4.6 Article

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

期刊

INTERNATIONAL JOURNAL OF CARDIOLOGY
卷 198, 期 -, 页码 187-195

出版社

ELSEVIER IRELAND LTD
DOI: 10.1016/j.ijcard.2015.06.070

关键词

MSCs; Fucoidan; MnSOD; Survival; Vascular repair

资金

  1. National Research Foundation - Korean government [NRF-2011-0009610]
  2. Korean Health Technology R&D Project, Ministry of Health and Welfare, Republic of Korea [HI14C2253]
  3. National Research Foundation of Korea (NRF) - Korea government (MSIP) [2005-0049416]
  4. Next-Generation BioGreen 21 Program [PJ011141]
  5. Rural Development Administration, Republic of Korea
  6. National Research Foundation of Korea [2005-0049416] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

向作者/读者索取更多资源

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.

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