Cargando…
miR-100-5p Promotes Epidermal Stem Cell Proliferation through Targeting MTMR3 to Activate PIP3/AKT and ERK Signaling Pathways
Skin epidermal stem cells (EpSCs) play a critical role in wound healing and are ideal seed cells for skin tissue engineering. Exosomes from human adipose-derived stem cells (ADSC-Exos) promote human EpSC proliferation, but the underlying mechanism remains unclear. Here, we investigated the effect of...
Autores principales: | , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9421352/ https://www.ncbi.nlm.nih.gov/pubmed/36045954 http://dx.doi.org/10.1155/2022/1474273 |
_version_ | 1784777573321932800 |
---|---|
author | Liu, Zhe Yang, Yuan Ju, Jihui Zhang, Guangliang Zhang, Ping Ji, Pengxiang Jin, Qianheng Cao, Gaobiao Zuo, Rui Wang, Hongyu Yu, Chenghao Zhang, Zhiqiang Le, Yingying Fu, Yi Hou, Ruixing |
author_facet | Liu, Zhe Yang, Yuan Ju, Jihui Zhang, Guangliang Zhang, Ping Ji, Pengxiang Jin, Qianheng Cao, Gaobiao Zuo, Rui Wang, Hongyu Yu, Chenghao Zhang, Zhiqiang Le, Yingying Fu, Yi Hou, Ruixing |
author_sort | Liu, Zhe |
collection | PubMed |
description | Skin epidermal stem cells (EpSCs) play a critical role in wound healing and are ideal seed cells for skin tissue engineering. Exosomes from human adipose-derived stem cells (ADSC-Exos) promote human EpSC proliferation, but the underlying mechanism remains unclear. Here, we investigated the effect of miR-100-5p, one of the most abundant miRNAs in ADSC-Exos, on the proliferation of human EpSCs and explored the mechanisms involved. MTT and BrdU incorporation assays showed that miR-100-5p mimic transfection promoted EpSC proliferation in a time-dependent manner. Cell cycle analysis showed that miR-100-5p mimic transfection significantly decreased the percentage of cells in the G1 phase and increased the percentage of cells in the G2/M phase. Myotubularin-related protein 3 (MTMR3), a lipid phosphatase, was identified as a direct target of miR-100-5p. Knockdown of MTMR3 in EpSCs by RNA interference significantly enhanced cell proliferation, decreased the percentage of cells in the G1 phase and increased the percentage of cells in the S phase. Overexpression of MTMR3 reversed the proproliferative effect of miR-100-5p on EpSCs, indicating that miR-100-5p promoted EpSC proliferation by downregulating MTMR3. Mechanistic studies showed that transfection of EpSCs with miR-100-5p mimics elevated the intracellular PIP3 level, induced AKT and ERK phosphorylation, and upregulated cyclin D1, E1, and A2 expression, which could be attenuated by MTMR3 overexpression. Consistently, intradermal injection of ADSC-Exos or miR-100-5p-enriched ADSC-Exos into cultured human skin tissues significantly reduced MTMR3 expression and increased the thickness of the epidermis and the number of EpSCs in the basal layer of the epidermis. The aforementioned effect of miR-100-5p-enriched ADSC-Exos was stronger than that of ADSC-Exos and was reversed by MTMR3 overexpression. Collectively, our findings indicate that miR-100-5p promotes EpSC proliferation through MTMR3-mediated elevation of PIP3 and activation of AKT and ERK. miR-100-5p-enriched ADSC-Exos can be used to treat skin wound and expand EpSCs for generating epidermal autografts and engineered skin equivalents. |
format | Online Article Text |
id | pubmed-9421352 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-94213522022-08-30 miR-100-5p Promotes Epidermal Stem Cell Proliferation through Targeting MTMR3 to Activate PIP3/AKT and ERK Signaling Pathways Liu, Zhe Yang, Yuan Ju, Jihui Zhang, Guangliang Zhang, Ping Ji, Pengxiang Jin, Qianheng Cao, Gaobiao Zuo, Rui Wang, Hongyu Yu, Chenghao Zhang, Zhiqiang Le, Yingying Fu, Yi Hou, Ruixing Stem Cells Int Research Article Skin epidermal stem cells (EpSCs) play a critical role in wound healing and are ideal seed cells for skin tissue engineering. Exosomes from human adipose-derived stem cells (ADSC-Exos) promote human EpSC proliferation, but the underlying mechanism remains unclear. Here, we investigated the effect of miR-100-5p, one of the most abundant miRNAs in ADSC-Exos, on the proliferation of human EpSCs and explored the mechanisms involved. MTT and BrdU incorporation assays showed that miR-100-5p mimic transfection promoted EpSC proliferation in a time-dependent manner. Cell cycle analysis showed that miR-100-5p mimic transfection significantly decreased the percentage of cells in the G1 phase and increased the percentage of cells in the G2/M phase. Myotubularin-related protein 3 (MTMR3), a lipid phosphatase, was identified as a direct target of miR-100-5p. Knockdown of MTMR3 in EpSCs by RNA interference significantly enhanced cell proliferation, decreased the percentage of cells in the G1 phase and increased the percentage of cells in the S phase. Overexpression of MTMR3 reversed the proproliferative effect of miR-100-5p on EpSCs, indicating that miR-100-5p promoted EpSC proliferation by downregulating MTMR3. Mechanistic studies showed that transfection of EpSCs with miR-100-5p mimics elevated the intracellular PIP3 level, induced AKT and ERK phosphorylation, and upregulated cyclin D1, E1, and A2 expression, which could be attenuated by MTMR3 overexpression. Consistently, intradermal injection of ADSC-Exos or miR-100-5p-enriched ADSC-Exos into cultured human skin tissues significantly reduced MTMR3 expression and increased the thickness of the epidermis and the number of EpSCs in the basal layer of the epidermis. The aforementioned effect of miR-100-5p-enriched ADSC-Exos was stronger than that of ADSC-Exos and was reversed by MTMR3 overexpression. Collectively, our findings indicate that miR-100-5p promotes EpSC proliferation through MTMR3-mediated elevation of PIP3 and activation of AKT and ERK. miR-100-5p-enriched ADSC-Exos can be used to treat skin wound and expand EpSCs for generating epidermal autografts and engineered skin equivalents. Hindawi 2022-08-21 /pmc/articles/PMC9421352/ /pubmed/36045954 http://dx.doi.org/10.1155/2022/1474273 Text en Copyright © 2022 Zhe Liu et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Liu, Zhe Yang, Yuan Ju, Jihui Zhang, Guangliang Zhang, Ping Ji, Pengxiang Jin, Qianheng Cao, Gaobiao Zuo, Rui Wang, Hongyu Yu, Chenghao Zhang, Zhiqiang Le, Yingying Fu, Yi Hou, Ruixing miR-100-5p Promotes Epidermal Stem Cell Proliferation through Targeting MTMR3 to Activate PIP3/AKT and ERK Signaling Pathways |
title | miR-100-5p Promotes Epidermal Stem Cell Proliferation through Targeting MTMR3 to Activate PIP3/AKT and ERK Signaling Pathways |
title_full | miR-100-5p Promotes Epidermal Stem Cell Proliferation through Targeting MTMR3 to Activate PIP3/AKT and ERK Signaling Pathways |
title_fullStr | miR-100-5p Promotes Epidermal Stem Cell Proliferation through Targeting MTMR3 to Activate PIP3/AKT and ERK Signaling Pathways |
title_full_unstemmed | miR-100-5p Promotes Epidermal Stem Cell Proliferation through Targeting MTMR3 to Activate PIP3/AKT and ERK Signaling Pathways |
title_short | miR-100-5p Promotes Epidermal Stem Cell Proliferation through Targeting MTMR3 to Activate PIP3/AKT and ERK Signaling Pathways |
title_sort | mir-100-5p promotes epidermal stem cell proliferation through targeting mtmr3 to activate pip3/akt and erk signaling pathways |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9421352/ https://www.ncbi.nlm.nih.gov/pubmed/36045954 http://dx.doi.org/10.1155/2022/1474273 |
work_keys_str_mv | AT liuzhe mir1005ppromotesepidermalstemcellproliferationthroughtargetingmtmr3toactivatepip3aktanderksignalingpathways AT yangyuan mir1005ppromotesepidermalstemcellproliferationthroughtargetingmtmr3toactivatepip3aktanderksignalingpathways AT jujihui mir1005ppromotesepidermalstemcellproliferationthroughtargetingmtmr3toactivatepip3aktanderksignalingpathways AT zhangguangliang mir1005ppromotesepidermalstemcellproliferationthroughtargetingmtmr3toactivatepip3aktanderksignalingpathways AT zhangping mir1005ppromotesepidermalstemcellproliferationthroughtargetingmtmr3toactivatepip3aktanderksignalingpathways AT jipengxiang mir1005ppromotesepidermalstemcellproliferationthroughtargetingmtmr3toactivatepip3aktanderksignalingpathways AT jinqianheng mir1005ppromotesepidermalstemcellproliferationthroughtargetingmtmr3toactivatepip3aktanderksignalingpathways AT caogaobiao mir1005ppromotesepidermalstemcellproliferationthroughtargetingmtmr3toactivatepip3aktanderksignalingpathways AT zuorui mir1005ppromotesepidermalstemcellproliferationthroughtargetingmtmr3toactivatepip3aktanderksignalingpathways AT wanghongyu mir1005ppromotesepidermalstemcellproliferationthroughtargetingmtmr3toactivatepip3aktanderksignalingpathways AT yuchenghao mir1005ppromotesepidermalstemcellproliferationthroughtargetingmtmr3toactivatepip3aktanderksignalingpathways AT zhangzhiqiang mir1005ppromotesepidermalstemcellproliferationthroughtargetingmtmr3toactivatepip3aktanderksignalingpathways AT leyingying mir1005ppromotesepidermalstemcellproliferationthroughtargetingmtmr3toactivatepip3aktanderksignalingpathways AT fuyi mir1005ppromotesepidermalstemcellproliferationthroughtargetingmtmr3toactivatepip3aktanderksignalingpathways AT houruixing mir1005ppromotesepidermalstemcellproliferationthroughtargetingmtmr3toactivatepip3aktanderksignalingpathways |