scholarly journals Activation of rape (Brassica napus L.) embryo during seed germination. IV. Germinating embryo. The first zones of mitoses, starch and DNA synthesis and their expansion pattern

2014 ◽  
Vol 55 (4) ◽  
pp. 539-563 ◽  
Author(s):  
Mieczysław Kuraś
Keyword(s):  
Dna Synthesis ◽  
Cell Activation ◽  
Starch Synthesis ◽  
Lower Boundary ◽  
Apical Part ◽  
Cell Number ◽  
Root Cap ◽  
Brassica Napus L ◽  
Cell Divisions ◽  
Cell Layers

The rape radicle is completely covered by the root cap. The successive lateral cell layers of the root cap are terminated by T-forming walls in the dermatogen layer in a statistically constant position. T-walls in dermatogen were utilized for delimitation of successive root sectors on longitudinal microtome sections at the succeeding germination stages. The length and the cell number of the corresponding sectors were studied and the starch and DNA synthesis sites as well as cell divisions localized. All these processes are initiated in a constant sequence and in specific embryo zones. The first symptom of activation of the embryo is starch synthesis. It begins in two centres: in the apical part of the radicle columella and in the hypoctyl dermalogen it moves deep into the cortex and in both directions along the columella the activation of starch synthesis shifts basipetally into the whole columella and the initial centre as well as the lateral parts of the root cap. From the hypocotyl dermatogen it moves into the cortex and in both directions along the embryo axis. In the root dermatogen and periblem the activation zone is first located in the basal sector and, then, gradually, in the lower ones. Just before germination the basal and apical zones of activation meet. Starch can then, be found throughout the root. During starch synthesis, in the basal part of the radicle. DNA synthesis and cell growth begin. In the root sectors which have already begun to grow and synthesize DNA, cell divisions start. The boundary of the dividing cells zone shifts acropetally at some distance above the lower boundary of DNA synthesis and the zone of cell premitotic growth. The acropetal shift of the mitotic activation zones can be described as wave expansion. Before the first mitotic wave reaches the promeristem it is followed by at least three acropetal waves, arising in the already activated basal sectors. and then the mitoses are asynchronised. Mitotic.: activation of the root cap is partly independent of the acropetal wave of cell activation and results from the expanding weaker basipetal wave.

scholarly journals Rape embryogenesis. IV. Appearance and disappearance of starch during embryo development

2014 ◽  
Vol 51 (3-4) ◽  
pp. 381-387 ◽  
Author(s):  
Teresa Tykarska
Keyword(s):  
Apical Part ◽  
Embryo Axis ◽  
Starch Grains ◽  
Cell Divisions ◽  
Embryo Cells ◽  
Dividing Cells ◽  
Gradual Accumulation ◽  
Black Seeds ◽  
Mother Cells ◽  
Storage Starch

Starch appears first in the suspensor of the proembryo with two-cell apical part. It is observed in the embryo proper from the octant stage. At first it is visible in all the embryo cells in the form of minute transient grains which disappear during cell divisions. But the columella mother cells and their derivatives have persistent large grains. When the embryo turns green in the heart stage a gradual accumulation of storage starch begins and lasts to the end of embryogenesis. Storage starch grains appear first in the auter cortex layers of the hypocotyl where the largest grains are to be found later, and afterwards in all the other tissues. Starch is usually absent in the frequently dividing cells, but even there it appears in the form of minute grains after the end of cell divisions. Disappearance of starch starts when the intensive green colour of the seed coat begins to fade. The first to disappear are the smallest granules in the regions where they were noted latest. In the embryo axis the starch grains remain deposited longest in dermatogen and cortex cells in the lower hypocotyl part. They are visible there, still when the seed turns brown. In black seeds starch may be only found in the columella the cells of which throughout embryogenesis contain amyloplasts filled with starch. These grains disappear completely at the time when the seeds become dry.

scholarly journals Antitumor activity of L-asparaginase from Erwinia Carotovora from against different leukemic and solid tumours cell lines

2013 ◽  
Vol 59 (5) ◽  
pp. 498-513 ◽  
Author(s):  
O.Yu. Abakumova ◽  
O.V. Podobed ◽  
P.A. Karalkin ◽  
L.I. Kondakova ◽  
N.N. Sokolov
Keyword(s):  
Dna Synthesis ◽  
Tumor Cells ◽  
Solid Tumor ◽  
Human Fibroblasts ◽  
Erwinia Carotovora ◽  
Cell Number ◽  
Jurkat Cells ◽  
Leukemic Cells ◽  
Cycle Phase ◽  
Tumor Cell Death

We have studied dose- and time-dependent antitumor and cytotoxic effects of Erwinia carotovora L-asparaginase (ECAR LANS) and Escherichia coli L-asparaginase (MEDAC) on human leukemic cells and human and animal solid tumor cells. We determined the sensitivity of tumor cells to L-asparaginases, as well the effect L-asparaginases on cell growth rate, protein and DNA synthesis per se and with addition of different cytostatics. The data obtained demonstrated that ECAR LANS L-asparaginase suppressed growth of all tested solid tumor cells. Evaluation of leukemic cell number after treatment with L-asparaginases for 24, 48 and 72 h demonstrated that asparagine deficiency did not kill cells but stopped normal cell division and had no effect on protein and DNA synthesis. Cytofluorometric study of solid and leukemic cells demonstrated that the treatment with L-asparaginase for 72 h did not change cell cycle phase distribution and did not increase the number of apoptotic cells. The HL-60 cell line was only exemption. At the same time, cells treatment with L-asparaginase and doxorubicin combination leaded to increase of apoptotypical cell number to 60% for MCF7 cells, to 40% for Jurkat cells and to 99% for HL-60 cells. We have excluded apoptosis as main reason for tumor cell death after asparaginase treatment because multi resistant Jurkat/A4 cells have been asparaginase sensitive. We have not found ECAR LANS L-asparaginase effect on normal human fibroblasts growth ability and we had come to conclusion that enzyme cytotoxcisity related only with asparagine deficiency.

scholarly journals Human leukemic B cell activation: functional consequence of membrane IgM interaction with anti-IgM ligand is an alterable cell characteristic

Blood ◽  
1987 ◽  
Vol 70 (4) ◽  
pp. 1193-1202 ◽  
Author(s):  
P Mongini ◽  
C Blessinger ◽  
S Seremetis ◽  
R Winchester ◽  
S Rudich
Keyword(s):  
Signal Transduction ◽  
T Cell ◽  
B Cells ◽  
Dna Synthesis ◽  
B Cell ◽  
Cell Activation ◽  
Functional Study ◽  
Normal Peripheral Blood ◽  
Activated T Cell ◽  
Cell Supernatant

Abstract A functional study of several human malignant B cell populations has indicated that occasional leukemic clones are extraordinarily sensitive to signal transduction through membrane IgM. One isolated hairy cell leukemia (HCL) with low background DNA synthesis was stimulated to significant levels of DNA synthesis when cultured with high (100 micrograms/mL) concentrations of soluble anti-IgM ligands. In contrast to the activation of normal peripheral blood polyclonal B cells, this DNA synthesis was completely independent of accessory T cell factors. Although the HCL clone could also be induced to enter S phase by incubation in media supplemented with only activated T cell supernatant, culture of the clone with activated T cell supernatant plus anti-IgM Ab resulted in DNA synthesis that was significantly less than that induced by either activator alone. Factor(s) in T cell supernatant appear to modulate the leukemic clone so that the binding of ligand to membrane IgM is perceived as an inhibitory rather than a stimulatory signal for DNA synthesis. In terms of Ig Fc independence and low ligand dose requirements, anti-IgM-mediated inhibitory signal transduction in the T cell supernatant-activated HCL clone was found to mimic anti-IgM mediated suppression of the spontaneous DNA synthesis of an alternative HCL clone. The functional results suggest that the type of signal transduced anti-Ig ligands may reflect differences in the activation state of receptive leukemic B cells.

scholarly journals Characterization of a photoproduct of 7,12-dimethylbenz[a]anthracene and its effects on chick-embryo cells in culture

1977 ◽  
Vol 164 (3) ◽  
pp. 481-486 ◽  
Author(s):  
D Warshawsky ◽  
E Kerns ◽  
M J Bissell ◽  
M Calvin
Keyword(s):  
Chick Embryo ◽  
Dna Synthesis ◽  
Oxidation Product ◽  
Biological Effects ◽  
Cell Number ◽  
Resonance Spectroscopy ◽  
Morphological Transformation ◽  
Morphological Alterations ◽  
Photo Oxidation ◽  
Embryo Cells

A common impurity of 7,12-dimethylbenz[alpha]anthracene was more effective than 7,12-dimethylbenz[alpha]anthracene in inducing morphological alterations, and in causing an increase in glucose uptake, DNA synthesis and cell number in chick-embryo fibroblasts. Gradual morphological transformation follows the increase in DNA synthesis after 2 days when either primary or secondary cultures are treated with 3 microgram of the compound/ml. The compound, isolated from 7,12-dimethylbenz[alpha]anthracene by alumina column chromatography, was characterized by t.l.c., mass spectroscopy, carbon-hydrogen analysis, u.v. and nuclear-magnetic-resonance spectroscopy and thermal decomposition. It was the photo-oxidation product of 7,12-dimethylbenz[alpha]anthracene, 7,12-epidioxy-7,12-dimethylbenz[alpha]anthracene. It is suggested that some of the biological effects observed after treatment of cultures with 7,12-dimethylbenz[alpha]anthracene may be due in part to the presence of the photo-oxidation product.

scholarly journals Induction of Cytotoxic T Lymphocyte Antigen 4 (Ctla-4) Restricts Clonal Expansion of Helper T Cells

2001 ◽  
Vol 194 (7) ◽  
pp. 893-902 ◽  
Author(s):  
Alden M. Doyle ◽  
Alan C. Mullen ◽  
Alejandro V. Villarino ◽  
Anne S. Hutchins ◽  
Frances A. High ◽  
...  
Keyword(s):  
T Cells ◽  
T Cell Activation ◽  
T Lymphocyte ◽  
Cd4 T Cells ◽  
Cell Activation ◽  
Cytotoxic T Lymphocyte ◽  
Clonal Expansion ◽  
Negative Regulator ◽  
Lymphocyte Antigen ◽  
Cell Divisions

Cytotoxic T lymphocyte antigen (CTLA)-4 plays an essential role in immunologic homeostasis. How this negative regulator of T cell activation executes its functions has remained controversial. We now provide evidence that CTLA-4 mediates a cell-intrinsic counterbalance to restrict the clonal expansion of proliferating CD4+ T cells. The regulation of CTLA-4 expression and function ensures that, after ∼3 cell divisions of expansion, most progeny will succumb to either proliferative arrest or death over the ensuing three cell divisions. The quantitative precision of the counterbalance hinges on the graded, time-independent induction of CTLA-4 expression during the first three cell divisions. In contrast to the limits imposed on unpolarized cells, T helper type 1 (Th1) and Th2 effector progeny may be rescued from proliferative arrest by interleukin (IL)-12 and IL-4 signaling, respectively, allowing appropriately stimulated progeny to proceed to the stage of tissue homing. These results suggest that the cell-autonomous regulation of CTLA-4 induction may be a central checkpoint of clonal expansion of CD4+ T cells, allowing temporally and spatially restricted growth of progeny to be dictated by the nature of the threat posed to the host.

scholarly journals Effects of tumour necrosis factor-α on BrdU incorporation in cultured human enterocytes

1995 ◽  
Vol 4 (1) ◽  
pp. 31-37 ◽  
Author(s):  
J. McDevitt ◽  
C. Feighery ◽  
C. O'Farrelly ◽  
G. Martin ◽  
D. G. Weir ◽  
...  
Keyword(s):  
Dna Synthesis ◽  
Cell Line ◽  
Cell Number ◽  
Brdu Incorporation ◽  
Similar Response ◽  
Proliferating Cells ◽  
Incorporated Brdu ◽  
Factor Α ◽  
Proliferation Assays ◽  
Necrosis Factor

Bromodeoxyuridine incorporation is a useful method for studying the pattern of DNA synthesis in proliferating cells. The distribution pattern of incorporated BrdU in villus enterocytes of duodenal explants was analysed after exposure to TNFα in organ culture. TNFα caused a consistent, low level uptake of BrdU in the portion of the nucleus close to the nuclear membrane, this pattern was absent from the control cultures. As these epithelial cells are terminally arrested in G0, the BrdU incorporation was thought not to be due to S phase DNA synthesis, but rather a response to the cytotoxic influence of TNFα. Microtitre plate proliferation assays of cell density and DNA synthesis were devised to study the effects of TNFα on confluent monolayers of the human foetal jejunal cell line I407 and the mouse fibrosarcoma cell line L929. Both cell lines showed a similar response to TNFα. Exposure to TNFα alone did not reduce cell numbers but did cause a significant increase in DNA synthesis (p < 0.05). When cycloheximtde was added in tandem with TNFα there was a significant reduction in cell number (p < 0.001) and level of DNA synthesis (p < 0.01) indicative of cell death. The DNA of cells exposed to TNFα and cycloheximide was fragmented when viewed on an electrophoresis gel. The results show that BrdU incorporation might be a good indicator of damage to the DNA of cells after cytotoxic insult. TNFα may be responsible for villus enterocyte damage in enteropathies such as coeliac disease and GVHR of the small bowel.

Effects of Ca-Containing Phosphate Glasses on T Lymphocytes In Vitro

2005 ◽  
Vol 284-286 ◽  
pp. 597-602 ◽  
Author(s):  
A. Kesisoglou ◽  
Jonathan C. Knowles ◽  
I. Olsen
Keyword(s):  
T Cells ◽  
T Lymphocytes ◽  
Dna Synthesis ◽  
T Cell Activation ◽  
Cell Activation ◽  
Human Peripheral Blood ◽  
Suppressor Cells ◽  
Phosphate Glasses ◽  
Activated T Cells

Calcium phosphate-based glasses (PG) are of interest as both scaffold and delivery materials for tissue rebuilding because of their chemical similarity to bone. Since it is essential that these materials exhibit local and systemic biocompatibility and do not adversely affect host tissues, the present study was undertaken to examine the effects of PG containing different amounts of Ca on human T lymphocytes in vitro. This was carried out by measuring the effects of extracts of the PG on the direct and mitogen-induced activation of T cells from human peripheral blood, as well as assessing CD4 and CD8, surface antigens which define T-helper and T-suppressor cells, respectively. The results showed that DNA synthesis by resting T lymphocytes was unaffected by all the PG. However, extracts of the PG containing 24 mol% of Ca caused a very marked inhibition of mitogen-induced T cell activation. This PG also reduced both the resting CD4+ and CD8+ T cells, as well as activated CD8+ cells. In contrast, high Ca-PG significantly augmented DNA synthesis by mitogen-activated T cells. These experiments show that PG containing differing levels of Ca can have pronounced and differential effects on the activation and function of T lymphocytes in vitro.

Growth factor stimulated cell proliferation is accompanied by an elevated labile intracellular pool of zinc in 3T3 cells

2002 ◽  
Vol 80 (8) ◽  
pp. 790-795 ◽  
Author(s):  
Shirley C Paski ◽  
Zhaoming Xu
Keyword(s):  
Cell Proliferation ◽  
Growth Factors ◽  
Growth Factor ◽  
Dna Synthesis ◽  
Cell Number ◽  
3T3 Cells ◽  
Intracellular Pool ◽  
Igf I ◽  
Epidermal Growth ◽  
Number Counts

Growth factors such as platelet-derived growth factor (PDGF), epidermal growth factor (EGF), and insulin-like growth factor-I (IGF-I) are required for quiescent 3T3 cells to proliferate, but zinc deprivation impairs IGF-I-induced DNA synthesis. We recently showed that labile intracellular pool of zinc is involved in cell proliferation. Our objective was to determine whether the labile intracellular pool of zinc plays a role in growth factor (PDGF, EGF, and IGF-I) - stimulated proliferation of 3T3 cells. Quiescent 3T3 cells were cultured in DMEM with or without growth factors. Labile intracellular pool of zinc, DNA synthesis, and cell proliferation were assessed using fluorescence microscopy, 3H-thymidine incorporation, and total cell number counts, respectively. After 24 h, growth factors stimulated DNA synthesis (24%) but not cell proliferation. After 48 h, growth factors stimulated both DNA synthesis (37%) and cell proliferation (89%). In response to growth factor stimulation, the labile intracellular pool of zinc was also elevated after 24 or 48 h of treatment. In summary, growth factor (PDGF, EGF, and IGF-I) - stimulated increase in DNA synthesis and cell proliferation were accompanied by an elevated labile intracellular pool of zinc in 3T3 cells. Since elevation of the labile intracellular pool of zinc occurred along with increased DNA synthesis, but cell proliferation remained unchanged, the elevation of the labile intracellular pool of zinc likely occurred during the S phase to provide the zinc needed to support DNA synthesis and ultimately cell proliferation.Key words: PDGF, EGF, IGF-I, labile intracellular pool of zinc, cell proliferation, DNA synthesis, 3T3 cells.

Rhizogénèse adventive dans l'épicotyle du Pois : initiation et structuration de la racine

1982 ◽  
Vol 60 (3) ◽  
pp. 261-280 ◽  
Author(s):  
A. Nougarède ◽  
P. Rondet
Keyword(s):  
Adventitious Roots ◽  
Root Meristem ◽  
Cell Layer ◽  
Cell Number ◽  
Root Cap ◽  
Root Initiation ◽  
Elongation Zone ◽  
No Formation ◽  
Depth Position ◽  
Growing Conditions

The ability of the first internode of Pisum sativum epicotylary axis to produce adventitious roots was examined with respect to dark and light growing conditions and depth position of the soaked seeds in vermiculite. Root initiation began on the 7th day and moved acropetally until the 16th day, with no formation of new roots between older ones. DNA synthesis in the diploid interfascicular cells followed the first mitoses of root initiation. The cell layer that would normally have differentiated into an endodermis reacted more slowly and built a primordial root cap, protecting the root as it grew through the cortex. When the new root emerged a new root cap – protoderm complex was rebuilt from the subapical cells of the root meristem. The increase in cell number was highest during the first 24 h following root initiation, and the cell cycle was extremely short with a very reduced G1 phase. Only the elongation zone of the mature adventitious root showed polyploidy.

Lateral bud growth on excised stem segments: effect of the stem

1975 ◽  
Vol 53 (3) ◽  
pp. 243-248 ◽  
Author(s):  
Carol A. Peterson ◽  
R. A. Fletcher
Keyword(s):  
Sucrose Solution ◽  
Apical Part ◽  
Endogenous Auxin ◽  
Cell Divisions ◽  
Cotyledonary Nodes ◽  
Lateral Buds ◽  
Lateral Bud ◽  
Bud Growth ◽  
Soybean Plants ◽  
Stem Segments

Lateral buds at the cotyledonary nodes of soybean plants grown under the conditions used in this study usually remain inhibited. These buds grow when the apical part of the plant is removed. They will grow, but less strongly, when the roots as well as the apex of the plant are removed and the basal end of the cut stem is placed in a mineral salt solution. Bud growth is further diminished by decreasing the length of stem left attached to the bud. The cotyledon is essential for bud growth on plant segments maintained in nutrient solution, but it can be replaced by a 1% sucrose solution during the early days of bud growth. Buds which are completely detached from the stem and placed in 1% sucrose do not elongate, but a small number of cell divisions are detectable, indicating that the early events of the release from inhibition have occurred. Buds elongate when they are apically or centrally located on stem segments. Increasing the length of the attached stem segments increases the growth of the buds. Additions of the cytokinin benzyladenine to plants causes a dramatic increase in bud growth when buds are attached to stem segments but does not stimulate growth of buds without stem segments. It is concluded that benzyladenine alone will not substitute for a factor(s) present in the stem which is necessary for bud growth. Increasing stem lengths above buds located at the basal ends of segments inhibits bud growth. It is suggested that this may be due to an accumulation of endogenous auxin at the site of the buds.

Sign in / Sign up

Export Citation Format

Share Document