OBJECTIVE: The objective was to study the effectiveness of a commercially available collagen conduit filled with fibrin-agarose hydrogels alone or with fibrin-agarose hydrogels containing autologous adipose-derived mesenchymal stem cells (ADMSCs) in a rat sciatic nerve injury model. APPROACH: A 10 mm gap was created in the sciatic nerve of 48 rats and repaired using saline-filled collagen conduits or collagen conduits filled with fibrin-agarose hydrogels alone (acellular conduits) or with hydrogels containing ADMSCs (ADMSC conduits). Nerve regeneration was assessed in clinical, electrophysiological and histological studies. MAIN RESULTS: Clinical and electrophysiological outcomes were more favorable with ADMSC conduits than with the acellular or saline conduits, evidencing a significant recovery of sensory and motor functions. Histological analysis showed that ADMSC conduits produce more effective nerve regeneration by Schwann cells, with higher remyelination and properly oriented axonal growth that reached the distal areas of the grafted conduits, and with intensely positive expressions of S100, neurofilament and laminin. Extracellular matrix was also more abundant and better organized around regenerated nerve tissues with ADMSC conduits than those with acellular or saline conduits. SIGNIFICANCE: Clinical, electrophysiological and histological improvements obtained with tissue-engineered ADMSC conduits may contribute to enhancing axonal regeneration by Schwann cells.
OBJECTIVE: The objective was to study the effectiveness of a commercially available collagen conduit filled with fibrin-agarose hydrogels alone or with fibrin-agarose hydrogels containing autologous adipose-derived mesenchymal stem cells (ADMSCs) in a ratsciatic nerve injury model. APPROACH: A 10 mm gap was created in the sciatic nerve of 48 rats and repaired using saline-filled collagen conduits or collagen conduits filled with fibrin-agarose hydrogels alone (acellular conduits) or with hydrogels containing ADMSCs (ADMSC conduits). Nerve regeneration was assessed in clinical, electrophysiological and histological studies. MAIN RESULTS: Clinical and electrophysiological outcomes were more favorable with ADMSC conduits than with the acellular or saline conduits, evidencing a significant recovery of sensory and motor functions. Histological analysis showed that ADMSC conduits produce more effective nerve regeneration by Schwann cells, with higher remyelination and properly oriented axonal growth that reached the distal areas of the grafted conduits, and with intensely positive expressions of S100, neurofilament and laminin. Extracellular matrix was also more abundant and better organized around regenerated nerve tissues with ADMSC conduits than those with acellular or saline conduits. SIGNIFICANCE: Clinical, electrophysiological and histological improvements obtained with tissue-engineered ADMSC conduits may contribute to enhancing axonal regeneration by Schwann cells.
Authors: Cristina Gila-Vilchez; Mari C Mañas-Torres; Rafael Contreras-Montoya; Miguel Alaminos; Juan D G Duran; Luis Álvarez de Cienfuegos; Modesto T Lopez-Lopez Journal: Philos Trans A Math Phys Eng Sci Date: 2019-04-22 Impact factor: 4.226
Authors: D Durand-Herrera; F Campos; B D Jaimes-Parra; J D Sánchez-López; R Fernández-Valadés; M Alaminos; A Campos; V Carriel Journal: Histochem Cell Biol Date: 2018-06-11 Impact factor: 4.304
Authors: Laura García-Martínez; Fernando Campos; Carlos Godoy-Guzmán; María Del Carmen Sánchez-Quevedo; Ingrid Garzón; Miguel Alaminos; Antonio Campos; Víctor Carriel Journal: Histochem Cell Biol Date: 2016-09-01 Impact factor: 4.304
Authors: Deanna Bousalis; Michaela W McCrary; Natalie Vaughn; Nora Hlavac; Ashley Evering; Shruti Kolli; Young Hye Song; Cameron Morley; Thomas E Angelini; Christine E Schmidt Journal: J Biomed Mater Res A Date: 2021-09-29 Impact factor: 4.396
Authors: Frances M Walocko; Roger K Khouri; Melanie G Urbanchek; Benjamin Levi; Paul S Cederna Journal: Microsurgery Date: 2015-09-07 Impact factor: 2.425
Authors: Jasper Iske; Yeqi Nian; Ryoichi Maenosono; Max Maurer; Igor M Sauer; Stefan G Tullius Journal: Cell Mol Immunol Date: 2019-03-06 Impact factor: 11.530