Exosomes from LPS-Stimulated hDPSCs Activated the Angiogenic Potential of HUVECs In Vitro
Background. Exosomes from human dental pulp stem cells (hDPSCs) were indicated to play a positive role in vascular regeneration processes. But the angiogenic capabilities of exosomes from inflammatory hDPSCs and the underlying mechanism remain unknown. In this study, the inflammatory factor lipopoly...
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| Format: | Article |
| Language: | English |
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Wiley
2021-01-01
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| Series: | Stem Cells International |
| Online Access: | http://dx.doi.org/10.1155/2021/6685307 |
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| author | Xiangyu Huang Wei Qiu Yuhua Pan Jianjia Li Zhao Chen Kaiying Zhang Yifei Luo Buling Wu Wenan Xu |
| author_facet | Xiangyu Huang Wei Qiu Yuhua Pan Jianjia Li Zhao Chen Kaiying Zhang Yifei Luo Buling Wu Wenan Xu |
| author_sort | Xiangyu Huang |
| collection | DOAJ |
| description | Background. Exosomes from human dental pulp stem cells (hDPSCs) were indicated to play a positive role in vascular regeneration processes. But the angiogenic capabilities of exosomes from inflammatory hDPSCs and the underlying mechanism remain unknown. In this study, the inflammatory factor lipopolysaccharide (LPS) was used to stimulate hDPSCs, and exosomes were extracted from these hDPSCs. The proangiogenic potential of exosomes was examined, and the underlying mechanism was studied. Method. Exosomes were isolated from hDPSCs with or without LPS stimulation (N-EXO and LPS-EXO) and cocultured with human umbilical vein endothelial cells (HUVECs). The proangiogenic potential of exosomes was evaluated by endothelial cell proliferation, migration, and tube formation abilities in vitro. To investigate the proangiogenic mechanism of LPS-EXO, microRNA sequencing was performed to explore the microRNA profile of N-EXO and LPS-EXO. Gene Ontology (GO) analysis was used to study the functions of the predicted target genes. Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis was used to estimate the signaling pathways associated with the inflammation-induced angiogenesis process. Result. Compared to the uptake of N-EXO, uptake of LPS-EXO activated the angiogenic potential of HUVECs by promoting the proliferation, migration, and tube formation abilities in vitro. The mRNA expression levels of vascular endothelial growth factor (VEGF) and kinase-insert domain-containing receptor (KDR) in the LPS-EXO group were significantly higher than those in the N-EXO group. MicroRNA sequencing showed that 10 microRNAs were significantly changed in LPS-EXO. Pathway analysis showed that the genes targeted by differentially expressed microRNAs were involved in multiple angiogenesis-related pathways. Conclusion. This study revealed that exosomes derived from inflammatory hDPSCs possessed better proangiogenic potential in vitro. This is the first time to explore the role of exosomal microRNA from hDPSCs in inflammation-induced angiogenesis. This finding sheds new light on the effect of inflammation-stimulated hDPSCs on tissue regeneration. |
| format | Article |
| id | doaj-art-7c16c9e5ad3946d0bc31a7ae5b2bb253 |
| institution | Kabale University |
| issn | 1687-966X 1687-9678 |
| language | English |
| publishDate | 2021-01-01 |
| publisher | Wiley |
| record_format | Article |
| series | Stem Cells International |
| spelling | doaj-art-7c16c9e5ad3946d0bc31a7ae5b2bb2532025-02-03T05:49:26ZengWileyStem Cells International1687-966X1687-96782021-01-01202110.1155/2021/66853076685307Exosomes from LPS-Stimulated hDPSCs Activated the Angiogenic Potential of HUVECs In VitroXiangyu Huang0Wei Qiu1Yuhua Pan2Jianjia Li3Zhao Chen4Kaiying Zhang5Yifei Luo6Buling Wu7Wenan Xu8Department of Stomatology, Nanfang Hospital, Southern Medical University, School of Stomatology, 1838 Guangzhou Avenue North, Guangzhou 510515, ChinaDepartment of Stomatology, Nanfang Hospital, Southern Medical University, School of Stomatology, 1838 Guangzhou Avenue North, Guangzhou 510515, ChinaDepartment of Stomatology, Nanfang Hospital, Southern Medical University, School of Stomatology, 1838 Guangzhou Avenue North, Guangzhou 510515, ChinaDepartment of Stomatology, Nanfang Hospital, Southern Medical University, School of Stomatology, 1838 Guangzhou Avenue North, Guangzhou 510515, ChinaShenzhen Stomatology Hospital (Pingshan), Southern Medical University, 143 Dongzong Road, Pingshan District, Shenzhen 518118, ChinaDepartment of Stomatology, Nanfang Hospital, Southern Medical University, School of Stomatology, 1838 Guangzhou Avenue North, Guangzhou 510515, ChinaDepartment of Stomatology, Nanfang Hospital, Southern Medical University, School of Stomatology, 1838 Guangzhou Avenue North, Guangzhou 510515, ChinaDepartment of Stomatology, Nanfang Hospital, Southern Medical University, School of Stomatology, 1838 Guangzhou Avenue North, Guangzhou 510515, ChinaDepartment of Stomatology, Nanfang Hospital, Southern Medical University, School of Stomatology, 1838 Guangzhou Avenue North, Guangzhou 510515, ChinaBackground. Exosomes from human dental pulp stem cells (hDPSCs) were indicated to play a positive role in vascular regeneration processes. But the angiogenic capabilities of exosomes from inflammatory hDPSCs and the underlying mechanism remain unknown. In this study, the inflammatory factor lipopolysaccharide (LPS) was used to stimulate hDPSCs, and exosomes were extracted from these hDPSCs. The proangiogenic potential of exosomes was examined, and the underlying mechanism was studied. Method. Exosomes were isolated from hDPSCs with or without LPS stimulation (N-EXO and LPS-EXO) and cocultured with human umbilical vein endothelial cells (HUVECs). The proangiogenic potential of exosomes was evaluated by endothelial cell proliferation, migration, and tube formation abilities in vitro. To investigate the proangiogenic mechanism of LPS-EXO, microRNA sequencing was performed to explore the microRNA profile of N-EXO and LPS-EXO. Gene Ontology (GO) analysis was used to study the functions of the predicted target genes. Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis was used to estimate the signaling pathways associated with the inflammation-induced angiogenesis process. Result. Compared to the uptake of N-EXO, uptake of LPS-EXO activated the angiogenic potential of HUVECs by promoting the proliferation, migration, and tube formation abilities in vitro. The mRNA expression levels of vascular endothelial growth factor (VEGF) and kinase-insert domain-containing receptor (KDR) in the LPS-EXO group were significantly higher than those in the N-EXO group. MicroRNA sequencing showed that 10 microRNAs were significantly changed in LPS-EXO. Pathway analysis showed that the genes targeted by differentially expressed microRNAs were involved in multiple angiogenesis-related pathways. Conclusion. This study revealed that exosomes derived from inflammatory hDPSCs possessed better proangiogenic potential in vitro. This is the first time to explore the role of exosomal microRNA from hDPSCs in inflammation-induced angiogenesis. This finding sheds new light on the effect of inflammation-stimulated hDPSCs on tissue regeneration.http://dx.doi.org/10.1155/2021/6685307 |
| spellingShingle | Xiangyu Huang Wei Qiu Yuhua Pan Jianjia Li Zhao Chen Kaiying Zhang Yifei Luo Buling Wu Wenan Xu Exosomes from LPS-Stimulated hDPSCs Activated the Angiogenic Potential of HUVECs In Vitro Stem Cells International |
| title | Exosomes from LPS-Stimulated hDPSCs Activated the Angiogenic Potential of HUVECs In Vitro |
| title_full | Exosomes from LPS-Stimulated hDPSCs Activated the Angiogenic Potential of HUVECs In Vitro |
| title_fullStr | Exosomes from LPS-Stimulated hDPSCs Activated the Angiogenic Potential of HUVECs In Vitro |
| title_full_unstemmed | Exosomes from LPS-Stimulated hDPSCs Activated the Angiogenic Potential of HUVECs In Vitro |
| title_short | Exosomes from LPS-Stimulated hDPSCs Activated the Angiogenic Potential of HUVECs In Vitro |
| title_sort | exosomes from lps stimulated hdpscs activated the angiogenic potential of huvecs in vitro |
| url | http://dx.doi.org/10.1155/2021/6685307 |
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