TY - JOUR
T1 - Compartmental microfluidic system for studying muscle-neuron communication and neuromuscular junction maintenance
AU - Ionescu, Ariel
AU - Zahavi, Eitan Erez
AU - Gradus, Tal
AU - Ben-Yaakov, Keren
AU - Perlson, Eran
N1 - Publisher Copyright:
© 2015 Elsevier GmbH.
PY - 2016
Y1 - 2016
N2 - Molecular communication between the motoneuron and the muscle is vital for neuromuscular junction (NMJ) formation and maintenance. Disruption in the structure and function of NMJs is a hallmark of various neurodegenerative processes during both development and pathological events. Still due to the complexity of this process, it is very difficult to elucidate the cellular mechanisms underlying it, generating a keen interest for developing better tools for investigating it. Here we describe a simplified method to study mechanisms of NMJs formation, maintenance and disruption. A spinal cord explant from mice expressing the Hb9::GFP motoneuron marker is plated on one side of a compartmental chamber, and myotubes derived from muscle satellite progenitor cells are plated on the other. The GFP labeled motoneurons extend their axons via microgrooves in the chamber to innervate the muscle cells and to form functional in-vitro NMJs. Next we provide procedures to measure axon growth and to reliably quantify NMJ activity using imaging of both muscle contractions and fast intracellular calcium changes. This platform allows precise control, monitoring and manipulation of subcellular microenvironments. Specifically, it enables to distinguish local from retrograde signaling mechanisms and allows restricted experimental intervention in local compartments along the muscle-neuron route.
AB - Molecular communication between the motoneuron and the muscle is vital for neuromuscular junction (NMJ) formation and maintenance. Disruption in the structure and function of NMJs is a hallmark of various neurodegenerative processes during both development and pathological events. Still due to the complexity of this process, it is very difficult to elucidate the cellular mechanisms underlying it, generating a keen interest for developing better tools for investigating it. Here we describe a simplified method to study mechanisms of NMJs formation, maintenance and disruption. A spinal cord explant from mice expressing the Hb9::GFP motoneuron marker is plated on one side of a compartmental chamber, and myotubes derived from muscle satellite progenitor cells are plated on the other. The GFP labeled motoneurons extend their axons via microgrooves in the chamber to innervate the muscle cells and to form functional in-vitro NMJs. Next we provide procedures to measure axon growth and to reliably quantify NMJ activity using imaging of both muscle contractions and fast intracellular calcium changes. This platform allows precise control, monitoring and manipulation of subcellular microenvironments. Specifically, it enables to distinguish local from retrograde signaling mechanisms and allows restricted experimental intervention in local compartments along the muscle-neuron route.
KW - Axonal transport
KW - Microfluidic-chamber
KW - Motoneuron
KW - Neuromuscular Junction
KW - Neurotrophic factors
UR - http://www.scopus.com/inward/record.url?scp=84949670719&partnerID=8YFLogxK
U2 - 10.1016/j.ejcb.2015.11.004
DO - 10.1016/j.ejcb.2015.11.004
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AN - SCOPUS:84949670719
SN - 0171-9335
VL - 95
SP - 69
EP - 88
JO - European Journal of Cell Biology
JF - European Journal of Cell Biology
IS - 2
ER -