Osteogenic capacity of mesenchymal stem cells from patients with osteoporotic hip fractures in vivo

ABSTRACT

Purpose

Human mesenchymal stem cells (MSCs) have the ability to differentiate into bone-forming osteoblasts. The aim of this study was to elucidate if MSCs from patients with OP show a senescent phenotype and explore their bone-forming ability in vivo.

Materials and methods

MSCs from patients with OP and controls with osteoarthritis (OA) were implanted into the subcutaneous tissue of immunodeficient mice for histological analysis and expression of human genes by RT-PCR. The expression of senescence-associated phenotype (SASP) genes, as well as p16, p21, and galactosidase, was studied in cultures of MSCs.

Results

In vivo bone formation was evaluated in 103 implants (47 OP, 56 OA). New bone was observed in 45% of the implants with OP cells and 46% of those with OA cells (p = 0.99). The expression of several bone-related genes (collagen, osteocalcin, alkaline phosphatase, sialoprotein) was also similar in both groups. There were no differences between groups in SASP gene expression, p16, and p21 expression, or in senescence-associated galactosidase activity.

Conclusion

Senescence markers and the osteogenic capacity in vivo of MSCs from patients with OP are not inferior to that of cells from controls of similar age with OA. This supports the interest of future studies to evaluate the potential use of autologous MSCs from OP patients in bone regeneration procedures.

KEYWORDS:

• Bone formation
• osteoblasts
• mesenchymal stem cells
• cell senescence
• bone nodules
• in vivo

Acknoledgements

We acknowledge the excellent technical work of Alicia Martin-Rebollo.

Disclosure statement

Authors declare that they do not have competing interests

Additional information

Funding

This study was supported by a grant from Instituto de Salud Carlos III [PI16-915], which can be cofounded by EU Feder funds.