间充质干细胞
细胞生物学
移植
下调和上调
自噬
体内
球体
先天免疫系统
癌症研究
上睑下垂
间质细胞
生物
细胞凋亡
免疫系统
化学
免疫学
炎症
细胞培养
炎症体
医学
生物化学
外科
生物技术
基因
遗传学
作者
Duc‐Vinh Pham,Prakash Shrestha,Thi-Kem Nguyen,Junhyeung Park,Mahesh Pandit,Jae‐Hoon Chang,Soo Young Kim,Dong‐Young Choi,Sung Soo Han,Inho Choi,Gyu Hwan Park,Jee‐Heon Jeong,Pil-Hoon Park
标识
DOI:10.1016/j.ymthe.2022.12.014
摘要
Mesenchymal stem cells (MSCs) are ubiquitous multipotent cells that exhibit significant therapeutic potentials in a variety of disorders. Nevertheless, their clinical efficacy is limited owing to poor survival, low rate of engraftment, and impaired potency upon transplantation. Spheroidal three-dimensional (3D) culture of MSCs (MSC3D) has been proven to better preserve their in vivo functional properties. However, the molecular mechanisms underlying the improvement in MSC function by spheroid formation are not clearly understood. NLRP3 inflammasomes, a key component of the innate immune system, have recently been shown to play a role in cell fate decision of MSCs. The present study examined the role of NLRP3 inflammasomes in the survival and potency of MSC spheroids. We found that MSC3D led to decreased activation of NLRP3 inflammasomes through alleviation of ER stress in an autophagy-dependent manner. Importantly, downregulation of NLRP3 inflammasomes signaling critically contributes to the enhanced survival rate in MSC3D through modulation of pyroptosis and apoptosis. The critical role of NLRP3 inflammasome suppression in the enhanced therapeutic efficacy of MSC spheroids was further confirmed in an in vivo mouse model of DSS-induced colitis. These findings suggest that 3D culture confers survival and functional advantages to MSCs by suppressing NLRP3 inflammasome activation.
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