in the initial fine structural changes which precede cell division in the cultured lens.


In a recent communication on the Defensive Spines of Fishes, published in the Philosophical Transactions (Series B, vol. 212), I described the glandular structure in the lateral groove of the caudal spine of Trygon ; and on p. 7 I gave a drawing of a transverse section of the distal portion of the spine, showing lateral processes or projections which appeared to overlap a space containing isolated masses of epithelial cells. The suggestion was made that these lateral flaps of tissue were intended to protect the glandular epithelium in that part of the spine which did not lie in contact with the opposing tail. But it was pointed out that sections showing the epithelium completely filling the space beneath the processes were wanting, and it seemed necessary for the completion of this research that sections should be obtained confirming this point. Through the kindness of Mr. Thomas More, of the Sungei Bulch Estate, Kuala Selangor, Federated Malay States, I received, in very good condition, three small ikan pari in June, 1923. According to Gimlette, in his book Malay Poisons and Charm Cures (p. 117), is the native Malay name for fish, and pari is used collectively for the sting rays, eagle rays and electric rays. The specimens I received were those of the sting ray ( Sengat pari ), and after six months of careful decalcification the spines were ready to imbed and examine. The result of an examination of the sections confirmed the observations I had previously made on the special epithelial structure found in the lateral grooves near the base of the spine, and very fortunately, sections of the distal portion of one of the spines provided a complete picture of the tissue in the groove. These sections, as the accompanying figures will make clear, confirm my supposition as to the function of the lateral processes; the glandular tissue and small masses of secretion are seen completely filling the space which in previous sections only contained isolated groups of cells and secretion. Where the extremities of the processes meet, there is a small space through which portions of coagulated secretion have passed. The secreting cells have been caught in an active state, as in the cell mass are to be seen complete cells, some distended with secretion and others in which only the remnants of a nucleus remain; in fact, all stages of the secreting process can be observed.


Development ◽  
1963 ◽  
Vol 11 (2) ◽  
pp. 353-367
Author(s):  
L. N. Zhinkin ◽  
L. F. Andreeva

Despite a large number of investigations devoted to the development and regeneration of skeletal musculature, the problem of the mode of reproduction of the muscle nuclei remains unsolved (Boyd, 1960; Murray, 1960; Holtzer, 1961; and many others). The majority of investigators believe that the symplast nuclei reproduce by amitosis (Bücher, 1959). Only a few investigations have shown the presence of mitoses in developing muscle fibres. Purely morphological investigations of the development and regeneration of muscle tissue seem to be unable to solve this problem. The nuclei of muscle fibres developing in vitro have recently been shown to synthesize DNA, moreover, the experiments showed the synthesis of DNA by the nuclei to be antagonistic to that of specialized muscle proteins (Stockdale & Holtzer, 1961). Bintliff & Walker (1960) showed that a considerable percentage of de-differentiated nuclei synthesized DNA upon regeneration of the skeletal musculature.


Author(s):  
Gamal El-Sokkary

AbstractThe protective effect of melatonin against phenobarbital-induced oxidative stress in the rat liver was measured based on lipid peroxidation levels (malondialedyde and 4-hydroxyalkenals). Cellular proliferation, DNA synthesis and cell cycle duration were quantitated by the incorporation of 3H-thymidine, detected by autoradiography, into newly synthesized DNA. Two experiments were carried out in this study, each on four equal-sized groups of male rats (control, melatonin [10 mg/kg], phenobabital [20 mg/kg] and phenobarbital plus melatonin). Experiment I was designed to study the proliferative activity and rate of DNA synthesis, and measure the levels of lipid peroxidation, while experiment II was for cell cycle time determination. Relative to the controls, the phenobarbital-treated rats showed a significant increase (P < 0.01) in the lipid peroxidation levels (30.7%), labelling index (69.4%) and rate of DNA synthesis (37.8%), and a decrease in the cell cycle time. Administering melatonin to the phenobarbital-treated rats significantly reduced (P < 0.01) the lipid peroxidation levels (23.5%), labelling index (38.2%) and rate of DNA synthesis (29.0%), and increased the cell cycle time. These results seem to indicate that the stimulatory effect of phenobarbital on the oxidized lipids, proliferative activity, kinetics of DNA synthesis and cell cycle time alteration in the liver may be one of the mechanisms by which the non-genotoxic mitogen induces its carcinogenic action. Furthermore, melatonin displayed powerful protection against the toxic effect of phenobarbital.


1979 ◽  
Vol 57 (6) ◽  
pp. 1318-1332 ◽  
Author(s):  
W. D. Peek ◽  
J. H. Youson

The interlamellar areas of the gills of the anadromous sea lamprey, Petromyzon marinus, undergo structural modification during the process of metamorphosis of larvae to young adults. The initial changes involve a degeneration of presumed ion-absorptive superficial cells of the larvae and this is followed by a differentiation of adult-type chloride cells presumably from intermediate cells. Adult-type chloride cells are characterized primarily by the presence of an extensive tubular reticulum, which is continuous with lateral and basal plasma membranes. The tubules first appear in peripheral regions of intermediate cells and subsequent development involves a proliferation of the tubules toward the interior of the cell. Autoradiography with [3H]thymidine indicates that extensive DNA synthesis occurs synchronously in the interlamellar basal cells throughout the gill filaments. This DNA synthesis and division of both basal and intermediate cells is most common immediately preceding the first appearance of immature chloride cells. This suggests that cells are produced in apparent anticipation of a requirement for adult-type chloride cells and that they subsequently differentiate. The timing of differentiation of chloride cells is well correlated with developmental changes in other organs during metamorphosis.


Author(s):  
J. K. Maurin

Conductor, resistor, and dielectric patterns of microelectronic device are usually defined by exposure of a photosensitive material through a mask onto the device with subsequent development of the photoresist and chemical removal of the undesired materials. Standard optical techniques are limited and electron lithography provides several important advantages, including the ability to expose features as small as 1,000 Å, and direct exposure on the wafer with no intermediate mask. This presentation is intended to report how electron lithography was used to define the permalloy patterns which are used to manipulate domains in magnetic bubble memory devices.The electron optical system used in our experiment as shown in Fig. 1 consisted of a high resolution scanning electron microscope, a computer, and a high precision motorized specimen stage. The computer is appropriately interfaced to address the electron beam, control beam exposure, and move the specimen stage.


Sign in / Sign up

Export Citation Format

Share Document