Observations préliminaires sur l'organisation du cytosquelette des cellules végétales. Mise en évidence d'un “réseau microtrabéculaire”

1983 ◽  
Vol 61 (5) ◽  
pp. 1467-1475 ◽  
Author(s):  
Jean-Pierre Arsanto
Keyword(s):  
Actin Filaments ◽  
Close Relationships ◽  
Plant Cells ◽  
Ground Substance ◽  
Animal Cells ◽  
Electron Microscopic ◽  
Parenchyma Cells ◽  
Vascular Parenchyma ◽  
Cytoplasmic Ground Substance ◽  
Cellular Components

Electron microscopic observations of particularly favourable sections of pericycle and vascular parenchyma cells fixed with glutaraldéhyde have revealed the existence of a network of exceedingly fine filaments in the cytoplasmic ground substance of plant cells. This highly intricated structure to which polysomes seem to be attached interconnects the cytoskeletal fibers and the various other cellular components. It corresponds evidently to the "microtrabecular lattice" described in animal cells. Moreover, this report points out that microfilaments, which are 6- to 8-nm putative actin filaments, contract with microtubules or sheets of agranular reticulum, to form privileged close relationships whose functional significance is discussed.

scholarly journals Ultrastructural immunocytochemical localization of myosin in cultured fibroblastic cells.

1981 ◽  
Vol 29 (11) ◽  
pp. 1289-1301 ◽  
Author(s):  
M C Willingham ◽  
S S Yamada ◽  
P J Bechtel ◽  
A V Rutherford ◽  
I H Pastan
Keyword(s):  
Cell Function ◽  
Ground Substance ◽  
Nonmuscle Myosin ◽  
Electron Microscopic ◽  
Electron Microscopic Immunocytochemistry ◽  
Localization Method ◽  
Preferential Localization ◽  
Cytoplasmic Ground Substance ◽  
Fibroblastic Cells ◽  
Electron Microscopic Localization

Nonmuscle myosin in the cytoplasm of cultured fibroblastic cells has been localized using light and electron microscopic immunocytochemistry. Antibodies to purified fibroblast myosin were produced in goat and rabbit and purified by affinity chromatography. Light microscopic immunofluorescence localization showed patterns similar to those previously published. Electron microscopic localization using the ethyldimethyl aminopropyl carbodiimide-glutaraldehyde-saponin (EGS) fixation-permeabilization procedure and the ferritin bridge localization method produced quantifiable localization in intracellular sites with well-preserved ultrastructural morphology. Myosin was found to be a major component of the cytosol. It was distributed diffusely with no preferential localization on membranous organelles. Myosin was found to be slightly concentrated on the surface of microfilament-containing structures, including the subplasmalemmal microfilament mat and stress fibers, occasionally with an interrupted periodicity. However, no myosin was found in surface ruffles or microvilli. Morphometric quantitation showed that the majority of the cell's myosin was in the cytosol. This location is compatible with myosin being a component of the microtrabecular lattice of the cytoplasmic ground substance. The concentration of myosin in association with microfilaments was only twice that of the cytosol. This interpretation must be somewhat tempered by the possibility that some myosin bound to tightly packed actin may be inaccessible. The significance of this distribution of myosin in cell function is discussed.

Organisation in the Structure of the Cytoplasmic Ground Substance

1978 ◽  
Vol 36 (3) ◽  
pp. 627-639
Author(s):  
K.R. Porter
Keyword(s):  
Endoplasmic Reticulum ◽  
Golgi Complex ◽  
Random Distribution ◽  
Ground Substance ◽  
The Matrix ◽  
Cell Processes ◽  
Cytoplasmic Ground Substance

Most types of cells are known from their structure and overall form to possess a characteristic organization. In some instances this is evident in the non-random disposition of organelles and such system subunits as cisternae of the endoplasmic reticulum or the Golgi complex. In others it appears in the distribution and orientation of cytoplasmic fibrils. And in yet others the organization finds expression in the non-random distribution and orientation of microtubules, especially as found in highly anisometric cells and cell processes. The impression is unavoidable that in none of these cases is the organization achieved without the involvement of the cytoplasmic ground substance (CGS) or matrix. This impression is based on the fact that a matrix is present and that in all instances these formed structures, whether membranelimited or filamentous, are suspended in it. In some well-known instances, as in arrays of microtubules which make up axonemes and axostyles, the matrix resolves itself into bridges (and spokes) between the microtubules, bridges which are in some cases very regularly disposed and uniform in size (Mcintosh, 1973; Bloodgood and Miller, 1974; Warner and Satir, 1974).

Freeze-Fracture Replication in the Ultrastructure of Blue-Green Algae

1967 ◽  
Vol 25 ◽  
pp. 74-75
Author(s):  
L. V. Leak
Keyword(s):  
Cell Wall ◽  
Electron Microscope ◽  
Green Algae ◽  
Three Dimensional ◽  
Freeze Fracture ◽  
Electron Microscopic ◽  
Photosynthetic Membranes ◽  
Blue Green Algae ◽  
Cell Biol ◽  
Cellular Components

Electron microscopic observations of freeze-fracture replicas of Anabaena cells obtained by the procedures described by Bullivant and Ames (J. Cell Biol., 1966) indicate that the frozen cells are fractured in many different planes. This fracturing or cleaving along various planes allows one to gain a three dimensional relation of the cellular components as a result of such a manipulation. When replicas that are obtained by the freeze-fracture method are observed in the electron microscope, cross fractures of the cell wall and membranes that comprise the photosynthetic lamellae are apparent as demonstrated in Figures 1 & 2.A large portion of the Anabaena cell is composed of undulating layers of cytoplasm that are bounded by unit membranes that comprise the photosynthetic membranes. The adjoining layers of cytoplasm are closely apposed to each other to form the photosynthetic lamellae. Occassionally the adjacent layers of cytoplasm are separated by an interspace that may vary in widths of up to several 100 mu to form intralamellar vesicles.

Confocal microscopy of the cytoskeleton in living plant cells following microinjection of fluorescent probes

1993 ◽  
Vol 51 ◽  
pp. 130-131
Author(s):  
Ann Cleary
Keyword(s):  
Cell Division ◽  
Fluorescent Probes ◽  
Actin Filaments ◽  
Intracellular Transport ◽  
Cell Structure ◽  
Plant Cells ◽  
Cell Plate ◽  
Cell Cortex ◽  
Living Plant ◽  
Rhodamine Phalloidin

Microinjection of fluorescent probes into living plant cells reveals new aspects of cell structure and function. Microtubules and actin filaments are dynamic components of the cytoskeleton and are involved in cell growth, division and intracellular transport. To date, cytoskeletal probes used in microinjection studies have included rhodamine-phalloidin for labelling actin filaments and fluorescently labelled animal tubulin for incorporation into microtubules. From a recent study of Tradescantia stamen hair cells it appears that actin may have a role in defining the plane of cell division. Unlike microtubules, actin is present in the cell cortex and delimits the division site throughout mitosis. Herein, I shall describe actin, its arrangement and putative role in cell plate placement, in another material, living cells of Tradescantia leaf epidermis.The epidermis is peeled from the abaxial surface of young leaves usually without disruption to cytoplasmic streaming or cell division. The peel is stuck to the base of a well slide using 0.1% polyethylenimine and bathed in a solution of 1% mannitol +/− 1 mM probenecid.

scholarly journals Mechanism of the formation of contractile ring in dividing cultured animal cells. II. Cortical movement of microinjected actin filaments.

1990 ◽  
Vol 111 (5) ◽  
pp. 1905-1911 ◽  
Author(s):  
L G Cao ◽  
Y L Wang
Keyword(s):  
Actin Filaments ◽  
Average Rate ◽  
Rat Kidney ◽  
Equatorial Region ◽  
Cell Cortex ◽  
Polar Regions ◽  
Cortical Actin ◽  
Animal Cells ◽  
Contractile Ring ◽  
Directional Movement

The contractile ring in dividing animal cells is formed primarily through the reorganization of existing actin filaments (Cao, L.-G., and Y.-L. Wang. 1990. J. Cell Biol. 110:1089-1096), but it is not clear whether the process involves a random recruitment of diffusible actin filaments from the cytoplasm, or a directional movement of cortically associated filaments toward the equator. We have studied this question by observing the distribution of actin filaments that have been labeled with fluorescent phalloidin and microinjected into dividing normal rat kidney (NRK) cells. The labeled filaments are present primarily in the cytoplasm during prometaphase and early metaphase, but become associated extensively with the cell cortex 10-15 min before the onset of anaphase. This process is manifested both as an increase in cortical fluorescence intensity and as movements of discrete aggregates of actin filaments toward the cortex. The concentration of actin fluorescence in the equatorial region, accompanied by a decrease of fluorescence in polar regions, is detected 2-3 min after the onset of anaphase. By directly tracing the distribution of aggregates of labeled actin filaments, we are able to detect, during anaphase and telophase, movements of cortical actin filaments toward the equator at an average rate of 1.0 micron/min. Our results, combined with previous observations, suggest that the organization of actin filaments during cytokinesis probably involves an association of cytoplasmic filaments with the cortex, a movement of cortical filaments toward the cleavage furrow, and a dissociation of filaments from the equatorial cortex.

Cysts of unknown etiology in marine fishes of the Northwest Atlantic and Gulf of Mexico

1987 ◽  
Vol 65 (2) ◽  
pp. 296-303 ◽  
Author(s):  
Sharon A. MacLean ◽  
Carol M. Morrison ◽  
Robert A. Murchelano ◽  
Sherie Everline ◽  
Joyce J. Evans
Keyword(s):  
Unknown Etiology ◽  
Ground Substance ◽  
Structural Components ◽  
Electron Microscopic ◽  
Sand Lance ◽  
Atlantic Mackerel ◽  
The Core ◽  
Sudan Black B ◽  
Silver Hake ◽  
Feulgen Technique

Results of light and electron microscopic examinations of cysts of unknown etiology (CUEs) occurring in the gills of Atlantic mackerel, red hake, white hake, cod, haddock, and silver hake are presented. CUEs were found also in gills and viscera of winter flounder, Atlantic croaker, spot, windowpane flounder, and sand lance. CUEs measured 150–400 μm in diameter and consisted of an external fibrous cuticle, usually a thick median band, and a central core that frequently contained eosinophilic vesicles. Structures resembling mitochondria were found in the band and in vesicles of the core, but no other organelles were apparent. Cytochemical staining and ultramicroscopy revealed aggregates of glycogen in the core ground substance; no structural components were stained with Sudan black B or by the Feulgen technique. Extensive encapsulation of CUEs by fibroblasts was typical. Of 717 mackerel examined, 76.8% had CUEs in the gills; numbers ranged from 1 to 353 per fish. The prevalence and intensity of occurrence of CUEs increased with the age of the mackerel.

scholarly journals FIXATION OF NEURAL TISSUES FOR ELECTRON MICROSCOPY BY PERFUSION WITH SOLUTIONS OF OSMIUM TETROXIDE

1962 ◽  
Vol 12 (2) ◽  
pp. 385-410 ◽  
Author(s):  
Sanford L. Palay ◽  
S. M. McGee-Russell ◽  
Spencer Gordon ◽  
Mary A. Grillo
Keyword(s):  
Electron Microscopy ◽  
Nervous System ◽  
Osmium Tetroxide ◽  
Microscopic Level ◽  
Electron Microscopic Level ◽  
Electron Microscopic ◽  
Vascular Perfusion ◽  
Neural Tissues ◽  
Structural Relations ◽  
Cellular Components

This paper describes in detail a method for obtaining nearly uniform fixation of the nervous system by vascular perfusion with solutions of osmium tetroxide. Criteria are given for evaluating the degree of success achieved in the preservation of all the cellular components of the nervous system. The method permits analysis of the structural relations between cells at the electron microscopic level to an extent that has not been possible heretofore.

Progression of partial experimental injury to peripheral nerve

1975 ◽  
Vol 42 (1) ◽  
pp. 15-22 ◽  
Author(s):  
Alan R. Hudson ◽  
David G. Kline
Keyword(s):  
Recovery Of Function ◽  
Electron Microscopic Examination ◽  
Ground Substance ◽  
Electron Microscopic ◽  
Early Recovery ◽  
Content Type ◽  
Proximal Stimulus ◽  
Late Recovery ◽  
Fine Print ◽  
Experimental Injury

✓ Biopsies from partially lacerated nerves were taken at the sites of proximal stimulus, laceration, and distal recording, and from stimuli and recording sites of control nerves. Electron microscopic examination of the partially lacerated major fasciculus revealed three zones of injury. The laceration zone showed neurotemetic changes, the adjacent or intermediate zone, partial degeneration, and the zone most peripheral to the laceration, changes in ground substance. Progression of the original injury is apparently due to ongoing changes in the intermediate and peripheral zones while much of the relative early recovery is due to reversal of changes in these zones. Regeneration through the laceration or neurotemetic zone is limited but does account for a small amount of late recovery of function.

scholarly journals Laser Scanning Confocal Microcopy for Arabidopsis Epidermal, Mesophyll, and Vascular Parenchyma Cells

BIO-PROTOCOL ◽  
2017 ◽  
Vol 7 (5) ◽  
Author(s):  
Christian Elowsky ◽  
Yashitola Wamboldt ◽  
Sally Mackenzie
Keyword(s):  
Laser Scanning ◽  
Parenchyma Cells ◽  
Vascular Parenchyma

Experimental Investigation of Effects of Extrusion Pressure on Cell Growth of Bioprinted Algae Cells in Green Bioprinting

2020 ◽  
Author(s):  
Laura Jerpseth ◽  
Ketan Thakare ◽  
Zhijian Pei ◽  
Hongmin Qin
Keyword(s):  
Cell Growth ◽  
Cell Count ◽  
Plant Cells ◽  
Extrusion Pressure ◽  
Layer By Layer ◽  
Animal Cells ◽  
Physical Damage ◽  
The Third ◽  
Cell Counts ◽  
The Difference

Abstract In bioprinting, biomaterials are deposited layer-by-layer to fabricate structures. Bioprinting has many potential applications in drug screening, tissue engineering, and regenerative medicine. Both animal cells and plant cells can be used to synthesize bioinks. Green bioprinting uses bioinks that have been synthesized using plant cells. Constructs fabricated via green bioprinting contain immobilized plant cells, with these cells arranged at desired locations. The constructs provide scaffolds for cell growth. Printing parameters affecting the growth of cells in green bioprinted constructs include print speed, needle diameter, extrusion temperature, and extrusion pressure. This paper reports a study to examine effects of extrusion pressure on cell growth (measured by cell count) in bioprinted constructs, using bioink containing Chlamydomonas reinhardtii algae cells. Three levels of extrusion pressure were used: 3, 5, and 7 bar. Cell counts in the bioprinted constructs were measured on the third and sixth days after bioprinting. It was found that, as extrusion pressure increased, cell count decreased on both the third and sixth days after bioprinting. Furthermore, the difference in cell counts between the third and the sixth days decreased as extrusion pressure increased. These trends suggest that increasing extrusion pressure during green bioprinting negatively affects cell growth. A possible reason for these trends is physical damage to or death of cells in the bioprinted constructs when extrusion pressure became higher.

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