Liang Changxiang, Liang Guoyan, Zheng Xiaoqing, Huang Yongxiong, Huang Shuaihao, Yin Dong
Department of Spinal Surgery, Guangdong Provincial People's Hospital, Guangzhou, China 510080.
Stem Cells Int. 2020 Apr 6;2020:7073805. doi: 10.1155/2020/7073805. eCollection 2020.
Mesenchymal stem cells (MSCs) are multipotent stem cells that have a strong osteogenic differentiation capacity. However, the molecular mechanism underlying the osteogenic differentiation of MSCs remains largely unknown and thus hinders further development of MSC-based cell therapies for bone repair in the clinic. RSP5, also called NEDD4L (NEDD4-like E3 ubiquitin protein ligase), belongs to the HECT (homologous to E6-AP carboxyl terminus) domain-containing E3 ligase family. Nevertheless, although many studies have been conducted to elucidate the role of RSP5 in various biological processes, its effect on osteogenesis remains elusive. In this study, we demonstrated that the expression of RSP5 was elevated during the osteogenesis of MSCs and positively regulated the osteogenic capacity of MSCs by inducing K63-linked polyubiquitination and activation of the Akt pathway. Taken together, our findings suggest that RSP5 may be a promising target to improve therapeutic efficiency by using MSCs for bone regeneration and repair.
间充质干细胞(MSCs)是具有强大成骨分化能力的多能干细胞。然而,MSCs成骨分化的分子机制在很大程度上仍不清楚,因此阻碍了基于MSCs的细胞疗法在临床上用于骨修复的进一步发展。RSP5,也称为NEDD4L(NEDD4样E3泛素蛋白连接酶),属于含HECT(与E6-AP羧基末端同源)结构域的E3连接酶家族。然而,尽管已经进行了许多研究来阐明RSP5在各种生物学过程中的作用,但其对成骨的影响仍然难以捉摸。在本研究中,我们证明RSP5在MSCs成骨过程中表达升高,并通过诱导K63连接的多聚泛素化和激活Akt途径来正向调节MSCs的成骨能力。综上所述,我们的研究结果表明,RSP5可能是一个有前景的靶点,可通过使用MSCs进行骨再生和修复来提高治疗效率。