Cargando…
Exosome-guided bone targeted delivery of Antagomir-188 as an anabolic therapy for bone loss
The differentiation shift from osteogenesis to adipogenesis of bone marrow mesenchymal stem cells (BMSCs) characterizes many pathological bone loss conditions. Stromal cell-derived factor-1 (SDF1) is highly enriched in the bone marrow for C-X-C motif chemokine receptor 4 (CXCR4)-positive hematopoiet...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
KeAi Publishing
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7917458/ https://www.ncbi.nlm.nih.gov/pubmed/33718671 http://dx.doi.org/10.1016/j.bioactmat.2021.02.014 |
_version_ | 1783657703930855424 |
---|---|
author | Hu, Yan Li, Xiaoqun Zhang, Qin Gu, Zhengrong Luo, Ying Guo, Jiawei Wang, Xiuhui Jing, Yingying Chen, Xiao Su, Jiacan |
author_facet | Hu, Yan Li, Xiaoqun Zhang, Qin Gu, Zhengrong Luo, Ying Guo, Jiawei Wang, Xiuhui Jing, Yingying Chen, Xiao Su, Jiacan |
author_sort | Hu, Yan |
collection | PubMed |
description | The differentiation shift from osteogenesis to adipogenesis of bone marrow mesenchymal stem cells (BMSCs) characterizes many pathological bone loss conditions. Stromal cell-derived factor-1 (SDF1) is highly enriched in the bone marrow for C-X-C motif chemokine receptor 4 (CXCR4)-positive hematopoietic stem cell (HSC) homing and tumor bone metastasis. In this study, we displayed CXCR4 on the surface of exosomes derived from genetically engineered NIH-3T3 cells. CXCR4(+) exosomes selectively accumulated in the bone marrow. Then, we fused CXCR4(+) exosomes with liposomes carrying antagomir-188 to produce hybrid nanoparticles (NPs). The hybrid NPs specifically gathered in the bone marrow and released antagomir-188, which promoted osteogenesis and inhibited adipogenesis of BMSCs and thereby reversed age-related trabecular bone loss and decreased cortical bone porosity in mice. Taken together, this study presents a novel way to obtain bone-targeted exosomes via surface display of CXCR4 and a promising anabolic therapeutic approach for age-related bone loss. |
format | Online Article Text |
id | pubmed-7917458 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | KeAi Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-79174582021-03-12 Exosome-guided bone targeted delivery of Antagomir-188 as an anabolic therapy for bone loss Hu, Yan Li, Xiaoqun Zhang, Qin Gu, Zhengrong Luo, Ying Guo, Jiawei Wang, Xiuhui Jing, Yingying Chen, Xiao Su, Jiacan Bioact Mater Article The differentiation shift from osteogenesis to adipogenesis of bone marrow mesenchymal stem cells (BMSCs) characterizes many pathological bone loss conditions. Stromal cell-derived factor-1 (SDF1) is highly enriched in the bone marrow for C-X-C motif chemokine receptor 4 (CXCR4)-positive hematopoietic stem cell (HSC) homing and tumor bone metastasis. In this study, we displayed CXCR4 on the surface of exosomes derived from genetically engineered NIH-3T3 cells. CXCR4(+) exosomes selectively accumulated in the bone marrow. Then, we fused CXCR4(+) exosomes with liposomes carrying antagomir-188 to produce hybrid nanoparticles (NPs). The hybrid NPs specifically gathered in the bone marrow and released antagomir-188, which promoted osteogenesis and inhibited adipogenesis of BMSCs and thereby reversed age-related trabecular bone loss and decreased cortical bone porosity in mice. Taken together, this study presents a novel way to obtain bone-targeted exosomes via surface display of CXCR4 and a promising anabolic therapeutic approach for age-related bone loss. KeAi Publishing 2021-02-23 /pmc/articles/PMC7917458/ /pubmed/33718671 http://dx.doi.org/10.1016/j.bioactmat.2021.02.014 Text en © 2021 [The Author/The Authors] http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Hu, Yan Li, Xiaoqun Zhang, Qin Gu, Zhengrong Luo, Ying Guo, Jiawei Wang, Xiuhui Jing, Yingying Chen, Xiao Su, Jiacan Exosome-guided bone targeted delivery of Antagomir-188 as an anabolic therapy for bone loss |
title | Exosome-guided bone targeted delivery of Antagomir-188 as an anabolic therapy for bone loss |
title_full | Exosome-guided bone targeted delivery of Antagomir-188 as an anabolic therapy for bone loss |
title_fullStr | Exosome-guided bone targeted delivery of Antagomir-188 as an anabolic therapy for bone loss |
title_full_unstemmed | Exosome-guided bone targeted delivery of Antagomir-188 as an anabolic therapy for bone loss |
title_short | Exosome-guided bone targeted delivery of Antagomir-188 as an anabolic therapy for bone loss |
title_sort | exosome-guided bone targeted delivery of antagomir-188 as an anabolic therapy for bone loss |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7917458/ https://www.ncbi.nlm.nih.gov/pubmed/33718671 http://dx.doi.org/10.1016/j.bioactmat.2021.02.014 |
work_keys_str_mv | AT huyan exosomeguidedbonetargeteddeliveryofantagomir188asananabolictherapyforboneloss AT lixiaoqun exosomeguidedbonetargeteddeliveryofantagomir188asananabolictherapyforboneloss AT zhangqin exosomeguidedbonetargeteddeliveryofantagomir188asananabolictherapyforboneloss AT guzhengrong exosomeguidedbonetargeteddeliveryofantagomir188asananabolictherapyforboneloss AT luoying exosomeguidedbonetargeteddeliveryofantagomir188asananabolictherapyforboneloss AT guojiawei exosomeguidedbonetargeteddeliveryofantagomir188asananabolictherapyforboneloss AT wangxiuhui exosomeguidedbonetargeteddeliveryofantagomir188asananabolictherapyforboneloss AT jingyingying exosomeguidedbonetargeteddeliveryofantagomir188asananabolictherapyforboneloss AT chenxiao exosomeguidedbonetargeteddeliveryofantagomir188asananabolictherapyforboneloss AT sujiacan exosomeguidedbonetargeteddeliveryofantagomir188asananabolictherapyforboneloss |