| Literature DB >> 31042075 |
Yixiong Tan1,2, Wei Nie1,2,3, Cheng Chen1,2, Xuesong He1,2, Yuzhi Xu1,2, Xiaoqian Ma1,2,3, Juan Zhang1,2, Mengqun Tan3, Pengfei Rong1,2, Wei Wang1,2,3.
Abstract
IMPACT STATEMENT: The utilization of mesenchymal stem cells (MSCs) is a promising approach to serve as adjuvant therapy for islet transplantation. But the inability to translate promising preclinical results into sound therapeutic effects in human subjects indicates a lack of key knowledge of MSC-islet interactions that warrant further research. Hypoxia and oxidative stress are critical factors which lead to a tremendous loss of islet grafts. However, previous studies mainly focused on other aspects of MSC protection such as inducing revascularization, enhancing insulin secretion, and reducing islet apoptosis. In this study, we aim to investigate whether MSC can protect islet cells from hypoxic damage by inhibiting ROS production and the potential underlying pathways involved. We also explore the effects of MSC-derived exosomes and IL-6 on hypoxia-injured islets. Our data provide new molecular targets for developing MSC applications, and this may ultimately promote the efficiency of clinical islet transplantation.Entities:
Keywords: Islet transplantation; exosome; hypoxia; mesenchymal stem cells; oxidative stress; the ERK pathway
Mesh:
Substances:
Year: 2019 PMID: 31042075 PMCID: PMC6567589 DOI: 10.1177/1535370219844472
Source DB: PubMed Journal: Exp Biol Med (Maywood) ISSN: 1535-3699