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Axonal outgrowth in muscle grafts made acellular by chemical extraction
13
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0
References
2000
Year
Tissue EngineeringRegenerationEngineeringPeripheral Nerve InjuryTissue TransplantationPeripheral NerveBiomedical EngineeringPeripheral NervesOrgan RegenerationOrthopaedic SurgerySkin RegenerationRegenerative MedicineNeuroregenerationRegenerative BiomaterialsRat Sciatic NerveNerve GraftingTissue RepairMechanobiologyNerve RegenerationMedicineFunctional Tissue EngineeringNeural Tissue EngineeringMicrosurgical Nerve RepairTissue RegenerationDevelopmental BiologyExtracted Muscle GraftsWound HealingTissue CultureSoft Tissue ReconstructionMuscle GraftsPlastic SurgeryExtracellular Matrix
Purpose: To compare nerve regeneration in autologous detergent extracted and freeze-thawed muscle grafts and to electrophoretically characterize the grafts. Methods: Autologous acellular muscie grafts were created either by freeze/thawing or by detergent extraction and then used to bridge a 10 mm gap in rat sciatic nerve. The autologous grafts were compared with respect to protein content, using electrophoresis preimplantation, and axonal outgrowth, Schwann cell and macrophage content, using immunocytochemistry (neurofilaments, S-100 protein, ED 1 macrophages) at 5-20 days postimplantation. Results: The extracted muscle grafts were elastic, but the amount of several proteins was reduced and laminin was still present at a position of basal laminae of the muscle fibers. The freeze/thawed grafts were brittle and lacked elasticity, but resulted in minor changes in major proteins. The axons regenerated through both types of grafts (initial delay 6 days and rate 0.7-0.8 mm/day), which shrunk in length by 25%. There were no apparent differences with respect to Schwann cells and macrophages. Conclusions: The results suggest that detergent extracted muscle tissue, in which some basal lamina proteins remain but cells are removed, could present a new favourable option for nerve grafting.