Culture medium and protein supplementation affect sensitivity of the mouse embryo assay in detecting Triton X-100

IF 3.7 2区 医学 Q1 OBSTETRICS & GYNECOLOGY Reproductive biomedicine online Pub Date : 2024-05-18 DOI:10.1016/j.rbmo.2024.104120
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Abstract

Research question

To what extent does the type and concentration of protein and the type of culture medium affect the sensitivity of the mouse embryo assay (MEA) to detect Triton X-100 (TX-100) in culture media?

Design

The effect of the concentration of bovine serum albumin (BSA) and human serum albumin (HSA) was assessed by supplementing media with 0.5 or 5 mg/ml. Potassium-supplemented simplex optimized medium (KSOM) and human tubal fluid (HTF) were used as complex and simple formulation media, respectively. Variables were combined, forming study groups where embryos were cultured in test media spiked with a sublethal TX-100 concentration. The conditions of greatest sensitivity were determined by statistical comparison of blastocyst formation rates and total cell counts between groups.

Results

Although all of the study groups showed equal capacity for sustaining proper embryo development, the reported sensitivity of the MEA differed between groups when subjected to TX-100. HTF conferred significantly greater sensitivity than KSOM regardless of the type and concentration of protein used, and medium supplementation with 5 mg/ml BSA rather than 0.5 mg/ml BSA resulted in significantly higher sensitivity regardless of the type of medium used. This increase in concentration also resulted in higher sensitivity when supplementing HTF with HSA. The BSA groups provided more sensitivity than their HSA counterparts, except for the KSOM + 0.5 mg/ml BSA group. Cell count analysis did not provide further significant conclusions.

Conclusions

For TX-100 detection within culture medium, the type and concentration of protein and the type of culture medium have a direct effect on MEA sensitivity. These results could help to standardize the MEA protocol, and increase its ability to detect sublethal concentrations of embryotoxic substances, especially TX-100, thus avoiding possible clinical harmful effects.

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培养基和蛋白质补充对小鼠胚胎测定法检测 Triton X-100 灵敏度的影响
研究问题蛋白质的类型和浓度以及培养基的类型在多大程度上影响小鼠胚胎测定法(MEA)检测培养基中Triton X-100(TX-100)的灵敏度? 设计通过在培养基中添加0.5或5 mg/ml的牛血清白蛋白(BSA)和人血清白蛋白(HSA)来评估其浓度的影响。钾补充的单克隆优化培养基(KSOM)和人类输卵管液(HTF)分别用作复合培养基和简单配方培养基。将各种变量进行组合,形成研究组,在这些研究组中,胚胎在添加了亚致死浓度 TX-100 的测试培养基中进行培养。结果虽然所有研究组在维持胚胎正常发育方面都表现出同等能力,但各组对 TX-100 的敏感性却不尽相同。无论使用哪种类型和浓度的蛋白质,HTF 的灵敏度都明显高于 KSOM;无论使用哪种类型的培养基,在培养基中添加 5 mg/ml BSA 而不是 0.5 mg/ml BSA 的灵敏度都明显更高。在 HTF 中添加 HSA 时,浓度的增加也会导致更高的灵敏度。除 KSOM + 0.5 mg/ml BSA 组外,BSA 组的灵敏度均高于 HSA 组。结论对于在培养基中检测 TX-100,蛋白质的类型和浓度以及培养基的类型会直接影响 MEA 的灵敏度。这些结果有助于规范 MEA 方案,提高其检测亚致死浓度胚胎毒性物质(尤其是 TX-100)的能力,从而避免可能的临床危害。
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来源期刊
Reproductive biomedicine online
Reproductive biomedicine online 医学-妇产科学
CiteScore
7.20
自引率
7.50%
发文量
391
审稿时长
50 days
期刊介绍: Reproductive BioMedicine Online covers the formation, growth and differentiation of the human embryo. It is intended to bring to public attention new research on biological and clinical research on human reproduction and the human embryo including relevant studies on animals. It is published by a group of scientists and clinicians working in these fields of study. Its audience comprises researchers, clinicians, practitioners, academics and patients. Context: The period of human embryonic growth covered is between the formation of the primordial germ cells in the fetus until mid-pregnancy. High quality research on lower animals is included if it helps to clarify the human situation. Studies progressing to birth and later are published if they have a direct bearing on events in the earlier stages of pregnancy.
期刊最新文献
Ultra-fast vitrification and rapid elution of human oocytes: part I. germinal vesicle model validation. Ultra-fast vitrification and rapid elution of human oocytes: Part II - verification of blastocyst development from mature oocytes. Inside Front Cover - Affiliations and First page of TOC Front Matter - Continued TOC Outside Back Cover - Editorial Board
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