Circular RNA AFF4 modulates osteogenic differentiation in BM-MSCs by activating SMAD1/5 pathway through miR-135a-5p/FNDC5/Irisin axis

Abstract Bone marrow-derived mesenchymal stem cells (BM-MSCs), the common progenitor cells of adipocytes and osteoblasts, have been recognized as the key mediator during bone formation. Herein, our study aim to investigate molecular mechanisms underlying circular RNA (circRNA) AFF4 (circ_AFF4)-regul...

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Main Authors: Chao Liu, An-Song Liu, Da Zhong, Cheng-Gong Wang, Mi Yu, Hao-Wei Zhang, Han Xiao, Jian-Hua Liu, Jian Zhang, Ke Yin
Format: Article
Language:English
Published: Nature Publishing Group 2021-06-01
Series:Cell Death and Disease
Online Access:https://doi.org/10.1038/s41419-021-03877-4
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spelling doaj-52eae0a7fc9443d495ea1f19f877d19d2021-06-20T11:05:05ZengNature Publishing GroupCell Death and Disease2041-48892021-06-0112711710.1038/s41419-021-03877-4Circular RNA AFF4 modulates osteogenic differentiation in BM-MSCs by activating SMAD1/5 pathway through miR-135a-5p/FNDC5/Irisin axisChao Liu0An-Song Liu1Da Zhong2Cheng-Gong Wang3Mi Yu4Hao-Wei Zhang5Han Xiao6Jian-Hua Liu7Jian Zhang8Ke Yin9Department of Orthopedics, The First Affiliated Hospital of University of South ChinaDepartment of Orthopedics, The First Affiliated Hospital of University of South ChinaDepartment of Orthopedics, Xiangya Hospital, Central South UniversityDepartment of Orthopedics, Xiangya Hospital, Central South UniversityMedical College of University of South ChinaDepartment of Orthopedics, The First Affiliated Hospital of University of South ChinaDepartment of Orthopedics, The First Affiliated Hospital of University of South ChinaDepartment of Hematology, The First Affiliated Hospital of University of South ChinaDepartment of Orthopedics, The First Affiliated Hospital of University of South ChinaDepartment of Orthopedics, The First Affiliated Hospital of University of South ChinaAbstract Bone marrow-derived mesenchymal stem cells (BM-MSCs), the common progenitor cells of adipocytes and osteoblasts, have been recognized as the key mediator during bone formation. Herein, our study aim to investigate molecular mechanisms underlying circular RNA (circRNA) AFF4 (circ_AFF4)-regulated BM-MSCs osteogenesis. BM-MSCs were characterized by FACS, ARS, and ALP staining. Expression patterns of circ_AFF4, miR-135a-5p, FNDC5/Irisin, SMAD1/5, and osteogenesis markers, including ALP, BMP4, RUNX2, Spp1, and Colla1 were detected by qRT-PCR, western blot, or immunofluorescence staining, respectively. Interactions between circ_AFF4 and miR-135a-5p, FNDC5, and miR-135a-5p were analyzed using web tools including TargetScan, miRanda, and miRDB, and further confirmed by luciferase reporter assay and RNA pull-down. Complex formation between Irisin and Integrin αV was verified by Co-immunoprecipitation. To further verify the functional role of circ_AFF4 in vivo during bone formation, we conducted animal experiments harboring circ_AFF4 knockdown, and born samples were evaluated by immunohistochemistry, hematoxylin and eosin, and Masson staining. Circ_AFF4 was upregulated upon osteogenic differentiation induction in BM-MSCs, and miR-135a-5p expression declined as differentiation proceeds. Circ_AFF4 knockdown significantly inhibited osteogenesis potential in BM-MSCs. Circ_AFF4 stimulated FNDC5/Irisin expression through complementary binding to its downstream target molecule miR-135a-5p. Irisin formed an intermolecular complex with Integrin αV and activated the SMAD1/5 pathway during osteogenic differentiation. Our work revealed that circ_AFF4, acting as a sponge of miR-135a-5p, triggers the promotion of FNDC5/Irisin via activating the SMAD1/5 pathway to induce osteogenic differentiation in BM-MSCs. These findings gained a deeper insight into the circRNA-miRNA regulatory system in the bone marrow microenvironment and may improve our understanding of bone formation-related diseases at physiological and pathological levels.https://doi.org/10.1038/s41419-021-03877-4
collection DOAJ
language English
format Article
sources DOAJ
author Chao Liu
An-Song Liu
Da Zhong
Cheng-Gong Wang
Mi Yu
Hao-Wei Zhang
Han Xiao
Jian-Hua Liu
Jian Zhang
Ke Yin
spellingShingle Chao Liu
An-Song Liu
Da Zhong
Cheng-Gong Wang
Mi Yu
Hao-Wei Zhang
Han Xiao
Jian-Hua Liu
Jian Zhang
Ke Yin
Circular RNA AFF4 modulates osteogenic differentiation in BM-MSCs by activating SMAD1/5 pathway through miR-135a-5p/FNDC5/Irisin axis
Cell Death and Disease
author_facet Chao Liu
An-Song Liu
Da Zhong
Cheng-Gong Wang
Mi Yu
Hao-Wei Zhang
Han Xiao
Jian-Hua Liu
Jian Zhang
Ke Yin
author_sort Chao Liu
title Circular RNA AFF4 modulates osteogenic differentiation in BM-MSCs by activating SMAD1/5 pathway through miR-135a-5p/FNDC5/Irisin axis
title_short Circular RNA AFF4 modulates osteogenic differentiation in BM-MSCs by activating SMAD1/5 pathway through miR-135a-5p/FNDC5/Irisin axis
title_full Circular RNA AFF4 modulates osteogenic differentiation in BM-MSCs by activating SMAD1/5 pathway through miR-135a-5p/FNDC5/Irisin axis
title_fullStr Circular RNA AFF4 modulates osteogenic differentiation in BM-MSCs by activating SMAD1/5 pathway through miR-135a-5p/FNDC5/Irisin axis
title_full_unstemmed Circular RNA AFF4 modulates osteogenic differentiation in BM-MSCs by activating SMAD1/5 pathway through miR-135a-5p/FNDC5/Irisin axis
title_sort circular rna aff4 modulates osteogenic differentiation in bm-mscs by activating smad1/5 pathway through mir-135a-5p/fndc5/irisin axis
publisher Nature Publishing Group
series Cell Death and Disease
issn 2041-4889
publishDate 2021-06-01
description Abstract Bone marrow-derived mesenchymal stem cells (BM-MSCs), the common progenitor cells of adipocytes and osteoblasts, have been recognized as the key mediator during bone formation. Herein, our study aim to investigate molecular mechanisms underlying circular RNA (circRNA) AFF4 (circ_AFF4)-regulated BM-MSCs osteogenesis. BM-MSCs were characterized by FACS, ARS, and ALP staining. Expression patterns of circ_AFF4, miR-135a-5p, FNDC5/Irisin, SMAD1/5, and osteogenesis markers, including ALP, BMP4, RUNX2, Spp1, and Colla1 were detected by qRT-PCR, western blot, or immunofluorescence staining, respectively. Interactions between circ_AFF4 and miR-135a-5p, FNDC5, and miR-135a-5p were analyzed using web tools including TargetScan, miRanda, and miRDB, and further confirmed by luciferase reporter assay and RNA pull-down. Complex formation between Irisin and Integrin αV was verified by Co-immunoprecipitation. To further verify the functional role of circ_AFF4 in vivo during bone formation, we conducted animal experiments harboring circ_AFF4 knockdown, and born samples were evaluated by immunohistochemistry, hematoxylin and eosin, and Masson staining. Circ_AFF4 was upregulated upon osteogenic differentiation induction in BM-MSCs, and miR-135a-5p expression declined as differentiation proceeds. Circ_AFF4 knockdown significantly inhibited osteogenesis potential in BM-MSCs. Circ_AFF4 stimulated FNDC5/Irisin expression through complementary binding to its downstream target molecule miR-135a-5p. Irisin formed an intermolecular complex with Integrin αV and activated the SMAD1/5 pathway during osteogenic differentiation. Our work revealed that circ_AFF4, acting as a sponge of miR-135a-5p, triggers the promotion of FNDC5/Irisin via activating the SMAD1/5 pathway to induce osteogenic differentiation in BM-MSCs. These findings gained a deeper insight into the circRNA-miRNA regulatory system in the bone marrow microenvironment and may improve our understanding of bone formation-related diseases at physiological and pathological levels.
url https://doi.org/10.1038/s41419-021-03877-4
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