Autologous Marrow Mesenchymal Stem Cell Driving Bone Regeneration in a Rabbit Model of Femoral Head Osteonecrosis

被引:8
作者
Mastrolia, Ilenia [1 ]
Giorgini, Andrea [2 ]
Murgia, Alba [3 ]
Loschi, Pietro [4 ]
Petrachi, Tiziana [3 ]
Rasini, Valeria [1 ]
Pinelli, Massimo [5 ]
Pinto, Valentina [5 ]
Lolli, Francesca [5 ]
Chiavelli, Chiara [1 ]
Grisendi, Giulia [1 ]
Baschieri, Maria Cristina [1 ]
De Santis, Giorgio [5 ]
Catani, Fabio [2 ]
Dominici, Massimo [1 ,3 ]
Veronesi, Elena [1 ,3 ]
机构
[1] Univ Modena & Reggio Emilia, Dept Med & Surg Sci Children & Adults, Div Oncol, Lab Cellular Therapy, I-41124 Modena, Italy
[2] Univ Hosp Modena & Reggio Emilia, Dept Med & Surg Sci Children & Adults, Div Orthoped, I-41124 Modena, Italy
[3] Technopole Mirandola TPM, I-41037 Modena, Italy
[4] Dardano Clin, I-41036 Modena, Italy
[5] Univ Hosp Modena & Reggio Emilia, Dept Med & Surg Sci Children & Adults, Div Plast Surg, I-41124 Modena, Italy
关键词
osteonecrosis; femoral head; bone marrow; mesenchymal stromal; stem cells; bone regeneration; cell therapy; CORTICOSTEROID-INDUCED OSTEONECROSIS; ENDOCHONDRAL OSSIFICATION; STROMAL/STEM CELLS; NECROSIS; INJECTION; APOPTOSIS; DELIVERY; THERAPY; REPAIR;
D O I
10.3390/pharmaceutics14102127
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Osteonecrosis of the femoral head (ONFH) is a progressive degenerative disease that ultimately requires a total hip replacement. Mesenchymal stromal/stem cells (MSCs), particularly the ones isolated from bone marrow (BM), could be promising tools to restore bone tissue in ONFH. Here, we established a rabbit model to mimic the pathogenic features of human ONFH and to challenge an autologous MSC-based treatment. ON has been originally induced by the synergic combination of surgery and steroid administration. Autologous BM-MSCs were then implanted in the FH, aiming to restore the damaged tissue. Histological analyses confirmed bone formation in the BM-MSC treated rabbit femurs but not in the controls. In addition, the model also allowed investigations on BM-MSCs isolated before (ON-BM-MSCs) and after (ON+BM-MSCs) ON induction to dissect the impact of ON damage on MSC behavior in an affected microenvironment, accounting for those clinical approaches foreseeing MSCs generally isolated from affected patients. BM-MSCs, isolated before and after ON induction, revealed similar growth rates, immunophenotypic profiles, and differentiation abilities regardless of the ON. Our data support the use of ON+BM-MSCs as a promising autologous therapeutic tool to treat ON, paving the way for a more consolidated use into the clinical settings.
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页数:16
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