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具有费城染色体阳性的人慢性粒细胞白血病细胞系。

Human chronic myelogenous leukemia cell-line with positive Philadelphia chromosome.

作者信息

Lozzio C B, Lozzio B B

出版信息

Blood. 1975 Mar;45(3):321-34.

PMID:163658
Abstract

A cell-line derived from a patient with chronic myelogenous leukemia (CML) is described. The new cell-line, which has over 175 serial passanges in a 3 1/2-yr period, has the following characteristics: (1) CML cells started to proliferate actively since they were first incubated in culture media. A threefold increase in the total number of cells was observed during the first seven passages; the cell population increased by a factor of 10 to 20 every 7 days from passage 8 through 85; from 20 to 40 times from passage 86 through 150, and more than 40 times after 150 passages. (2) The majority of the nononucleated cells are undifferentiated blasts. (3) The karyotype of all the cells examined show the Philadelphia (Ph1) chromosome and a long acrocentric marker plus aneuploidy. The Giemsa-banding studies identified the Ph1 chromosome as a terminal deletion of the long arm of chromosome 22:del(22)(q12) and the long acrocentric marker as an unbalanced reciprocal translocation of one chromosome 17 and the long arm of one chromosome 15. (4) The CML cells do not produce immunoglobulins, are free of mycoplasma, Epstein-Barr virus, and herpes-like virus particles. (5) CML cells have no alkaline phosphatase and myeloperoxidase activities and did not engulf inert particles. (6) Cultured CML cells provide a constant source of a specific antigen. This CML cell-line represents a unique source of CML cells with meaningful indicators of malignancy for clinical and experimental studies.

摘要

本文描述了一种源自慢性粒细胞白血病(CML)患者的细胞系。该新细胞系在3年半的时间里已连续传代175次以上,具有以下特征:(1)CML细胞自首次接种于培养基中后便开始活跃增殖。在最初的7次传代过程中,细胞总数增加了两倍;从第8代到第85代,细胞群体每7天增加10至20倍;从第86代到第150代增加20至40倍,150代之后增加超过40倍。(2)大多数无核细胞为未分化的原始细胞。(3)所有检测细胞的核型均显示有费城(Ph1)染色体、一条长近端着丝粒标记染色体以及非整倍体。吉姆萨显带研究确定Ph1染色体为22号染色体长臂的末端缺失:del(22)(q12),长近端着丝粒标记染色体为一条17号染色体与一条15号染色体长臂的不平衡相互易位。(4)CML细胞不产生免疫球蛋白,无支原体、EB病毒和疱疹样病毒颗粒。(5)CML细胞无碱性磷酸酶和髓过氧化物酶活性,不吞噬惰性颗粒。(6)培养的CML细胞可提供特定抗原的恒定来源。该CML细胞系代表了一种独特的CML细胞来源,具有对临床和实验研究有意义的恶性指标。

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