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首页> 外文期刊>The Journal of Immunology: Official Journal of the American Association of Immunologists >Cutting edge: The B cell chemokine CXC chemokine ligand 13/B lymphocyte chemoattractant is expressed in the high endothelial venules of lymph nodes and Peyer's patches and affects B cell trafficking across high endothelial venules.
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Cutting edge: The B cell chemokine CXC chemokine ligand 13/B lymphocyte chemoattractant is expressed in the high endothelial venules of lymph nodes and Peyer's patches and affects B cell trafficking across high endothelial venules.

机译:前沿:B细胞趋化因子CXC趋化因子配体13 / B淋巴细胞趋化因子在淋巴结和Peyer斑块的高内皮微静脉中表达,并影响跨高内皮微静脉的B细胞运输。

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摘要

While CCR7 ligands direct T cell trafficking into lymph nodes (LNs) and Peyer's patches (PPs), chemokines that regulate B cell trafficking across high endothelial venules (HEVs) remain to be fully elucidated. Here we report that CXC chemokine ligand (CXCL)13 (B lymphocyte chemoattractant) is detected immunohistologically in the majority of HEVs in LNs and PPs of nonimmunized mice. Systemically administered anti-CXCL13 Ab bound to the surface of approximately 50% of HEVs in LNs and PPs, but not to other types of blood vessels, indicating that CXCL13 is expressed in the HEV lumen. In CXCL13-null mice, B cells rarely adhered to PP HEVs, whereas T cells did efficiently. Superfusion of CXCL13-null PPs with CXCL13 restored the luminal presentation of CXCL13 and also B cell arrest in PP HEVs at least partially. Collectively, these results indicate that CXCL13 expressed in the HEV lumen plays a crucial role in B cell trafficking into secondary lymphoid tissues such as PPs.
机译:虽然CCR7配体将T细胞运输引导到淋巴结(LN)和Peyer斑块(PPs)中,但调节B细胞在高内皮小静脉(HEV)上运输的趋化因子仍有待充分阐明。在这里,我们报告在未免疫小鼠的LN和PP中,大多数HEV的免疫组织学检测到CXC趋化因子配体(CXCL)13(B淋巴细胞趋化因子)。全身施用的抗CXCL13 Ab与LN和PP中大约50%的HEV表面结合,但不与其他类型的血管结合,表明CXCL13在HEV腔中表达。在无CXCL13的小鼠中,B细胞很少粘附于PP HEV,而T细胞则有效。 CXCL13-null PP与CXCL13的融合至少部分恢复了CXCL13的腔内表现,也恢复了B HEV中的B细胞停滞。总体而言,这些结果表明,HEV管腔中表达的CXCL13在B细胞向次级淋巴组织(如PP)的运输中起着至关重要的作用。

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