Silver nanoparticles (AgNPs) internalization and passage through the Lactuca sativa (Asteraceae) outer cell wall

2021 ◽  
Author(s):  
Sergimar Kennedy de Paiva Pinheiro ◽  
Thaiz Batista Azevedo Rangel Miguel ◽  
Marlos de Medeiros Chaves ◽  
Francisco Claudio de Freitas Barros ◽  
Camila Pessoa Farias ◽  
...  
1974 ◽  
Vol 52 (9) ◽  
pp. 2033-2036 ◽  
Author(s):  
N. C. Lyon ◽  
W. C. Mueller

Leaf tissue of Phaseolus vulgaris L. and Plantago major L. was prepared by the freeze-etch technique and examined in the electron microscope for the presence of ectodesmata. No structures analagous to ectodesmata observed with light microscopy could be found in freeze-etched preparations of chemically unfixed material or in material fixed only in glutaraldehyde. Objects appearing as broad, shallow, granular areas in the epidermal cell wall beneath the cuticle were observed in leaf replicas after fixation in complete sublimate fixative, the acid components of the sublimate fixative, or mercuric chloride alone. Because of their distribution and location, these objects can be considered analagous to ectodesmata observed by light microscopists. Because these areas occur only in chemically fixed walls and are localized within the walls in discrete areas, their presence supports the contention that ectodesmata are sites in the outer cell wall with defined physicochemical characteristics.


eLife ◽  
2020 ◽  
Vol 9 ◽  
Author(s):  
CJ Cambier ◽  
Steven M Banik ◽  
Joseph A Buonomo ◽  
Carolyn R Bertozzi

Several virulence lipids populate the outer cell wall of pathogenic mycobacteria. Phthiocerol dimycocerosate (PDIM), one of the most abundant outer membrane lipids, plays important roles in both defending against host antimicrobial programs and in evading these programs altogether. Immediately following infection, mycobacteria rely on PDIM to evade Myd88-dependent recruitment of microbicidal monocytes which can clear infection. To circumvent the limitations in using genetics to understand virulence lipids, we developed a chemical approach to track PDIM during Mycobacterium marinum infection of zebrafish. We found that PDIM's methyl-branched lipid tails enabled it to spread into host epithelial membranes to prevent immune activation. Additionally, PDIM’s affinity for cholesterol promoted this phenotype; treatment of zebrafish with statins, cholesterol synthesis inhibitors, decreased spreading and provided protection from infection. This work establishes that interactions between host and pathogen lipids influence mycobacterial infectivity and suggests the use of statins as tuberculosis preventive therapy by inhibiting PDIM spread.


2012 ◽  
Vol 60 (1) ◽  
pp. 85-93 ◽  
Author(s):  
Agata Konarska

The seedlings of the red pepper (<i>Capsicum annuum</i> L.) cv. Trapez grown in water culture for a period of 14 days with Al (0, 10, 20 and 40 mg·dm<sup>-3</sup> AlCl<sub>3</sub>·6 H<sub>2</sub>O). Some morphological and anatomical features of red pepper shoots were analyzed. Reduction in height and diameter of stems as well as decrease in fresh mass of shoots were observed after Al-treatment. In the hypocotyl the thickness of cortex parenchyma layer and the size of their cells were reduced. The aluminum treatment resulted in the increased in thickness of the epidermis outer cell wall. Under Al stress in the cotrex and the central cylinder parenchyma cells were present numerous enlarge plastids which contained large grains of starch and dark little bodies which were possible aluminum deposits. They weren`t observed in control seedlings.


Hybridoma ◽  
1994 ◽  
Vol 13 (1) ◽  
pp. 45-51 ◽  
Author(s):  
FRANCOISE TALBOT ◽  
GEORGES ROBREAU ◽  
FRANCOISE GUEGUEN ◽  
ROGER MALCOSTE

2003 ◽  
Vol 69 (3) ◽  
pp. 1581-1588 ◽  
Author(s):  
Sophie Paris ◽  
Jean-Paul Debeaupuis ◽  
Reto Crameri ◽  
Marilyn Carey ◽  
Franck Charlès ◽  
...  

ABSTRACT The surface of Aspergillus fumigatus conidia, the first structure recognized by the host immune system, is covered by rodlets. We report that this outer cell wall layer contains two hydrophobins, RodAp and RodBp, which are found as highly insoluble complexes. The RODA gene was previously characterized, and ΔrodA conidia do not display a rodlet layer (N. Thau, M. Monod, B. Crestani, C. Rolland, G. Tronchin, J. P. Latgé, and S. Paris, Infect. Immun. 62:4380-4388, 1994). The RODB gene was cloned and disrupted. RodBp was highly homologous to RodAp and different from DewAp of A. nidulans. ΔrodB conidia had a rodlet layer similar to that of the wild-type conidia. Therefore, unlike RodAp, RodBp is not required for rodlet formation. The surface of ΔrodA conidia is granular; in contrast, an amorphous layer is present at the surface of the conidia of the ΔrodA ΔrodB double mutant. These data show that RodBp plays a role in the structure of the conidial cell wall. Moreover, rodletless mutants are more sensitive to killing by alveolar macrophages, suggesting that RodAp or the rodlet structure is involved in the resistance to host cells.


2000 ◽  
Vol 14 (3) ◽  
pp. 225-229 ◽  
Author(s):  
Leonard Amaral ◽  
Jette E Kristiansen ◽  
Villy Frølund Thomsen ◽  
Bogooljub Markovich

Author(s):  
John Maynard Smith ◽  
Eors Szathmary

The basic structures of a bacterial and a eukaryotic cell are shown in Fig. 8.1. The differences whose origins call for an explanation are as follows: • The bacterial cell has a rigid outer cell wall, usually made of the peptidoglycan, murein. In eukaryotes, the rigid cell wall is not universal, and cell shape is maintained primarily by an internal cytoskeleton of filaments and microtubules. • Eukaryotic cells have a complex system of internal membranes, including the nuclear envelope, endoplasmic reticulum and lysosomes. • Bacteria have a single circular chromosome, attached to the rigid outer cell wall. In eukaryotes, linear chromosomes are contained within a nuclear envelope, which separates transcription from translation: communication between nucleus and cytoplasm is via pores in the nuclear envelope. • Eukaryotes have a complex cytoskeleton. The actomyosin system powers cell division, phagocytosis, amoeboid motion and the overall contractility to resist osmotic swelling. Microtubules and the associated motor proteins (kinesin, dynein and dynamin) ensure the accurate segregation of chromosomes in mitosis, ciliary motility and the movement of transport vesicles. Intermediate filaments form the structural basis for the association of the endomembranes and nuclear-pore complexes with the chromatin to form the nuclear envelope, while other intermediate filaments help to anchor the nucleus in the cytoplasm. One crucial difference between prokaryotes and most eukaryotes has been omitted from Fig. 8.1: this is the presence of mitochondria, and, in plants and algae, of chloroplasts. The reason for the omission is that, on the scenario for eukaryote origins that seems to us most plausible, these intracellular organelles originated later in time than the structures shown in the figure. The differences between these cell types justifies the recognition of two empires of life (above the kingdom level): Bacteria and Eukaryota (Cavalier-Smith, 199la; Table 8.1). (It is interesting that this taxonomic rank was recognized by Linnaeus.) Within each of the empires, there are two major categories: Bacteria consist of the kingdoms Eubacteria and Archaebacteria, and Eukaryota are divided into the superkingdoms Archaezoa and Metakaryota. The justification for these divisions is as follows. The Archaebacteria, in contrast to the Eubacteria, never have murein cell walls, and their single cell membrane contains isoprenoidal ether rather than acyl ester lipids.


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