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NOD-SCID 小鼠携带与艾滋病相关的 Burkitt 淋巴瘤细胞系 2F7 时,其鼠源 CXCL13 水平显著升高,但人源 CXCL13 水平则不然。

Levels of murine, but not human, CXCL13 are greatly elevated in NOD-SCID mice bearing the AIDS-associated Burkitt lymphoma cell line, 2F7.

机构信息

Department of Obstetrics & Gynecology, David Geffen School of Medicine at UCLA, University of California Los Angeles, Los Angeles, California, United States of America.

出版信息

PLoS One. 2013 Aug 2;8(8):e72414. doi: 10.1371/journal.pone.0072414. Print 2013.

Abstract

Currently, few rodent models of AIDS-associated non-Hodgkin's lymphoma (AIDS-NHL) exist. In these studies, a novel mouse/human xenograft model of AIDS-associated Burkitt lymphoma (AIDS-BL) was created by injecting cells of the human AIDS-BL cell line, 2F7, intraperitoneally into NOD-SCID mice. Mice developed tumors in the peritoneal cavity, with metastases to the spleen, thymus, and mesenteric lymph nodes. Expression of the chemokine receptor, CXCR5, was greatly elevated in vivo on BL tumor cells in this model, as shown by flow cytometry. CXCL13 is the ligand for CXCR5, and serum and ascites levels of murine, but not human, CXCL13 showed a striking elevation in tumor-bearing mice, with levels as high as 200,000 pg/ml in ascites, as measured by ELISA. As shown by immunohistochemistry, murine CXCL13 was associated with macrophage-like tumor-infiltrating cells that appeared to be histiocytes. Blocking CXCR5 on 2F7 cells with neutralizing antibodies prior to injection into the mice substantially delayed tumor formation. The marked elevations in tumor cell CXCR5 expression and in murine CXCL13 levels seen in the model may potentially identify an important link between tumor-interacting histiocytes and tumor cells in AIDS-BL. These results also identify CXCL13 as a potential biomarker for this disease, which is consistent with previous studies showing that serum levels of CXCL13 were elevated in human subjects who developed AIDS-lymphoma. This mouse model may be useful for future studies on the interactions of the innate immune system and AIDS-BL tumor cells, as well as for the assessment of potential tumor biomarkers for this disease.

摘要

目前,针对艾滋病相关非霍奇金淋巴瘤(AIDS-NHL)的啮齿动物模型较少。在这些研究中,通过将人 AIDS-BL 细胞系 2F7 的细胞腹腔内注射到 NOD-SCID 小鼠中,创建了一种新型的 AIDS 相关伯基特淋巴瘤(AIDS-BL)的小鼠/人异种移植模型。小鼠在腹腔内形成肿瘤,并转移到脾、胸腺和肠系膜淋巴结。流式细胞术显示,该模型中 BL 肿瘤细胞体内趋化因子受体 CXCR5 的表达大大升高。CXCL13 是 CXCR5 的配体,ELISA 检测显示,肿瘤荷瘤小鼠血清和腹水中小鼠而非人 CXCL13 的水平显著升高,腹水水平高达 200,000pg/ml。免疫组化显示,小鼠 CXCL13 与巨噬细胞样肿瘤浸润细胞相关,这些细胞似乎是组织细胞。在将 2F7 细胞注射到小鼠体内之前,用中和抗体阻断 CXCR5 可显著延迟肿瘤形成。在该模型中观察到肿瘤细胞 CXCR5 表达和小鼠 CXCL13 水平的显著升高,这可能潜在地确定了 AIDS-BL 中肿瘤相互作用的组织细胞与肿瘤细胞之间的重要联系。这些结果还表明 CXCL13 是该疾病的潜在生物标志物,这与先前的研究一致,即血清 CXCL13 水平升高的人类发生 AIDS-淋巴瘤。这种小鼠模型可能对研究先天免疫系统与 AIDS-BL 肿瘤细胞的相互作用以及评估该疾病的潜在肿瘤生物标志物有用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c89/3732224/e1403b7d0459/pone.0072414.g001.jpg

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