scholarly journals Involvement of microtubules and 10-nm filaments in the movement and positioning of nuclei in syncytia.

1979 ◽  
Vol 83 (2) ◽  
pp. 320-337 ◽  
Author(s):  
E Wang ◽  
R K Cross ◽  
P W Choppin

Previous studies (Holmes, K.V., and P.W. Choppin. J. Exp. Med. 124:501-520; J. Cell Biol. 39:526-543) showed that infection of baby hamster kidney (BHK21-F) cells with the parainfluenza virus SV5 causes extensive cell fusion, that nuclei migrate in the syncytial cytoplasm and align in tightly-packed rows, and that microtubules are involved in nuclear movement and alignment. The role of microtubules, 10-nm filaments, and actin-containing microfilaments in this process has been investigated by immunofluorescence microscopy using specific antisera, time-lapse cinematography, and electron microscopy. During cell fusion, micro tubules and 10-nm filaments from many cells form large bundles which are localized between rows of nuclei. No organized bundles of actin fibers were detected in these areas, although actin fibers were observed in regions away from the aligned nuclei. Although colchicine disrupts microtubules and inhibits nuclear movement, cytochalasin B (CB; 20-50 microgram/ml) does not inhibit cell fusion or nuclear movement. However, CB alters the shape of the syncytium, resulting in long filamentous processes extending from a central region. When these processes from neighboring cells make contact, fusion occurs, and nuclei migrate through the channels which are formed. Electron and immunofluorescence microscopy reveal bundles of microtubules and 10-nm filaments in parallel arrays within these processes, but no bundles of microfilaments were detected. The effect of CB on the structural integrity of microfilaments at this high concentration (20 microgram/ml) was demonstrated by the disappearance of filaments interacting with heavy meromyosin. Cycloheximide (20 microgram/ml) inhibits protein synthesis but does not affect cell fusion, the formation of microtubules and 10-nm filament bundles, or nuclear migration and alignment; thus, continued protein synthesis is not required. The association of microtubules and 10-nm filaments with nuclear migration and alignment suggests that microtubules and 10-nm filaments are two components in a system which serves both cytoskeletal and force-generating functions in intracellular movement and position of nuclei.

2002 ◽  
Vol 115 (8) ◽  
pp. 1717-1732 ◽  
Author(s):  
Reinhard Windoffer ◽  
Monika Borchert-Stuhlträger ◽  
Rudolf E. Leube

Desmosomes are prominent cell adhesion structures that are major stabilizing elements, together with the attached cytoskeletal intermediate filament network, of the cytokeratin type in epithelial tissues. To examine desmosome dynamics in tightly coupled cells and in situations of decreased adhesion, fluorescent desmosomal cadherin desmocollin 2a (Dsc2a) chimeras were stably expressed in human hepatocellular carcinoma-derived PLC cells (clone PDc-13) and in Madin-Darby canine kidney cells (clone MDc-2) for the continuous monitoring of desmosomes in living cells. The hybrid polypeptides integrated specifically and without disturbance into normal-appearing desmosomes that occurred in association with typical cytokeratin filament bundles. Tracking of labeled adhesion sites throughout the cell cycle by time-lapse fluorescence microscopy revealed that they were immobile and that they maintained their structural integrity for long periods of time. Time-space diagrams further showed that desmosomal positioning was tightly controlled, even during pronounced cell shape changes, although the desmosomal arrays extended and contracted, suggesting that they were interconnected by a flexible system with intrinsic elasticity. Double-fluorescence microscopy detecting Dsc2a chimeras together with fluorescent cytokeratin 18 chimeras revealed the association and synchronous movement of labeled desmosomes and fluorescent cytokeratin filaments. Only a minor destabilization of desmosomes was observed during mitosis, demonstrated by increased diffuse plasma membrane fluorescence and the fusion of desmosomes into larger structures. Desmosomes did not disappear completely at any time in any cell, and residual cytokeratin filaments remained in association with adhesion sites throughout cell division. On the other hand, a rapid loss of desmosomes was observed upon calcium depletion, with irreversible uptake of some desmosomal particles. Simultaneously, diffusely distributed desmosomal cadherins were detected in the plasma membrane that retained the competence to nucleate the reformation of desmosomes after the cells were returned to a standard calcium-containing medium. To examine the molecular stability of desmosomes, exchange rates of fluorescent chimeras were determined by fluorescence recovery after photobleaching, thereby identifying considerable Dsc2a turnover with different rates of fluorescence recovery for PDc-13 cells (36±17% recovery after 30 minutes) and MDc-2 cells (60±20% recovery after 30 minutes). Taken together, our observations suggest that desmosomes are pliable structures capable of fine adjustment to functional demands despite their overall structural stability and relative immobility.


1970 ◽  
Vol 16 (10) ◽  
pp. 959-963 ◽  
Author(s):  
R. W. Detroy ◽  
C. W. Hesseltine

The effect of two inhibitors on the formation of aflatoxin B1 synthetase activity in strain NRRL 2999 Aspergillus parasiticus has been studied. Aflatoxin B1 synthesizing activity was measured in vivo by incorporation of the 14C-methionine methyl group into aflatoxin B1. Cycloheximide at a concentration of 150 μg/ml blocks protein synthesis completely. If addition of cycloheximide is made before B1 synthetase appears, no activity accumulates; if added during accumulation, activity is frozen at the level reached at the time of addition. The cycloheximide effect is reversible since morphogenesis, total protein synthesis, and aflatoxin B1 synthetase activity all resume after removal of the inhibitor.DL-p-Fluorophenylalanine partially inhibits aflatoxin B1 synthesis in vivo; however, its effect upon macromolecular synthesis is incomplete even at high concentration levels. Once formed, the aflatoxin synthetase appears to maintain B1 synthesis when further protein synthesis is blocked; i.e., it is not rapidly degraded.


1979 ◽  
Vol 183 (1) ◽  
pp. 73-81 ◽  
Author(s):  
R Felix ◽  
H Fleisch

1. Dichloromethanediphosphonate and to a lesser degree 1-hydroxyethane-1,1-diphosphonate, two compounds characterized by a P-C-P bond, increased the alkaline phosphatase activity of cultured rat calvaria cells up to 30 times in a dose-dependent fashion. 2. Both diphosphonates also slightly inhibited the protein synthesis in these cells. 3. Thymidine, an inhibitor of cell division, did not inhibit the induction of the enzyme, indicating that the increase in enzyme activity was not due to the formation of a specific population of cells with high alkaline phosphatase activity. 4. The effect on alkaline phosphatase was suppressed by the addition of cycloheximide, an inhibitor of protein synthesis. 5. After subculturing the stimulated cells in medium without diphosphonates, the enzyme activity fell almost to the control value. 6. Bovine parathyrin diminished the enzyme activity of the control cells and the cells treated with dichloromethanediphosphonate; however, at high concentration the effect of parathyrin was greater on the diphosphonate-treated cells than on the control cells. 7. The electrophoretic behaviour, heat inactivation, inhibition by bromotetramisole or by phenylalanine, and the Km value of the induced enzyme were identical with that of the control enzyme.


1995 ◽  
Vol 73 (S1) ◽  
pp. 364-368 ◽  
Author(s):  
Takashi Kamada ◽  
Shigeru Tanabe

Coprinus cinereus exhibits conspicuous nuclear movement and precise nuclear positioning during its life cycle. Examples include transhyphal migration of nuclei in compatible mating giving rise to a dikaryon, nuclear positioning relative to the hyphal apex in the dikaryon, the close spacing in interphase and conjugate division of the two nuclei in the dikaryon, and the migration of nuclei from the basidium into developing spores. We have investigated the roles of the cytoskeleton in these processes using cytoskeleton mutants as well as fluorescence microscopy. Some of the α1- and β1-tubulin mutations examined blocked nuclear migration in dikaryosis and disturbed nuclear pairing in the dikaryon, demonstrating that microtubules are involved in these processes. The same mutations, however, did not affect the positioning of nuclei in interphase nor in conjugate division in the dikaryon, nor the migration of nuclei into the developing spores. Immunofluorescence microscopy revealed that these mutations inhibit the formation of asters of the mitotic apparatus in conjugate division, providing evidence against direct involvement of astral microtubules in nuclear movement during conjugate division. Actin was concentrated in hyphal regions where the nuclei sit in early phases of conjugate division, suggesting the involvement of actin in conjugate division. Key words: Coprinus cinereus, dikaryon, nuclear movement, microtubules, aster, actin.


Development ◽  
2021 ◽  
Vol 148 (10) ◽  
Author(s):  
Jun Yu ◽  
Marilyn Janice Oentaryo ◽  
Chi Wai Lee

ABSTRACT Upon the stimulation of extracellular cues, a significant number of proteins are synthesized distally along the axon. Although local protein synthesis is crucial for various stages throughout neuronal development, its involvement in presynaptic differentiation at developing neuromuscular junctions remains unknown. By using axon severing and microfluidic chamber assays, we first showed that treatment of a protein synthesis inhibitor, cycloheximide, inhibits agrin-induced presynaptic differentiation in cultured Xenopus spinal neurons. Newly synthesized proteins are prominently detected, as revealed by the staining of click-reactive cell-permeable puromycin analog O-propargyl-puromycin, at agrin bead-neurite contacts involving the mTOR/4E-BP1 pathway. Next, live-cell time-lapse imaging demonstrated the local capturing and immobilization of ribonucleoprotein granules upon agrin bead stimulation. Given that our recent study reported the roles of membrane-type 1 matrix metalloproteinase (MT1-MMP) in agrin-induced presynaptic differentiation, here we further showed that MT1-MMP mRNA is spatially enriched and locally translated at sites induced by agrin beads. Taken together, this study reveals an essential role for axonal MT1-MMP translation, on top of the well-recognized long-range transport of MT1-MMP proteins synthesized from neuronal cell bodies, in mediating agrin-induced presynaptic differentiation.


2020 ◽  
Author(s):  
Daniel León-Periñán ◽  
Alfonso Fernández-Álvarez

ABSTRACTAs one of the main events occurring during meiotic prophase, the dynamics of meiotic chromosome movement is not yet well understood. Currently, although it is well-established that chromosome movement takes an important role during meiotic recombination promoting the pairing between homologous chromosomes and avoiding excessive chromosome associations, it is mostly unclear whether those movements follow a particular fixed pattern, or are stochastically distributed. Using Schizosaccharomyces pombe as a model organism, which exhibits dramatic meiotic nuclear oscillations, we have developed a computationally automatized statistical analysis of three-dimensional time-lapse fluorescence information in order to characterize nuclear trajectories and morphological patterns during meiotic prophase. This approach allowed us to identify a patterned oscillatory microvariation during the meiotic nuclear motion. Additionally, we showed evidence suggesting that this unexpected oscillatory motif might be due to the detection of persistent DNA damage during the nuclear movement, supporting how the nucleus also regulates its oscillations. Our computationally automatized tool will be useful for the identification of new patterns of nuclear oscillations during gametogenesis.


1997 ◽  
Vol 30 (5/6) ◽  
pp. 593-599 ◽  
Author(s):  
Hiroshi Kogo ◽  
Mariko Shioya ◽  
Yukiko Takahashi ◽  
Toyoshi Fujimoto

2020 ◽  
Vol 114 (3) ◽  
pp. e44
Author(s):  
Alice J. Shapiro ◽  
Lindsay Kroener ◽  
Nicholas J. Jackson ◽  
Zachary Haimowitz ◽  
Alin Lina Akopians ◽  
...  

Author(s):  
Michele Andreani

The presence of hydrogen stratification in a NPP containment in the case of a severe accident is a source of concern, as pockets of the gas in high concentration could lead to a deflagration or detonation risk, which might challenge the containment structural integrity. These issues, as well as the capability of various computer codes to predict the evolution of a representative accident, are addressed in the coordinated projects ERCOSAM of the 7th EURATOM FWP and the project SAMARA sponsored by ROSATOM. The projects aim to establish whether in a test sequence representative of a severe accident in a LWR hydrogen stratification can be established during the initial transient following a loss of coolant accident (LOCA) and whether and how this stratification can be broken down by the operation of Severe Accident Management systems (SAMs): sprays, coolers and Passive Auto-catalytic Recombiners (PARs). Experiments with helium (as simulant of hydrogen) have been performed at “small scale” in TOSQAN (IRSN, Saclay), and “medium scale” in the MISTRA (CEA, Saclay), PANDA (PSI, Villigen) and SPOT ((JSC “Afrikantov OKBM”, Nizhny Novgorod) facilities. The present paper presents the analysis of the initial transient of some tests in the PANDA, TOSQAN and SPOT facilities using the GOTHIC computer code. The work therefore addresses the capability of the code and a relatively coarse mesh to simulate the pressurisation and build-up of steam and helium stratification for conditions representative of a postulated severe accident scenario, properly scaled to the various facilities. The prediction of the pressurisation is excellent, and the position of the gas concentration stratification front at the end of the steam and helium releases is generally well captured.


2002 ◽  
Vol 13 (4) ◽  
pp. 1366-1380 ◽  
Author(s):  
Dominic Hoepfner ◽  
Florian Schaerer ◽  
Arndt Brachat ◽  
Achim Wach ◽  
Peter Philippsen

Nuclear migration and positioning in Saccharomyces cerevisiae depend on long astral microtubules emanating from the spindle pole bodies (SPBs). Herein, we show by in vivo fluorescence microscopy that cells lacking Spc72, the SPB receptor of the cytoplasmic γ-tubulin complex, can only generate very short (<1 μm) and unstable astral microtubules. Consequently, nuclear migration to the bud neck and orientation of the anaphase spindle along the mother-bud axis are absent in these cells. However,SPC72 deletion is not lethal because elongated but misaligned spindles can frequently reorient in mother cells, permitting delayed but otherwise correct nuclear segregation. High-resolution time-lapse sequences revealed that this spindle reorientation was most likely accomplished by cortex interactions of the very short astral microtubules. In addition, a set of double mutants suggested that reorientation was dependent on the SPB outer plaque and the astral microtubule motor function of Kar3 but not Kip2/Kip3/Dhc1, or the cortex components Kar9/Num1. Our observations suggest that Spc72 is required for astral microtubule formation at the SPB half-bridge and for stabilization of astral microtubules at the SPB outer plaque. In addition, our data exclude involvement of Spc72 in spindle formation and elongation functions.


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