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人精子 DNA 碎片化:单链和双链 DNA 断裂及其各自动态行为反应的简单评估。

DNA fragmentation of human spermatozoa: Simple assessment of single- and double-strand DNA breaks and their respective dynamic behavioral response.

机构信息

Genetics Unit, INIBIC-Complexo Hospitalario Universitario A Coruña (CHUAC), A Coruña, Spain.

HM Maternidad Belén, A Coruña, Spain.

出版信息

Andrology. 2020 Sep;8(5):1287-1303. doi: 10.1111/andr.12819. Epub 2020 Jun 15.

Abstract

BACKGROUND

Procedures to detect sperm DNA fragmentation (SDF), like the sperm chromatin dispersion (SCD) test, determine the "global" SDF without discriminating between spermatozoa with single-strand DNA breaks only (SDF-SSBs) and those containing double-strand DNA breaks (SDF-DSBs).

OBJECTIVES

(a) To validate a test to distinguish human spermatozoa with massive DSBs (DSB-SCD assay), (b) to study the baseline SDF-SSBs and SDF-DSBs, and (c) to assess their dynamics in vitro.

MATERIALS AND METHODS

(a) SDF-DSBs were determined by visualization of diffused DNA fragments from spermatozoa lysed under non-denaturing conditions. This was validated by in vitro incubation with DNase I and the comet assay. (b) Baseline SDF-DSBs and SDF-SSBs were determined in ejaculates from 95 males. (c) Their dynamic appearance was studied in samples untreated or exposed to hyperthermia, acidic pH, nitric oxide released by sodium nitroprusside (SNP), and the metabolic energy inhibitors 2-deoxy-D-glucose and antimycin A.

RESULTS

(a) DNase I and comet assay experiments confirmed that the assay successfully determined SDF-DSBs. (b) The higher the SDF of the semen sample, the higher the frequency of SSBs, whereas DSBs behaved independently. Abnormal samples showed higher SDF than normozoospermic, the difference being only significant for SDF-SSBs. (c) During the first hours of incubation, the linear rate of increase in SDF-SSBs was 3.7 X higher than that of SDF-DSBs. All hazardous agents accelerated the SDF rate when compared to untreated spermatozoa, primarily being associated with SDF-SSBs. SNP treatment was the most damaging, rapidly inducing spermatozoa with SSBs which progressively evolved to DSBs. Remarkably, this phenomenon was also evidenced after acute SNP exposure, revealing cryptic sperm damage.

CONCLUSION

The DSBs-SCD is an easy complement for SDF assessment. The dynamic study of SSBs and DSBs may improve the evaluation of sperm quality in clinical settings, particularly "unmasking" the presence of non-specific cryptic sperm damage that might otherwise go undetected.

摘要

背景

检测精子 DNA 碎片化(SDF)的方法,如精子染色质扩散(SCD)测试,可确定“整体”SDF,而不区分仅具有单链 DNA 断裂的精子(SDF-SSBs)和具有双链 DNA 断裂的精子(SDF-DSBs)。

目的

(a)验证一种区分具有大量 DSB 的人类精子的测试(DSB-SCD 检测),(b)研究基线 SDF-SSBs 和 SDF-DSBs,并(c)评估它们在体外的动力学。

材料和方法

(a)通过在非变性条件下裂解精子后扩散的 DNA 片段的可视化来确定 SDF-DSBs。通过体外用 DNA 酶 I 和彗星试验孵育来验证。(b)在 95 名男性的精液中确定基线 SDF-DSBs 和 SDF-SSBs。(c)在未处理或暴露于高温、酸性 pH、硝普钠释放的一氧化氮(SNP)以及代谢能量抑制剂 2-脱氧-D-葡萄糖和抗霉素 A 的样品中研究其动态出现。

结果

(a)DNA 酶 I 和彗星试验证实,该试验成功地确定了 SDF-DSBs。(b)精液样本的 SDF 越高,SSBs 的频率越高,而 DSBs 则独立表现。异常样本的 SDF 高于正常精子,差异仅在 SDF-SSBs 上有统计学意义。(c)在孵育的最初几小时内,SDF-SSBs 的线性增加率比 SDF-DSBs 高 3.7 倍。与未处理的精子相比,所有有害剂都加速了 SDF 率,主要与 SDF-SSBs 相关。SNP 处理最具破坏性,迅速诱导具有 SSBs 的精子,这些 SSBs 逐渐演变为 DSBs。值得注意的是,这种现象在 SNP 急性暴露后也得到了证实,显示出隐匿性精子损伤。

结论

DSB-SCD 是 SDF 评估的一种简单补充。SSBs 和 DSBs 的动态研究可以改善临床环境中精子质量的评估,特别是“揭示”否则可能未被发现的非特异性隐匿性精子损伤的存在。

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