Excision repair of UV damage in human fibroblasts reversibly permeabilized by lysolecithin

Jeffrey D. Lorenz, John F. Watkins, Michael J. Smerdon
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引用次数: 10

Abstract

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 [α35S]dNTPs occurred at a lysolecithin concentration (∼ 80 μg/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 tottal cell population incorporated significant levels of 35S into DNA. This result presumably reflected the fact that ∼ 20% of the total cell population remained permeable for much longer periods of time (up to 2 h) than the remaining cell population (< 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.

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溶卵磷脂可逆渗透人成纤维细胞紫外线损伤的切除修复
我们研究了溶卵磷脂渗透的融合人二倍体成纤维细胞中核苷酸切除修复的合成。在12 J/m2的紫外线照射剂量下,溶卵磷脂浓度(~ 80 μg/ml)时,[α35S]dNTPs的最大掺入,其中略多于90%的细胞最初可渗透到台泛蓝。然而,在溶卵磷脂浓度下通透的细胞放射自显影显示,只有约20%的总细胞群将显著水平的35S纳入DNA。这一结果可能反映了这样一个事实,即总细胞群中约20%的细胞保持渗透性的时间(长达2小时)比其余细胞群(<20分钟)。紫外线照射的通透性细胞与dNTPs的结合似乎是真正的切除修复合成,因为:(1)在未照射的通透性细胞和照射的通透性修复缺陷细胞中,dNTPs完全不存在结合。(2) BrdUTP存在时纳入的核苷酸与正常密度DNA相关。(3)所有4种dNTPs的表观Km均为50-100 nM,与过去关于细胞裂解不可逆渗透的人成纤维细胞的报道一致。(4)与新合并的dNTPs相关的DNA在染色质结构中进行了类似于在完整的人类细胞中观察到的结扎和重排。在紫外线照射和渗透后的前2小时内,dNTPs的修复结合是快速和线性的。在此之后,合并停止或继续以慢得多的速度进行。细胞活力实验和放射自显影表明,渗透到[3H]dNTPs的细胞能够进行DNA复制和细胞分裂。因此,融合的人二倍体成纤维细胞可以被溶卵磷脂可逆地渗透到标记的dNTPs中,用于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,只有一小部分细胞在较长时间内保持可渗透性。
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