2 research outputs found

    Comparison of synthetic routes for large-scale synthesis of spherical BiVOâ‚„ with photocatalytic and superhydrophobic properties

    No full text
    Abstract The spherical BiVO4 in tetragonal and monoclinic scheelite phases have been prepared through five general methods by using K6V10O28·9H2O as self-sacrifice templates. The morphology of these BiVO4 is kept spherical because of K6V10O28·9H2O as self-sacrifice templates. The microwave-assisted synthesis of tetragonal BiVO4 is convenient, and ultrasonic synthesis is the best choice for the synthesis of monoclinic BiVO4. BiVO4 has been prepared by five general methods using decavanadate (K6V10O28·9H2O) as vanadium source. And the morphology of these BiVO4 is spherical

    Protein phosphatase 2A propels follicular T helper cell development in lupus

    No full text
    Follicular helper T (Tfh) cells are important for generating humoral immune responses by helping B cells form germinal centers (GCs) and the production of high-affinity antibodies. However, aberrant Tfh cell expansion also contributes to the generation of self-reactive autoantibodies and promotes autoantibody-mediated autoimmune diseases such as systemic lupus erythematosus (SLE). Protein phosphatase 2A catalytic subunit alpha isoform (PP2A Cα) expression levels are elevated in peripheral T cells of SLE patients and positively correlate with autoantibody titers and disease activity. Here, we demonstrate a critical role of PP2A in Tfh differentiation by using T cell restricted PP2A Cα deficient mice. We observed impaired Tfh differentiation and GC response in two different classical Tfh induction models. Mechanistic studies revealed that downregulation of protein translation of the Tfh lineage transcription factor BCL6 in PP2A deficient T cells. Importantly, we found that PP2A deficiency by either gene knockout or chemical inhibition alleviated lupus severity in mice. Lastly, we confirmed a positive correlation between PP2A Cα and BCL6 protein levels in human CD4 T cells from patients with SLE. In summary, our study revealed a critical role of PP2A in regulating Tfh cells and suggests it is a potential therapeutic target for lupus
    corecore