Pore forming toxins (PFT) are important virulence factors produced by bacteria to kill eukaryotic cells by forming holes in the cellular membrane. They represent a diverse group of proteins with a wide range of target cells. Although the amino acid sequence is not conserved among the different PFT, many of them share some aspects of their mechanism of action. In general, the mode of action of PFT involves receptor recognition, activation by proteases, and aggregation into oligomeric-structures that insert into the membrane to form ionic pores. Beside the pore formation activity, PFT may have other effects during its interaction with their target cells such as intra-cellular signaling or transport of other enzymatic components, as in the case of anthrax or diphtheria toxins produced by Bacillus anthracis and Corynebacterium diphtheria, respectively (Parker and Feil, 2005). Although PFT have evolved as a pathogenic mechanism, some of them have great impact in society since they have different applications in biotechnology or are used as therapeutic agents, or as tools in the study of cell biology (Schiavo and van der Goot, 2001). On the other side, their target organisms have evolved different mechanisms to counter toxin action. Understanding the mechanism of action of PFT as well as the host responses to toxin action would provide ways to deal with these pathogens or with emerging pathogens and more importantly to improve the action of toxins that have biotechnological applications. In this review we will describe the intracellular effects induced by some PFT and the cellular responses evolved by eukaryotic cell to overcome PFT action.
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http://dx.doi.org/10.5661/bger-26-65 | DOI Listing |
Dev Biol
December 2024
Stowers Institute for Medical Research, Kansas City, Missouri 64110, USA; Howard Hughes Medical Institute, Stowers Institute for Medical Research, Kansas City, Missouri 64110, USA. Electronic address:
The cell nuclei of Ophisthokonts, the eukaryotic supergroup defined by fungi and metazoans, is remarkable in the constancy of their double-membraned structure in both somatic and germ cells. Such remarkable structural conservation underscores common and ancient evolutionary origins. Yet, the dynamics of disassembly and reassembly displayed by Ophisthokont nuclei vary extensively.
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December 2024
School of Resources & Safety Engineering, Central South University, Changsha, 410083, Hunan, China.
To explore the mechanism of water inrush from the mine roof strata, a series of seepage-acoustic emission (SAE) experiments on red sandstone disc samples were carried out. The effects of the height to diameter ratio (H/D) and pore pressure on the mechanical, hydraulic and crack propagation properties of red sandstones were investigated. Test results show that, the peak load of rock samples declines with the decreasing H/D and increasing pore pressure.
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December 2024
Corrosion and Surface Engineering CSIR, National Metallurgical Laboratory, Jamshedpur, India.
Chloride-induced corrosion of steel rebars embedded in mortar was effectively controlled by blending of gallic acid in wet mixture. Mixing of optimized concentration of gallic acid (GA) inhibitor (0.125%) in mortars considerably increased the charge transfer resistance of embedded rebars (80.
View Article and Find Full Text PDFToxins (Basel)
December 2024
Department of Pathology and Experimental Therapeutics, Faculty of Medicine and Health Sciences-Campus Bellvitge, University of Barcelona, 08907 Barcelona, Spain.
Epsilon toxin (ETX) from is a pore-forming toxin (PFT) that crosses the blood-brain barrier and binds to myelin structures. In in vitro assays, ETX causes oligodendrocyte impairment, subsequently leading to demyelination. In fact, ETX has been associated with triggering multiple sclerosis.
View Article and Find Full Text PDFNanomaterials (Basel)
December 2024
Personalized Medicine Centre, Almazov National Medical Research Centre, Akkuratova Str. 2, 197341 St. Petersburg, Russia.
This study addresses issues in developing spatially controlled magnetic fields for particle guidance, synthesizing biocompatible and chemically stable MNPs and enhancing their specificity to pathological cells through chemical modifications, developing personalized adjustments, and highlighting the potential of tumor-on-a-chip systems, which can simulate tissue environments and assess drug efficacy and dosage in a controlled setting. The research focused on two MNP types, uncoated magnetite nanoparticles (mMNPs) and carboxymethyl dextran coated superparamagnetic nanoparticles (CD-SPIONs), and evaluated their transport properties in microfluidic systems and porous media. The original uncoated mMNPs of bimodal size distribution and the narrow size distribution of the fractions (23 nm and 106 nm by radii) were demonstrated to agglomerate in magnetically driven microfluidic flow, forming a stable stationary web consisting of magnetic fibers within 30 min.
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