Use of poly(DL-lactide-ε-caprolactone) membranes and mesenchymal stem cells from the Wharton's jelly of the umbilical cord for promoting nerve regeneration in axonotmesis: In vitro and in vivo analysis

被引:49
作者
Gaertner, A. [1 ,2 ]
Pereira, T. [1 ,2 ]
Armada-da-Silva, P. A. S. [3 ]
Amorim, I. [1 ]
Gomes, R. [1 ,2 ]
Ribeiro, J. [1 ,2 ]
Franca, M. L. [1 ,2 ]
Lopes, C. [1 ]
Porto, B. [1 ]
Sousa, R. [1 ]
Bombaci, A. [4 ,5 ]
Ronchi, G. [4 ,5 ]
Fregnan, F. [4 ,5 ]
Varejao, A. S. P. [6 ]
Luis, A. L. [1 ,2 ]
Geuna, S. [4 ,5 ]
Maurico, A. C. [1 ,2 ]
机构
[1] Porto Univ UP, ICBAS, P-4050313 Oporto, Portugal
[2] Univ Porto, Food & Agr Sci & Technol Inst ICETA, Anim Sci & Study Ctr CECA, P-4051401 Oporto, Portugal
[3] Tech Univ Lisbon UTL, Dept Human Kinet FMH, P-1499002 Lisbon, Portugal
[4] Neurosci Inst Cavalieri Ottolenghi, I-10043 Turin, Italy
[5] Univ Turin, Dept Clin & Biol Sci, I-10043 Turin, Italy
[6] Univ Tras Os Montes & Alto Douro UTAD, CIDESD, Dept Vet Sci, P-5001801 Vila Real, Portugal
关键词
Axonotmesis; Stem cells; Mesenchymal stem cells; Neuroglial-like cells; Nerve regeneration; Wharton jelly; RAT SCIATIC-NERVE; MARROW STROMAL CELLS; PERIPHERAL-NERVE; BONE-MARROW; SCHWANN-CELLS; SPINAL-CORD; N1E-115; CELLS; CRUSH INJURY; MATRIX CELLS; ADULT RATS;
D O I
10.1016/j.diff.2012.10.001
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cellular systems implanted into an injured nerve may produce growth factors or extracellular matrix molecules, modulate the inflammatory process and eventually improve nerve regeneration. In the present study, we evaluated the therapeutic value of human umbilical cord matrix MSCs (HMSCs) on rat sciatic nerve after axonotmesis injury associated to Vivosorb (R) membrane. During HMSCs expansion and differentiation in neuroglial-like cells, the culture medium was collected at 48, 72 and 96h for nuclear magnetic resonance (NMR) analysis in order to evaluate the metabolic profile. To correlate the HMSCs ability to differentiate and survival capacity in the presence of the Vivosorb (R) membrane, the [Ca(2+)]i of undifferentiated HMSCs or neuroglial-differentiated HMSCs was determined by the epifluorescence technique using the Fura-2AM probe. The Vivosorb (R) membrane proved to be adequate and used as scaffold associated with undifferentiated HMSCs or neuroglial-differentiated HMSCs. In vivo testing was carried out in adult rats where a sciatic nerve axonotmesis injury was treated with undifferentiated HMSCs or neuroglial differentiated HMSCs with or without the Vivosorb (R) membrane. Motor and sensory functional recovery was evaluated throughout a healing period of 12 weeks using sciatic functional index (SFI), extensor postural thrust (EPT), and withdrawal reflex latency (WRL). Stereological analysis was carried out on regenerated nerve fibers. In vitro investigation showed the formation of typical neuroglial cells after differentiation, which were positively stained for the typical specific neuroglial markers such as the GFAP, the GAP-43 and NeuN. NMR showed clear evidence that HMSCs expansion is glycolysis-dependent but their differentiation requires the switch of the metabolic profile to oxidative metabolism. In vivo studies showed enhanced recovery of motor and sensory function in animals treated with transplanted undifferentiated and differentiated HMSCs that was accompanied by an increase in myelin sheath. Taken together, HMSC from the umbilical cord Wharton jelly might be useful for improving the clinical outcome after peripheral nerve lesion. (C) 2012 International Society of Differentiation. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:355 / 365
页数:11
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