scholarly journals Sodium cacodylate as antimitotic agent

2014 ◽  
Vol 57 (3) ◽  
pp. 329-340
Author(s):  
Jadwiga A. Tarkowska
Keyword(s):  
Allium Cepa ◽  
Mitotic Spindle ◽  
Sodium Cacodylate ◽  
Antimitotic Agent ◽  
Ultrastructural Studies ◽  
Meristematic Cells ◽  
Cacodylate Buffer ◽  
Root Meristematic Cells ◽  
Dividing Cells

The effect of pure sodium cacodylate on dividing cells was studied. The root meristematic cells of <em>Allium cepa</em> L. (the roots were squashed in acetoorcein) and endosperm cells of <em>Haemanthus katherinae</em> Bak. (<em>in vitro</em> observations) were used. Serious disturbances in karyokinesis and cytokinesis were found that led most often to the formation of polyploid or multinucleate (<em>A. cepa</em>) cells. These results point to damage of the mitotic spindle and phragmoplast. Careful use of cacodylate buffer in ultrastructural studies of microtubules is advised.

scholarly journals Investigations in vitro on the behaviour of chromosomes and the mitotic apparatus in endosperm cells of Haemanthus katherinae Baker treated with oleander glycosides

2015 ◽  
Vol 45 (3) ◽  
pp. 271-283
Author(s):  
J. A. Tarkowska
Keyword(s):  
Cell Division ◽  
Mitotic Spindle ◽  
Strong Tendency ◽  
Mitotic Apparatus ◽  
Meristematic Cells ◽  
Root Meristematic Cells ◽  
Chromosome Pattern ◽  
Chromosome Movements

The effect of oleander glycosides on dividing endosperm cells of <i>Haemanthus katherine</i> was investigated in vitro. The disturbances in the successive cell division phases were analysed in reference to cytokinesis. A strong tendency was noted to restitution nuclei formation in all phases of mitosis, and particularly in prophase. The observed chromosome pattern is the result of disturbances in prometaphase and anaphase chromosome movements owing to disturbances in the function of 'the 'mitotic spindle. It is probable that oleander glycosides inhibit formatiom of 'the microtubules of the mitotic spindle and disorganize the already formed spindle. They cause minor disturbances in cytokinesis, although frequently cell plates arise in quite unexpected places. The results of the present study are compared with those obtained in the case of root meristematic cells (Tarkowska, 1971a, b).

Structural integrity after cold storage of human epidermal model in hypothermosol: A correlative ultrastructural and fluorescent assay

1994 ◽  
Vol 52 ◽  
pp. 270-271
Author(s):  
Henry H. Eichelberger ◽  
John G. Baust ◽  
Robert G. Van Buskirk
Keyword(s):  
Cold Storage ◽  
Structural Integrity ◽  
Culture Media ◽  
Cell Structure ◽  
Natural State ◽  
Sodium Cacodylate ◽  
Ruthenium Tetroxide ◽  
Cacodylate Buffer ◽  
Before And After

For research in cell differentiation and in vitro toxicology it is essential to provide a natural state of cell structure as a benchmark for interpreting results. Hypothermosol (Cryomedical Sciences, Rockville, MD) has proven useful in insuring the viability of synthetic human epidermis during cold-storage and in maintaining the epidermis’ ability to continue to differentiate following warming.Human epidermal equivalent, EpiDerm (MatTek Corporation, Ashland, MA) consisting of fully differentiated stratified human epidermal cells were grown on a microporous membrane. EpiDerm samples were fixed before and after cold-storage (4°C) for 5 days in Hypothermosol or skin culture media (MatTek Corporation) and allowed to recover for 7 days at 37°C. EpiDerm samples were fixed 1 hour in 2.5% glutaraldehyde in sodium cacodylate buffer (pH 7.2). A secondary fixation with 0.2% ruthenium tetroxide (Polysciences, Inc., Warrington, PA) in sodium cacodylate was carried out for 3 hours at 4°C. Other samples were similarly fixed, but with 1% Osmium tetroxide in place of ruthenium tetroxide. Samples were dehydrated through a graded acetone series, infiltrated with Spurrs resin (Polysciences Inc.) and polymerized at 70°C.

scholarly journals Action of Ponceau 4R (E-124) food dye on root meristematic cells of Allium cepa L.

2015 ◽  
Vol 37 (1) ◽  
pp. 101 ◽  
Author(s):  
Gleuvânia Santana Marques ◽  
Josefa Janaína do Anjos Sousa ◽  
Ana Paula Peron
Keyword(s):  
Allium Cepa ◽  
Meristematic Cells ◽  
Food Dye ◽  
Root Meristematic Cells ◽  
Ponceau 4R

Ultrastructural association of the chromatin-containing lacunar spaces with the vacuolar component of the interphase nucleolus in Allium cepa

1982 ◽  
Vol 60 (12) ◽  
pp. 2624-2628 ◽  
Author(s):  
L. A. Chouinard
Keyword(s):  
Granular Material ◽  
Allium Cepa ◽  
Ultrastructural Level ◽  
Observational Evidence ◽  
The Other ◽  
Active Chromatin ◽  
Meristematic Cells ◽  
Fibrillar Material ◽  
Nucleolar Organizing Region ◽  
Root Meristematic Cells

At the ultrastructural level, some of the chromatin-containing lacunar spaces of the interphase nucleolus in root meristematic cells of Allium cepa are seen to be walled off, on one side, by dense-fibrillar material and to be contiguous, on the other side, to electron-transparent areas, of variable sizes and shapes, bordered by dense-granular material continuous with and indistinguishable from the dense-granular component of the nucleolar mass. These electron-transparent areas associated with the lacunar spaces are equated with nucleolar vacuoles since they contain scattered preribosomal-like granules and fibrils and are rimmed by dense-granular material. The relevant observational evidence would be consistent with the view that loops of transcriptionnally active chromatin emanating from the nucleolar organizing region project radially into either only the dense-fibrillar or both the dense-fibrillar and the interior of the electron-transparent vacuolar areas seen to be contiguous to the lacunar spaces in question. In relation to this problem, it is of interest to note that the vacuolar spaces of the interphase nucleolus in Allium cepa occasionally display within their confines discrete masses of fibrillar material, possibly chromatinic in character, and in various states of condensation and configuration.

scholarly journals Characterization of proteins immunologically related to brain microtubule-associated protein MAP-1B in non-neural cells

1989 ◽  
Vol 92 (4) ◽  
pp. 607-620
Author(s):  
J. Diaz-Nido ◽  
J. Avila
Keyword(s):  
Mitotic Spindle ◽  
Polyclonal Antibodies ◽  
Microtubule Assembly ◽  
Neural Cells ◽  
Microtubule Network ◽  
Cytoplasmic Microtubule ◽  
Protein Map ◽  
Dividing Cells

Brain microtubule-associated protein MAP-1 is composed of at least two polypeptides, MAP-1A and MAP-1B, which are among the main components of the neural cytoskeleton. Specific monoclonal and polyclonal antibodies against MAP-1B stain nuclei, mitotic spindles, centrosomes and the cytoplasmic microtubule network of different non-neural cells studied by immunofluorescence microscopy. It appears that these cells contain two proteins of 325K and 220K (K = 10(3) Mr), which are immunologically related to brain MAP-1B. The 325K protein, which is localized to the cytoplasmic microtubule network, the centrosome and the mitotic spindle, seems to be structurally related to the neural MAP-1B, as judged from their similar peptide maps and phosphorylation patterns. The 220K protein, which is localized to the nuclear matrix in interphase cells and to the mitotic spindle in dividing cells, has a proteolytic profile different from that of neural MAP-1B and is phosphorylated to a much lesser extent than the 325K protein. Both proteins bind tubulin in vitro, which suggests that they may participate in microtubule assembly in vivo; the 325K protein could perform such a role during the entire cell cycle, while the 220K protein could be implicated in the formation of the mitotic spindle.

scholarly journals TH588 and Low-Dose Nocodazole Impair Chromosome Congression by Suppressing Microtubule Turnover within the Mitotic Spindle

Cancers ◽  
2021 ◽  
Vol 13 (23) ◽  
pp. 5995
Author(s):  
Girish Rajendraprasad ◽  
Susana Eibes ◽  
Claudia Guasch Boldú ◽  
Marin Barisic
Keyword(s):  
Mitotic Spindle ◽  
Low Dose ◽  
Microtubule Dynamics ◽  
Anticancer Properties ◽  
Microtubule Targeting Agents ◽  
Depth Analysis ◽  
Dividing Cells ◽  
Targeting Ability ◽  
The Impact

Microtubule-targeting agents (MTAs) have been used for decades to treat different hematologic and solid cancers. The mode of action of these drugs mainly relies on their ability to bind tubulin subunits and/or microtubules and interfere with microtubule dynamics. In addition to its MTH1-inhibiting activity, TH588 has been recently identified as an MTA, whose anticancer properties were shown to largely depend on its microtubule-targeting ability. Although TH588 inhibited tubulin polymerization in vitro and reduced microtubule plus-end mobility in interphase cells, its effect on microtubule dynamics within the mitotic spindle of dividing cells remained unknown. Here, we performed an in-depth analysis of the impact of TH588 on spindle-associated microtubules and compared it to the effect of low-dose nocodazole. We show that both treatments reduce microtubule turnover within the mitotic spindle. This microtubule-stabilizing effect leads to premature formation of kinetochore-microtubule end-on attachments on uncongressed chromosomes, which consequently cannot be transported to the cell equator, thereby delaying cell division and leading to cell death or division with uncongressed chromosomes.

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