scholarly journals Progress in perisynaptic Schwann cell and neuromuscular junction research

2022 ◽  
Vol 17 (6) ◽  
pp. 1273
Author(s):  
ChandlerL Walker
Glia ◽  
2020 ◽  
Vol 68 (6) ◽  
pp. 1182-1200 ◽  
Author(s):  
Albina Jablonka‐Shariff ◽  
Chuieng‐Yi Lu ◽  
Katherine Campbell ◽  
Kelly R. Monk ◽  
Alison K. Snyder‐Warwick

1998 ◽  
Vol 92 (5-6) ◽  
pp. 450-452
Author(s):  
J. Koenig ◽  
S. De La Porte ◽  
J. Chapron

2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Robert Louis Hastings ◽  
Michelle Mikesh ◽  
Young il Lee ◽  
Wesley J. Thompson

1968 ◽  
Vol 169 (1016) ◽  
pp. 289-306 ◽  

(1) Intracellular micro-electrodes and electron-microscopy were used to study normal and denervated end-plates in rat diaphragm muscle fibres. (2) In normal muscles 84.5 to 100% of the micro-electrode insertions were sufficiently close to the neuromuscular junction to detect miniature end-plate potentials. The structure of the normal neuromuscular junction had the usual 3-cell arrangement: muscle with synaptic folds, axon and Schwann cell. (3) Within one day after section of the phrenic nerve, the axon disintegrated and miniature end-plate potentials ceased to occur. Subsequently, miniature potentials were not observed at denervated end-plates, except during the third week after denervation, at which time a low-frequency discharge was seen in eight out of 770 fibres. The miniature potentials at these end-plates resembled those at normal junctions, and were presumably also due to acetylcholine acting on the muscle membrane. (4) The synaptic folds remain for several months after denervation, and serve to identify electron-microscopically the denervated end-plate. After prolonged denervation (> 3 weeks), when miniature end-plate potentials were never observed, there was generally no cell overlying the synaptic folds. (5) During the first 3 weeks after denervation, a nucleated cell, presumably the Schwann cell, was in close contact with the muscle. ‘Schwann-muscle' contacts were observed in muscle without miniature end-plate potentials. (6) Electron microscopy of a portion of denervated muscle, which included a fibre with miniature potentials, showed that the fibre had extensive ‘Schwann-muscle’ contacts. (7) It is concluded that the Schwann cell is the source of the packages of acetylcholine which evoke miniature end-plate potentials in denervated muscle. Since the Schwann cell was in contact with muscle fibres without miniature potentials, it appears that the presence of the Schwann cell is a necessary, but not a sufficient, condition for the production of miniature potentials at denervated end-plates.


2019 ◽  
Vol 515 (1) ◽  
pp. 50-56 ◽  
Author(s):  
Shi-Jie Zhang ◽  
Xiao-Xiao Li ◽  
Yuyu Yu ◽  
Amy P. Chiu ◽  
Lilian H. Lo ◽  
...  

1998 ◽  
Vol 92 (3-4) ◽  
pp. 153-155 ◽  
Author(s):  
Jeanine Koenig ◽  
Sabine De La Porte ◽  
Jacquline Chapron

1999 ◽  
Vol 19 (24) ◽  
pp. RC46-RC46 ◽  
Author(s):  
Jane L. Lubischer ◽  
David M. Bebinger

Author(s):  
R.L. Martuza ◽  
T. Liszczak ◽  
A. Okun ◽  
T-Y Wang

Neurofibromatosis (NF) is an autosomal dominant genetic disorder with a prevalence of 1/3,000 births. The NF mutation causes multiple abnormalities of various cells of neural crest origin. Schwann cell tumors (neurofibromas, acoustic neuromas) are the most common feature of neurofibromatosis although meningiomas, gliomas, and other neoplasms may be seen. The schwann cell tumors commonly develop from the schwann cells associated with sensory or sympathetic nerves or their ganglia. Schwann cell tumors on ventral spinal roots or motor cranial nerves are much less common. Since the sensory neuron membrane is known to contain a mitogenic factor for schwann cells, we have postulated that neurofibromatosis may be due to an abnormal interaction between the nerve and the schwann cell and that this interaction may be hormonally modulated. To test this possibility a system has been developed in which an enriched schwannoma cell culture can be obtained and co-cultured with pure neurons.


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