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人B淋巴细胞系

Human B-lymphoid cell lines.

作者信息

Nilsson K

机构信息

Department of Pathology, University of Uppsala.

出版信息

Hum Cell. 1992 Mar;5(1):25-41.

PMID:1329931
Abstract

The collective efforts during almost three decades by hematologists, tumor biologists and immunologists have provided a collection of established human hematopoietic cell lines, representing most of the hematopoietic cell lineages. The representativity of cell lines derived from the B cell differentiation lineage, however, is the most impressive. Human B-lymphoid cell lines are extensively used world wide as models in studies of various aspects of B cell biology and as tools in research on the etiology, pathogenesis and the biology of leukemia and lymphoma. Lymphoblastoid cell lines (LCL) carrying the Epstein-Barr Virus (EBV) are of particular importance. These lines can be established spontaneously from blood and lymphoid tissue from any EBV positive individual by special techniques, and from all individuals by EBV infection of peripheral blood B cells by EBV infection in vitro. At spontaneous establishment B cells, latently infected by EBV in vivo, will release EBV which subsequently infects normal EBV-negative B cells and immortalizes them into LCL cells, but direct outgrowth of the latently infected B cells as LCLs has also been documented. The target B cells for the EBV infection in vitro are not fully defined-most are mature B cells but also pro-B and pre-B and some B-blasts can be infected. Apart from their capacity for infinite growth, LCL cells have non-malignant properties, e. g. they are diploid, do not grow in agarose and do not form tumors upon inoculation subcutaneously in nude mice. LCLs have a phenotype corresponding to activated B cells (B-blasts) and have been used as "the E. Coli" of eukaryotic cells for about two decades. LCLs are derived at a high frequency also from tumor biopsies of EBV positive patients with leukemia and lymphoma. However, tumor cell lines are available from most of the B cell lineage-derived leukemias, B-lymphomas and myeloma. The frequency of successful establishment has been particularly high from EBV positive Burkitt's lymphoma (BL). From EBV genome negative BL and other B-lymphoma and B-leukemia biopsies the frequency of successful, spontaneous establishment is low (5-10%), and such lines have, with rare exceptions, been derived from pleural effusions and ascitis of patients with advanced, chemotherapy resistant, disease. Many of the cell lines therefore do not represent the clinically most common types of leukemia and lymphoma. No authentic malignant cell lines have been established from chronic lymphocytic leukemia (CLL), prolymphocytic leukemia (PLL) and Waldenström's disease.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

血液学家、肿瘤生物学家和免疫学家近三十年来的共同努力,已建立起一系列成熟的人类造血细胞系,涵盖了大多数造血细胞谱系。然而,源自B细胞分化谱系的细胞系的代表性最为突出。人类B淋巴细胞系在全球范围内被广泛用作研究B细胞生物学各个方面的模型,以及白血病和淋巴瘤病因、发病机制及生物学研究的工具。携带爱泼斯坦-巴尔病毒(EBV)的淋巴母细胞系(LCL)尤为重要。这些细胞系可通过特殊技术从任何EBV阳性个体的血液和淋巴组织中自发建立,也可通过体外EBV感染外周血B细胞从所有个体中建立。在自发建立过程中,体内潜伏感染EBV的B细胞会释放EBV,随后感染正常的EBV阴性B细胞并使其永生化成为LCL细胞,但也有文献记载潜伏感染的B细胞可直接生长为LCL。体外EBV感染的靶B细胞尚未完全明确——大多数是成熟B细胞,但前B细胞和一些B母细胞也可被感染。除了具有无限生长能力外,LCL细胞还具有非恶性特性,例如它们是二倍体,不在琼脂糖中生长,皮下接种到裸鼠体内也不形成肿瘤。LCL具有与活化B细胞(B母细胞)相对应的表型,在大约二十年里一直被用作真核细胞的“大肠杆菌”。LCL也高频源自EBV阳性白血病和淋巴瘤患者的肿瘤活检。然而,大多数源自B细胞谱系的白血病、B淋巴瘤和骨髓瘤都有可用的肿瘤细胞系。从EBV阳性伯基特淋巴瘤(BL)成功建立细胞系的频率特别高。从EBV基因组阴性的BL以及其他B淋巴瘤和B白血病活检中,成功自发建立细胞系的频率较低(5%-10%),而且这些细胞系除极少数外,均源自晚期、化疗耐药患者的胸腔积液和腹水。因此,许多细胞系并不代表临床上最常见的白血病和淋巴瘤类型。尚未从慢性淋巴细胞白血病(CLL)、幼淋巴细胞白血病(PLL)和瓦尔登斯特伦病中建立出真正的恶性细胞系。(摘要截选至400字)

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