Jayne E Wiarda, Adrienne L Shircliff, Sage R Becker, Judith B Stasko, Sathesh K Sivasankaran, Mark R Ackermann, Crystal L Loving
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引用次数: 0
Abstract
Peyer's patches (PPs) are B cell-rich sites of intestinal immune induction, yet PP-associated B cell signaling, activation, and differentiation are poorly defined. Single-cell and spatial transcriptomics were completed to study B cells from porcine jejunum and ileum containing PPs. Intestinal locations had distinct immune landscapes, including more follicular B cells in ileum and increased MHC-II-encoding gene expression in jejunal B cells. Despite distinct landscapes, conserved B cell dynamics were detected across intestinal locations, including B cell signaling to CD4+ macrophages that are putative phagocytic, cytotoxic, effector cells and deduced routes of B cell activation/differentiation, including resting B cells migrating into follicles to replicate/divide or differentiate into antibody-secreting cells residing in intestinal crypts. A six-biomarker panel recapitulated transcriptomics findings of B cell phenotypes, frequencies, and spatial locations via ex vivo and in situ staining. Findings convey conserved B cell dynamics across intestinal locations containing PPs, despite location-specific immune environments. Results establish a benchmark of B cell dynamics for understanding intestinal immune induction important to promoting gut/overall health.
佩耶氏斑块(PPs)是肠道免疫诱导中B细胞丰富的部位,但与PPs相关的B细胞信号传导、活化和分化尚不明确。我们完成了单细胞和空间转录组学研究,以研究猪空肠和回肠中含有PPs的B细胞。肠道位置具有不同的免疫景观,包括回肠中更多的滤泡 B 细胞和空肠 B 细胞中更多的 MHC-II 编码基因表达。尽管肠道位置不同,但检测到的 B 细胞动态是一致的,包括 B 细胞向 CD4+ 巨噬细胞发出信号,CD4+ 巨噬细胞是潜在的吞噬细胞、细胞毒性细胞和效应细胞,以及推断出的 B 细胞活化/分化途径,包括静止的 B 细胞迁移到滤泡中复制/分裂或分化成驻留在肠隐窝的分泌抗体的细胞。通过体外和原位染色,一个六种生物标记物面板再现了B细胞表型、频率和空间位置的转录组学发现。研究结果表明,尽管存在特定位置的免疫环境,但在含有PPs的肠道中,B细胞的动态变化是一致的。研究结果为了解对促进肠道/整体健康非常重要的肠道免疫诱导建立了一个 B 细胞动态基准。
期刊介绍:
Mucosal Immunology, the official publication of the Society of Mucosal Immunology (SMI), serves as a forum for both basic and clinical scientists to discuss immunity and inflammation involving mucosal tissues. It covers gastrointestinal, pulmonary, nasopharyngeal, oral, ocular, and genitourinary immunology through original research articles, scholarly reviews, commentaries, editorials, and letters. The journal gives equal consideration to basic, translational, and clinical studies and also serves as a primary communication channel for the SMI governing board and its members, featuring society news, meeting announcements, policy discussions, and job/training opportunities advertisements.