Nasto Luigi A, Ngo Kevin, Leme Adriana S, Robinson Andria R, Dong Qing, Roughley Peter, Usas Arvydas, Sowa Gwendolyn A, Pola Enrico, Kang James, Niedernhofer Laura J, Shapiro Steven, Vo Nam V
Department of Orthopaedic Surgery, Ferguson Laboratory for Orthopaedic Research, University of Pittsburgh School of Medicine, Pittsburgh, PA 15261, USA; Department of Orthopaedic Surgery, Catholic University of Rome School of Medicine, "A. Gemelli" University Hospital, l.go Agostino Gemelli 8, 00168 Roma, Italy.
Department of Orthopaedic Surgery, Ferguson Laboratory for Orthopaedic Research, University of Pittsburgh School of Medicine, Pittsburgh, PA 15261, USA.
Spine J. 2014 Mar 1;14(3):416-23. doi: 10.1016/j.spinee.2013.08.034. Epub 2013 Nov 6.
Tobacco smoking is a key risk factor for spine degeneration. However, the underlying mechanism by which smoking induces degeneration is not known. Recent studies implicate DNA damage as a cause of spine and intervertebral disc degeneration. Because tobacco smoke contains many genotoxins, we hypothesized that tobacco smoking promotes spine degeneration by inducing cellular DNA damage.
To determine if DNA damage plays a causal role in smoking-induced spine degeneration.
To compare the effect of chronic tobacco smoke inhalation on intervertebral disc and vertebral bone in normal and DNA repair-deficient mice to determine the contribution of DNA damage to degenerative changes.
Two-month-old wild-type (C57BL/6) and DNA repair-deficient Ercc1(-/Δ) mice were exposed to tobacco smoke by direct inhalation (4 cigarettes/day, 5 days/week for 7 weeks) to model first-hand smoking in humans. Total disc proteoglycan (PG) content (1,9-dimethylmethylene blue assay), PG synthesis ((35)S-sulfate incorporation assay), aggrecan proteolysis (immunoblotting analysis), and vertebral bone morphology (microcomputed tomography) were measured.
Exposure of wild-type mice to tobacco smoke led to a 19% increase in vertebral porosity and a 61% decrease in trabecular bone volume. Intervertebral discs of smoke-exposed animals also showed a 2.6-fold decrease in GAG content and an 8.1-fold decrease in new PG synthesis. These smoking-induced degenerative changes were similar but not worse in Ercc1(-/Δ) mice.
Short-term exposure to high levels of primary tobacco smoke inhalation promotes degeneration of vertebral bone and discs. Disc degeneration is primarily driven by reduced synthesis of proteoglycans needed for vertebral cushioning. Degeneration was not exacerbated in congenic DNA repair-deficient mice, indicating that DNA damage per se does not have a significant causal role in driving smoke-induced spine degeneration.
吸烟是脊柱退变的一个关键风险因素。然而,吸烟诱发退变的潜在机制尚不清楚。最近的研究表明DNA损伤是脊柱和椎间盘退变的一个原因。由于烟草烟雾含有多种基因毒素,我们推测吸烟通过诱导细胞DNA损伤促进脊柱退变。
确定DNA损伤在吸烟诱发的脊柱退变中是否起因果作用。
比较慢性吸入烟草烟雾对正常小鼠和DNA修复缺陷小鼠椎间盘及椎骨的影响,以确定DNA损伤对退变改变的作用。
将2月龄野生型(C57BL/6)和DNA修复缺陷型Ercc1(-/-Δ)小鼠通过直接吸入(每天4支香烟,每周5天,共7周)暴露于烟草烟雾中,以模拟人类的直接吸烟。测量椎间盘总蛋白聚糖(PG)含量(1,9-二甲基亚甲基蓝法)、PG合成(35S-硫酸盐掺入法)、聚集蛋白聚糖蛋白水解(免疫印迹分析)和椎骨形态(微型计算机断层扫描)。
野生型小鼠暴露于烟草烟雾导致椎体孔隙率增加19%,小梁骨体积减少61%。暴露于烟雾的动物的椎间盘也显示糖胺聚糖(GAG)含量减少2.6倍,新PG合成减少8.1倍。这些吸烟诱导的退变改变在Ercc1(-/-Δ)小鼠中相似但并不更严重。
短期高剂量直接吸入烟草烟雾可促进椎骨和椎间盘退变。椎间盘退变主要是由椎骨缓冲所需蛋白聚糖合成减少所致。在同基因DNA修复缺陷小鼠中退变并未加剧,表明DNA损伤本身在驱动烟雾诱导的脊柱退变中没有显著的因果作用。