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Updated: Apr 17, 2026

Studying Organelle Dynamics in B Cells During Immune Synapse Formation
Published on: June 1, 2019
The potential mechanism of bursal-derived BP8 on B cell developments
Xiao-Dong Liu1, Fu-Bo Zhang, Hu Shan
1College of Animal Science and Veterinary Medicine, Qingdao Agricultural University, Qingdao, 266109, China.
Abstract:
The bursa of Fabricius, the key humoral immune organ unique to birds, is critical for B cell differentiation and antibody production. BP8 (AGHTKKAP) is a novel immunomodulatory peptide that regulates B-cell development. Gene microarray was used to investigate the mechanism of BP8 on B cell development. BP8 regulated expressions of 1,570 genes that were involved in retinol metabolism, the Wnt signaling pathway, MAPK pathway, Jak-Stat pathway, Notch signaling pathway, cytokine-cytokine receptor interaction, and Ca(2+) signals. Finally, BP8 triggered ADH7 and RDH10 expression, interacted with retinol binding protein, and regulated retinol uptake in vitro and vivo. These data reveal a bursal-derived multifunctional factor, BP8, as a novel biomaterial which is essential for the development of the immune system and represents an important linker between the B cell development and retinol metabolism. This study elucidates the mechanisms involved in humoral immune system and has implications in treating human diseases.
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