Rasekh Hosein, Hoseini Farahi Mehdi, Mehrabani Davood, Massoumi Seyed Jalil, Ramzi Mani, Acker Jason P
Department of Horticultural Sciences, Yasooj Branch, Islamic Azad University, Yasooj, Iran.
Stem Cell Technology Research Center, Department of Pathology, Shiraz University of Medical Sciences, Shiraz, Iran.
World J Plast Surg. 2020 Sep;9(3):313-320. doi: 10.29252/wjps.9.3.313.
Feijoa is widely used in medicine due to their anti-inflammatory, antioxidant, antimicrobial and antitumor properties. The current investigation studied the proliferative and regenerative effect of acetonic extract of on stem cells.
Acetone extract of Feijoa was prepared using percolator and rotary machines. Human bone marrow stem cells (hBMSCs) were used as experimental model and characterized morphologically, by flowcytometry, and differentiation properties. The toxicity of the extract on hBMSCs was determined by MTT assay. The viability and growth kinetics of hBMSCs treated to Feijoa was determined. Real time PCR was used for changes in expression of proliferative and apoptotic genes on day 7.
MTT assay demondtrated that Feijoa at doses less than 200 ng/ml did not show any cytotoxic effect on hBMSCs and increased the cell proliferation until day 3 followed by a non-significant slow decreasing trend until day 7. Population doubling time (PDT) showed a decline until day 3 followed by an increase until day 7. A significant rise in expression of Bax and decline in Bcl-2 expression were noted on day 7.
The modulatory activity of Feijoa may be responsible for its increasing effect on cell proliferation till day 3. Therefore, when faster proliferation during a shorter time period is targeted, Feijoa can be safely added to the culture media in the first three days.
费约果因其抗炎、抗氧化、抗菌和抗肿瘤特性而被广泛应用于医学领域。本研究探讨了费约果丙酮提取物对干细胞的增殖和再生作用。
使用渗滤器和旋转机器制备费约果的丙酮提取物。以人骨髓干细胞(hBMSCs)作为实验模型,通过形态学、流式细胞术和分化特性进行表征。采用MTT法测定提取物对hBMSCs的毒性。测定经费约果处理的hBMSCs的活力和生长动力学。在第7天使用实时PCR检测增殖和凋亡基因表达的变化。
MTT分析表明,剂量低于200 ng/ml的费约果对hBMSCs未显示任何细胞毒性作用,在第3天前细胞增殖增加,随后直到第7天呈无显著意义的缓慢下降趋势。群体倍增时间(PDT)在第3天前下降,随后直到第7天增加。在第7天观察到Bax表达显著升高,Bcl-2表达下降。
费约果的调节活性可能是其在第3天前对细胞增殖产生增加作用的原因。因此,当目标是在较短时间内实现更快增殖时,可在头三天将费约果安全添加到培养基中。