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霍奇金和里德-斯腾伯格细胞中CCL5/RANTES的表达及其在肥大细胞募集至淋巴瘤组织中的可能作用。

Expression of CCL5/RANTES by Hodgkin and Reed-Sternberg cells and its possible role in the recruitment of mast cells into lymphomatous tissue.

作者信息

Fischer Marie, Juremalm Mikael, Olsson Niclas, Backlin Carin, Sundström Christer, Nilsson Kenneth, Enblad Gunilla, Nilsson Gunnar

机构信息

Department of Oncology, Radiology and Clinical Immunology, Uppsala University, Uppsala, Sweden.

出版信息

Int J Cancer. 2003 Nov 1;107(2):197-201. doi: 10.1002/ijc.11370.

DOI:10.1002/ijc.11370
PMID:12949794
Abstract

HL is a malignant lymphoma characterized by a small number of malignant HRS cells among a major population of infiltrating reactive cells, e.g., lymphocytes and eosinophils. We previously reported that mast cells are present in HL-affected lymph nodes and therein are the predominant CD30L-expressing cells. The CD30L expressed on mast cells is functionally active and can provide stimulatory signals to HRS cells. Thus, mast cells constitute an important portion of the infiltrating reactive cells that contribute to tumor progression in HL. Control of the recruitment of this previously unrecognized cell and its interactions with tumor cells are essentially unknown. To elucidate if mast cells might be specifically attracted to the tumor area by chemokines produced by HRS cells, we investigated chemokine expression in HL cell lines and in vivo. By RNase protection assay, mRNA expression of several chemokines could be detected in the cell lines. Despite the heterogeneous expression profile exhibited by the cell lines, 4 of 5 expressed CCL5 (RANTES) mRNA. RT-PCR and immunohistochemistry confirmed expression of CCL5 in vivo. Furthermore, secreted CCL5 was detected in conditioned media from 3 of the cell lines. In a migration assay, we found that CCL5 present in conditioned medium could induce mast cell migration. Taken together, our results suggest that CCL5 produced by HRS cells is one mechanism by which mast cells can be attracted into the tumor tissue in HL.

摘要

霍奇金淋巴瘤(HL)是一种恶性淋巴瘤,其特征是在大量浸润的反应性细胞(如淋巴细胞和嗜酸性粒细胞)中存在少量恶性霍奇金和里德􀅰斯腾伯格(HRS)细胞。我们之前报道过肥大细胞存在于受HL影响的淋巴结中,并且是其中主要表达CD30配体(CD30L)的细胞。肥大细胞上表达的CD30L具有功能活性,能够向HRS细胞提供刺激信号。因此,肥大细胞构成了浸润性反应性细胞的重要部分,促进了HL中的肿瘤进展。此前对这种未被认识的细胞的募集及其与肿瘤细胞相互作用的控制基本上还不清楚。为了阐明肥大细胞是否可能被HRS细胞产生的趋化因子特异性吸引到肿瘤区域,我们研究了HL细胞系和体内趋化因子的表达。通过核糖核酸酶保护分析,在细胞系中可检测到几种趋化因子的信使核糖核酸(mRNA)表达。尽管细胞系表现出异质性表达谱,但5个细胞系中有4个表达了CC趋化因子配体5(CCL5,又称调节激活正常T细胞表达和分泌因子,RANTES)mRNA。逆转录聚合酶链反应(RT-PCR)和免疫组织化学证实了CCL5在体内的表达。此外,在3个细胞系的条件培养基中检测到了分泌的CCL5。在迁移试验中,我们发现条件培养基中存在的CCL5可诱导肥大细胞迁移。综上所述,我们的结果表明,HRS细胞产生的CCL5是肥大细胞能够被吸引到HL肿瘤组织中的一种机制。

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