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归巢受体再探讨:小鼠淋巴细胞内皮细胞黏附分子-1(MEL-14抗原)参与淋巴细胞向肠道相关淋巴组织的迁移。

Homing receptors reexamined: mouse LECAM-1 (MEL-14 antigen) is involved in lymphocyte migration into gut-associated lymphoid tissue.

作者信息

Hamann A, Jablonski-Westrich D, Jonas P, Thiele H G

机构信息

Department of Immunology, I. Medizinische Klinik, Universitätskrankenhaus, Eppendorf, Hamburg, FRG.

出版信息

Eur J Immunol. 1991 Dec;21(12):2925-9. doi: 10.1002/eji.1830211205.

DOI:10.1002/eji.1830211205
PMID:1721022
Abstract

Specific recognition molecules ("homing receptors") on lymphocytes are thought to direct selective entry of cells into different organs. The lectin-related cell adhesion molecule LECAM-1 has previously been supposed to mediate lymphocyte entry into peripheral lymph nodes and, partially, mesenteric nodes but not into Peyer's patches. Here we present evidence that in vivo the molecule is also implicated in homing of mouse lymphocytes to Peyer's patches and may have a more general role as homing receptor for high endothelial venules-bearing lymphoid tissue, but not for most non-lymphoid tissue.

摘要

淋巴细胞上的特异性识别分子(“归巢受体”)被认为可引导细胞选择性进入不同器官。此前认为凝集素相关细胞黏附分子LECAM-1介导淋巴细胞进入外周淋巴结,部分介导进入肠系膜淋巴结,但不介导进入派氏结。在此我们提供证据表明,在体内该分子也与小鼠淋巴细胞归巢至派氏结有关,并且可能作为带有高内皮微静脉的淋巴组织的归巢受体发挥更广泛的作用,但对大多数非淋巴组织不起作用。

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Homing receptors reexamined: mouse LECAM-1 (MEL-14 antigen) is involved in lymphocyte migration into gut-associated lymphoid tissue.归巢受体再探讨:小鼠淋巴细胞内皮细胞黏附分子-1(MEL-14抗原)参与淋巴细胞向肠道相关淋巴组织的迁移。
Eur J Immunol. 1991 Dec;21(12):2925-9. doi: 10.1002/eji.1830211205.
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B and T lymphocyte subsets enter peripheral lymph nodes and Peyer's patches without preference in vivo: no correlation occurs between their localization in different types of high endothelial venules and the expression of CD44, VLA-4, LFA-1, ICAM-1, CD2 or L-selectin.B淋巴细胞和T淋巴细胞亚群在体内无偏好地进入外周淋巴结和派尔集合淋巴结:它们在不同类型的高内皮微静脉中的定位与CD44、VLA-4、LFA-1、ICAM-1、CD2或L-选择素的表达之间不存在相关性。
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Organ specificity of lymphocyte migration: mediation by highly selective lymphocyte interaction with organ-specific determinants on high endothelial venules.淋巴细胞迁移的器官特异性:通过淋巴细胞与高内皮微静脉上的器官特异性决定簇的高度选择性相互作用介导。
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