Banfalvi G, Gacsi M, Nagy G, Kiss Z B, Basnakian A G
Department of Animal Anatomy and Physiology, University of Debrecen, Debrecen 4032, Hungary.
Apoptosis. 2005 May;10(3):631-42. doi: 10.1007/s10495-005-1897-9.
CHO cells were grown in the presence of 1 mu M CdCl(2) and subjected to ATP-dependent replicative DNA synthesis after permeabilization. By decreasing the density of the cell culture replicative DNA synthesis was diminishing. At higher than 2 x 10(6) cell/ml concentration Cd had virtually no effect on the rate of DNA replication. Growth at higher cell concentrations could be suppressed by increasing Cd concentration. After Cd treatment cells were synchronized by counterflow centrifugal elutriation. Cadmium toxicity on cell growth in early and mid S phase led to the accumulation of enlarged cells in late S phase. Flow cytometry showed increased cellular and nuclear sizes after Cd treatment. As the cells progressed through the S phase, 11 subpopulations of nuclear sizes were distinguished. Apoptotic chromatin changes were visualized by fluorescent microscopy in a cell cycle dependent manner. In the control untreated cells the main transitory forms of chromatin corresponded to those we have published earlier (veil-like, supercoiled chromatin, fibrous, ribboned structures, chromatin strings, elongated prechromosomes, precondensed chromosomes). Cadmium treatment caused: (a) the absence of decondensed veil-like structures and premature chromatin condensation in the form of apoptotic bodies in early S phase (2.2-2.4 average C-value), (b) the absence of fibrous structures, the lack of supercoiled chromatin, the appearance of uncoiled ribboned chromatin and perichromatin semicircles, in early mid S phase (2.5-2.9 C), (c) the presence of perichromatin fibrils and chromatin bodies in mid S phase (2.9-3.2 C), (d) early intra-nuclear inclusions, elongated forms of premature chromosomes, the extrusion and rupture of nuclear membrane later in mid S phase (3.3-3.4 C), (e) the exclusion of chromatin bodies and the formation of clusters of large-sized perichromatin granules in late S phase (3.5-3.8 C) and (f) large extensive disruptions and holes in the nuclear membrane and the clumping of incompletely folded chromosomes (3.8-4. C).
CHO细胞在1 μM CdCl₂存在的情况下生长,并在透化后进行依赖ATP的复制性DNA合成。通过降低细胞培养物的密度,复制性DNA合成减少。当细胞浓度高于2×10⁶个细胞/毫升时,镉对DNA复制速率几乎没有影响。通过提高镉浓度可以抑制更高细胞浓度下的生长。镉处理后,细胞通过逆流离心淘析进行同步化。镉对S期早期和中期细胞生长的毒性导致S期后期出现增大的细胞积累。流式细胞术显示镉处理后细胞和细胞核大小增加。随着细胞在S期的进展,可以区分出11个核大小的亚群。通过荧光显微镜以细胞周期依赖性方式观察到凋亡染色质变化。在未处理的对照细胞中,染色质的主要过渡形式与我们之前发表的一致(面纱样、超螺旋染色质、纤维状、带状结构、染色质丝、拉长的前染色体、预凝聚染色体)。镉处理导致:(a) 在S期早期(平均C值为2.2 - 2.4),不存在解凝聚的面纱样结构,并且以凋亡小体形式出现过早的染色质凝聚;(b) 在S期早期至中期(2.5 - 2.9 C),不存在纤维状结构,缺乏超螺旋染色质,出现解螺旋的带状染色质和染色质周半圆;(c) 在S期中期(2.9 - 3.2 C),存在染色质周纤维和染色质体;(d) 在S期中期后期(3.3 - 3.4 C),早期核内包涵体、过早染色体的拉长形式、核膜的挤出和破裂;(e) 在S期后期(3.5 - 3.8 C),染色质体的排除和大型染色质周颗粒簇的形成;以及(f) 在核膜中出现大量广泛的破坏和孔洞,以及不完全折叠染色体的聚集(3.8 - 4. C)。