Conditioned medium derived from rat amniotic epithelial cells confers protection against inflammation, cancer, and senescence

被引:18
作者
Di Germanio, Clara [1 ,2 ]
Bernier, Michel [2 ]
Petr, Michael [2 ]
Mattioli, Mauro [1 ,3 ]
Barboni, Barbara [1 ]
de Cabo, Rafael [2 ]
机构
[1] Univ Teramo, Fac Vet Med, Teramo, Italy
[2] NIA, Translat Gerontol Branch, NIH, Baltimore, MD 21224 USA
[3] Ist Zooprofilatt Sperimentale Abruzzo & Molise G, Teramo, Italy
基金
美国国家卫生研究院;
关键词
amniotic epithelial cells; inflammation; tumorigenesis; senescence; SASP; Gerotarget; STEM-CELLS; SECRETORY PHENOTYPE; CELLULAR SENESCENCE; HUMAN FIBROBLASTS; IN-VITRO; MEMBRANE; DIFFERENTIATION; POLARIZATION; PLACENTA; TRANSPLANTATION;
D O I
10.18632/oncotarget.9694
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Amniotic epithelial cells (AECs) are a class of fetal stem cells that derives from the epiblast and resides in the amnion until birth. AECs are suitable candidates for regenerative medicine because of the ease of collection, their low immunogenicity and inability to form tumors after transplantation. Even though human AECs have been widely investigated, the fact remains that very little is known about AECs isolated from rat, one of the most common animal models in medical testing. In this study, we showed that rat AECs retained stemness properties and plasticity, expressed the pluripotency markers Sox2, Nanog, and Oct4 and were able to differentiate toward the osteogenic lineage. The addition of conditioned medium collected from rat AECs to lipopolysaccharide-activated macrophages elicited anti-inflammatory properties through a decrease of Tnfa expression and slowed tumor cell proliferation in vitro and in vivo. The senescence-associated secretory phenotype was also significantly lower upon incubation of senescent human IMR-90 fibroblast cells with conditioned medium from rat AECs. These results confirm the potential of AECs in the modulation of inflammatory mechanisms and open new therapeutic possibilities for regenerative medicine and anti-aging therapies as well.
引用
收藏
页码:39051 / 39064
页数:14
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