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Real‐Time H 2 O 2 Measurements in Bone Marrow Mesenchymal Stem Cells (MSCs) Show Increased Antioxidant Capacity in Cells From Osteoporotic Women
Author(s) -
Román Flavia,
Urra Carla,
Porras Omar,
Pino Ana María,
Rosen Clifford J.,
Rodríguez Juan Pablo
Publication year - 2017
Publication title -
journal of cellular biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.028
H-Index - 165
eISSN - 1097-4644
pISSN - 0730-2312
DOI - 10.1002/jcb.25739
Subject(s) - mesenchymal stem cell , reactive oxygen species , oxidative stress , superoxide dismutase , intracellular , bone marrow , catalase , microbiology and biotechnology , stem cell , cell , chemistry , antioxidant , biology , immunology , biochemistry
Oxidative stress (OS) derived from an increase in intracellular reactive oxygen species (ROS) is a major determinant of aging and lifespan. It has also been associated with several age‐related disorders, like postmenopausal osteoporosis of Mesenchymal stem cells (MSCs). MSCs are the common precursors for osteoblasts and adipocytes; appropriate commitment and differentiation of MSCs into a specific phenotype is modulated, among other factors, by ROS balance. MSCs have shown more resistance to ROS than differentiated cells, and their redox status depends on complex and abundant anti‐oxidant mechanisms. The purpose of this work was to analyze in real time, H 2 O 2 signaling in individual h‐MSCs, and to compare the kinetic parameters of H 2 O 2 management by cells derived from both control (c‐) and osteoporotic (o‐) women. For these purposes, cells were infected with a genetically encoded fluorescent biosensor named HyPer, which is specific for detecting H 2 O 2 inside living cells. Subsequently, cells were sequentially challenged with 50 and 500 μM H 2 O 2 pulses, and the cellular response was recorded in real time. The results demonstrated adequate expression of the biosensor allowing registering fluorescence from HyPer at a single cell level. Comparison of the response of c‐ and o‐MSCs to the oxidant challenges demonstrated improved antioxidant activity in o‐MSCs. This was further corroborated by measuring the relative expression of mRNAs for catalase, superoxide dismutase‐1, thioredoxine, and peroxiredoxine, as well as by cell‐surviving capacity under short‐term H 2 O 2 treatment. We conclude that functional differences exist between healthy and osteoporotic human MSCs. The mechanism for these differences requires further study. J. Cell. Biochem. 118: 585–593, 2017. © 2016 Wiley Periodicals, Inc.