Acute Hypoxic Stress Affects Migration Machinery of Tissue O2-Adapted Adipose Stromal Cells

The ability of mesenchymal stromal (stem) cells (MSCs) to be mobilised from their local depot towards sites of injury and to participate in tissue repair makes these cells promising candidates for cell therapy. Physiological O2 tension in an MSC niche in vivo is about 4–7%. However, most in vitro st...

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Main Authors: Olga O. Udartseva, Margarita V. Lobanova, Elena R. Andreeva, Sergey V. Buravkov, Irina V. Ogneva, Ludmila B. Buravkova
Format: Article
Language:English
Published: Wiley 2016-01-01
Series:Stem Cells International
Online Access:http://dx.doi.org/10.1155/2016/7260562
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author Olga O. Udartseva
Margarita V. Lobanova
Elena R. Andreeva
Sergey V. Buravkov
Irina V. Ogneva
Ludmila B. Buravkova
author_facet Olga O. Udartseva
Margarita V. Lobanova
Elena R. Andreeva
Sergey V. Buravkov
Irina V. Ogneva
Ludmila B. Buravkova
author_sort Olga O. Udartseva
collection DOAJ
description The ability of mesenchymal stromal (stem) cells (MSCs) to be mobilised from their local depot towards sites of injury and to participate in tissue repair makes these cells promising candidates for cell therapy. Physiological O2 tension in an MSC niche in vivo is about 4–7%. However, most in vitro studies of MSC functional activity are performed at 20% O2. Therefore, this study focused on the effects of short-term hypoxic stress (0.1% O2, 24 h) on adipose tissue-derived MSC motility at tissue-related O2 level. No significant changes in integrin expression were detected after short-term hypoxic stress. However, O2 deprivation provoked vimentin disassembly and actin polymerisation and increased cell stiffness. In addition, hypoxic stress induced the downregulation of ACTR3, DSTN, MACF1, MID1, MYPT1, NCK1, ROCK1, TIAM1, and WASF1 expression, the products of which are known to be involved in leading edge formation and cell translocation. These changes were accompanied by the attenuation of targeted and nontargeted migration of MSCs after short-term hypoxic exposure, as demonstrated in scratch and transwell migration assays. These results indicate that acute hypoxic stress can modulate MSC function in their native milieu, preventing their mobilisation from sites of injury.
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spelling doaj-art-7f2de871bf09412983ee697ad1f69c382025-08-20T03:35:40ZengWileyStem Cells International1687-966X1687-96782016-01-01201610.1155/2016/72605627260562Acute Hypoxic Stress Affects Migration Machinery of Tissue O2-Adapted Adipose Stromal CellsOlga O. Udartseva0Margarita V. Lobanova1Elena R. Andreeva2Sergey V. Buravkov3Irina V. Ogneva4Ludmila B. Buravkova5Institute of Biomedical Problems, Russian Academy of Science, Khoroshevskoe Shosse 76A, Moscow 123007, RussiaInstitute of Biomedical Problems, Russian Academy of Science, Khoroshevskoe Shosse 76A, Moscow 123007, RussiaInstitute of Biomedical Problems, Russian Academy of Science, Khoroshevskoe Shosse 76A, Moscow 123007, RussiaLomonosov Moscow State University, Faculty of Fundamental Medicine, Lomonosovsky Prospect 31-5, Moscow 117192, RussiaInstitute of Biomedical Problems, Russian Academy of Science, Khoroshevskoe Shosse 76A, Moscow 123007, RussiaInstitute of Biomedical Problems, Russian Academy of Science, Khoroshevskoe Shosse 76A, Moscow 123007, RussiaThe ability of mesenchymal stromal (stem) cells (MSCs) to be mobilised from their local depot towards sites of injury and to participate in tissue repair makes these cells promising candidates for cell therapy. Physiological O2 tension in an MSC niche in vivo is about 4–7%. However, most in vitro studies of MSC functional activity are performed at 20% O2. Therefore, this study focused on the effects of short-term hypoxic stress (0.1% O2, 24 h) on adipose tissue-derived MSC motility at tissue-related O2 level. No significant changes in integrin expression were detected after short-term hypoxic stress. However, O2 deprivation provoked vimentin disassembly and actin polymerisation and increased cell stiffness. In addition, hypoxic stress induced the downregulation of ACTR3, DSTN, MACF1, MID1, MYPT1, NCK1, ROCK1, TIAM1, and WASF1 expression, the products of which are known to be involved in leading edge formation and cell translocation. These changes were accompanied by the attenuation of targeted and nontargeted migration of MSCs after short-term hypoxic exposure, as demonstrated in scratch and transwell migration assays. These results indicate that acute hypoxic stress can modulate MSC function in their native milieu, preventing their mobilisation from sites of injury.http://dx.doi.org/10.1155/2016/7260562
spellingShingle Olga O. Udartseva
Margarita V. Lobanova
Elena R. Andreeva
Sergey V. Buravkov
Irina V. Ogneva
Ludmila B. Buravkova
Acute Hypoxic Stress Affects Migration Machinery of Tissue O2-Adapted Adipose Stromal Cells
Stem Cells International
title Acute Hypoxic Stress Affects Migration Machinery of Tissue O2-Adapted Adipose Stromal Cells
title_full Acute Hypoxic Stress Affects Migration Machinery of Tissue O2-Adapted Adipose Stromal Cells
title_fullStr Acute Hypoxic Stress Affects Migration Machinery of Tissue O2-Adapted Adipose Stromal Cells
title_full_unstemmed Acute Hypoxic Stress Affects Migration Machinery of Tissue O2-Adapted Adipose Stromal Cells
title_short Acute Hypoxic Stress Affects Migration Machinery of Tissue O2-Adapted Adipose Stromal Cells
title_sort acute hypoxic stress affects migration machinery of tissue o2 adapted adipose stromal cells
url http://dx.doi.org/10.1155/2016/7260562
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