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携带人类T细胞白血病病毒的各种人类细胞系的细胞表面表型及病毒抗原表达

Cell surface phenotypes and expression of viral antigens of various human cell lines carrying human T-cell leukemia virus.

作者信息

Sugamura K, Fujii M, Kannagi M, Sakitani M, Takeuchi M, Hinuma Y

出版信息

Int J Cancer. 1984 Aug 15;34(2):221-8. doi: 10.1002/ijc.2910340213.

Abstract

Human T-cell leukemia/lymphoma virus (HTLV)-carrying cells from various origins were characterized by cell surface markers and expression of HTLV antigens. Eight cell lines named TCL were obtained by transformation of peripheral blood leukocytes (PBL) of healthy donors or HTLV carriers in cocultures with HTLV-producer MT-2 cells. Nine cell lines named ILT were interleukin 2 (IL2)-dependent cell lines cloned from PBL of ATL patients and healthy HTLV-carriers. Tc-Kan9 cell line was also an IL2-dependent cell line clonally established from PBL culture stimulated with autologous TCL cells. Five cell lines named TL were established in vitro directly from PBL of an adult T-cell leukemia (ATL) patient and from ILT cells of an ATL patient and three HTLV-carriers, respectively, to grow autonomously without IL2. All the TCLs, ILTs, TLs and Tc-Kan9 possessed Leu-I antigen, a pan-T-cell marker. Leu3a antigen, a helper/inducer T-cell marker, was expressed on five of eight TCLs and all of the ILTs and TLs. Leu-2a, a cytotoxic/suppressor T-cell marker, was detected only on Tc-Kan9 but not others. Fresh ATL leukemic cells of patients had a helper/inducer T-cell marker. Ia, OKT9 and Tac antigens, markers for activated and differentiated T cells, were strongly expressed on all of the cell lines tested and fresh ATL leukemic cells were weakly positive for these antigens. Expression of HTLV antigens detected by mouse monoclonal antibodies and an ATL-patient serum varied among these cell lines. One TL, two ILTs and most of the fresh ATL leukemic cells did not express HTLV antigens on the cell surface. The other cell lines were all positive for the surface viral antigens. However, molecular species of antigens defined by radioimmunoprecipitation with an ATL-patient serum were not always identical among the cell lines. Molecular weights of polypeptides detectable in most of the cell lines were 62K, 46K, 40K, 24K, 21K and 19K which could never be detected in several control T-cell lines. 68K and 28K polypeptides were frequently detected in MT-2 and TGLs. GIN14, a mouse monoclonal antibody against HTLV core protein (p19) detected not only p19 in various cell lines but also p28, p29, p31 or p40 in certain cell lines tested. B-cell lines named LCL were established and cloned from PBL of two HTLV-carriers by EB-virus-induced transformation and they also expressed HTLV antigens, Ia, OKT9 and Tac antigens.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

通过细胞表面标志物和人T细胞白血病/淋巴瘤病毒(HTLV)抗原的表达对来自不同来源的携带HTLV的细胞进行了表征。通过将健康供体或HTLV携带者的外周血白细胞(PBL)与产生HTLV的MT - 2细胞共培养,获得了8个名为TCL的细胞系。9个名为ILT的细胞系是从成人T细胞白血病(ATL)患者和健康HTLV携带者的PBL中克隆得到的白细胞介素2(IL2)依赖细胞系。Tc - Kan9细胞系也是从用自体TCL细胞刺激的PBL培养物中克隆建立的IL2依赖细胞系。5个名为TL的细胞系分别直接从一名ATL患者的PBL以及一名ATL患者和三名HTLV携带者的ILT细胞体外建立,可在无IL2的情况下自主生长。所有的TCL、ILT、TL和Tc - Kan9都具有全T细胞标志物Leu - I抗原。辅助/诱导性T细胞标志物Leu3a抗原在8个TCL中的5个以及所有的ILT和TL中表达。细胞毒性/抑制性T细胞标志物Leu - 2a仅在Tc - Kan9中检测到,其他细胞系未检测到。患者新鲜的ATL白血病细胞具有辅助/诱导性T细胞标志物。Ia、OKT9和Tac抗原是活化和分化T细胞的标志物,在所有测试的细胞系中均强烈表达,新鲜的ATL白血病细胞对这些抗原呈弱阳性。用小鼠单克隆抗体和一名ATL患者血清检测到的HTLV抗原在这些细胞系中的表达各不相同。一个TL、两个ILT以及大多数新鲜的ATL白血病细胞在细胞表面不表达HTLV抗原。其他细胞系的表面病毒抗原均为阳性。然而,用一名ATL患者血清通过放射免疫沉淀法确定的抗原分子种类在细胞系之间并不总是相同的。大多数细胞系中可检测到的多肽分子量为62K、46K、40K、24K、21K和19K,在几个对照T细胞系中从未检测到。68K和28K多肽在MT - 2和TGL中经常检测到。针对HTLV核心蛋白(p19)的小鼠单克隆抗体GIN14不仅在各种细胞系中检测到p19,在某些测试的细胞系中还检测到p28、p29、p31或p40。通过EB病毒诱导转化从两名HTLV携带者的PBL中建立并克隆了名为LCL的B细胞系,它们也表达HTLV抗原、Ia、OKT9和Tac抗原。(摘要截取自400字)

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