Mutation Reduction of Alopecia-Related Genes in hiPSC Using miR-520d-5p
Background: iPSCs, with many mutations or epigenetic modifications, are in a unique aging state and have pluripotent properties. Previously, we reported that hsa-miR-520d-5p reverted fibroblasts to mesenchymal stem cells (MSCs) and converted approximately half of the mutations in cancer cells back t...
| 出版年: | Re:GEN Open |
|---|---|
| 主要な著者: | , |
| フォーマット: | 論文 |
| 言語: | 英語 |
| 出版事項: |
Mary Ann Liebert
2022-10-01
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| 主題: | |
| オンライン・アクセス: | https://www.liebertpub.com/doi/full/10.1089/REGEN.2022.0042 |
| _version_ | 1850146181638782976 |
|---|---|
| author | Norimasa Miura Norimasa Miura Keigo Miura Keigo Miura |
| author_facet | Norimasa Miura Norimasa Miura Keigo Miura Keigo Miura |
| author_sort | Norimasa Miura |
| collection | DOAJ |
| container_title | Re:GEN Open |
| description | Background: iPSCs, with many mutations or epigenetic modifications, are in a unique aging state and have pluripotent properties. Previously, we reported that hsa-miR-520d-5p reverted fibroblasts to mesenchymal stem cells (MSCs) and converted approximately half of the mutations in cancer cells back to wild-type alleles.
Objective: We focused on the genes involved in the hair life cycle comprising 4 phases and examined whether 520d-5p can convert iPSCs with mutation(s) to less-mutated status during the differentiation to MSCs.
Materials and methods: Using next-generation sequencing analysis, we compared the effect of 520d-5p on the mutation level in 177 hair life cycle-related genes in iPSCs to that in iPSC-differentiated MSCs.
Results: Transfection by hsa-miR-520d-5p induced genetic improvement in 79.7% (141/177) of the genes and reverted 17.7% (25/141) to wild type; the average conversion rate was 54.4%. The hsa-miR-520d-5p-induced genes, including the function of dermal papilla cells or bulge stem cells closer to intact status. Interestingly, the dramatic changes of nucleotide extended to non-target genes as well as target genes.
Conclusions: Thus, hsa-miR-520d-5p is useful for studying hair or scalp conditioning and developing therapy against aging or hair diseases such as alopecia. |
| format | Article |
| id | doaj-art-5fafb2fe30ce449ba4a8564d3a57f12e |
| institution | Directory of Open Access Journals |
| issn | 2766-2705 |
| language | English |
| publishDate | 2022-10-01 |
| publisher | Mary Ann Liebert |
| record_format | Article |
| spelling | doaj-art-5fafb2fe30ce449ba4a8564d3a57f12e2025-08-19T23:47:22ZengMary Ann LiebertRe:GEN Open2766-27052022-10-012113614410.1089/REGEN.2022.0042Mutation Reduction of Alopecia-Related Genes in hiPSC Using miR-520d-5pNorimasa Miura0Norimasa Miura1Keigo Miura2Keigo Miura3Tokyo Mibyou CenterR&D Center, LIVIUS Pte LtdTokyo Mibyou CenterR&D Center, LIVIUS Pte LtdBackground: iPSCs, with many mutations or epigenetic modifications, are in a unique aging state and have pluripotent properties. Previously, we reported that hsa-miR-520d-5p reverted fibroblasts to mesenchymal stem cells (MSCs) and converted approximately half of the mutations in cancer cells back to wild-type alleles. Objective: We focused on the genes involved in the hair life cycle comprising 4 phases and examined whether 520d-5p can convert iPSCs with mutation(s) to less-mutated status during the differentiation to MSCs. Materials and methods: Using next-generation sequencing analysis, we compared the effect of 520d-5p on the mutation level in 177 hair life cycle-related genes in iPSCs to that in iPSC-differentiated MSCs. Results: Transfection by hsa-miR-520d-5p induced genetic improvement in 79.7% (141/177) of the genes and reverted 17.7% (25/141) to wild type; the average conversion rate was 54.4%. The hsa-miR-520d-5p-induced genes, including the function of dermal papilla cells or bulge stem cells closer to intact status. Interestingly, the dramatic changes of nucleotide extended to non-target genes as well as target genes. Conclusions: Thus, hsa-miR-520d-5p is useful for studying hair or scalp conditioning and developing therapy against aging or hair diseases such as alopecia.https://www.liebertpub.com/doi/full/10.1089/REGEN.2022.0042mutationiPSCMSC520d-5phair life cyclegene expression |
| spellingShingle | Norimasa Miura Norimasa Miura Keigo Miura Keigo Miura Mutation Reduction of Alopecia-Related Genes in hiPSC Using miR-520d-5p mutation iPSC MSC 520d-5p hair life cycle gene expression |
| title | Mutation Reduction of Alopecia-Related Genes in hiPSC Using miR-520d-5p |
| title_full | Mutation Reduction of Alopecia-Related Genes in hiPSC Using miR-520d-5p |
| title_fullStr | Mutation Reduction of Alopecia-Related Genes in hiPSC Using miR-520d-5p |
| title_full_unstemmed | Mutation Reduction of Alopecia-Related Genes in hiPSC Using miR-520d-5p |
| title_short | Mutation Reduction of Alopecia-Related Genes in hiPSC Using miR-520d-5p |
| title_sort | mutation reduction of alopecia related genes in hipsc using mir 520d 5p |
| topic | mutation iPSC MSC 520d-5p hair life cycle gene expression |
| url | https://www.liebertpub.com/doi/full/10.1089/REGEN.2022.0042 |
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