IgM, IgG, and IgA Influenza-Specific Plasma Cells Express Divergent Transcriptomes
| Autor: | Christopher D. Scharer, Jeremy M. Boss, John E. Bradley, Madeline J. Price, Troy D. Randall, Sakeenah L. Hicks |
|---|---|
| Rok vydání: | 2019 |
| Předmět: |
animal diseases
Immunology Population Plasma Cells chemical and pharmacologic phenomena Biology Article Transcriptome Mice Immune system Gene expression Influenza Human medicine Tumor Cells Cultured Immunology and Allergy Animals Humans education B cell education.field_of_study breakpoint cluster region hemic and immune systems Cell sorting Isotype Complementarity Determining Regions eye diseases Cell biology Immunoglobulin A Mice Inbred C57BL medicine.anatomical_structure Immunoglobulin M Immunoglobulin G |
| Zdroj: | J Immunol |
| ISSN: | 1550-6606 |
| Popis: | Ab-secreting cells (ASC) or plasma cells are essential components of the humoral immune system. Although Abs of different isotypes have distinct functions, it is not known if the ASC that secrete each isotype are also distinct. ASC downregulate their surface BCR upon differentiation, hindering analyses that couple BCR information to other molecular characteristics. In this study, we developed a methodology using fixation, permeabilization, and intracellular staining coupled with cell sorting and reversal of the cross-links to allow RNA sequencing of isolated cell subsets. Using hemagglutinin and nucleoprotein Ag-specific B cell tetramers and intracellular staining for IgM, IgG, and IgA isotypes, we were able to derive and compare the gene expression programs of ASC subsets that were responding to the same Ags following influenza infection in mice. Intriguingly, whereas a shared ASC signature was identified, each ASC isotype-specific population expressed distinct transcriptional programs controlling cellular homing, metabolism, and potential effector functions. Additionally, we extracted and compared BCR clonotypes and found that each ASC isotype contained a unique, clonally related CDR3 repertoire. In summary, these data reveal specific complexities in the transcriptional programming of Ag-specific ASC populations. |
| Databáze: | OpenAIRE |
| Externí odkaz: |
|