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不同保存液低温保存卵巢组织过程中的代谢活性证据。

Evidence of metabolic activity during low-temperature ovarian tissue preservation in different media.

机构信息

Pôle de Recherche en Gynécologie, Institut de Recherche Expérimentale et Clinique, Université Catholique de Louvain, Avenue Mounier 52, bte B1.52.02, 1200, Brussels, Belgium.

Gynecology Department, Cliniques Universitaires Saint Luc, 1200, Brussels, Belgium.

出版信息

J Assist Reprod Genet. 2020 Oct;37(10):2477-2486. doi: 10.1007/s10815-020-01935-y. Epub 2020 Sep 4.

Abstract

PURPOSE

Although ovarian tissue transportation has been validated for up to 24 h, there is no standard protocol to date. We aimed to elucidate how existing media currently used for ovarian tissue transportation affect ovarian tissue metabolism and cell viability.

METHODS

Cow ovarian fragments were immersed in 0.9% NaCl solution, IVF medium, Leibovitz 15 medium (L-15), or PBS for 1, 4, or 24 h at 4 °C. Media were analyzed for pH, lactate dehydrogenase (LDH) activity, and glucose, pyruvate, and lactate concentrations, while apoptosis was assessed by TUNEL assays in fixed fragments. Viability rates were assessed by flow cytometry (FACS).

RESULTS

There were lower pH levels in NaCl at all time points compared with other media. LDH activity increased with time and was lowest in NaCl at 1 and 4 h. There was no significant difference in glucose levels, but a significant pyruvate decrease in L-15 and a significant lactate increase in all media. TUNEL showed apoptosis rates ranging from 0 to 5%. FACS showed a mean of 4% necrotic cells and 15-19% apoptotic cells after 1 h of incubation, but less than 1% necrotic cells and 2-6% apoptotic cells after 24 h in all media.

CONCLUSION

Our results indicate marked metabolic activity in ovarian tissue at 4 °C and suggest that cells use internal sources of energy, which may influence transplantation outcomes. This highlights the importance of better understanding whole tissue dynamics to develop a standard protocol for ovarian tissue transportation. Graphical abstract.

摘要

目的

尽管已经验证了卵巢组织运输可长达 24 小时,但目前尚无标准方案。本研究旨在阐明目前用于卵巢组织运输的现有培养基如何影响卵巢组织代谢和细胞活力。

方法

将牛卵巢组织片段浸入 0.9% NaCl 溶液、IVF 培养基、Leibovitz 15 培养基(L-15)或 PBS 中,4°C 下分别孵育 1、4 或 24 小时。分析培养基的 pH 值、乳酸脱氢酶(LDH)活性以及葡萄糖、丙酮酸和乳酸浓度,同时通过固定组织片段的 TUNEL 检测评估细胞凋亡情况。通过流式细胞术(FACS)评估存活率。

结果

与其他培养基相比,所有时间点的 NaCl 中的 pH 值均较低。LDH 活性随时间增加,在 1 和 4 小时的 NaCl 中最低。葡萄糖水平无显著差异,但 L-15 中的丙酮酸显著减少,所有培养基中的乳酸显著增加。TUNEL 显示凋亡率在 0 到 5%之间。FACS 显示,孵育 1 小时后,所有培养基中的平均有 4%的坏死细胞和 15-19%的凋亡细胞,但孵育 24 小时后,坏死细胞少于 1%,凋亡细胞为 2-6%。

结论

我们的结果表明,4°C 下卵巢组织的代谢活性明显,提示细胞利用内部能源,这可能会影响移植结果。这凸显了更好地理解整个组织动力学以开发卵巢组织运输标准方案的重要性。

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