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引流淋巴的 T 细胞和树突状细胞利用不同的趋化因子受体 CCR7 依赖性途径进入淋巴结和淋巴结内迁移。

Afferent lymph-derived T cells and DCs use different chemokine receptor CCR7-dependent routes for entry into the lymph node and intranodal migration.

机构信息

Institute of Immunology, Hannover Medical School, Hannover, Germany.

出版信息

Nat Immunol. 2011 Aug 14;12(9):879-87. doi: 10.1038/ni.2085.


DOI:10.1038/ni.2085
PMID:21841786
Abstract

Little is known about the molecular mechanisms that determine the entry into the lymph node and intranodal positioning of lymph-derived cells. By injecting cells directly into afferent lymph vessels of popliteal lymph nodes, we demonstrate that lymph-derived T cells entered lymph-node parenchyma mainly from peripheral medullary sinuses, whereas dendritic cells (DCs) transmigrated through the floor of the subcapsular sinus on the afferent side. Transmigrating DCs induced local changes that allowed the concomitant entry of T cells at these sites. Signals mediated by the chemokine receptor CCR7 were absolutely required for the directional migration of both DCs and T cells into the T cell zone but were dispensable for the parenchymal entry of lymph-derived T cells and dendrite probing of DCs. Our findings provide insight into the molecular and structural requirements for the entry into lymph nodes and intranodal migration of lymph-derived cells of the immune system.

摘要

目前对于决定淋巴来源细胞进入淋巴结和在淋巴结内定位的分子机制知之甚少。通过将细胞直接注入到腘窝淋巴结的输入淋巴管中,我们证明了淋巴来源的 T 细胞主要从外周髓质窦进入淋巴结实质,而树突状细胞(DC)则通过输入淋巴管侧的被膜下窦底部穿越。穿越的 DC 诱导了局部变化,允许 T 细胞同时在这些部位进入。趋化因子受体 CCR7 介导的信号对于 DC 和 T 细胞向 T 细胞区的定向迁移是绝对必需的,但对于淋巴来源的 T 细胞进入淋巴结实质和 DC 的树突探测是可有可无的。我们的发现为了解免疫系统中淋巴来源细胞进入淋巴结和在淋巴结内迁移的分子和结构要求提供了线索。

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本文引用的文献

[1]
The outs and the ins of sphingosine-1-phosphate in immunity.

Nat Rev Immunol. 2011-5-6

[2]
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Proc Natl Acad Sci U S A. 2010-11-8

[3]
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J Exp Med. 2009-12-7

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J Exp Med. 2009-11-23

[7]
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J Immunol. 2009-10-1

[8]
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Nat Immunol. 2009-1

[9]
CXCL12 is essential for migration of activated Langerhans cells from epidermis to dermis.

Eur J Immunol. 2008-11

[10]
Rapid leukocyte migration by integrin-independent flowing and squeezing.

Nature. 2008-5-1

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