Logothetou-Rella H
Department of Experimental Physiology, Medical School, University of Athens, Greece.
Histol Histopathol. 1996 Oct;11(4):943-63.
This is the first study on the in situ cytogenetic morphology and analysis of malignant bone marrow cells, growing attached on a culture vessel surface. It was documented that bone marrow cells, in different types of hematological malignancies, divide by meiosis giving rise to a non-repetitive aneuploidy. Male and female gametes are formed by meiosis and fertilization occurs in a life cycle of: [sequence see text] Immature and mature somatic oocytes were evidenced by prophase stages of the first and diploid or hypodiploid or haploid metaphases identical to those of the second human, ovarian oocytic meiotic division, showing "XX" or "XY" sex chromosomes in female or male patients respectively. Nuclear vlimata were the male gametes showing a condensed head with tail morphology. Metaphases of nuclear vlimata were aneuploid, keeping the head with tail shape, carrying chromosomes identical to those of human spermatogonia. Somatic metaphases identical to those of human spermatocytes in meiosis II and spermatogonia were demonstrated. The process of fertilization was documented by nuclear vlima invasion into host cell metaphases, by metaphases of fertilized oocyte showing both the female chromosome "0" and the male chromatids "s" and hybrid metaphases of oocytic with somatic chromosomes. Meiosis was characterized by nuclear extrusion of chromosomes, meiotic, condensed chromosomes, nuclear vlimata, metaphase and nuclear fusion, hybrid metaphases, nuclear budding, nuclear conglomerates, nuclear bridges, chromosomal fusion substance, transfer of chromosomes and non-repetitive aneuploidy. Meiotic, Double Minute, ring and minute chromosomes extruded by nuclei were loaded with glycoproteins, glycosaminoglycans and calcium-activated neutral proteinase, distinguishing them from mitotic chromosomes. The main characteristic events of meiosis, observed in malignant bone marrow cells, were also demonstrated in fungal and rat testicular cells, known to divide by meiosis.
这是第一项关于附着在培养容器表面生长的恶性骨髓细胞的原位细胞遗传学形态及分析的研究。据记载,在不同类型的血液系统恶性肿瘤中,骨髓细胞通过减数分裂进行分裂,产生非重复性非整倍体。雄性和雌性配子通过减数分裂形成,受精发生在以下生命周期中:[序列见原文]未成熟和成熟的体细胞卵母细胞通过第一次减数分裂前期阶段以及与人类卵巢卵母细胞第二次减数分裂相同的二倍体、亚二倍体或单倍体中期得以证实,分别在女性或男性患者中显示出“XX”或“XY”性染色体。核鞭毛是显示出头部浓缩且带有尾部形态的雄性配子。核鞭毛的中期是非整倍体,保持头部带尾的形状,携带与人精原细胞相同的染色体。证实了与人类减数分裂II期精母细胞和精原细胞相同的体细胞中期。受精过程通过核鞭毛侵入宿主细胞中期、受精卵母细胞中期显示出雌性染色体“0”和雄性染色单体“s”以及卵母细胞与体细胞染色体的杂交中期得以记录。减数分裂的特征在于染色体的核挤出、减数分裂期浓缩染色体、核鞭毛、中期和核融合、杂交中期、核出芽、核聚集、核桥、染色体融合物质、染色体转移和非重复性非整倍体。由细胞核挤出的减数分裂期双微体、环状和微小染色体负载有糖蛋白、糖胺聚糖和钙激活中性蛋白酶,这使其与有丝分裂染色体区分开来。在恶性骨髓细胞中观察到的减数分裂的主要特征事件,在已知通过减数分裂进行分裂的真菌和大鼠睾丸细胞中也得到了证实。