Enhancing Bone Formation Through bFGF-Loaded Mesenchymal Stromal Cell Spheroids During Fracture Healing in Mice

This study aimed to evaluate the osteogenic potential of mesenchymal stromal cell (MSC) spheroids combined with the basic fibroblast growth factor (bFGF) in a mouse femur fracture model. To begin, MSC spheroids were generated, and the expression of key trophic factors (<i>bFGF Bmp2</i>, and <i>Vegfa</i>) was assessed using quantitative PCR (qPCR). A binding assay confirmed the interaction between the bFGF and the spheroids' extracellular matrix. The spheroid cultures significantly upregulated <i>bFGF</i>, <i>Bmp2</i>, and <i>Vegfa</i> expression compared to the monolayers (<i>p</i> < 0.001), and the binding assay demonstrated effective bFGF binding to the MSC spheroids. Following these in vitro assessments, the mice were divided into five groups for the in vivo study: (1) no treatment (control), (2) spheroids alone, (3) bFGF alone, (4) bFGF-loaded spheroids (bFGF-spheroids), and (5) non-viable (frozen) bFGF-loaded spheroids (bFGF-dSpheroids). Bone formation was analyzed by a micro-CT, measuring the bone volume (BV) and bone mineral content (BMC) of the mice four weeks post-fracture. A high dose of the bFGF (10 µg) significantly promoted bone formation regardless of the presence of spheroids, as evidenced by the increases in BV (bFGF, <i>p</i> = 0.010; bFGF-spheroids, <i>p</i> = 0.006; bFGF-dSpheroids, <i>p</i> = 0.032) and BMC (bFGF, <i>p</i> = 0.023; bFGF-spheroids, <i>p</i> = 0.004; bFGF-dSpheroids, <i>p</i> = 0.014), compared to the controls. In contrast, a low dose of the bFGF (1 µg) combined with the MSC spheroids significantly increased BV and BMC compared to the control (BV, <i>p</i> = 0.012; BMC, <i>p</i> = 0.015), bFGF alone (BV, <i>p</i> = 0.012; BMC, <i>p</i> = 0.008), and spheroid (BV, <i>p</i> < 0.001; BMC, <i>p</i> < 0.001) groups. A low dose of the bFGF alone did not significantly promote bone formation (<i>p</i> > 0.05). The non-viable (frozen) spheroids loaded with a low dose of the bFGF resulted in a higher BV and BMC compared to the spheroids alone (BV, <i>p</i> = 0.003; BMC, <i>p</i> = 0.017), though the effect was less pronounced than in the viable spheroids. These findings demonstrate the synergistic effect of the bFGF and MSC spheroids on bone regeneration. The increased expression of the BMP-2 and VEGF observed in the initial experiments, coupled with the enhanced bone formation in vivo, highlight the therapeutic potential of this combination. Future studies will aim to elucidate the underlying molecular mechanisms and assess the long-term outcomes for bone repair strategies.

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Journal
Bioengineering
Published
2024-10-18
DOI
https://doi.org/10.3390/bioengineering11101041
Citations
1
Primary Topic
Mesenchymal stem cell research
Type
article
Field-Weighted Citation Impact
0.44

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article

Enhancing Bone Formation Through bFGF-Loaded Mesenchymal Stromal Cell Spheroids During Fracture Healing in Mice

Masayuki Miyagi, Masashi Takaso, Shintaro Shoji, Gen Inoue et al.
1 citations
Bioengineering
Mesenchymal stem cell research
0.44
article

Enhancing Bone Formation Through bFGF-Loaded Mesenchymal Stromal Cell Spheroids During Fracture Healing in Mice

Masayuki Miyagi, Masashi Takaso, Shintaro Shoji, Gen Inoue, Masanobu Ujihira, Hiroki Saito, Kentaro Uchida, Hiroyuki Sekiguchi, Kugo Takeda, Mitsuyoshi Matsumoto
article en
1 citations

Abstract

This study aimed to evaluate the osteogenic potential of mesenchymal stromal cell (MSC) spheroids combined with the basic fibroblast growth factor (bFGF) in a mouse femur fracture model. To begin, MSC spheroids were generated, and the expression of key trophic factors (<i>bFGF Bmp2</i>, and <i>Vegfa</i>) was assessed using quantitative PCR (qPCR). A binding assay confirmed the interaction between the bFGF and the spheroids' extracellular matrix. The spheroid cultures significantly upregulated <i>bFGF</i>, <i>Bmp2</i>, and <i>Vegfa</i> expression compared to the monolayers (<i>p</i> < 0.001), and the binding assay demonstrated effective bFGF binding to the MSC spheroids. Following these in vitro assessments, the mice were divided into five groups for the in vivo study: (1) no treatment (control), (2) spheroids alone, (3) bFGF alone, (4) bFGF-loaded spheroids (bFGF-spheroids), and (5) non-viable (frozen) bFGF-loaded spheroids (bFGF-dSpheroids). Bone formation was analyzed by a micro-CT, measuring the bone volume (BV) and bone mineral content (BMC) of the mice four weeks post-fracture. A high dose of the bFGF (10 µg) significantly promoted bone formation regardless of the presence of spheroids, as evidenced by the increases in BV (bFGF, <i>p</i> = 0.010; bFGF-spheroids, <i>p</i> = 0.006; bFGF-dSpheroids, <i>p</i> = 0.032) and BMC (bFGF, <i>p</i> = 0.023; bFGF-spheroids, <i>p</i> = 0.004; bFGF-dSpheroids, <i>p</i> = 0.014), compared to the controls. In contrast, a low dose of the bFGF (1 µg) combined with the MSC spheroids significantly increased BV and BMC compared to the control (BV, <i>p</i> = 0.012; BMC, <i>p</i> = 0.015), bFGF alone (BV, <i>p</i> = 0.012; BMC, <i>p</i> = 0.008), and spheroid (BV, <i>p</i> < 0.001; BMC, <i>p</i> < 0.001) groups. A low dose of the bFGF alone did not significantly promote bone formation (<i>p</i> > 0.05). The non-viable (frozen) spheroids loaded with a low dose of the bFGF resulted in a higher BV and BMC compared to the spheroids alone (BV, <i>p</i> = 0.003; BMC, <i>p</i> = 0.017), though the effect was less pronounced than in the viable spheroids. These findings demonstrate the synergistic effect of the bFGF and MSC spheroids on bone regeneration. The increased expression of the BMP-2 and VEGF observed in the initial experiments, coupled with the enhanced bone formation in vivo, highlight the therapeutic potential of this combination. Future studies will aim to elucidate the underlying molecular mechanisms and assess the long-term outcomes for bone repair strategies.

BioengineeringVol. 11(10)
Shonan University of Medical Sciences (JP), Kitasato University (JP)
Kitasato University, General Insurance Association of Japan
Openalex Percentile: Top 32%
Mesenchymal stem cell research
0.44
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