Brachova Pavla, Alvarez Nehemiah S, Van Voorhis Bradley J, Christenson Lane K
Department of Molecular and Integrative Physiology, University of Kansas Medical Center, Kansas City, KS 66160, United States.
Department of Pathology and Laboratory Medicine, University of Kansas Medical Center, Kansas City, KS 66160, United States.
Gynecol Oncol. 2017 Jun;145(3):577-583. doi: 10.1016/j.ygyno.2017.02.017. Epub 2017 Feb 16.
Ovarian carcinomas that originate from fallopian epithelial cells are suggested to arise due to repeated exposure to ovulatory follicular fluid (FF). Mechanistic explanation(s) for how this occurs are unknown. Here, we sought to understand if FF exposure to fallopian epithelial cells could induce DNA damage and expression of a known family of DNA mutators, apolipoprotein B mRNA editing enzyme, catalytic polypeptide (APOBEC) cytidine deaminases.
Follicular fluid and matched patient plasma samples were obtained from donors. Fallopian epithelial cells (FT33-TAg, FT189, FT190, and FT194) were cultured with FF or plasma for 24h, and cell proliferation and DNA damage were assessed. Effects of FF on Apobec gene expression were determined by qRT-PCR and western blot analyses. Fallopian epithelial cells were transfected with an APOBEC3A expression vector and DNA damage was assessed.
Follicular fluid exposure increased epithelial cell proliferation as measured by three independent methods, and DNA damage accumulation as assessed using three independent measures. This effect was specific to FF, as matched patient plasma did not have the same effects. Increased expression of Apobec3a was observed in fallopian epithelial cells following exposure to 5 of 8 patient FF samples, and transient overexpression of APOBEC3A was sufficient to induce double strand DNA breaks.
Follicular fluid can induce cell proliferation and DNA damage accumulation in cultured fallopian epithelial cells. Increased expression of APOBEC3A, a known DNA mutator, may explain the high incidence of DNA damage after FF exposure. The role of Apobec3a in ovulation-induced inflammation warrants further investigation.
起源于输卵管上皮细胞的卵巢癌被认为是由于反复接触排卵滤泡液(FF)而发生的。关于其发生机制尚不清楚。在此,我们试图了解FF暴露于输卵管上皮细胞是否会诱导DNA损伤以及已知的DNA突变家族载脂蛋白B mRNA编辑酶、催化多肽(APOBEC)胞苷脱氨酶的表达。
从供体获取滤泡液和匹配的患者血浆样本。将输卵管上皮细胞(FT33 - TAg、FT189、FT190和FT194)与FF或血浆培养24小时,评估细胞增殖和DNA损伤。通过qRT - PCR和蛋白质印迹分析确定FF对Apobec基因表达的影响。用APOBEC3A表达载体转染输卵管上皮细胞并评估DNA损伤。
通过三种独立方法测量,滤泡液暴露增加了上皮细胞增殖,并通过三种独立测量评估了DNA损伤积累。这种效应是FF特有的,因为匹配的患者血浆没有相同的作用。在暴露于8个患者FF样本中的5个后,输卵管上皮细胞中观察到Apobec3a表达增加,并且APOBEC3A的瞬时过表达足以诱导双链DNA断裂。
滤泡液可诱导培养的输卵管上皮细胞中的细胞增殖和DNA损伤积累。已知的DNA突变体APOBEC3A表达增加可能解释了FF暴露后DNA损伤的高发生率。Apobec3a在排卵诱导的炎症中的作用值得进一步研究。