Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/69395
Title: A microfluidic neuronal platform for neuron axotomy and controlled regenerative studies
Author: Tong, Z.
Segura-Feliu, M.
Seira, Oscar
Homs Corbera, Antoni
Río Fernández, José Antonio del
Samitier i Martí, Josep
Keywords: Lesions medul·lars
Regeneració del sistema nerviós
Medul·la espinal
Neurones
Spinal cord injuries
Nervous system regeneration
Spinal cord
Neurons
Issue Date: 20-Aug-2015
Publisher: Royal Society of Chemistry
Abstract: Understanding the basic mechanisms of neural regeneration after injury is a pre-requisite for developing appropriate treatments. Traditional approaches to model axonal lesions, such as high intensity power laser ablation or sharp metal scratching, are complex to implement, have low throughputs, and generate cuts that are difficult to modulate. We present here a novel reproducible microfluidic approach to model in vitro mechanical lesion of tens to hundreds of axons simultaneously in a controlled manner. The dimensions of the induced axonal injury and its distance from the neuronal cell body are precisely controlled while preserving both the proximal and distal portions of axons. We have observed that distal axons undergo Wallerianlike anterograde degeneration after axotomy; in contrast, proximal portions of the axons remain un-degenerated, possessing the potential to re-grow. More importantly, surpassing the previous axotomy methods performed in petridish in which local microenvironments cannot be tailored, our platform holds the capability to implement fine-tuned treatments to lesioned axon stumps in a local, controlled manner. Specifically, molecules such as chondroitin sulphate proteoglycans and its degrading enzyme Chondroitinase ABC, hydrogels, and supporting cells have been shown to be deliverable to the lesioned site of injured axons. In addition, this system also permits double interventions at the level of the lesioned axons and the perikaryon. This proves the potentiality of our model by demonstrating how axonal regrowth can be evaluated under circumstances that are better mimicking biological problems. We believe that this novel mechanical microfluidic axotomy approach is easy to perform, yields high throughput axon lesions, is physiologically relevant, and offers a simplified platform for screening of potential new neurological drugs.
Note: Reproducció del document publicat a: http://dx.doi.org/10.1039/C5RA11522A
It is part of: RSC Advances, 2015, vol. 5, p. 73457-73466
Related resource: http://dx.doi.org/10.1039/C5RA11522A
URI: http://hdl.handle.net/2445/69395
ISSN: 2046-2069
Appears in Collections:Articles publicats en revistes (Biologia Cel·lular, Fisiologia i Immunologia)
Articles publicats en revistes (Electrònica)
Articles publicats en revistes (Institut de Bioenginyeria de Catalunya (IBEC))

Files in This Item:
File Description SizeFormat 
653931.pdf3.76 MBAdobe PDFView/Open


This item is licensed under a Creative Commons License Creative Commons