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体细胞裂解缓冲液对纯化实验用鼠精子效果有限。

Limited efficacy of somatic cell lysis buffer to purify laboratory mouse sperm.

机构信息

Molecular & Cellular Cognition, German Center for Neurodegenerative Diseases, Bonn, Germany.

出版信息

Epigenomics. 2018 Jun;10(6):689-694. doi: 10.2217/epi-2018-0015.

Abstract

AIM

Epigenetic analyses of sperm require pure samples devoid of diploid cell contamination. We sought to determine the efficacy of somatic cell lysis buffer (SCLB) treatment to purify mouse epididymis sperm samples.

MATERIALS & METHODS: Sperm cell concentration, sperm purity, small RNA contents and sperm and somatic marker gene expression was compared in SCLB-treated sperm samples and two different control conditions.

RESULTS

The SCLB condition as well as the control condition mimicking the additional pelleting and re-suspension steps resulted in substantial cell loss without evidence of enhanced purification of sperm cells as compared with epididymis-derived sperm samples that were not manipulated further.

CONCLUSION

Molecular analyses focused on sperm cells require high levels of purity in order to avoid high-confounding RNA and cytosolic contributions of nonsperm cells. Our findings advocate gradient or cell sorting-based purification approaches where pure samples are required for sensitive molecular assays.

摘要

目的

对精子进行表观遗传学分析需要纯净的样本,避免二倍体细胞污染。我们旨在确定体细胞裂解缓冲液(SCLB)处理方法纯化小鼠附睾精子样本的效果。

材料与方法

比较 SCLB 处理的精子样本与两种不同对照条件下的精子浓度、精子纯度、小 RNA 含量以及精子和体细胞标记基因的表达。

结果

SCLB 条件以及模拟额外沉淀和重悬浮步骤的对照条件导致大量细胞丢失,但与未进一步处理的来源于附睾的精子样本相比,并未显示出精子细胞的净化效果增强。

结论

如果要对精子细胞进行分子分析,则需要高纯度,以避免非精子细胞的高混杂 RNA 和胞质成分的影响。我们的研究结果主张使用基于梯度或细胞分选的纯化方法,在需要进行敏感分子检测时获得纯净的样本。

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