miR-27b represses migration of mouse MSCs to burned margins and prolongs wound repair through silencing SDF-1a.

BACKGROUND: Interactions between stromal cell-derived factor-1α (SDF-1α) and its cognate receptor CXCR4 are crucial for the recruitment of mesenchymal stem cells (MSCs) from bone marrow (BM) reservoirs to damaged tissues for repair during alarm situations. MicroRNAs are differentially expressed in s...

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Main Authors: Mu-Han Lü, Chang-Jiang Hu, Ling Chen, Xi Peng, Jian Chen, Jiong-Yu Hu, Miao Teng, Guang-Ping Liang
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3718818?pdf=render
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author Mu-Han Lü
Chang-Jiang Hu
Ling Chen
Xi Peng
Jian Chen
Jiong-Yu Hu
Miao Teng
Guang-Ping Liang
author_facet Mu-Han Lü
Chang-Jiang Hu
Ling Chen
Xi Peng
Jian Chen
Jiong-Yu Hu
Miao Teng
Guang-Ping Liang
author_sort Mu-Han Lü
collection DOAJ
description BACKGROUND: Interactions between stromal cell-derived factor-1α (SDF-1α) and its cognate receptor CXCR4 are crucial for the recruitment of mesenchymal stem cells (MSCs) from bone marrow (BM) reservoirs to damaged tissues for repair during alarm situations. MicroRNAs are differentially expressed in stem cell niches, suggesting a specialized role in stem cell regulation. Here, we gain insight into the molecular mechanisms involved in regulating SDF-1α. METHODS: MSCs from green fluorescent protein transgenic male mice were transfused to irradiated recipient female C57BL/6 mice, and skin burn model of bone marrow-chimeric mice were constructed. Six miRNAs with differential expression in burned murine skin tissue compared to normal skin tissue were identified using microarrays and bioinformatics. The expression of miR-27b and SDF-1α was examined in burned murine skin tissue using quantitative real-time PCR (qPCR) and immunohistochemistry (IHC), enzyme-linked immunosorbent assay (ELISA). The Correlation of miR-27b and SDF-1α expression was analyzed by Pearson analysis Correlation. miRNAs suppressed SDF-1α protein expression by binding directly to its 3'UTR using western blot and luciferase reporter assay. The importance of miRNAs in MSCs chemotaxis was further estimated by decreasing SDF-1α in vivo and in vitro. RESULTS: miR-23a, miR-27a and miR-27b expression was significantly lower in the burned skin than in the normal skin (p<0.05). We also found that several miRNAs suppressed SDF-1α protein expression, while just miR-27a and miR-27b directly bound to the SDF-1α 3'UTR. Moreover, the forced over-expression of miR-27a and miR-27b significantly reduced the directional migration of mMSCs in vitro. However, only miR-27b in burn wound margins significantly inhibited the mobilization of MSCs to the epidermis. CONCLUSION: miR-27b may be a unique signature of the stem cell niche in burned mouse skin and can suppress the directional migration of mMSCs by targeting SDF-1α by binding directly to its 3'UTR.
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spelling doaj.art-f0180423896543acab3626133264e8572022-12-21T20:30:21ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0187e6897210.1371/journal.pone.0068972miR-27b represses migration of mouse MSCs to burned margins and prolongs wound repair through silencing SDF-1a.Mu-Han LüChang-Jiang HuLing ChenXi PengJian ChenJiong-Yu HuMiao TengGuang-Ping LiangBACKGROUND: Interactions between stromal cell-derived factor-1α (SDF-1α) and its cognate receptor CXCR4 are crucial for the recruitment of mesenchymal stem cells (MSCs) from bone marrow (BM) reservoirs to damaged tissues for repair during alarm situations. MicroRNAs are differentially expressed in stem cell niches, suggesting a specialized role in stem cell regulation. Here, we gain insight into the molecular mechanisms involved in regulating SDF-1α. METHODS: MSCs from green fluorescent protein transgenic male mice were transfused to irradiated recipient female C57BL/6 mice, and skin burn model of bone marrow-chimeric mice were constructed. Six miRNAs with differential expression in burned murine skin tissue compared to normal skin tissue were identified using microarrays and bioinformatics. The expression of miR-27b and SDF-1α was examined in burned murine skin tissue using quantitative real-time PCR (qPCR) and immunohistochemistry (IHC), enzyme-linked immunosorbent assay (ELISA). The Correlation of miR-27b and SDF-1α expression was analyzed by Pearson analysis Correlation. miRNAs suppressed SDF-1α protein expression by binding directly to its 3'UTR using western blot and luciferase reporter assay. The importance of miRNAs in MSCs chemotaxis was further estimated by decreasing SDF-1α in vivo and in vitro. RESULTS: miR-23a, miR-27a and miR-27b expression was significantly lower in the burned skin than in the normal skin (p<0.05). We also found that several miRNAs suppressed SDF-1α protein expression, while just miR-27a and miR-27b directly bound to the SDF-1α 3'UTR. Moreover, the forced over-expression of miR-27a and miR-27b significantly reduced the directional migration of mMSCs in vitro. However, only miR-27b in burn wound margins significantly inhibited the mobilization of MSCs to the epidermis. CONCLUSION: miR-27b may be a unique signature of the stem cell niche in burned mouse skin and can suppress the directional migration of mMSCs by targeting SDF-1α by binding directly to its 3'UTR.http://europepmc.org/articles/PMC3718818?pdf=render
spellingShingle Mu-Han Lü
Chang-Jiang Hu
Ling Chen
Xi Peng
Jian Chen
Jiong-Yu Hu
Miao Teng
Guang-Ping Liang
miR-27b represses migration of mouse MSCs to burned margins and prolongs wound repair through silencing SDF-1a.
PLoS ONE
title miR-27b represses migration of mouse MSCs to burned margins and prolongs wound repair through silencing SDF-1a.
title_full miR-27b represses migration of mouse MSCs to burned margins and prolongs wound repair through silencing SDF-1a.
title_fullStr miR-27b represses migration of mouse MSCs to burned margins and prolongs wound repair through silencing SDF-1a.
title_full_unstemmed miR-27b represses migration of mouse MSCs to burned margins and prolongs wound repair through silencing SDF-1a.
title_short miR-27b represses migration of mouse MSCs to burned margins and prolongs wound repair through silencing SDF-1a.
title_sort mir 27b represses migration of mouse mscs to burned margins and prolongs wound repair through silencing sdf 1a
url http://europepmc.org/articles/PMC3718818?pdf=render
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