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小鼠淋巴瘤对淋巴结(而非脾脏)的侵袭既依赖CD44又依赖透明质酸盐。

Lymph node (but not spleen) invasion by murine lymphoma is both CD44- and hyaluronate-dependent.

作者信息

Zahalka M A, Okon E, Gosslar U, Holzmann B, Naor D

机构信息

Lautenberg Center for General and Tumor Immunology, Hebrew University, Hadassah Medical School, Jerusalem, Israel.

出版信息

J Immunol. 1995 May 15;154(10):5345-55.

PMID:7537306
Abstract

Similar to activated T cells, LB T cell lymphoma expresses the CD44 cell surface Ag. In addition, the vast majority of LB cells also express the beta 2 (CD18) and alpha L (CD11a) chains of LFA-1 integrin. In view of the finding that anti-CD18 mAb blocked spleen, but not lymph node invasion by LB cells inoculated s.c. into BALB/c mice, we tested the ability of anti-CD44 mAb (IM 7.8.1) to block the infiltration of LB cells into the lymph nodes. We found that, as opposed to anti-CD18 mAb, anti-CD44 mAb, as well as its F(ab')2 or Fab fragment, prevented lymph node infiltration but had no effect on spleen invasion. This conclusion was based on histologic examination and [3H]thymidine incorporation into proliferating LB cells invading the lymphoid organs. Histologic analysis further demonstrated that LB cells invade the lymph node via the afferent lymphatics. The surface expression of CD44 molecules on LB cells was enhanced after PMA activation. PMA activation also enabled in vitro binding of the lymphoma to hyaluronic acid (HA), a known ligand of CD44. Because anti-CD44 mAb, its F(ab')2 or Fab fragment, and hyaluronidase blocked this binding, we also tested the ability of the enzyme to inhibit lymph node invasion by LB cells. We established through histologic examination and [3H]thymidine incorporation that hyaluronidase protected the lymph node, but not the spleen, from invasion by the lymphoma.

摘要

与活化的T细胞相似,淋巴母细胞性T细胞淋巴瘤表达CD44细胞表面抗原。此外,绝大多数淋巴母细胞还表达淋巴细胞功能相关抗原1(LFA-1)整合素的β2(CD18)和αL(CD11a)链。鉴于抗CD18单克隆抗体可阻断皮下接种到BALB/c小鼠体内的淋巴母细胞对脾脏的侵袭,但不能阻断其对淋巴结的侵袭这一发现,我们测试了抗CD44单克隆抗体(IM 7.8.1)阻断淋巴母细胞浸润淋巴结的能力。我们发现,与抗CD18单克隆抗体不同,抗CD44单克隆抗体及其F(ab')2或Fab片段可阻止淋巴结浸润,但对脾脏侵袭没有影响。这一结论基于组织学检查以及对侵入淋巴器官的增殖性淋巴母细胞的[3H]胸苷掺入情况。组织学分析进一步表明,淋巴母细胞通过输入淋巴管侵入淋巴结。经佛波酯(PMA)激活后,淋巴母细胞上CD44分子的表面表达增强。PMA激活还使淋巴瘤在体外能够与透明质酸(HA,CD44的已知配体)结合。由于抗CD44单克隆抗体及其F(ab')2或Fab片段以及透明质酸酶可阻断这种结合,我们还测试了该酶抑制淋巴母细胞侵袭淋巴结能力。通过组织学检查和[3H]胸苷掺入实验,我们证实透明质酸酶可保护淋巴结免受淋巴瘤侵袭,但对脾脏无此作用。

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