Role of the Peripheral Nervous System in Skeletal Development and Regeneration: Controversies and Clinical Implications.

Bone regeneration Denervation Fracture healing NGF/TrkA Peripheral nerve Skeletal development

Journal

Current osteoporosis reports
ISSN: 1544-2241
Titre abrégé: Curr Osteoporos Rep
Pays: United States
ID NLM: 101176492

Informations de publication

Date de publication:
10 2023
Historique:
accepted: 25 07 2023
medline: 4 10 2023
pubmed: 14 8 2023
entrez: 14 8 2023
Statut: ppublish

Résumé

This review examines the diverse functional relationships that exist between the peripheral nervous system (PNS) and bone, including key advances over the past century that inform our efforts to translate these discoveries for skeletal repair. The innervation of the bone during development, homeostasis, and regeneration is highly patterned. Consistent with this, there have been nearly 100 studies over the past century that have used denervation approaches to isolate the effects of the different branches of the PNS on the bone. Overall, a common theme of balance emerges whereby an orchestration of both local and systemic neural functions must align to promote optimal skeletal repair while limiting negative consequences such as pain. An improved understanding of the functional bidirectional pathways linking the PNS and bone has important implications for skeletal development and regeneration. Clinical advances over the next century will necessitate a rigorous identification of the mechanisms underlying these effects that is cautious not to oversimplify the in vivo condition in diverse states of health and disease.

Identifiants

pubmed: 37578676
doi: 10.1007/s11914-023-00815-5
pii: 10.1007/s11914-023-00815-5
pmc: PMC10543521
doi:

Types de publication

Journal Article Review Research Support, U.S. Gov't, Non-P.H.S. Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

503-518

Subventions

Organisme : NIDCR NIH HHS
ID : R01 DE027957
Pays : United States
Organisme : NIAMS NIH HHS
ID : R56 AR081251
Pays : United States
Organisme : NIAMS NIH HHS
ID : T32-AR060719
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK132073
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01-DK132073
Pays : United States
Organisme : NIAMS NIH HHS
ID : P30-AR074992
Pays : United States
Organisme : NIAMS NIH HHS
ID : R56-AR081251
Pays : United States
Organisme : NIDCR NIH HHS
ID : R01-DE027957
Pays : United States
Organisme : NIDCR NIH HHS
ID : R21 DE032420
Pays : United States

Informations de copyright

© 2023. The Author(s).

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Auteurs

Mohamed G Hassan (MG)

Department of Medicine, Division of Bone and Mineral Diseases, Washington University, 660 South Euclid Avenue, Campus Box 8301, St. Louis, MO, 63110, USA.

Allison L Horenberg (AL)

Department of Biomedical Engineering, Johns Hopkins University, Baltimore, MD, USA.
Translational Tissue Engineering Center, Johns Hopkins University, Baltimore, MD, USA.

Ariella Coler-Reilly (A)

Department of Medicine, Division of Bone and Mineral Diseases, Washington University, 660 South Euclid Avenue, Campus Box 8301, St. Louis, MO, 63110, USA.

Warren L Grayson (WL)

Department of Biomedical Engineering, Johns Hopkins University, Baltimore, MD, USA.
Translational Tissue Engineering Center, Johns Hopkins University, Baltimore, MD, USA.
Department of Chemical and Biomolecular Engineering, Johns Hopkins University, Baltimore, MD, USA.
Department of Materials Science and Engineering, Johns Hopkins University, Baltimore, MD, USA.
Institute for Nanobiotechnology, Johns Hopkins University, Baltimore, MD, USA.

Erica L Scheller (EL)

Department of Medicine, Division of Bone and Mineral Diseases, Washington University, 660 South Euclid Avenue, Campus Box 8301, St. Louis, MO, 63110, USA. scheller@wustl.edu.
Department of Biomedical Engineering, Washington University, MO, St. Louis, USA. scheller@wustl.edu.
Department of Cell Biology and Physiology, Washington University, MO, St. Louis, USA. scheller@wustl.edu.

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