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不同冷冻速率对绵羊精原干细胞解冻后活力、增殖及干性的影响比较

Comparison of different freezing rates on post-thaw viability, proliferation, and stemness of sheep spermatogonial stem cells.

作者信息

Binsila Balakrishnan, Tomcy Tomy A, Krishnappa Balaganur, Sadikh Muhammed, Ramachandran Natesan, Kolte Atul P, Selvaraju Sellappan

机构信息

Animal Physiology Division, ICAR-National Institute of Animal Nutrition and Physiology, Adugodi, Bangalore, India, 560030.

Animal Physiology Division, ICAR-National Institute of Animal Nutrition and Physiology, Adugodi, Bangalore, India, 560030.

出版信息

Cryobiology. 2025 Mar;118:105203. doi: 10.1016/j.cryobiol.2025.105203. Epub 2025 Feb 11.

Abstract

The application of spermatogonial stem cells (SSC) will be more effective and feasible following the successful cryopreservation and transfer of SSCs in livestock. Like other cells, SSCs are also sensitive to cryoinjury; hence composition of the cryomedia and freezing protocols need to be optimized. The present study aims to optimize the best freezing rates by minimising the ice crystallization and dehydration effect in order to maximize the post-thaw SSCs survivability and stemness characteristics. Three different freezing protocols with varied cooling profiles, cooling profile 1 (isopropanol based freezing): 1 °C/min from 0 °C to -10 °C, 0.5 °C/min up to -40 °C, further reduced to 0.25 °C/min up to -50 °C and 0.1 °C/min to -60 °C; cooling profile 2 (using programmable freezer): 1 °C/min up to 4 °C, 0.3 °C/min up to -8 °C, and cooled at 0.5 °C/min to -50 °C, further decrease to -90 °C (8 °C/min) and cooling profile 3 (uncontrolled rapid freezing): 3.3 °C/min from 0 °C to -10 °C, 5 °C/min up to -40 °C, 2 °C/min to -50 °C and 1.2 °C/min up to -60 °C, were compared for cryopreservation efficiency. The overall viability (91.41 ± 2.00 % Vs 74.59 ± 2.34 %), stemness activity (1.34 ± 0.095 OD units Vs 0.356 ± 0.026 OD units), and proliferation rate (0.849 ± 0.019 OD units Vs 0.749 ± 0.015 OD units) of post-thaw SSC culture irrespective of the freezing regimes were significantly decreased when compared to pre-freeze SSC culture characteristics. The post-thaw viability was significantly greater in cooling profile 1 (79.64 ± 4.1 %) when compared to cooling profile 2 (69.72 ± 2.4 %) and cooling profile 3 (75.43 ± 4.8 %). Also, cooling profile 1 yielded greater (p < 0.05) post-thaw stemness activity (0.456 ± 0.044 OD units) when compared to other methods. The study suggests that the cooling profile 1 using isopropanol based freezing can be recommended for preservation of viability and stemness characteristics of SSCs.

摘要

在成功实现家畜精原干细胞(SSC)的冷冻保存和移植后,SSC的应用将更有效且可行。与其他细胞一样,SSC对冷冻损伤也很敏感;因此,需要优化冷冻培养基的成分和冷冻方案。本研究旨在通过最小化冰晶形成和脱水效应来优化最佳冷冻速率,以最大化解冻后SSC的存活率和干性特征。比较了三种具有不同冷却曲线的不同冷冻方案,冷却曲线1(基于异丙醇的冷冻):从0°C到-10°C为1°C/分钟,到-40°C为0.5°C/分钟,进一步降至-50°C为0.25°C/分钟,到-60°C为0.1°C/分钟;冷却曲线2(使用程序降温冷冻仪):到4°C为1°C/分钟,到-8°C为0.3°C/分钟,以0.5°C/分钟冷却至-50°C,再降至-90°C(8°C/分钟);冷却曲线3(无控制快速冷冻):从0°C到-10°C为3.3°C/分钟,到-40°C为5°C/分钟,到-50°C为2°C/分钟,到-60°C为1.2°C/分钟,比较其冷冻保存效率。与冷冻前SSC培养特征相比,无论冷冻方案如何,解冻后SSC培养物的总体存活率(91.41±2.00%对74.59±2.34%)、干性活性(1.34±0.095 OD单位对0.356±0.026 OD单位)和增殖率(0.849±0.019 OD单位对0.749±0.015 OD单位)均显著降低。与冷却曲线2(69.72±2.4%)和冷却曲线3(75.43± 4.8%)相比,冷却曲线1解冻后的存活率显著更高(79.64±4.1%)。此外,与其他方法相比,冷却曲线1解冻后的干性活性更高(p<0.05)(0.456±0.044 OD单位)。该研究表明,基于异丙醇冷冻的冷却曲线1可推荐用于保存SSC的活力和干性特征。

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