Abdanipour Alireza, Dadkhah Masoud, Alipour Mohsen, Feizi Hadi
Department of Anatomical Sciences, Faculty of Medicine, Zanjan University of Medical Sciences, Zanjan, Iran.
Department of Physiology and Pharmacology, Faculty of Medicine, Zanjan University of Medical Sciences, Zanjan, Iran.
Adv Pharm Bull. 2018 Aug;8(3):429-435. doi: 10.15171/apb.2018.050. Epub 2018 Aug 29.
The antiapoptotic effect of ghrelin in various cell lines including bone marrow stromal cells (BMSCs) has been proved. However, the real mechanism of this effect is not clear. Caspase3 and Bcl2 are well-known pro- and antiapoptotic regulatory genes in eukaryotes. The aim of the study was to find out the effect of ghrelin on Caspase 3 and Bcl2 change in BMSCs. Rat BMSCs were cultivated in DMEM. Passage 3 BMSCs were treated with ghrelin 100 μM for 48 h. Real-time PCR for Caspase 3 and Bcl2 was carried out from B (untreated BMSCs), BH (BMSCs treated with 125 µM H2O2), BGH (BMSCs treated with 100 µM ghrelin then 125 µM H2O2) and BG (BMSCs treated with 100 µM ghrelin) groups. For immunofluorescence, cells were incubated with anti Caspase 3 and Bcl2monoclonal antibodies. Primary antibodies were visualized using the FITC method. All data are presented as means ± SEM. Values of P<0.05 were considered statistically significant. Ghrelin decreased mRNA expressions of Caspase-3 significantly as compared to the BH group (P<0.05). Also, Bcl-2 gene expression showed an increment in BG group as compare with BH and BGH groups (P<0.05). A high present of Bcl-2 positive cells were observed in the BGH group while Caspase-3 positive cells were significantly decreased in the BGH group compared with the BH group (P<0.05). Ghrelin probably enhances BMSCs viability through regulation of pro- and antiapoptotic genes Caspase 3 and Bcl2. However the signaling pathway of this effect should be elucidated in the future.
已证实胃饥饿素在包括骨髓基质细胞(BMSCs)在内的多种细胞系中具有抗凋亡作用。然而,这种作用的真正机制尚不清楚。半胱天冬酶3(Caspase3)和Bcl2是真核生物中众所周知的促凋亡和抗凋亡调节基因。本研究的目的是探究胃饥饿素对骨髓基质细胞中Caspase 3和Bcl2变化的影响。大鼠骨髓基质细胞在DMEM中培养。将第3代骨髓基质细胞用100μM胃饥饿素处理48小时。对B组(未处理的骨髓基质细胞)、BH组(用125µM过氧化氢处理的骨髓基质细胞)、BGH组(先用100µM胃饥饿素处理然后用125µM过氧化氢处理的骨髓基质细胞)和BG组(用100µM胃饥饿素处理的骨髓基质细胞)进行Caspase 3和Bcl2的实时定量聚合酶链反应。对于免疫荧光,细胞与抗Caspase 3和Bcl2单克隆抗体孵育。使用异硫氰酸荧光素(FITC)方法观察一抗。所有数据均以平均值±标准误表示。P<0.05的值被认为具有统计学意义。与BH组相比,胃饥饿素显著降低了Caspase-3的mRNA表达(P<0.05)。此外,与BH组和BGH组相比,BG组中Bcl-2基因表达增加(P<0.05)。在BGH组中观察到大量Bcl-2阳性细胞,而与BH组相比,BGH组中Caspase-3阳性细胞显著减少(P<0.05)。胃饥饿素可能通过调节促凋亡和抗凋亡基因Caspase 3和Bcl2来增强骨髓基质细胞的活力。然而,这种作用的信号通路有待未来阐明。