颗粒细胞的优化原代培养和传代培养

Nadia Fallah, Maryam Paktinat, Milad Rasouli, M. Nabiuni, E. Amini
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引用次数: 0

摘要

背景:原始卵泡包括被一层称为颗粒细胞(GCs)的体细胞包围的卵母细胞。GCs,也被称为护理细胞,是卵母细胞生长和存活的重要保护因子。卵母细胞缺乏一些代谢过程,它们的发育需要颗粒细胞。目的:阐述从NMRI小鼠卵巢中提取GCs原代培养物的方法。方法:采用两种不同培养基的方法选择最佳方案,以获得更多gc,加快工艺流程。采用苏木精和伊红(H&E)染色和流式细胞术分析卵巢提取细胞的类型。此外,我们通过MTT法评估了藏红花素和DPP作为伊朗常见的两种天然产物对这些细胞增殖的影响。结果:根据实验结果选择第二方案法和α - mem培养基。我们从HE染色和流式细胞术的发现证实了培养的gc在烧瓶中的百分比。此外,MTT评估表明,高剂量的藏红花素对颗粒细胞有毒性作用,而椰枣花粉(DPP)则刺激颗粒细胞增殖。结论:修改该方案是为了提高原代培养和传代培养中GCs的增殖、一致性和质量。关于这两种天然产物对颗粒细胞的作用,我们可以提到藏红花素和DPP在增殖中的双边增强作用。
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Optimized Primary Culture and Subculture of Granulosa Cells
Background: Primordial follicle includes an oocyte surrounded by a layer of somatic cells called Granulosa Cells (GCs). GCs, also known as nurse cells, are an important protective element for the growth and survival of oocytes. Oocytes, which lack some of the metabolic processes, require granulosa cells for their development. Objectives: This manuscript was provided to explain the protocol of GCs primary culture extracted from NMRI mice ovaries. Methods: For choosing the optimum protocol, we used two methods with different culture mediums to obtain more GCs and expedite the process. Hematoxylin and Eosin (H&E) staining and flow cytometry were used to analyze the type of extracted cells from ovaries. Besides, we evaluated the effect of crocin and DPP as two common natural products in Iran on the proliferation of these cells via MTT assay. Results: Second protocol method and alpha-MEM culture medium were chosen based on the results. Our findings from HE staining and flow cytometry proved the percentage of cultured GCs in the flask. Further, MTT assessment demonstrated that crocin at high doses had a toxic effect on granulosa cells, whereas date palm pollen (DPP) stimulated them to proliferation. Conclusion: Modifying this protocol is for the improvement of proliferation, coherence, and quality of GCs in primary culture and subculture. Regarding the effect of these two natural products on granulosa cells, we can mention the bilateral effect of crocin and DPP enhancement in proliferation.
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