miR?148a controls metabolic programming and survival of mature CD19?negative plasma cells in mice
نویسندگان
چکیده
Long-lived antibody-secreting plasma cells are essential to establish humoral memory against pathogens. While a regulatory transcription factor network has been established in cell differentiation, the role of miRNAs remains enigmatic. We have recently identified miR-148a as most abundant miRNA primary mouse and human cells. To determine whether this signature controls vivo development B into long-lived cells, we mice with genomic, conditional, inducible deletions miR-148a. The analysis miR-148a-deficient revealed reduced serum Ig, decreased numbers newly formed plasmablasts CD19-negative, CD93-positive Transcriptome metabolic an impaired glucose uptake, oxidative phosphorylation-based energy metabolism, altered abundance homing receptors CXCR3 (increase) CXCR4 (reduction) These findings support positive regulator maintenance
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ژورنال
عنوان ژورنال: European Journal of Immunology
سال: 2021
ISSN: ['1521-4141', '0014-2980']
DOI: https://doi.org/10.1002/eji.202048993