Cell-cell and cell-matrix adhesions are fundamental in all multicellular organisms. They play a key role in cellular growth, differentiation, pattern formation and migration. Cell-cell adhesion is substantial in the immune response, pathogen-host interactions, and tumor development. The success of tissue engineering and stem cell implantations strongly depends on the fine control of live cell adhesion on the surface of natural or biomimetic scaffolds. Therefore, the quantitative and precise measurement of the adhesion strength of living cells is critical, not only in basic research but in modern technologies, too. Several techniques have been developed or are under development to quantify cell adhesion. All of them have their pros and cons, which has to be carefully considered before the experiments and interpretation of the recorded data. Current review provides a guide to choose the appropriate technique to answer a specific biological question or to complete a biomedical test by measuring cell adhesion.
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http://dx.doi.org/10.1016/j.cis.2019.05.005 | DOI Listing |
Food Microbiol
August 2025
College of Food Science and Engineering, Northwest A&F University, 22 Xinong Road, Yangling, 712100, Shaanxi, China. Electronic address:
The aim of the present study was to evaluate the mechanism of antimicrobial action of Lysine (Lys) against Escherichia coli (E. coli) O157:H7. Lys alters the permeability and morphology of bacterial cell membranes, leading to leakage of intracellular material.
View Article and Find Full Text PDFJ Immunother Cancer
March 2025
Team "Biologie des Infections à Polyomavirus", UMR1282, Tours, France.
The cell adhesion protein CD56 has been identified as a potential therapeutic target in several solid tumors and hematological malignancies. Recently, we developed a CD56-directed antibody-drug conjugate (ADC), called Adcitmer and demonstrated its antitumor properties in preclinical models of the rare and aggressive skin cancer Merkel cell carcinoma (MCC).The present study aims to further optimize Adcitmer to overcome the therapeutic limitations observed with previously evaluated CD56-targeting ADCs, which were partially related to toxic effects on leukocytes.
View Article and Find Full Text PDFJ Thromb Haemost
March 2025
Department of Health Sciences, Università del Piemonte Orientale, Novara, ITALY; Department of Integrated Activities and Research Innovation, University Hospital SS. Antonio and Biagio and Cesare Arrigo, Alessandria, ITALY. Electronic address:
Background: Factor VIII (FVIII), an essential coagulation co-factor and independent cancer associated thrombotic risk factor, has recently been shown to be synthesized directly by a broad profile of cancers. With evident extra-coagulative functions, it remains to understand if FVIII can play a functional role in cancer.
Objectives: Establish if FVIII plays a direct role in bladder cancer cell models.
Dev Comp Immunol
March 2025
College of Life Science & Technology, Heilongjiang Bayi Agricultural University. Daqing 163319, Heilongjiang Province, P. R. China. Electronic address:
CD169, a salivary acid adhesion receptor on macrophages, plays a crucial role in enhancing the phagocytic response to pathogenic bacteria and in antibacterial immunity. To explore its potential in targeted veterinary drug applications, we used phage display technology to biopan peptide fragments specific to CD169. After several rounds of screening, 45 phage clones were selected for ELISA testing, resulting in 21 high-affinity clones.
View Article and Find Full Text PDFJ Colloid Interface Sci
March 2025
College of Physics, Sichuan University, Chengdu 610065, China. Electronic address:
This study presents a dual-layer artificial dura mater, a hierarchically structured fibrous membrane composed of poly(p-dioxanone) (PPDO) and bioactive glass (BG), fabricated using electrospinning and melt-casting techniques. Designed to address the challenges of dura mater repair, the membrane features a dense outer PPDO layer for mechanical resilience and an electrospun inner layer embedded with BG to enable controlled ion release, promoting tissue regeneration and angiogenesis. We evaluated the fibrous membrane's surface morphology, mechanical properties, hydrophilicity, and in vitro degradation, demonstrating that increasing BG content enhances hydrophilicity, reduces crystallinity, and modulates degradation kinetics.
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