Singh Bibhuti N, Hayes Gary R, Lucas John J, Beach David H, Gilbert Robert O
Department of Biochemistry and Molecular Biology, SUNY Upstate Medical University, Syracuse, NY 13210, USA.
Am J Vet Res. 2005 Jul;66(7):1181-6. doi: 10.2460/ajvr.2005.66.1181.
To evaluate the cytopathic effects of Tritrichomonas foetus and a purified cysteine protease (ie, CP30) of T foetus on cultured bovine uterine epithelial cells (BUECs) in vitro.
10 reproductive tracts were obtained from late-term bovine fetuses at a commercial abattoir.
An in vitro culture system of BUECs was developed to study the cytopathic effects of T foetus and purified CP30 of T foetus on host cells. Cytotoxicity of T foetus or CP30 on exposed BUECs was determined. Fluorescence microscopy and flow cytometry analyses were used to detect apoptosis. A fluorometric assay was used to detect BUEC caspase 3 activation. The CP inhibitor E-64 and a caspase inhibitor were used to inhibit apoptosis.
Cytopathic effects were observed in BUECs treated with parasites or CP30 and were concentration and time dependent. The BUECs underwent apoptosis in the presence of parasites or CP30. The specific CP inhibitor E-64 abolished the induction of apoptosis in BUECs by CP30. The caspase inhibitor reduced the amount of apoptosis in BUECs.
T foetus and its CP30 induce apoptosis in cultured BUECs in vitro. Induction of apoptosis by CP30 is correlated with protease activity. Endometrial cell death as a result of a T foetus infection is likely to be more important in mediating infertility than a direct effect on the conceptus. Provoking an apoptotic reaction in the host may mitigate an inflammatory reaction or immune response and therefore favor survival of the parasite in a chronic infection.
评估胎儿三毛滴虫及其纯化的半胱氨酸蛋白酶(即CP30)对体外培养的牛子宫上皮细胞(BUECs)的细胞病变效应。
从一家商业屠宰场的晚期牛胎儿获取10个生殖道。
建立BUECs体外培养系统,以研究胎儿三毛滴虫及其纯化的CP30对宿主细胞的细胞病变效应。测定胎儿三毛滴虫或CP30对暴露的BUECs的细胞毒性。使用荧光显微镜和流式细胞术分析检测细胞凋亡。采用荧光测定法检测BUECs半胱天冬酶3的激活。使用半胱氨酸蛋白酶抑制剂E-64和半胱天冬酶抑制剂抑制细胞凋亡。
在用寄生虫或CP30处理的BUECs中观察到细胞病变效应,且呈浓度和时间依赖性。在存在寄生虫或CP30的情况下,BUECs发生凋亡。特异性半胱氨酸蛋白酶抑制剂E-64消除了CP30对BUECs凋亡的诱导作用。半胱天冬酶抑制剂减少了BUECs中的凋亡量。
胎儿三毛滴虫及其CP30在体外诱导培养的BUECs凋亡。CP30诱导的凋亡与蛋白酶活性相关。胎儿三毛滴虫感染导致的子宫内膜细胞死亡在介导不孕方面可能比直接影响孕体更为重要。在宿主中引发凋亡反应可能减轻炎症反应或免疫反应,因此有利于寄生虫在慢性感染中的存活。