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1. |
A quantitative comparison of cellular motile systems |
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Cell Motility,
Volume 4,
Issue 1,
1984,
Page 1-5
R. Bruce Nicklas,
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摘要:
AbstractCellular motile systems as diverse as muscle and the mitotic spindle have been compared by their specific power output: the maximum power they develop per unit of engine volume. Striated muscles and flagella have high specific output; their performance is comparable to that of typical automobile engines. The cytokinetic furrow and the mitotic spindle have very much lower specific power output. The furrow's output is 7,000 times lower than muscle and the spindle's is 300,000 times lower. Different macromolecules have been used to generate power in systems with similar output (muscles and flagella) and, conversely, the same macromolecular motor has been used in systems with very different output (muscles and cytokinetic furrows). The common feature amid this diversity is adaptation to a particular biological role, which specific power output reflects very well. High values are found where a powerful, compact engine should be advantageous, while low values are found where precision, not power, matters most.
ISSN:0271-6585
DOI:10.1002/cm.970040102
出版商:Wiley Subscription Services, Inc., A Wiley Company
年代:1984
数据来源: WILEY
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2. |
Rheological properties of living cytoplasm: A preliminary investigation of squid axoplasm (Loligo pealei) |
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Cell Motility,
Volume 4,
Issue 1,
1984,
Page 7-23
Masahiko Sato,
Terence Z. Wong,
Douglas T. Brown,
Robert D. Allen,
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摘要:
AbstractA magnetic sphere viscoelastometer has been developed to peform rheological experiments in living axoplasm of Loligo pealei. The technique includes the use of a calibrated magnetic sphere viscoelastometer on surgically implanted ferro‐magnetic spheres in intact squid giant axons. The axoplasm was discerned to be “living” by the biological criterion of tubulovesicular organelle motility, which was observed before and after experimentation. From these in vivo experiments, new structural characteristics of the axoplasm have been identified. First, analysis of magnetic sphere trajectories has shown the axoplasm to be a complex viscoelastic fluid. Directional experimentation showed that this material is structurally anisotropic, with a greater elastic modulus in the direction parallel to the axon long axis. Second, both magnetic sphere and in vivo capillary experiments suggested that the axoplasm is tenaciously anchored to the axolemma. Third, it was found that axoplasm could be modelled as a linear viscoelastic material in the low shear rate range of 0.0001 to 0.004 s−1. The simplest mechanical model incorporating the discovered properties of the material in this range is Burger'
ISSN:0271-6585
DOI:10.1002/cm.970040103
出版商:Wiley Subscription Services, Inc., A Wiley Company
年代:1984
数据来源: WILEY
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3. |
Observations of exocytosis in fucus vesiculosus gametes using video‐enhanced light microscopy: A video report |
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Cell Motility,
Volume 4,
Issue 1,
1984,
Page 25-27
Nina Strömgren Allen,
Susan H. Brawley,
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ISSN:0271-6585
DOI:10.1002/cm.970040104
出版商:Wiley Subscription Services, Inc., A Wiley Company
年代:1984
数据来源: WILEY
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4. |
Microfilament rearrangements during fibroblast‐induced contraction of three‐dimensional hydrated collagen gels |
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Cell Motility,
Volume 4,
Issue 1,
1984,
Page 29-40
Jamila M. A. Farsi,
Jane E. Aubin,
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摘要:
AbstractIn vitro models have been developed recently to study the ability of fibroblasts to generate tensile force within collagen gels. The present study was initiated to assess the role of the cytoskeleton in the cell shape changes and force generation in one such model system. Porcine periodontal ligament fibroblasts (PPLF) were cultured within three‐dimensional collagen gels attached to glass coverslips. Fluorescence microscopy, using nitrobenzooxadizole (NBD)‐phallacidin labeling for microfilaments and tubulin antibody staining for microtubules, was combined with phase and Nomarski optics to determine the intra‐ and extracellular architecture of the cells and collagen fibers. Samples were observed from 30 minutes to 24 hours after initiation of cell attachment. During attachment and spreading, NBD‐phallacidin staining changed dramatically until large microfilament bundles became prominent. Collagen fiber alignment, compaction, and finally tearing from the coverslip occurred during this time. After release of tension, microfilament bundles were no longer evident. The change in microtubule distribution during these processes was less dramatic, appearing to follow the change in cell shape. These results indicate that microfilaments play an essential role in generating force to align and compact collagen, while microtubules may have a secondary ro
ISSN:0271-6585
DOI:10.1002/cm.970040105
出版商:Wiley Subscription Services, Inc., A Wiley Company
年代:1984
数据来源: WILEY
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5. |
An unusual mechanism of cell contraction: Leptodiscinae Dinoflagellates |
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Cell Motility,
Volume 4,
Issue 1,
1984,
Page 41-55
Jean Cachon,
Monique Cachon,
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摘要:
AbstractThe Leptodiscinae, a group of marine Dinoflagellates, are good material for the study of contraction though they cannot be collected in abundance. Their cell bodies are flattened anteroposteriorly (Leptodiscus, Leptophyllus, and Leptospathium) and are able to contract suddenly when the surrounding water is disturbed.Electron microscopical observations have shown that the structures responsible for the contraction consist of a layer of parallel filaments located beneath the cell membrane of some specialized parts of the body. These filaments seem to be nonactin (NAF) because of their diameter (2.5–3 nm) and because they are not decorated by heavy meromyosin (HMM). They appear helically coiled and doubly twisted, and form tubular structures when contracte
ISSN:0271-6585
DOI:10.1002/cm.970040106
出版商:Wiley Subscription Services, Inc., A Wiley Company
年代:1984
数据来源: WILEY
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6. |
Induction of shape transformation in sea urchin coelomocytes by the calcium ionophore A23187 |
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Cell Motility,
Volume 4,
Issue 1,
1984,
Page 57-71
Hilary A. Hyatt,
Michael S. Shure,
David A. Begg,
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摘要:
AbstractWe have investigated the ability of the Ca+ +ionophore A23187 to induce the transformation of petaloid sea urchin coleomocytes to the filopodial form. The response of individual cells to different media was observed with time‐lapse phasecontrast video microscopy. In the presence of 1 mM CaCl2, isotonic medium containing 1–5 μM A23187 produces a similar shape transformation to that caused by hypotonic shock. Higher concentrations of ionophore (10–20 μM) induce the formation of filopodia that are thinner and less rigid than those generated by hypotonic shock or low doses of ionophore. A23187 also induces shape transformation in highly flattened cells that do not respond fully to hypotonic shock. The induction of cytoplasmic alkalinization by NH4Cl, methylamine‐HCl, or the Na+ionophore monensin does not induce shape transformation, suggesting that increased intracellular pH is not the stimulus for this process. Ultrastructural changes in cytoskeletal organization were examined in negatively stained detergent‐extracted cells. Low doses of ionophore produce filopodia that are indistin‐guishable from those of hypotonically shocked cells, with actin filament bundles that are straight and cohesive along their entire length. High concentrations of ionophore produce filopodia with filament bundles that branch repeatedly and splay apart near their tips, forming loops and irregular curves. These results suggest that an increase in intracellular free Ca+ +concentration acts as the trigger that stimulates coelomocyte shape transformation, but that abnormally high concentrations of intracellular Ca+ +, produced by high doses of ionophore, interfere with actin fila
ISSN:0271-6585
DOI:10.1002/cm.970040107
出版商:Wiley Subscription Services, Inc., A Wiley Company
年代:1984
数据来源: WILEY
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7. |
Announcement |
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Cell Motility,
Volume 4,
Issue 1,
1984,
Page 76-76
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ISSN:0271-6585
DOI:10.1002/cm.970040108
出版商:Wiley Subscription Services, Inc., A Wiley Company
年代:1984
数据来源: WILEY
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8. |
Masthead |
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Cell Motility,
Volume 4,
Issue 1,
1984,
Page -
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PDF (82KB)
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ISSN:0271-6585
DOI:10.1002/cm.970040101
出版商:Wiley Subscription Services, Inc., A Wiley Company
年代:1984
数据来源: WILEY
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