Karimi Mohammad Hossein, Barzkar Zahra, Babaee Maryam, Naghdi Majid
Transplant Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
Noncommunicable Diseases Research Center, Fasa University of Medical Sciences, Fasa, Iran.
Adv Pharm Bull. 2016 Jun;6(2):179-86. doi: 10.15171/apb.2016.025. Epub 2016 Jun 30.
Mesenchymal stem cells (MSCs) are multipotent cells and recent findings suggest immunomodulatory effect of them on immune cells including T cells and dendritic cells (DCs). DCs are the most potent antigen presenting cells. It seems because of immunoregulatory properties of MSCs, they can affect the maturation and differentiation of DCs. DCs express a kind of surface receptors called toll-like receptors (TLRs) and play a key role in maturation process and activation of DCs. The aim of this study was to evaluate expression of TLR2 and TLR4 on DCs after exposure to mesenchymal stem cell's supernatant in culture media containing LPS and devoid of it.
In this experimental study, MSCs and DCs were extracted from adult Balb/c mouse bone marrow and spleen, respectively. MSCs supernatant were collected 24 and 48 h after 5(th) passage, and in adjusted with DCs culture. Isolated DCs were co-cultured with MSCs supernatant, incubation time were 24 and 48 hours. mRNA levels of TLR2 and TLR4 were evaluated using real time PCR technique.
The results demonstrated that although, expressions of these two receptors were up-regulated in culture media lacking LPS in comparison with the control group but the increase was not significant. There were no significant associations between LPS stimulated DCs with and without MSCs supernatants.
According to the results presented here, it appears that TLR2 and TLR4 gene expressions on the DCs are not affected by MSCs supernatant.
间充质干细胞(MSCs)是多能细胞,最近的研究结果表明它们对包括T细胞和树突状细胞(DCs)在内的免疫细胞具有免疫调节作用。DCs是最有效的抗原呈递细胞。由于MSCs的免疫调节特性,它们似乎可以影响DCs的成熟和分化。DCs表达一种称为Toll样受体(TLRs)的表面受体,并在DCs的成熟过程和激活中起关键作用。本研究的目的是评估在含有LPS和不含LPS的培养基中,DCs暴露于间充质干细胞上清液后TLR2和TLR4的表达情况。
在本实验研究中,分别从成年Balb/c小鼠的骨髓和脾脏中提取MSCs和DCs。在第5代培养24小时和48小时后收集MSCs上清液,并与DCs培养进行调整。将分离的DCs与MSCs上清液共培养,孵育时间为24小时和48小时。使用实时PCR技术评估TLR2和TLR4的mRNA水平。
结果表明,与对照组相比,在缺乏LPS的培养基中这两种受体的表达上调,但增加不显著。有或没有MSCs上清液刺激的LPS刺激的DCs之间没有显著关联。
根据此处给出的结果,似乎DCs上的TLR2和TLR4基因表达不受MSCs上清液的影响。