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鸡中类别转换B细胞的特征分析。

Characterization of class-switched B cells in chickens.

作者信息

von La Roche Dominik, Schumacher Magdalena, Kohn Marina, Trapp Johanna, Schusser Benjamin, Rautenschlein Silke, Härtle Sonja

机构信息

Department of Veterinary Sciences, AG Immunology, Ludwig-Maximilians-Universität München, Planegg, Germany.

Clinic for Poultry, University of Veterinary Medicine Hannover, Hannover, Germany.

出版信息

Front Immunol. 2024 Nov 21;15:1484288. doi: 10.3389/fimmu.2024.1484288. eCollection 2024.

DOI:10.3389/fimmu.2024.1484288
PMID:39640270
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11617357/
Abstract

While B cell development in the birds' primary B cell organ, the bursa Fabricius, is relatively well understood, very little is known about post bursal B cell differentiation into plasma and memory cells though these cells are essential for a protecting antibody response and so far, no specific markers for these cells were available. Since immunoglobulin class switch is one part of the B cell differentiation process, our objective was to conduct a first detailed investigation of class-switched chicken B cells. As only very few IgY and IgA expressing cells were detected in lymphoid organs of young chickens, we used CD40L and IL-10 to establish a prolonged culture system, which induces B cell proliferation, class switch to IgY and IgA and enhanced antibody secretion. This enabled a phenotypic analysis of differentiating B cells. Importantly, these cells lost surface expression of the B cell markers chB6 and BAFF-R. B cell receptor surface expression remained unchanged, showing that while differentiating toward plasma cells, B cells can be addressed by L chain staining. Newly generated potential plasma cell markers CD138 and TACI showed only a transient expression on cultured cells and rather act as markers for B cell activation than plasma/memory cells in general. CD57 upregulation was connected to activation and blast formation but not to class switch. We also examined potential changes in class-switched cells in different age groups and post vaccination. Surprisingly, bursa involution, laying and age had no distinct effects on the presence of class-switched cells, but we detected significantly more class-switched B cells post vaccination. Hence, we are now able to generate class-switched plasmablasts for a more detailed characterization and can address them under different conditions in chickens for further analysis of their B cell response.

摘要

虽然鸟类主要的B细胞器官法氏囊中B细胞的发育过程相对已被充分了解,但对于法氏囊后的B细胞分化为浆细胞和记忆细胞的情况却知之甚少,尽管这些细胞对于保护性抗体反应至关重要,而且到目前为止,还没有针对这些细胞的特异性标志物。由于免疫球蛋白类别转换是B细胞分化过程的一部分,我们的目标是首次对类别转换的鸡B细胞进行详细研究。由于在幼鸡的淋巴器官中仅检测到极少数表达IgY和IgA的细胞,我们使用CD40L和IL-10建立了一个长期培养系统,该系统可诱导B细胞增殖、类别转换为IgY和IgA并增强抗体分泌。这使得能够对分化中的B细胞进行表型分析。重要的是,这些细胞失去了B细胞标志物chB6和BAFF-R的表面表达。B细胞受体的表面表达保持不变,这表明在向浆细胞分化的过程中,B细胞可以通过轻链染色来识别。新产生的潜在浆细胞标志物CD138和TACI在培养细胞上仅短暂表达,总体上更像是B细胞活化的标志物而非浆细胞/记忆细胞的标志物。CD57的上调与活化和母细胞形成有关,但与类别转换无关。我们还研究了不同年龄组和接种疫苗后类别转换细胞的潜在变化。令人惊讶的是,法氏囊退化、产蛋和年龄对类别转换细胞的存在没有明显影响,但我们在接种疫苗后检测到显著更多的类别转换B细胞。因此,我们现在能够产生类别转换的浆母细胞以进行更详细的表征,并能够在鸡的不同条件下对其进行研究,以进一步分析它们的B细胞反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5882/11617357/38373d23f193/fimmu-15-1484288-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5882/11617357/8dd0f61873ba/fimmu-15-1484288-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5882/11617357/494947070ef9/fimmu-15-1484288-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5882/11617357/c113c5f5e7f0/fimmu-15-1484288-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5882/11617357/7d812c393e90/fimmu-15-1484288-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5882/11617357/bae1c1f8b705/fimmu-15-1484288-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5882/11617357/d444bfe0561f/fimmu-15-1484288-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5882/11617357/fd6ee195ab27/fimmu-15-1484288-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5882/11617357/62baa53d0b7c/fimmu-15-1484288-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5882/11617357/38373d23f193/fimmu-15-1484288-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5882/11617357/8dd0f61873ba/fimmu-15-1484288-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5882/11617357/494947070ef9/fimmu-15-1484288-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5882/11617357/c113c5f5e7f0/fimmu-15-1484288-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5882/11617357/7d812c393e90/fimmu-15-1484288-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5882/11617357/bae1c1f8b705/fimmu-15-1484288-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5882/11617357/d444bfe0561f/fimmu-15-1484288-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5882/11617357/fd6ee195ab27/fimmu-15-1484288-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5882/11617357/62baa53d0b7c/fimmu-15-1484288-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5882/11617357/38373d23f193/fimmu-15-1484288-g009.jpg

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