Distinct roles of ICOS and CD40L in human T-B cell adhesion and antibody production
Adult
CD4-Positive T-Lymphocytes
Male
0301 basic medicine
B-Lymphocytes
Adolescent
CD40 Ligand
Cell Communication
Middle Aged
Lymphocyte Activation
Inducible T-Cell Co-Stimulator Protein
Young Adult
03 medical and health sciences
Focal Adhesion Kinase 2
Immunoglobulin M
Immunoglobulin G
Antibody Formation
Cell Adhesion
Humans
Lupus Erythematosus, Systemic
Female
Cells, Cultured
DOI:
10.1016/j.cellimm.2021.104420
Publication Date:
2021-08-06T15:06:33Z
AUTHORS (9)
ABSTRACT
CD40-CD40L and inducible co-stimulatory molecule (ICOS)-ICOSL ligations are demonstrated to play critical roles in CD4+ T-B interaction for B cell activation differentiation mouse models. Herein, by using a micropipette adhesion assay an vitro coculture system simultaneously, we intended dissect their human IgG/IgM production. With the upregulation of CD40L ICOS expressions on T cells upon TCR/CD28 stimulation vitro, activated exhibited enhanced with autologous at single level when compared resting counterparts. Blockade dramatically damped between whereas less effect blockade was observed. On contrary, led dramatic decrease production were cocultured together induction CD19hi cells. However, displayed attenuation Distinct ICOS-ICOSL also observed lupus erythematosus patients. The CD40L, rather than ICOS, phosphorylation Pyk2 total Our study thus provides evidence that either or pathogenic state function diversely during interactions. While ligation is more likely be engaged adhesion, indispensable signal results indicative segregating costimulation differentiation, which might helpful dissection SLE pathogenesis.
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