mProX™ Human CD40LG Stable Cell Line
- Product Category:
- Membrane Protein Stable Cell Lines
- Subcategory:
- CD Cell Lines
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Published Data
Fig.1 Overexpressing CD40LG in human T cells.
Primary T cells from normal human donors were transfected with CD40LG cDNA, which had been cloned into the expression vector pEGFP-C1 (pEGFP-C1/CD40LG), while cells transfected with the empty vector were used as controls. The confirmation of transfection efficiency (≥ 40%) was carried out through flow cytometry for the GFP protein. CD40LG overexpression in transfected T cells was subsequently confirmed through the utilization of a fluorochrome-conjugated anti-CD40LG antibody in flow cytometry analysis.
Ref: Zhou, Ying, et al. "T cell CD40LG gene expression and the production of IgG by autologous B cells in systemic lupus erythematosus." Clinical immunology 132.3 (2009): 362-370.
Pubmed: 19520616
DOI: 10.1016/j.clim.2009.05.011
Research Highlights
H Wagner, A. et al. "Potential role of soluble CD40 receptor in chronic inflammatory diseases." Biochemical pharmacology, 2023.
The CD40 receptor and its ligand CD154 have a broad expression in immune-competent cells. The interaction between CD154 and CD40 is crucial for the growth and differentiation of B-cells, as well as immunoglobulin class switching. This co-stimulatory ligand-receptor pair also plays a significant role in the communication between various immune-competent cells involved in innate and adaptive immunity. The CD40-CD154 interaction has a significant involvement in the development of inflammatory and autoimmune diseases. Although both CD40 and CD154 are membrane-bound proteins, their soluble forms can be generated through proteolytic cleavage or alternative splicing. In this review, current knowledge about single nucleotide polymorphisms in the human CD40 gene and compensatory changes in the plasma level of soluble CD40 receptor (sCD40) isoform in related pro-inflammatory diseases will be summarized. Additionally, the regulation patterns of the disintegrin metalloprotease ADAM17 function, which leads to the shedding of transmembrane proteins, such as pro-inflammatory adhesion molecules or CD40, will be discussed. Finally, the potential of sCD40 as a biomarker for chronic inflammatory diseases will also be explored.
H Wagner, A. et al. "Potential role of soluble CD40 receptor in chronic inflammatory diseases." Biochemical pharmacology, 2023.
Pubmed:
37863325
DOI:
10.1016/j.bcp.2023.115858
B Jacobsen, Mads-Holger. et al. "Metabolic syndrome, soluble CD40L, and biomarkers of endothelial dysfunction in people living with HIV." APMIS : acta pathologica, microbiologica, et immunologica Scandinavica, 2023.
The aim of this present study was to investigate the relationship between soluble CD40 ligand (sCD40L), a marker of platelet activation, and soluble thrombomodulin and syndecan-1, both markers of endothelial dysfunction, with metabolic syndrome in a large cohort of well-treated people with HIV (PWH). The study included 862 PWH with undetectable viral replication. The authors used uni- and multivariable logistic regression models, adjusted for known confounders, to test their hypotheses. While there was no association found between soluble thrombomodulin and syndecan-1 with metabolic syndrome, high levels of sCD40L were significantly associated with increased risk of metabolic syndrome (adjusted odds ratio 1.54, 95% CI 1.07-2.22). These results suggest a potential role for sCD40L in the well-known link between cardiometabolic comorbidity and HIV infection, given its known association with vascular inflammation and endothelial damage.
B Jacobsen, Mads-Holger. et al. "Metabolic syndrome, soluble CD40L, and biomarkers of endothelial dysfunction in people living with HIV." APMIS : acta pathologica, microbiologica, et immunologica Scandinavica, 2023.
Pubmed:
37849049
DOI:
10.1111/apm.13354