1. Academic Validation
  2. Regulation of Osteogenic Differentiation of hBMSCs by the Overlay Angles of Bone Lamellae-like Matrices

Regulation of Osteogenic Differentiation of hBMSCs by the Overlay Angles of Bone Lamellae-like Matrices

  • ACS Appl Mater Interfaces. 2024 Oct 23;16(42):56801-56814. doi: 10.1021/acsami.4c12847.
Shuyun Zhang 1 2 3 Dengjian Qu 2 Bowen Luo 4 3 Lichen Wang 4 3 Hong Li 2 Hongjun Wang 4 3 5
Affiliations

Affiliations

  • 1 Guangdong Police College, Guangzhou 510440, Guangdong, China.
  • 2 College of Chemistry and Materials Science, Jinan University, 601 West Huangpu Avenue, Guangzhou 510632, Guangdong, China.
  • 3 Semcer Center for Healthcare Innovation, Stevens Institute of Technology, 1 Castle Point on the Hudson, Hoboken, New Jersey 07030, United States.
  • 4 Department of Biomedical Engineering, Stevens Institute of Technology, 1 Castle Point on the Hudson, Hoboken, New Jersey 07030, United States.
  • 5 Department of Chemistry and Chemical Biology, Stevens Institute of Technology, 1 Castle Point on the Hudson, Hoboken, New Jersey 07030, United States.
Abstract

Oriented fibers in bone lamellae are recognized for their contribution to the anisotropic mechanical performance of the cortical bone. While increasing evidence highlights that such oriented fibers also exhibit osteogenic induction to preosteoblasts, little is known about the effect of the overlay angle between lamellae on the osteogenic differentiation of bone marrow-derived mesenchymal stem cells (BMSCs). In this study, bone lamellae-like fibrous matrices composed of aligned core-shell [core: polycaprolactone (PCL)/type I collagen (Col I) + shell: Col I] nanofibers were seeded with human BMSCs (hBMSCs) and then laid over on each Other layer-by-layer (L-b-L) at selected angles (0 or 45°) to form three-dimensional (3D) constructs. Upon culture for 7 and 14 days, osteogenic differentiation of hBMSCs and mineralization within the lamellae assembly (LA) were characterized by Real-Time PCR, Western blot, immunofluorescent staining for osteogenic markers, and alizarin red staining for calcium deposition. Compared to those of random nanofibers (LA-RF) or aligned fibers with the overlay angle of 45° (LA-AF-45), the LA of aligned fibers at a 0° overlay angle (LA-AF-0) exhibited a noticeably higher osteogenic differentiation of hBMSCs, i.e., elevated gene expression of OPN, OCN, and RUNX2 and protein levels of ALP and RUNX2, while promoting mineral deposition as indicated by alizarin red staining and mechanical testing. Further analyses of hBMSCs within LA-AF-0 revealed an increase in both total and phosphorylated Integrin β1, which subsequently increased total focal adhesion kinase (FAK), phosphorylated FAK (p-FAK), and phosphorylated extracellular signal kinase ERK1/2 (p-ERK1/2). Inhibition of Integrin β1 and ERK1/2 activity effectively reduced the LA-AF-0-induced upregulation of p-FAK and osteogenic markers (OPN, OCN, and RUNX2), confirming the involvement of Integrin β1-FAK-ERK1/2 signaling. Altogether, the overlay angle of aligned core-shell nanofiber membranes regulates the osteogenic differentiation of hBMSCs via Integrin β1-FAK-ERK1/2 signaling, unveiling the effects of anisotropic fibers on bone tissue formation.

Keywords

core−shell nanofiber; hBMSC; integrin β1; layer-by-layer stacking; osteogenic differentiation.

Figures
Products
  • Cat. No.
    Product Name
    Description
    Target
    Research Area
  • HY-100506
    99.43%, 整合素受体拮抗剂