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Cell Adhesion Molecule 1 - DOAJ

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Last Updated: 10 September 2022

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Two Novel PET Radiopharmaceuticals for Endothelial Vascular Cell Adhesion Molecule-1 (VCAM-1) Targeting

Atherosclerosis is a chronic progressive disease characterized by inflammatory processes such as the overexpression of adhesion proteins, including the endothelial Vascular Cell Adhesion Molecule-1. DOTA's derivative of a DOTA derivative with the peptide is obtained from the direct conjugation of a DOTA derivative with the peptide, whereas NAMP is a biotin derivative intended to be used in a three-step pretargeting scheme that calls for the use of a double-chelating derivative of DOTA.

Source link: https://doi.org/10.3390/pharmaceutics13071025


Cell Adhesion Molecule 1 (CADM1) Is an Independent Prognostic Factor in Patients with Cutaneous Squamous Cell Carcinoma

Cell adhesion molecular 1 is a multifunctional cell adhesion molecule that belongs to the immunoglobulin superfamily, which blocks malignant solid tumor formation. However, the relationship between CADM1 expression and prognosis in cutaneous squamous cell carcinoma patients remains unclear. The degree of CADM1 expression in tumor cells in a retrospective analysis of 88 patients with cSCC at our hospital between January 2006 and December 2016 was determined by immunostaining.

Source link: https://doi.org/10.3390/diagnostics11050830


Platelet Endothelial Cell Adhesion Molecule 1 (CD31) Is Essential for Clostridium perfringens Beta-Toxin Mediated Cytotoxicity in Human Endothelial and Monocytic Cells

Using a CRISPR/Cas9 gene knockout and an antibody blocking strategy, we now investigate the role of CD31 in CPB cytotoxicity against human endothelial and monocytic cells. Human endothelial and monocytic cells were resistant to CPB and CPB oligomers that were only present in CD31-expressing cells, as shown by CD31-expressing cells. Endothelial and monocytic cells could be selectively enhanced out of a polyclonal cell population by exposing them to CPB. CPB's cell type specificity of CPB detected in vitro and corresponds to in vivo measurements in naturally diseased animals when combined with the CD31 molecule.

Source link: https://doi.org/10.3390/toxins13120893


Liver sinusoidal endothelial cell expressed vascular cell adhesion molecule 1 promotes liver fibrosis

Embethelial cell dysfunction, liver sinusoidal endothelial cell abnormalities, and capillarization can all contribute to liver fibrosis. In both NASH and liver fibrosis models, Lyve1's immunity was reduced in Vcam1fl/fl mice and restored in Vcam1fl/fl mice and restored in Vcam1u0394end mice. In areas lacking Lyve1, Co-immunostaining increased u03b1-smooth muscle actin in the livers of Vcam1fl/fl mice. In addition, scanning electron microscopy revealed reduced LSEC fenestrae in the Vcam1fl/fl mice but not in the Vcam1u0394end mice in both injury models, indicating that VCAM1 promotes LSEC capillarization during liver injury. When cocultured with LSECs from CD-HFD-fed Vcam1-u0394end mice relative to Vcam1fl/fl mice, HSCs profibrogenic markers were reduced.

Source link: https://doi.org/10.3389/fimmu.2022.983255

* Please keep in mind that all text is summarized by machine, we do not bear any responsibility, and you should always check original source before taking any actions

* Please keep in mind that all text is summarized by machine, we do not bear any responsibility, and you should always check original source before taking any actions