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Plant cell walls (PCWs) form the outer barrier of cells that give the plant strength and directly interact with the environment and other cells in the plant. PCWs are composed of several polysaccharides, of which cellulose forms the main fibrillar network. Enmeshed between these fibrils of cellulose are non-cellulosic polysaccharides (NCPs), pectins, and proteins. This study investigates the sequence, timing, patterning, and architecture of cell wall polysaccharide regeneration in suspension culture cells (SCC) of the grass species (). Confocal, superresolution, and electron microscopies were used in combination with cytochemical labeling to investigate polysaccharide deposition in SCC after protoplasting. Cellulose was the first polysaccharide observed, followed shortly thereafter by (1,3;1,4)-β-glucan, which is also known as mixed-linkage glucan (MLG), arabinoxylan (AX), and callose. Cellulose formed fibrils with AX and produced a filamentous-like network, whereas MLG formed punctate patches. Using colocalization analysis, cellulose and AX were shown to interact during early stages of wall generation, but this interaction reduced over time as the wall matured. AX and MLG interactions increased slightly over time, but cellulose and MLG were not seen to interact. Callose initially formed patches that were randomly positioned on the protoplast surface. There was no consistency in size or location over time. The architecture observed via superresolution microscopy showed similarities to the biophysical maps produced using atomic force microscopy and can give insight into the role of polysaccharides in PCWs.
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http://dx.doi.org/10.3390/cells10010127 | DOI Listing |
Cureus
August 2025
Stem Cell and Regenerative Biology Laboratory, Sri Ramachandra Institute of Higher Education and Research, Chennai, IND.
Introduction: The presence of stem cells in the ovary has been a topic of discussion due to their questionable existence. Isolation of stem cells has been possible by enzymatic digestion; however, the percentage of cells harvested and expanded has not been satisfactory. This could be due to the lack of optimal adhesion provided by the standard commercial culture dishes, which affects the initial attachment and further growth of cells.
View Article and Find Full Text PDFJ Appl Microbiol
September 2025
Graduate Institute of Medical Sciences, National Defense Medical University, Taipei City 114201, Taiwan (R.O.C.).
Aims: This study aims to develop and evaluate a rapid and high-multiplex pathogen detection method for clinical and food specimens to address the ongoing public health threat of foodborne infections and the limitations of conventional culture-based diagnostics.
Methods And Results: The foodborne bacteria (FBB) assay integrates multiplex PCR, T7 exonuclease hydrolysis, and a suspension bead array to simultaneously detect 16 genes from 13 major foodborne bacteria. Analytical performance was evaluated using reference strains, while diagnostic performance was assessed using clinical and food samples.
Tissue Eng Part A
September 2025
Department of Orthopaedic Surgery, McKay Orthopaedic Research Laboratory, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Cell and tissue engineering therapies provide promise for regenerating damaged intervertebral disc (IVD) tissue and resolving the low back pain that often accompanies it. However, these treatments remain experimental and unavailable for patients. Furthermore, the large body of work characterizing and utilizing mesenchymal stromal cells (MSCs) for these applications has, unfortunately, not resulted in any FDA-approved spinal therapies.
View Article and Find Full Text PDFJ Biophotonics
September 2025
Institute for Physical Research of National Academy of Sciences of Armenia, Ashtarak, Armenia.
We report the results of an experimental study of the movement and trapping of Gram-negative Escherichia coli (E. coli) bacteria in broth suspensions, under photovoltaic fields generated by an optical Bessel beam illumination of the surface of a lithium niobate crystal (photovoltaic tweezers). The study was performed using a phase-sensitive transmission microscope.
View Article and Find Full Text PDFAm J Infect Control
September 2025
Department of Infection Control and Prevention, The University of Tokyo Hospital, Japan. Electronic address:
Background: Adequate drying of endoscope channels following reprocessing is critical to inhibit microbial growth. This study evaluated residual moisture and bacterial contamination in endoscopes stored using different cabinets and storage methods.
Methods: EN-580T endoscopes were stored in three cabinets: TJ-908S and TJ-804S (both with active drying) and TM-804S (passive drying).