Fucoidan protects mesenchymal stem cells against oxidative stress and enhances vascular regeneration in a murine hindlimb ischemia model

被引:51
作者
Han, Yong-seok [1 ]
Lee, Jun Hee [3 ]
Jung, Jin Sup [4 ,5 ]
Noh, Hyunjin [6 ,7 ]
Baek, Moo Jun [8 ]
Ryu, Jung Min [9 ,10 ,11 ]
Yoon, Yeo Min [1 ]
Han, Ho Jae [9 ,10 ,11 ]
Lee, Sang Hun [1 ,2 ]
机构
[1] Soonchunhyang Univ, Med Sci Res Inst, Seoul Hosp, Seoul, South Korea
[2] Soonchunhyang Univ, Dept Biochem, Coll Med, Cheonan 330930, South Korea
[3] Pusan Natl Univ, Sch Med, Dept Physiol, Lab Vasc Med & Stem Cell Biol,Med Res Inst, Yangsan 626870, South Korea
[4] Pusan Natl Univ, Med Res Ctr Ischem Tissue Engn, Yangsan 626870, Gyeongnam, South Korea
[5] Pusan Natl Univ, Dept Physiol, Sch Med, Yangsan 626870, Gyeongnam, South Korea
[6] Soonchunhyang Univ, Dept Internal Med, Seoul, South Korea
[7] Soonchunhyang Univ, Hyonam Kidney Lab, Seoul, South Korea
[8] Soonchunhyang Univ, Sch Med, Dept Surg, Cheonan 330930, South Korea
[9] Seoul Natl Univ, Dept Vet Physiol, Coll Vet Med, Seoul 151741, South Korea
[10] Seoul Natl Univ, Res Inst Vet Sci, Seoul 151741, South Korea
[11] Seoul Natl Univ, PLUS Creat Vet Res Ctr BK21, Seoul 151741, South Korea
基金
新加坡国家研究基金会;
关键词
MSCs; Fucoidan; MnSOD; Survival; Vascular repair; DEPRIVATION-INDUCED APOPTOSIS; POSEIDON RANDOMIZED-TRIAL; COLONY-FORMING CELLS; BONE-MARROW; TRANSENDOCARDIAL INJECTION; IN-VITRO; HYPOXIA; THERAPY; REPAIR;
D O I
10.1016/j.ijcard.2015.06.070
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Background: Mesenchymal stem cells (MSCs) have the potential to differentiate into multiple cell lineages. Given this potential for tissue regeneration, MSC-based therapeutic applications have been considered in recent years. However, ischemia-induced apoptosis has been reported to be one of the main causes of MSC death following transplantation. The primary objective of this study was to determine whether a natural antioxidant, fucoidan, could protect MSCs from ischemia-induced apoptosis in vitro and in vivo. Furthermore, we investigated the mechanism of action of fucoidan's anti-ischemic effect in MSCs. Methods and result: Pre-treatment with fucoidan (10 mu g/mL) suppressed the increase in H2O2-induced reactive oxygen species (ROS) levels and drastically reduced apoptotic cell death in MSCs. Fucoidan inhibited the activation of the pro-apoptotic proteins p38-mitogen-activated protein kinase (MAPK), Jun N-terminal kinase (JNK), and caspase-3, and augmented the expression of the anti-apoptosis protein cellular inhibitor of apoptosis (cIAP). Moreover, fucoidan significantly increased manganese superoxide dismutase (MnSOD) expression and decreased cellular ROS levels via the Akt pathway, resulting in enhanced cell survival. In amurine hindlimb ischemia model, transplanted fucoidan-treated MSCs showed significantly enhanced cell survival and proliferation in ischemic tissues. Functional recovery and limb salvage also remarkably improved in mice injected with fucoidan-stimulated MSCs compared with mice injected with non-stimulated MSCs. Conclusion: Taken together, these results show that fucoidan protects MSCs from ischemia-induced cell death by modulation of apoptosis-associated proteins and cellular ROS levels through regulation of the MnSOD and Akt pathways, suggesting that fucoidan could be powerful therapeutic adjuvant for MSC-based therapy in ischemic diseases. (C) 2015 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:187 / 195
页数:9
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