B Cells Are Crucial for Both Development and Maintenance of the Splenic Marginal Zone1

B Cells Are Crucial for Both Development and Maintenance of the Splenic Marginal Zone1
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B 细胞对于脾边缘区的发育和维持至关重要1

DOI:
--
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发表时间:
2004
影响因子:
4.4
通讯作者:
R. Mebius
R. Mebius
中科院分区:
医学2区
文献类型:
--
作者:
M. Nolte;R. Arens;M. Kraus;M. V. van Oers;G. Kraal;R. V. van Lier;R. Mebius

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The splenic marginal zone is a unique compartment that separates the lymphoid white pulp from the surrounding red pulp. Due to the orchestration of specialized macrophages and B cells flanking a marginal sinus, this compartment plays an important role in uptake of blood-borne Ags and it gives the spleen its specialized function in antibacterial immunity. In this study, we demonstrate that both development and maintenance of this marginal zone is highly dependent on the presence of B cells. Spleens from B cell-deficient mice were found to lack both metallophilic and marginal zone macrophages as well as mucosal addressin cellular adhesion molecule-1+ sinus lining cells. Using an inducible Cre/loxP-driven mouse model in which mature B cells could be partially depleted by removal of the B cell receptor subunit Igα, we could show that the integrity and function of an established marginal zone was also dependent on the presence of B cells. This was confirmed in a transgenic model in which all B cells were gradually depleted due to overexpression of the TNF family member CD70. The loss of all cellular subsets from the marginal zone in these CD70 transgenic mice was effectively prevented by crossing these mice on a CD27−/− or TCRα−/− background, because this prohibited the ongoing B cell depletion. Therefore, we conclude that B cells are not only important for the development, but also for maintenance, of the marginal zone. This direct correlation between circulating B cells and the function of the spleen implies an increased risk for B cell lymphopenic patients with bacterial infections.
B7-1 转基因小鼠中揭示了 B7 的负调节功能。
DOI: 10.1016/1074-7613(94)90072-8
发表时间: 1994
期刊: Immunity
影响因子: 32.4
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DOI: --
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