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恶性核象的细胞遗传学分析与形态学。恶性细胞的生命周期。

Cytogenetic analysis and morphology of malignant nuclear vlimata. The life cycle of malignant cells.

作者信息

Logothetou-Rella H

机构信息

Department of Experimental Physiology, Medical School, University of Athens, Greece.

出版信息

Histol Histopathol. 1994 Oct;9(4):747-63.

PMID:7894147
Abstract

The karyotype of malignant nuclear vlimata (NVs) was investigated with the in situ and chromosomal spreading techniques. NV metaphases were recognised by the head with tail morphology, kept in situ and evaluated by the chromosomal spreading technique. It was shown that malignant NVs were produced by random, uncontrolled meiosis. NVs contain and carry single, hypodiploid, haploid, hypohaploid, hyperdiploid and atypical sets of chromosomes. NVs are unstable parasitic cellular elements, invading the cytoplasm or the nucleus of host cells, extruding and implanting their chromosomes in the host cell upon contact. Within a malignant cell culture, NVs play the role of chromosomal donors and host cells of chromosomal recipients. NVs were identified as episomatic on host cell nuclei or incorporated into host cell metaphases. The observations are discussed in terms of fertilization, viral infection and apoptosis. Comparison of malignant NVs with phytohaemagglutinin (PHA)-activated lymphocytic NVs is provided, as well as the life cycle of the malignant cells as follows: [Formula see text] cells (Logothetou-Rella, 1993). Phytohaemagglutinin (PHA)-activated lymphocytes also produced NVs by meiosis, carrying hypodiploid, haploid and hypohaploid sets of chromosomes (Logothetou-Rella, 1994a). In this study the cytogenetic analysis and morphology of malignant NVs are investigated, using a) the in situ cytogenetic technique, and b) the chromosomal spreading technique.

摘要

采用原位和染色体铺展技术对恶性核小体(NVs)的核型进行了研究。通过头端带尾形态识别NV中期相,将其保留在原位并用染色体铺展技术进行评估。结果表明,恶性NVs是由随机、不受控制的减数分裂产生的。NVs包含并携带单倍体、亚二倍体、单倍体、亚单倍体、超二倍体和非典型染色体组。NVs是不稳定的寄生细胞成分,侵入宿主细胞的细胞质或细胞核,接触时将其染色体挤出并植入宿主细胞。在恶性细胞培养中,NVs充当染色体供体,宿主细胞充当染色体受体。NVs被确定为宿主细胞核上的附加体或整合到宿主细胞中期相中。从受精、病毒感染和细胞凋亡的角度对这些观察结果进行了讨论。提供了恶性NVs与植物血凝素(PHA)激活的淋巴细胞NVs的比较,以及恶性细胞的生命周期如下:[公式见原文]细胞(洛戈泰托-雷拉,1993年)。植物血凝素(PHA)激活的淋巴细胞也通过减数分裂产生NVs,携带亚二倍体、单倍体和亚单倍体染色体组(洛戈泰托-雷拉,1994a)。在本研究中,使用a)原位细胞遗传学技术和b)染色体铺展技术对恶性NVs的细胞遗传学分析和形态进行了研究。

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