Diversified bursal medullary B cells survive and expand independently after depletion following neonatal infectious bursal disease virus infection
Autor: | David R. Withers, T. Fred Davison, John R. Young |
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Jazyk: | angličtina |
Rok vydání: | 2006 |
Předmět: |
Stromal cell
animal structures Immunology Immunoglobulin Variable Region Gene Expression Infectious bursal disease virus Infectious bursal disease Bursa of Fabricius Cytidine Deaminase medicine Activation-induced (cytidine) deaminase Immunology and Allergy Animals RNA Messenger Poultry Diseases B-Lymphocytes biology Lymphopoiesis Stem Cells Cell Differentiation Gene rearrangement Original Articles medicine.disease Birnaviridae Infections Virology Molecular biology Lymphatic system biology.protein Immunoglobulin Light Chains Stem cell Antibody Chickens |
Popis: | The primary immunoglobulin repertoire of chickens is generated not by gene rearrangement but by a subsequent process of gene conversion in proliferating immature B cells within the follicles of a specialized gut-associated lymphoid organ, the bursa of Fabricius. Neonatal infection with infectious bursal disease virus can eliminate almost the entire bursal B-cell compartment. Thereafter, two types of follicle reappear. Larger follicles, with rapidly proliferating B cells and normal structure, are correlated with partial recovery of antibody response. Smaller follicles, lacking distinct cortex and medulla, appear unable to produce antigen-responsive B cells. To understand the genesis of the two types of follicle, we analysed their VL sequences and activation-induced deaminase mRNA levels. The results provide a model of bursal repopulation in which surviving bursal stem cells generate new follicles with normal morphology and function, while surviving medullary B cells continue to proliferate slowly, under the influence of stromal cells, giving rise to the smaller follicles. The latter remain fixed in a stage of development incapable of further gene diversification. |
Databáze: | OpenAIRE |
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