Stress stimulation induced resistance of plant

During the course of pathogens penetrating the plant cell, besides of chemical secretion, the pathogens may cause mechanical signal by the physical pressure on the plant cell. In the current study, we took the stress as the mechanical signal elicitor to find the effect of plant resistance induced by stress. The results showed that an appropriate stress stimulation can evidently improve the plant resistance. However, disruption the plasma membrane–cell wall adhesion will absolutely eliminate this kind of inducement effect, which suggests that the plant resistance inducement by stress depend on the adhesion of plasma membrane–cell wall. Also we found that stress stimulation may cause synthesis of lignin and increase the activity of phenylalaninc ammonial lyase (PAL) chitinase and β-1,3-glucanase obviously. The results showed that stress stimulation may not only enhance ability of the plant cell resistant to pathogen penetration but also elicit the accumulation of pathogens suppression or antimicrobial chemical substance in the plant cell.     

Preliminary study on phytoalexin induction in cucumber

Inducer can induce new active composition and increase the content of the active composition in the plant. In this paper, we investigated the synthesis and accumulation of phytoalexin in cucumber seedlings which were induced by chemical inducer of the salicylic acid (SA) and physical inducer. Analyzed by experiment of antifungal activity, thin-layer chromatography (TLC) and high-performance liquid chromatography (HPLC), the result was that both SA and stress can induce the synthesis and accumulation of phytoalexin in cucumber seedlings. But the content of phytoalexin induced by SA was lower than it induced by stress. And in this paper, another conclusion was that the transduction of physical signal and the chemical signal in the plant depended on the adhesion between cell wall and plasma and active oxidative species producted by stimulation.     

Stress induced plant resistance and enzyme activity varying in cucumber

When pathogens penetrate plant cells, some chemical secretions are elicited, and the mechanical signals in plant cell may be induced by the simultaneous physical pressure to change. Based on the previous cognitions, we investigated the plant resistance and the variation of anti-disease enzyme activity in cucumber leaves after mechanical stress loading. Results showed that the appropriate mechanical stimulation could significantly improve plant resistance and alter the activity of phenylalanine ammonial lyases (PAL) and POD, leading to synthesis of lignin. However, we found that the effects of the stress on these cellular fundamental events were eliminated when the adhesion between plasma membrane and cell wall was disrupted. We speculated that mechanical signal transduction in plants depend on the adhesion of plasma membrane–cell wall.     

Stress stimulus induced resistance to Cladosporium cucumerinum in cucumber seeding

Up to date, the studies of plant induced resistance have become the focus in plant pathology and physiology. During the course of pathogens penetrating the plant cell, besides of chemical secretion, the pathogens may generate mechanical signal caused by the physical pressure on the plant cell. In the non-host resistance, both the chemical signal and the mechanical stress signal are considered to have contribution to the entire defense reaction acted by the plant. The penetration of pathogen Cladosporium cucumerinum to cucumber is thought to be one of the model in research of plant induced resistance. In the current study, as a mechanical signal elicitor, the appropriate stress stimulus was proved to effectually induce the resistance of cucumber seedling to C. cucumerinum. After the treatment of the stress stimulus on leaves, the activities of resistance-related enzymes were significantly increased, such as phenylanine ammonia lyase (PAL), peroxidase (POD). Also, we found that stress stimulation may cause synthesis of lignin, which acts as the physical barrier to defense the pathogens. The results suggest that stress stimulation may not only enhance ability of the plant cell resistance to pathogen penetration but also elicit the accumulation of pathogens suppression or antimicrobial chemical substance in the plant cell.     

Improved mesenchymal stem cell seeding on RGD-modified poly(L-lactic acid) scaffolds using flow perfusion

Arg-Gly-Asp (RGD) has been widely utilized to increase cell adhesion to three-dimensional scaffolds for tissue engineering. However, cell seeding on these scaffolds has only been carried out statically, which yields low cell seeding efficiencies. We have characterized, for the first time, the seeding of rat mesenchymal stem cells on RGD-modified poly(L-lactic acid) (PLLA) foams using oscillatory flow perfusion. The incorporation of RGD on the PLLA foams improves scaffold cellularity in a dose-dependent manner under oscillatory flow perfusion seeding. When compared to static seeding, oscillatory flow perfusion is the most efficient seeding technique. Cell detachment studies show that cell adhesion is dependent on the applied flow rate, and that cell attachment is strengthened at higher levels of RGD modification.     

Effect of local stress induction on resistance-related enzymes in cucumber seeding

In the current study, we found that the stress stimulus can act as a kind of elicitor, which can efficiently induce the resistance of cucumber against fungal pathogen. After the treatment of the stress stimulus on leaves, the activities of resistance-related enzymes were increased significantly. Such as phenylamine ammonia lyase (PAL), peroxidase (POD) and polyphenoloxidase (PPO), which are strongly associated with the plant disease resistance. Also the expression of pathogenesis-related protein (PR protein) were activated by stress stimulus, with the results that the activities of chitinase and beta-l,3-glucanase were increased obviously. The data showed that one of the mechanism of stress stimulus induction plant resistance may act via eliciting the metabolism related disease resistance within plant, which can produce many suppressing and antimicrobial compounds to against pathogens infection efficiently.     

Cell adhesion and growth to Peptide-patterned supported lipid membranes

Lipid vesicles displaying RGD peptide amphiphiles were fused with glass coverslips to control the ability of these surfaces to support cell adhesion and growth. Cell adhesion was prevented on phosphatidylcholine bilayers in the absence of RGD, whereas cells adhered and grew in the presence of accessible RGD amphiphiles. This specific interaction between cells and RGD peptides was further explored in a concentration-dependent fashion by creating surface composition arrays using microfluidics. For the range of concentrations studied adhesion and growth were favored by increased peptide concentration, but this concentration dependence was found to diminish in the higher concentration regions of the array. Developing peptide composition gradients in a membrane environment is demonstrated as an effective method to screen biological probes for cell adhesion and growth.     

Nitrogen-rich plasma-polymerized coatings on PET and PTFE surfaces improve endothelial cell attachment and resistance to shear flow

Low seeding efficiency and poor cell retention under flow-induced shear stress limit the effectiveness of in vitro endothelialization strategies for small-diameter vascular grafts. Primary-amine-rich plasma-polymerized coatings (PPE:N) deposited using low- and atmospheric-pressure plasma discharges on PET and PTFE are evaluated for their ability to improve endothelial cells' kinetics and strength of attachment. PPE:N coatings increase cell adhesion and adhesion rate, spreading, focal adhesion, and resistance to flow-induced shear compared with bare and gelatin-coated PET and PTFE. In particular, about 90% of the cells remain on coated surfaces after 1 h exposure to shear. These coatings, therefore, appear as a promising versatile approach to improve cell seeding strategies for vascular grafts.     

A Glycan Array-Based Assay for the Identification and Characterization of Plant Glycosyltransferases

Growing plants with modified cell wall compositions is a promising strategy to improve resistance to pathogens, increase biomass digestibility, and tune other important properties. In order to alter biomass architecture, a detailed knowledge of cell wall structure and biosynthesis is a prerequisite. We report here a glycan array-based assay for the high-throughput identification and characterization of plant cell wall biosynthetic glycosyltransferases (GTs). We demonstrate that different heterologously expressed galactosyl-, fucosyl-, and xylosyltransferases can transfer azido-functionalized sugar nucleotide donors to selected synthetic plant cell wall oligosaccharides on the array and that the transferred monosaccharides can be visualized “on chip” by a 1,3-dipolar cycloaddition reaction with an alkynyl-modified dye. The opportunity to simultaneously screen thousands of combinations of putative GTs, nucleotide sugar donors, and oligosaccharide acceptors will dramatically accelerate plant cell wall biosynthesis research.     

Elicitor-Induced Cellular and Molecular Events Are Responsible for Productivity Enhancement in Hairy Root Cultures: An Insight Study

A wide range of external stress stimuli triggers a plant cell to undergo a complex network of reactions that ultimately lead to the synthesis and accumulation of secondary metabolites. These secondary metabolites help the plant to survive under stress challenge. The potential of biotic and abiotic elicitors for the induction and enhancement of secondary metabolite production in various culture systems including hairy root (HR) cultures is well-known. The elicitor-induced defense responses involves signal perception of elicitor by a cell surface receptor followed by its transduction involving some major cellular and molecular events including activation of major secondary message signaling pathways. This result in induction of gene expressions escorting to the synthesis of various proteins mainly associated with plant defense responses and secondary metabolite synthesis and accumulation. The review discusses the elicitor-induced various cellular and molecular events and correlates them with enhanced secondary metabolite synthesis in HR systems. Further, this review also concludes that combining elicitation with in-silico approaches enhances the usefulness of this practice in better understanding and identifying the rate-limiting steps of biosynthetic pathways existing in HRs which in turn can contribute towards better productivity by utilizing metabolic engineering aspects.     

A Glycan Array‐Based Assay for the Identification and Characterization of Plant Glycosyltransferases

Growing plants with modified cell wall compositions is a promising strategy to improve resistance to pathogens, increase biomass digestibility, and tune other important properties. In order to alter biomass architecture, a detailed knowledge of cell wall structure and biosynthesis is a prerequisite. We report here a glycan array‐based assay for the high‐throughput identification and characterization of plant cell wall biosynthetic glycosyltransferases (GTs). We demonstrate that different heterologously expressed galactosyl‐, fucosyl‐, and xylosyltransferases can transfer azido‐functionalized sugar nucleotide donors to selected synthetic plant cell wall oligosaccharides on the array and that the transferred monosaccharides can be visualized “on chip” by a 1,3‐dipolar cycloaddition reaction with an alkynyl‐modified dye. The opportunity to simultaneously screen thousands of combinations of putative GTs, nucleotide sugar donors, and oligosaccharide acceptors will dramatically accelerate plant cell wall biosynthesis research.     

Block Copolymer Brushes for Completely Decoupled Control of Determinants of Cell–Surface Interactions

The known determinants for cell–surface interactions, comprising biochemical cues, patterns, passivating functionality, and control of tether mechanical properties, are fully decoupled in tailored block copolymer brushes synthesized by surface‐initiated atom transfer radical polymerization. Exploiting sequential polymerization of a passivating underlying polyacrylamide (PAAm) block with defined cross‐linking followed by a second poly(acrylic acid) block, which can be conjugated with a selective adhesion peptide, hierarchically structured brushes that can be micro‐patterned by soft lithography were obtained. The interaction of NIH 3T3 fibroblasts and PaTu 8988t pancreatic tumor cells with brushes that differed only in the stiffness of the hidden PAAm block or only in the peptide ligand, while keeping all other parameters constant, revealing profound differences in cell adhesion and morphology. In particular, cells could only attach well to stiff RGD presenting brushes.     

Protein adsorption and cell adhesion on RGD-functionalized silicon substrate surfaces

A method was developed to modify silicon surfaces with good protein resistance and specific cell attachment. A silicon surface was initially deposited using a block copolymer of N-vinylpyrrolidone (NVP) and 2-hydroxyethyl methacrylate (HEMA) (PVP-b-PHEMA) film through surface-initiated atom transfer radical polymerization and then further immobilized using a short arginine-glycine-aspartate (RGD) peptide. Our results demonstrate that the RGD-modified surfaces (Si-RGD) can suppress non-specific adsorption of proteins and induce the adhesion of L929 cells. The Si-RGD surface exhibited higher cell proliferation rates than the unmodified silicon surface. This research established a simple method for the fabrication of dual-functional silicon surface that combines antifouling and cell attachment promotion.     

Polyelectrolyte complex membranes for specific cell adhesion

The presentation of bioactive ligands on biomaterial surfaces is often confounded by the adsorption of proteins present in the biological milieu, rendering any type of cellular response nonspecific. We have engineered a polyelectrolyte complex membrane that demonstrates specific adhesion of various cell types for both two-dimensional (2D) and three-dimensional (3D) cell culture systems. Specific cell adhesion is achieved by a three-tiered structure: a silica cross-linked polycation as the bottom (first) tier, a nonfouling polyanion-poly(ethylene glycol) (PEG) conjugate as the intermediate (second) tier, and the cell-adhesion ligand as the top (third) tier. Each tier of the membrane was characterized in terms of chemical composition and dimensions. Epithelial cells (primary human cortical renal cells and a hepatocellular carcinoma cell line) cultured on the membranes exhibited little cell attachment on the polyanion-PEG second tier and good cell adhesion on the RGD-modified third tier. Thus, the second tier allowed the effect of cell adhesion due to the ligand (third tier) to be isolated and distinguished from nonspecific cell attachment to the first tier. For the culturing of cells in three dimensions, the three-tiered membrane system was applied using a highly swellable chitosan membrane as the first tier. The resulting cell-membrane construct was uniformly dispersed and centrifuged to form a matrix that interacted intimately with cells in the form of a pellet. Presentation of RGD in the latter format enhanced the viability of human mesenchymal stem cells (hMSCs) over controls without RGD.     

Cellular responses to patterned poly(acrylic acid) brushes

We use patterned poly(acrylic acid) (PAA) polymer brushes to explore the effects of surface chemistry and topography on cell-surface interactions. Most past studies of surface topography effects on cell adhesion have focused on patterned feature sizes that are larger than the dimensions of a cell, and PAA brushes have been characterized as cell repellent. Here we report cell adhesion studies for RBL mast cells incubated on PAA brush surfaces patterned with a variety of different feature sizes. We find that when patterned at subcellular dimensions on silicon surfaces, PAA brushes that are 30 or 15 nm thick facilitate cell adhesion. This appears to be mediated by fibronectin, which is secreted by the cells, adsorbing to the brushes and then engaging cell-surface integrins. The result is detectable accumulation of plasma membrane within the brushes, and this involves cytoskeletal remodeling at the cell-surface interface. By decreasing brush thickness, we find that PAA can be 'tuned' to promote cell adhesion with down-modulated membrane accumulation. We exemplify the utility of patterned PAA brush arrays for spatially controlling the activation of cells by modifying brushes with ligands that specifically engage IgE bound to high-affinity receptors on mast cells.     

Engineering of Covalently Immobilized Gradients of RGD Peptides on Hydrogel Scaffolds: Effect on Cell Behaviour

Summary: The aim of this study has been to design a system for the preparation of Polyethylene-glycol (PEG) based hydrogels with a controlled spatial distribution of covalently immobilised RGD adhesion signals in order to control and guide cell response for tissue engineering application. Gradients of immobilised RGD peptides were characterized by confocal microscopy analysis. Moreover, the effect of RGD spatial distribution on cell behaviour was evaluated by using mouse embryo fibroblasts NIH3T3. In particular, we observed cell adhesion and migration of fibroblasts seeded on RGD gradient compared to cells on control hydrogels having an uniform distribution of RGD. Our data suggest that a linear gradient of covalently immobilised adhesion signals affects cell behaviour. In particular, cells feel RGD gradient and oriented themselves and move along gradient direction.     

Efficient synthesis of brussalexin A, a remarkable phytoalexin from Brussels sprouts

The synthesis of brussalexin A, the first phytoalexin containing an allyl thiolcarbamate group, and its selective inhibitory activity against fungal plant pathogens is described.     

Controlling cell attachment selectively onto biological polymer-colloid templates using polymer-on-polymer stamping

A new patterning approach using polymer-on-polymer stamping (POPS) has been developed to fabricate polymer-colloid templates for controlling selective cell attachment. In this paper, a polyamine surface patterned onto a poly(acrylic acid)/poly(allylamine hydrochloride) (PAA/PAH) cell resistant multilayer platform serves as a template for the deposition of close- or loose-packed colloidal particles. Peptides containing the RGD adhesion sequence were used to modify the PAH/colloid surface for specific cell attachment. Cell behavior was studied by varying colloidal packing array density, pattern geometry, and surface chemistry. It was found that loose-packed RGD-modified colloidal arrays enhance cell adhesion, as observed through the development of focal adhesion contacts and orientation of actin stress fibers, but close-packed colloidal arrays induce a rounded and nonadhesive cell morphology and yield a smaller number of attached cells. On loose-packed arrays, cells adjust their shapes to the pattern geometry when the stripe width is smaller than 50 microm and increase their extent of attachment when the concentration of surface RGD peptides is increased. This new biomaterials system allows the examination of cell behavior as a function of RGD surface distribution on the molecular to micrometer scale and reveals cellular response to different surface roughnesses.     

Controlling mammalian cell interactions on patterned polyelectrolyte multilayer surfaces

A newly discovered class of cell resistant surfaces, specifically engineered polyelectrolyte multilayers, was patterned with varying densities of adhesion ligands to control attachment of mammalian cells and to study the effects of ligand density on cell activity. Cell adhesive patterns were created on cell resistant multilayer films composed of poly(acrylic acid) and polyacrylamide through polymer-on-polymer stamping of poly(allylamine hydrochloride) PAH and subsequent reaction of the amine functional groups with an adhesion ligand containing RGD (Arg-Gly-Asp). These cell patterns demonstrated great promise for long-term applications since they remained stable for over 1 month, unlike ethylene glycol functional surfaces. By changing the stamping conditions of PAH, it was possible to alter the number of available functional groups in the patterned regions, and as a result, control the ligand density. Cell spreading, morphology, and cytoskeletal organization were compared at four different RGD densities. The highest RGD density, approximately 152 000 molecules/microm2, was created by stamping PAH at a pH of 11.0. Lowering the stamping ink pH led to patterns with lower ligand surface densities (83 000 molecules/microm2 for pH 9.0, 53,000 molecules/ microm2 for pH 7.0, and 25 000 molecules/microm2 for pH 3.5). An increasing number of cells attached and spread as the RGD density of the patterns increased. In addition, more cells showed well-defined actin stress fibers and focal adhesions at higher levels of RGD density. Finally, we found that pattern geometry affected cytoskeletal protein organization. Well-formed focal adhesions and cell-spanning stress fibers were only found in cells on wider line patterns (at least 25 microm in width).     

Introductory remarks

Separate terms to distinguish the matrix between the cells that grow in vitro and the matrix that separates and surrounds cells in the living body are being proposed. The currently used designations: pericellular, extracellular, or intercellular matrix should be used only for the substance produced by cells in vitro (cultures). The well organized, highly specific, and stable structure with significant topographic variations between the cells of living tissues and organs should be called biological matrix or briefly as biomatrix. My experiments published in the early 1940s on plant cell walls illustrate some similarities between biomatrix of animal tissues and plant cell wall. When cells of plant epithelial membranes undergo plasmolysis, the space between the contracting cell and cellulose cell wall is filled with filaments called Hechtian filaments or strands. With silver impregnation, these filaments become a fibrous network, filling the space between the cell wall and the contracting plasma (cell) membrane. A similar extracellular fibrous network has been described earlier after silver impregnation in some animal tissues. I interpreted my finding that a pectin-like polysaccharide in the cell wall biomatrix and hyaluronan, the only polysaccharide present in the biomatrix of animal tissues, are responsible for this fibrous network artifact.