File Download

There are no files associated with this item.

  Links for fulltext
     (May Require Subscription)
Supplementary

Article: Lgr5-overexpressing mesenchymal stem cells augment fracture healing through regulation of Wnt/ERK signaling pathways and mitochondrial dynamics

TitleLgr5-overexpressing mesenchymal stem cells augment fracture healing through regulation of Wnt/ERK signaling pathways and mitochondrial dynamics
Authors
Keywordsangiogenesis
fission
GPCR
MSCs
osteogenic differentiation
Issue Date2019
Citation
FASEB Journal, 2019, v. 33, n. 7, p. 8565-8577 How to Cite?
AbstractFracture remains one of the most common traumatic conditions in orthopedic surgery. The use of mesenchymal stem cells (MSCs) to augment fracture repair is promising. Leucine-rich repeat-containing GPCR 5 (Lgr5), a transmembrane protein, has been identified as a novel adult stem cell marker in various organs and tissues. However, the roles of Lgr5 in MSCs are not fully understood. In this study, we investigated cellular functions of Lgr5 in MSCs and its potential implications in treating fracture. Lgr5-overexpressing MSCs (MSCLgr5) were established in murine SV40 promoter–driven luciferase reporter MSC line through virus transfection. Results of real-time quantitative PCR and Western blot analysis confirmed the increased expression of Lgr5 in MSCLgr5. MSCLgr5 exhibited increased osteogenic capacity, which may result from elevated expression of β-catenin and phosphorylated ERK1/2 within the nuclear region of cells. In contrast, inhibition of Lgr5 expression decreased the osteogenic differentiation ability of MSCs, accompanied with increased mitochondrial fragmentation and reduced expression of β-catenin. Local transplantation of MSCLgr5 at fracture sites accelerated fracture healing via enhanced osteogenesis and angiogenesis. MSCLgr5 stimulated the tube formation capacity of HUVECs in a Matrigel coculture system in vitro significantly. Taken together, results suggest that Lgr5 is implicated in the cellular processes of osteogenic differentiation of MSCs through regulation of Wnt and ERK signaling pathways and mitochondrial dynamics in fusion and fission. Inhibition of Lgr5 expression induced increased mitochondrial fragmentation and suppression of osteogenesis. MSCLgr5 exhibited enhanced therapeutic efficacy for fracture healing, which may serve as a superior cell source for bone tissue repair.—Lin, W., Xu, L., Pan, Q., Lin, S., Feng, L., Wang, B., Chen, S., Li, Y., Wang, H., Li, Y., Wang, Y., Lee, W. Y. W., Sun, D., Li, G. Lgr5-overexpressing mesenchymal stem cells augment fracture healing through regulation of Wnt/ERK signaling pathways and mitochondrial dynamics. FASEB J. 33, 8565–8577 (2019). www.fasebj.org.
Persistent Identifierhttp://hdl.handle.net/10722/363327
ISSN
2023 Impact Factor: 4.4
2023 SCImago Journal Rankings: 1.412

 

DC FieldValueLanguage
dc.contributor.authorLin, Weiping-
dc.contributor.authorXu, Liangliang-
dc.contributor.authorPan, Qi-
dc.contributor.authorLin, Sien-
dc.contributor.authorFeng, Lu-
dc.contributor.authorWang, Bin-
dc.contributor.authorChen, Shuxun-
dc.contributor.authorLi, Ying-
dc.contributor.authorWang, Haixing-
dc.contributor.authorLi, Yucong-
dc.contributor.authorWang, Yan-
dc.contributor.authorLee, Wayne Yuk Wai-
dc.contributor.authorSun, Dong-
dc.contributor.authorLi, Gang-
dc.date.accessioned2025-10-10T07:46:04Z-
dc.date.available2025-10-10T07:46:04Z-
dc.date.issued2019-
dc.identifier.citationFASEB Journal, 2019, v. 33, n. 7, p. 8565-8577-
dc.identifier.issn0892-6638-
dc.identifier.urihttp://hdl.handle.net/10722/363327-
dc.description.abstractFracture remains one of the most common traumatic conditions in orthopedic surgery. The use of mesenchymal stem cells (MSCs) to augment fracture repair is promising. Leucine-rich repeat-containing GPCR 5 (Lgr5), a transmembrane protein, has been identified as a novel adult stem cell marker in various organs and tissues. However, the roles of Lgr5 in MSCs are not fully understood. In this study, we investigated cellular functions of Lgr5 in MSCs and its potential implications in treating fracture. Lgr5-overexpressing MSCs (MSC<sup>Lgr5</sup>) were established in murine SV40 promoter–driven luciferase reporter MSC line through virus transfection. Results of real-time quantitative PCR and Western blot analysis confirmed the increased expression of Lgr5 in MSC<sup>Lgr5</sup>. MSC<sup>Lgr5</sup> exhibited increased osteogenic capacity, which may result from elevated expression of β-catenin and phosphorylated ERK1/2 within the nuclear region of cells. In contrast, inhibition of Lgr5 expression decreased the osteogenic differentiation ability of MSCs, accompanied with increased mitochondrial fragmentation and reduced expression of β-catenin. Local transplantation of MSC<sup>Lgr5</sup> at fracture sites accelerated fracture healing via enhanced osteogenesis and angiogenesis. MSC<sup>Lgr5</sup> stimulated the tube formation capacity of HUVECs in a Matrigel coculture system in vitro significantly. Taken together, results suggest that Lgr5 is implicated in the cellular processes of osteogenic differentiation of MSCs through regulation of Wnt and ERK signaling pathways and mitochondrial dynamics in fusion and fission. Inhibition of Lgr5 expression induced increased mitochondrial fragmentation and suppression of osteogenesis. MSC<sup>Lgr5</sup> exhibited enhanced therapeutic efficacy for fracture healing, which may serve as a superior cell source for bone tissue repair.—Lin, W., Xu, L., Pan, Q., Lin, S., Feng, L., Wang, B., Chen, S., Li, Y., Wang, H., Li, Y., Wang, Y., Lee, W. Y. W., Sun, D., Li, G. Lgr5-overexpressing mesenchymal stem cells augment fracture healing through regulation of Wnt/ERK signaling pathways and mitochondrial dynamics. FASEB J. 33, 8565–8577 (2019). www.fasebj.org.-
dc.languageeng-
dc.relation.ispartofFASEB Journal-
dc.subjectangiogenesis-
dc.subjectfission-
dc.subjectGPCR-
dc.subjectMSCs-
dc.subjectosteogenic differentiation-
dc.titleLgr5-overexpressing mesenchymal stem cells augment fracture healing through regulation of Wnt/ERK signaling pathways and mitochondrial dynamics-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1096/fj.201900082RR-
dc.identifier.pmid30991839-
dc.identifier.scopuseid_2-s2.0-85069237611-
dc.identifier.volume33-
dc.identifier.issue7-
dc.identifier.spage8565-
dc.identifier.epage8577-
dc.identifier.eissn1530-6860-

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats