scholarly journals Dynamic continuity of cytoplasmic and membrane compartments between plant cells.

1988 ◽  
Vol 106 (3) ◽  
pp. 715-721 ◽  
Author(s):  
O Baron-Epel ◽  
D Hernandez ◽  
L W Jiang ◽  
S Meiners ◽  
M Schindler
Keyword(s):  
Cell Communication ◽  
Plant Cells ◽  
Tumor Promoter ◽  
Ionophore A23187 ◽  
Animal Cells ◽  
Root Cells ◽  
Dynamic Membrane ◽  
Membrane Compartments ◽  
Intercellular Movement ◽  
Soybean Cell

Fluorescence photobleaching was employed to examine the intercellular movement of fluorescein and carboxyfluorescein between contiguous soybean root cells (SB-1 cell line) growing in tissue culture. Results of these experiments demonstrated movement of these fluorescent probes between cytoplasmic (symplastic) compartments. This symplastic transport was inhibited with Ca2+ in the presence of ionophore A23187, and also with the tumor promoter 12-O-tetradecanoyl-phorbol-13-acetate (TPA). Both of these agents have previously been demonstrated to inhibit gap junction-mediated cell-cell communication in animal cells. In a companion experiment, a fluorescent phospholipid analogue, N-4-nitrobenzo-2-oxa-1,3-diazole phosphatidylcholine (NBD-PC), was incorporated into soybean cell membranes to examine whether dynamic membrane continuity existed between contacting cells, a transport route not existing between animal cells. Photobleaching single soybean cells growing in a filamentous strand demonstrated that phospholipid did exchange between contiguous cells.

scholarly journals Plasmodesmata-dependent intercellular movement of bacterial effectors

2020 ◽  
Author(s):  
Zhongpeng Li ◽  
Haris Variz ◽  
Yani Chen ◽  
Su-Ling Liu ◽  
Kyaw Aung
Keyword(s):  
Pseudomonas Syringae ◽  
Cell Communication ◽  
Plant Cells ◽  
Host Cells ◽  
Host Immune Responses ◽  
Molecular Weights ◽  
Amino Acid Peptide ◽  
Pathogen Effectors ◽  
Intercellular Movement ◽  
Bacterial Effectors

AbstractPathogenic microorganisms deliver protein effectors into host cells to suppress host immune responses. Recent findings reveal that phytopathogens manipulate the function of plant cell-to-cell communication channels plasmodesmata (PD) to promote diseases. Several bacterial and filamentous pathogen effectors have been shown to regulate PD in their host cells. A few effectors of filamentous pathogens have been reported to move from the infected cells to neighboring plant cells through PD; however, it is unclear whether bacterial effectors can traffic through PD in plants. In this study, we systemically determined the intercellular movement of Pseudomonas syringae pv. tomato (Pst) DC3000 effectors between adjoining plant cells in Nicotiana benthamiana. We observed that at least 16 Pst DC3000 effectors move from transformed cells to the surrounding plant cells. The movement of the effectors is largely dependent on their molecular weights. The expression of PD regulators, Arabidopsis PD-located protein PDLP5 and PDLP7, lead to PD closure and inhibits the PD-dependent movement of a bacterial effector in N. benthamiana. Similarly, a 22-amino acid peptide of bacterial flagellin (flg22) treatment induces PD closure and suppresses the movement of a bacterial effector in N. benthamiana. Together, our findings demonstrated that bacterial effectors are able to move intercellularly through PD in plants.

Invasion of Soybean Root Cells in Culture by Rhizobium japonicum.

1975 ◽  
Vol 33 ◽  
pp. 582-583
Author(s):  
Dan Raveed ◽  
Minocher Reporter ◽  
Grace Norris
Keyword(s):  
Cell Walls ◽  
Plant Cells ◽  
Culture Conditions ◽  
Final Concentration ◽  
Rhizobium Japonicum ◽  
Symbiotic Association ◽  
Extracellular Material ◽  
Root Cells ◽  
Soybean Root ◽  
Soybean Cell

The initiation of association between cultured soybean root cells and Rhizobia shows specificity under proper conditions of culture. The establishment of these culture conditions for symbiotic association have been described previously. The compatible plant cells produced a filamentous extracellular material which was capable of trapping Rhizobia. Non-compatible cells did not produce extracellular material and were not invaded. In this presentation we have followed the effect of Rhizobial invasion on the wall morphology of the soybean root cells in suspension cultures. Changes in the morphology of the soybean cell walls were then examined as follows.Harosoy root cells were grown in liquid culture in Gamborg's B-5 medium for two weeks. Rhizobium japonicum strain 138 was added to the culture for another 3 days. For this purpose, fixation was carried out by adding glutaraldehyde to the medium to a final concentration of 2%. The cell clumps were fixed 1 hr.

scholarly journals Plasmodesmata-Dependent Intercellular Movement of Bacterial Effectors

2021 ◽  
Vol 12 ◽  
Author(s):  
Zhongpeng Li ◽  
Haris Variz ◽  
Yani Chen ◽  
Su-Ling Liu ◽  
Kyaw Aung
Keyword(s):  
Pseudomonas Syringae ◽  
Cell Communication ◽  
Plant Cells ◽  
Host Cells ◽  
Host Immune Responses ◽  
Molecular Weights ◽  
Amino Acid Peptide ◽  
Pathogen Effectors ◽  
Intercellular Movement ◽  
Bacterial Effectors

Pathogenic microorganisms deliver protein effectors into host cells to suppress host immune responses. Recent findings reveal that phytopathogens manipulate the function of plant cell-to-cell communication channels known as plasmodesmata (PD) to promote diseases. Several bacterial and filamentous pathogen effectors have been shown to regulate PD in their host cells. A few effectors of filamentous pathogens have been reported to move from the infected cells to neighboring plant cells through PD; however, it is unclear whether bacterial effectors can traffic through PD in plants. In this study, we determined the intercellular movement of Pseudomonas syringae pv. tomato (Pst) DC3000 effectors between adjoining plant cells in Nicotiana benthamiana. We observed that at least 16 Pst DC3000 effectors have the capacity to move from transformed cells to the surrounding plant cells. The movement of the effectors is largely dependent on their molecular weights. The expression of PD regulators, Arabidopsis PD-located protein PDLP5 and PDLP7, leads to PD closure and inhibits the PD-dependent movement of a bacterial effector in N. benthamiana. Similarly, a 22-amino acid peptide of bacterial flagellin (flg22) treatment induces PD closure and suppresses the movement of a bacterial effector in N. benthamiana. Among the mobile effectors, HopAF1 and HopA1 are localized to the plasma membrane (PM) in plant cells. Interestingly, the PM association of HopAF1 does not negatively affect the PD-dependent movement. Together, our findings demonstrate that bacterial effectors are able to move intercellularly through PD in plants.

scholarly journals The Endoplasmic Reticulum and the Golgi Structures in Maize Root Cells

1959 ◽  
Vol 5 (3) ◽  
pp. 501-506 ◽  
Author(s):  
W. Gordon Whaley ◽  
Hilton H. Mollenhauer ◽  
Joyce E. Kephart
Keyword(s):  
Endoplasmic Reticulum ◽  
Cell Wall ◽  
Electron Microscope ◽  
Nuclear Envelope ◽  
Epoxy Resin ◽  
Maize Root ◽  
Root Tips ◽  
Animal Cells ◽  
Root Cells ◽  
Vesicular Structure

Maize root tips were fixed in potassium permanganate, embedded in epoxy resin, sectioned to show silver interference color, and studied with the electron microscope. All the cells were seen to contain an endoplasmic reticulum and apparently independent Golgi structures. The endoplasmic reticulum is demonstrated as a membrane-bounded, vesicular structure comparable in many aspects to that of several types of animal cells. With the treatment used here the membranes appear smooth surfaced. The endoplasmic reticulum is continuous with the nuclear envelope and, by contact at least, with structures passing through the cell wall. The nuclear envelope is characterized by discontinuities, as previously reported for animal cells. The reticula of adjacent cells seem to be in contact at or through the plasmodesmata. Because of these contacts the endoplasmic reticulum of a given cell appears to be part of an intercellular system. The Golgi structures appear as stacks of platelet-vesicles which apparently may, under certain conditions, produce small vesicles around their edges. Their form changes markedly with development of the cell.

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.

The pH of Plant Cells The pH of Animal Cells

1955 ◽  
Author(s):  
James Small ◽  
Floyd J. Wiercinski
Keyword(s):  
Plant Cells ◽  
Animal Cells

scholarly journals THE STRUCTURE OF SOME CYTOPLASMIC COMPONENTS OF PLANT CELLS IN RELATION TO THE BIOCHEMICAL PROPERTIES OF ISOLATED PARTICLES

1957 ◽  
Vol 3 (1) ◽  
pp. 61-70 ◽  
Author(s):  
A. J. Hodge ◽  
E. M. Martin ◽  
R. K. Morton
Keyword(s):  
Endoplasmic Reticulum ◽  
Wheat Root ◽  
Dense Material ◽  
Animal Cells ◽  
Wheat Roots ◽  
Root Cells ◽  
Intact Cells ◽  
Thin Sections ◽  
Isolated Mitochondria ◽  
Silver Beet

1. Electron micrographs of thin sections of material fixed with buffered osmium tetroxide have been used for comparison of the fine structure of isolated cytoplasmic particles from silver beet petioles and roots of germinating wheat with that of the cytoplasm of the intact cells. 2. Mitochondria of wheat roots have an external double membrane and poorly oriented internal double membranes. As compared with the structures seen in situ, the isolated mitochondria showed evidence of some disorganisation of the fine internal structure, probably due to osmotic effects. The possible influence of such changes on the enzymic properties of the isolated mitochondria is discussed. 3. The isolated plant microsomes are mainly spherical vesicular structures consisting of (a) an outer membrane enclosing (b) either an homogeneous slightly dense material (wheat root microsomes) or some granular dense material (silver beet microsomes) and (c) small dense particles, mostly associated with the vesicle membranes. 4. The cytoplasm of the wheat root cells does not contain any structures similar to the isolated microsomes but has a very dense reticular network, consisting of membranes with associated small dense particles, here called the endoplasmic reticulum. The observations indicate that the isolated microsomes arise mainly by rupture and transformation of the membranes of this structure. The effects of such extensive changes in the lipoprotein membranes on the enzymic activities of the endoplasmic reticulum, as studied in isolated microsomes, is discussed. 5. Meristematic wheat root cells contain structures which consist of smooth membranes with associated vacuoles and are similar to the Golgi zones of animal cells. The membranes of these zones probably contribute to the microsomal fraction under the conditions of preparation used for the enzymic and chemical studies previously reported.

scholarly journals Potential of Peptides as Inhibitors and Mimotopes: Selection of Carbohydrate-Mimetic Peptides from Phage Display Libraries

2012 ◽  
Vol 2012 ◽  
pp. 1-15 ◽  
Author(s):  
Teruhiko Matsubara
Keyword(s):  
Phage Display ◽  
Protein Interactions ◽  
Cell Communication ◽  
Carbohydrate Binding ◽  
Animal Cells ◽  
Phage Display Technology ◽  
Diverse Range ◽  
Phage Display Libraries ◽  
Mimetic Peptides ◽  
Peptide Mimotopes

Glycoconjugates play various roles in biological processes. In particular, oligosaccharides on the surface of animal cells are involved in virus infection and cell-cell communication. Inhibitors of carbohydrate-protein interactions are potential antiviral drugs. Several anti-influenza drugs such as oseltamivir and zanamivir are derivatives of sialic acid, which inhibits neuraminidase. However, it is very difficult to prepare a diverse range of sugar derivatives by chemical synthesis or by the isolation of natural products. In addition, the pathogenic capsular polysaccharides of bacteria are carbohydrate antigens, for which a safe and efficacious method of vaccination is required. Phage-display technology has been improved to enable the identification of peptides that bind to carbohydrate-binding proteins, such as lectins and antibodies, from a large repertoire of peptide sequences. These peptides are known as “carbohydrate-mimetic peptides (CMPs)” because they mimic carbohydrate structures. Compared to carbohydrate derivatives, it is easy to prepare mono- and multivalent peptides and then to modify them to create various derivatives. Such mimetic peptides are available as peptide inhibitors of carbohydrate-protein interactions and peptide mimotopes that are conjugated with adjuvant for vaccination.

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