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本文引用的文献

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Lymph node cortical sinus organization and relationship to lymphocyte egress dynamics and antigen exposure.淋巴结皮质窦的组织及其与淋巴细胞迁出动力学和抗原暴露的关系。
Proc Natl Acad Sci U S A. 2010 Nov 23;107(47):20447-52. doi: 10.1073/pnas.1009968107. Epub 2010 Nov 8.
2
Fine-tuning immune surveillance by fever-range thermal stress.热应激微调免疫监视。
Immunol Res. 2010 Mar;46(1-3):177-88. doi: 10.1007/s12026-009-8122-9.
3
B lymphocytes exit lymph nodes through cortical lymphatic sinusoids by a mechanism independent of sphingosine-1-phosphate-mediated chemotaxis.B淋巴细胞通过一种独立于1-磷酸鞘氨醇介导的趋化作用的机制,经皮质淋巴窦离开淋巴结。
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Deletion of the developmentally essential gene ATR in adult mice leads to age-related phenotypes and stem cell loss.在成年小鼠中删除发育必需基因ATR会导致与年龄相关的表型和干细胞丢失。
Cell Stem Cell. 2007 Jun 7;1(1):113-126. doi: 10.1016/j.stem.2007.03.002.
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Follicular dendritic cell networks of primary follicles and germinal centers: phenotype and function.初级滤泡和生发中心的滤泡树突状细胞网络:表型与功能
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The "mode" of lymphocyte extravasation through HEV of Peyer's patches and its role in normal homing and inflammation.淋巴细胞通过派氏结的高内皮微静脉渗出的“方式”及其在正常归巢和炎症中的作用。
Microvasc Res. 2008 Mar;75(2):227-37. doi: 10.1016/j.mvr.2007.09.003. Epub 2007 Oct 4.
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Fibroblastic reticular cells in lymph nodes regulate the homeostasis of naive T cells.淋巴结中的成纤维网状细胞调节初始T细胞的稳态。
Nat Immunol. 2007 Nov;8(11):1255-65. doi: 10.1038/ni1513. Epub 2007 Sep 23.
8
CCR7 ligands control basal T cell motility within lymph node slices in a phosphoinositide 3-kinase-independent manner.CCR7配体以一种不依赖磷脂酰肌醇3激酶的方式控制淋巴结切片内的基础T细胞运动。
J Exp Med. 2007 May 14;204(5):1167-79. doi: 10.1084/jem.20062079. Epub 2007 May 7.
9
CCR7 ligands stimulate the intranodal motility of T lymphocytes in vivo.CCR7配体在体内刺激T淋巴细胞的结内运动。
J Exp Med. 2007 Mar 19;204(3):489-95. doi: 10.1084/jem.20061706. Epub 2007 Feb 26.
10
CC chemokine receptor 7 contributes to Gi-dependent T cell motility in the lymph node.C-C趋化因子受体7有助于淋巴结中依赖Gi的T细胞运动。
J Immunol. 2007 Mar 1;178(5):2973-8. doi: 10.4049/jimmunol.178.5.2973.

高内皮静脉作为交通控制点,维持淋巴结中淋巴细胞群体的平衡。

High endothelial venules as traffic control points maintaining lymphocyte population homeostasis in lymph nodes.

机构信息

Centre d'Immunologie de Marseille Luminy, Aix-Marseille University, Marseille, France.

出版信息

Blood. 2011 Dec 1;118(23):6115-22. doi: 10.1182/blood-2011-07-367409. Epub 2011 Sep 21.

DOI:10.1182/blood-2011-07-367409
PMID:21937697
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3234668/
Abstract

Millions of lymphocytes enter and exit mammal lymph nodes (LNs) each day, accessing the parenchyma via high endothelial venules (HEVs) and egressing via lymphatics. Despite this high rate of cellular flux and the many entry and exit sites within a given LN, the number of lymphocytes present in a resting LN is extraordinary stable over time, raising the question of how this steady-state is maintained. Here we have examined the anatomic details of lymphocyte movement in HEVs, finding that HEVs create pockets within which lymphocytes reside for several minutes before entering the LN proper. The function of these pockets was revealed in experiments performed under conditions in which lymphocyte egress from the LN was compromised by any of several approaches. Under such conditions, the HEVs pockets behaved as "waiting areas" in which lymphocytes were held until space was made available to them for entry into the parenchyma. Thus, rather than being simple entry ports, HEVs act as gatekeepers able to stack, hold and grant lymphocytes access to LN parenchyma in proportion to the rate of lymphocyte egress from the LN, enabling the LN to maintain a constant steady-state cellularity while supporting the extensive cellular trafficking necessary for repertoire scanning.

摘要

数以百万计的淋巴细胞每天进出哺乳动物淋巴结 (LNs),通过高内皮小静脉 (HEVs) 进入实质,通过淋巴管离开。尽管存在如此高的细胞通量和给定 LN 内的许多进入和离开部位,但在休息的 LN 中存在的淋巴细胞数量在很长一段时间内非常稳定,这引发了一个问题,即如何维持这种稳定状态。在这里,我们检查了淋巴细胞在 HEVs 中移动的解剖细节,发现 HEVs 在将淋巴细胞进入 LN 之前在其中形成了口袋,淋巴细胞在这些口袋中停留数分钟。在通过几种方法损害 LN 中淋巴细胞离开的条件下进行的实验揭示了这些口袋的功能。在这种情况下,HEV 口袋充当“等候区”,淋巴细胞在那里被扣留,直到为它们进入实质腾出空间。因此,HEVs 不仅仅是简单的入口,它们还充当门控器,能够根据从 LN 中离开的淋巴细胞的速度来堆积、保留和允许淋巴细胞进入 LN 实质,从而使 LN 能够维持恒定的稳定细胞状态,同时支持用于库扫描的广泛细胞运输。