Open this publication in new window or tab >>Translational Medicine R&D Center, Institute of Biomedical and Health Engineering, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, PR China.
Musculoskeletal Research Laboratory of the Department of Orthopedics and Traumatology, Faculty of Medicine, Chinese University of Hong Kong, Hong Kong, China; Innovative Orthopedic Biomaterial and Drug Translational Research Laboratory, Li Ka Shing Institute of Health Sciences, Chinese University of Hong Kong, Hong Kong, China.
School of Biomedical Engineering, Sun Yat-sen University, Guangzhou, PR China.
Musculoskeletal Research Laboratory of the Department of Orthopedics and Traumatology, Faculty of Medicine, Chinese University of Hong Kong, Hong Kong, China; Innovative Orthopedic Biomaterial and Drug Translational Research Laboratory, Li Ka Shing Institute of Health Sciences, Chinese University of Hong Kong, Hong Kong, China.
Department of Orthopedic Surgery, Beijing Hospital, Beijing, PR China.
Musculoskeletal Research Laboratory of the Department of Orthopedics and Traumatology, Faculty of Medicine, Chinese University of Hong Kong, Hong Kong, China.
Musculoskeletal Research Laboratory of the Department of Orthopedics and Traumatology, Faculty of Medicine, Chinese University of Hong Kong, Hong Kong, China.
Linköping University, Department of Biomedical and Clinical Sciences, Division of Surgery, Orthopedics and Oncology. Linköping University, Faculty of Medicine and Health Sciences. Region Östergötland, Center for Surgery, Orthopaedics and Cancer Treatment, Department of Orthopaedics in Linköping.
Department of Orthopedic Surgery, Washington University School of Medicine, St. Louis, MO, USA.
Musculoskeletal Research Laboratory of the Department of Orthopedics and Traumatology, Faculty of Medicine, Chinese University of Hong Kong, Hong Kong, China; Innovative Orthopedic Biomaterial and Drug Translational Research Laboratory, Li Ka Shing Institute of Health Sciences, Chinese University of Hong Kong, Hong Kong, China; Translational Medicine R&D Center, Institute of Biomedical and Health Engineering, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, PR China.
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2022 (English)In: Materials Today, ISSN 1369-7021, E-ISSN 1873-4103, Vol. 52, p. 43-62Article in journal (Refereed) Published
Abstract [en]
Bisphosphonates (BPs)-associated atypical femoral fractures (AFFs) present with impaired fracture healing, yet the underlying mechanism is unclear, which prevents the development of effective therapy. Peripheral sensory nerve has been shown to regulate fracture healing via releasing neuropeptides. Here we show that long-term BPs pre-treatment leads to fracture non-union in rats, characterized by reduced expression of calcitonin gene-related peptide (CGRP, a predominant type of neuropeptides) and abundant fibrous tissues in the non-bridged fracture gap, mimicking clinical AFFs. By using single-cell RNA-sequencing, long-term BPs treatment was identified to promote transition of progenitor cells into a specific cluster of fibroblasts that actively deposit dense extracellular matrix (ECM) to prevent fracture callus bridging. Administration of exogenous CGRP at early stages of fracture repair, in contrast, eliminates the ECM-secreting fibroblast cluster, attenuates fibrogenesis, and facilitates callus bridging, suggesting CGRP is a promising agent to facilitate AFF healing. Accordingly, we have developed an innovative magnesium (Mg) containing hybrid intramedullary nail fixation system (Mg-IMN) to effectively rescue BPs-impaired fracture healing via elevating CGRP synthesis and release. Such device optimizes the fracture healing in BPs-pretreated rats, comparable to direct administration of CGRP. These findings address the indispensable role of CGRP in advancing the healing of AFFs and develop translational strategies to accelerate AFF healing by taking advantage of the CGRP-stimulating effect of Mg-based biodegradable orthopedic implant. The study also indicates fibrosis could be targeted by augmenting CGRP expression to accelerate fracture healing even under challenging scenarios where fibroblasts are aberrantly activated.
Place, publisher, year, edition, pages
Elsevier, 2022
Keywords
Atypical femoral fractures (AFFs), Bisphosphonates (BPs), Calcitonin gene-related peptide (CGRP), Magnesium (Mg), Single-cell RNA-sequencing
National Category
Orthopaedics
Identifiers
urn:nbn:se:liu:diva-182450 (URN)10.1016/j.mattod.2021.11.028 (DOI)000840325900007 ()
Note
Funding: Research Grants Council of Hong Kong SAR [T13-402/17-N]; Research Grants Council of Hong Kong SAR grants [14121918, 14173917]; Innovation and Technology Commission Funding [ITS/208/18FX]; National Natural Science Foundation of China [81802152, 81702165]; Natural Science Fund of Guangdong province [2019A1515012224, 2019A1515011404]; Health and Medical Research Fund of Hong Kong [18190481]; Early Career Scheme of Hong Kong [24104517]
2022-01-202022-01-202022-08-31Bibliographically approved