Collagen structures of demineralized bone paper direct mineral metabolism.

bone matrix collagen matrix mineralization osteoblasts osteoclasts

Journal

JBMR plus
ISSN: 2473-4039
Titre abrégé: JBMR Plus
Pays: England
ID NLM: 101707013

Informations de publication

Date de publication:
Aug 2024
Historique:
received: 18 12 2023
revised: 28 05 2024
accepted: 12 06 2024
medline: 11 7 2024
pubmed: 11 7 2024
entrez: 11 7 2024
Statut: epublish

Résumé

Bone is a dynamic mineralized tissue that undergoes continuous turnover throughout life. While the general mechanism of bone mineral metabolism is documented, the role of underlying collagen structures in regulating osteoblastic mineral deposition and osteoclastic mineral resorption remains an active research area, partly due to the lack of biomaterial platforms supporting accurate and analytical investigation. The recently introduced osteoid-inspired demineralized bone paper (DBP), prepared by 20-μm thin sectioning of demineralized bovine compact bone, holds promise in addressing this challenge as it preserves the intrinsic bony collagen structure and retains semi-transparency. Here, we report on the impact of collagen structures on modulating osteoblast and osteoclast-driven bone mineral metabolism using vertical and transversal DBPs that exhibit a uniaxially aligned and a concentric ring collagen structure, respectively. Translucent DBP reveals these collagen structures and facilitates longitudinal tracking of mineral deposition and resorption under brightfield microscopy for at least 3 wk. Genetically labeled primary osteogenic cells allow fluorescent monitoring of these cellular processes. Osteoblasts adhere and proliferate following the underlying collagen structures of DBPs. Osteoblastic mineral deposition is significantly higher in vertical DBP than in transversal DBP. Spatiotemporal analysis reveals notably more osteoblast adhesion and faster mineral deposition in vascular regions than in bone regions. Subsequent osteoclastic resorption follows these mineralized collagen structures, directing distinct trench and pit-type resorption patterns. In vertical DBP, trench-type resorption occurs at an 80% frequency, whereas transversal DBP shows 35% trench-type and 65% pit-type resorption. Our studies substantiate the importance of collagen structures in regulating mineral metabolism by osteogenic cells. DBP is expected to serve as an enabling biomaterial platform for studying various aspects of cellular and extracellular bone remodeling biology.

Identifiants

pubmed: 38989259
doi: 10.1093/jbmrpl/ziae080
pii: ziae080
pmc: PMC11235081
doi:

Types de publication

Journal Article

Langues

eng

Pagination

ziae080

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press on behalf of the American Society for Bone and Mineral Research.

Déclaration de conflit d'intérêts

J.L., Y.P., and J.K. are inventors of a pending patent application (US20220152274A1) entitled “Demineralized Bone Paper” that was filed by the University of Massachusetts-Amherst. H.Y. declares no competing interest.

Auteurs

Hyejin Yoon (H)

Department of Biochemistry and Molecular Biology, University of Massachusetts, Amherst, MA 01003, United States.
Molecular and Cellular Biology Graduate Program, University of Massachusetts, Amherst, MA 01003, United States.

Yongkuk Park (Y)

Department of Chemical Engineering, University of Massachusetts, Amherst, MA 01003, United States.

Jun-Goo Kwak (JG)

Molecular and Cellular Biology Graduate Program, University of Massachusetts, Amherst, MA 01003, United States.

Jungwoo Lee (J)

Molecular and Cellular Biology Graduate Program, University of Massachusetts, Amherst, MA 01003, United States.
Department of Chemical Engineering, University of Massachusetts, Amherst, MA 01003, United States.
Department of Biomedical Engineering, University of Massachusetts, Amherst, MA 01003, United States.

Classifications MeSH