Lorenz J D, Watkins J F, Smerdon M J
Biochemistry/Biophysics Program, Washington State University, Pullman 99164-4660.
Mutat Res. 1988 Mar;193(2):167-79. doi: 10.1016/0167-8817(88)90047-8.
We have examined nucleotide excision repair synthesis in confluent human diploid fibroblasts permeabilized with lysolecithin. Following a UV dose of 12 J/m2, maximal incorporation of [alpha 35S]dNTPs occurred at a lysolecithin concentration (approximately 80 micrograms/ml) where slightly more than 90% of the cells were initially permeable to trypan blue. However, autoradiography of cells, permeabilized at this lysolecithin concentration, demonstrated that only about 20% of the total cell population incorporated significant levels of 35S into DNA. This result presumably reflected the fact that approximately 20% of the total cell population remained permeable for much longer periods of time (up to 2 h) than the remaining cell population (less than 20 min). The incorporation of dNTPs by UV-irradiated, permeabilized cells appeared to be bona fide excision repair synthesis since: (1) Incorporation was completely absent in unirradiated, permeabilized cells and in irradiated, permeabilized repair-deficient cells. (2) Nucleotides incorporated in the presence of BrdUTP were associated with normal density DNA. (3) The apparent Km for all 4 dNTPs was 50-100 nM, in agreement with past reports on human fibroblasts irreversibly permeabilized by cell lysis. (4) DNA associated with the newly incorporated dNTPs underwent ligation and rearrangements in chromatin structure analogous to what is observed in intact human cells. Repair incorporation of dNTPs was rapid and linear during the first 2 h after UV irradiation and permeabilization. After this time, incorporation ceased or continued at a much slower rate. Cell viability experiments and autoradiography demonstrated that the cells permeabilized to [3H]dNTPs were capable of carrying out DNA replication and cell division. Thus, confluent human diploid fibroblasts can be reversibly permeabilized to labeled dNTPs by lysolecithin for the study of excision repair following physiologic doses of UV radiation. However, under these conditions, only a fraction of the cells remain permeable for an extended period of time.
我们检测了用溶血卵磷脂通透处理的汇合的人二倍体成纤维细胞中的核苷酸切除修复合成。在紫外线剂量为12 J/m²后,[α³⁵S]dNTPs的最大掺入量出现在溶血卵磷脂浓度(约80微克/毫升)时,此时略多于90%的细胞最初可被台盼蓝通透。然而,对在此溶血卵磷脂浓度下通透处理的细胞进行放射自显影显示,仅约20%的总细胞群体将显著水平的³⁵S掺入DNA。该结果可能反映了这样一个事实,即约20%的总细胞群体保持通透的时间(长达2小时)比其余细胞群体(少于20分钟)长得多。紫外线照射且通透处理的细胞对dNTPs的掺入似乎是真正的切除修复合成,因为:(1)未照射且通透处理的细胞以及照射且通透处理的修复缺陷细胞中完全没有掺入。(2)在BrdUTP存在下掺入的核苷酸与正常密度的DNA相关。(3)所有4种dNTPs的表观Km为50 - 100 nM,这与过去关于通过细胞裂解不可逆通透处理的人成纤维细胞的报道一致。(4)与新掺入的dNTPs相关的DNA在染色质结构中经历连接和重排,类似于在完整人细胞中观察到的情况。紫外线照射和通透处理后的最初2小时内,dNTPs的修复掺入迅速且呈线性。在此之后,掺入停止或继续的速度要慢得多。细胞活力实验和放射自显影表明能够对[³H]dNTPs通透的细胞能够进行DNA复制和细胞分裂。因此,溶血卵磷脂可使汇合的人二倍体成纤维细胞对标记的dNTPs进行可逆性通透处理,以研究生理剂量紫外线辐射后的切除修复。然而,在这些条件下,只有一部分细胞在较长时间内保持通透。