Neural Network Formation and the Activity of an Aggregate of Dissociated Hydra Cells

Author(s):  
T. Itayama ◽  
Y. Sawada

Author(s):  
Satish Bodakuntla ◽  
Hana Nedozralova ◽  
Nirakar Basnet ◽  
Naoko Mizuno

Axon branching is a critical process ensuring a high degree of interconnectivity for neural network formation. As branching occurs at sites distant from the soma, it is necessary that axons have a local system to dynamically control and regulate axonal growth. This machinery depends on the orchestration of cellular functions such as cytoskeleton, subcellular transport, energy production, protein- and membrane synthesis that are adapted for branch formation. Compared to the axon shaft, branching sites show a distinct and dynamic arrangement of cytoskeleton components, endoplasmic reticulum and mitochondria. This review discusses the regulation of axon branching in the context of cytoskeleton and membrane remodeling.



1988 ◽  
Vol 1 ◽  
pp. 260 ◽  
Author(s):  
T. Itayama ◽  
O. Koizumi ◽  
Y. Sawada


1987 ◽  
Vol 97 (2) ◽  
pp. 280-288 ◽  
Author(s):  
F van Huizen ◽  
H.J Romijn ◽  
A.M.M.C Habets ◽  
P van den Hooff


2011 ◽  
Vol 88 (8) ◽  
pp. 1707-1710 ◽  
Author(s):  
ChunXiong Luo ◽  
Li Liu ◽  
XiaoFang Ni ◽  
Li Wang ◽  
Shinichiro M. Nomura ◽  
...  


2019 ◽  
Author(s):  
Ranmal A. Samarasinghe ◽  
Osvaldo A. Miranda ◽  
Simon Mitchell ◽  
Isabella Ferando ◽  
Momoko Watanabe ◽  
...  

ABSTRACTHuman brain organoids represent a powerful tool for the study of human neurological diseases particularly those that impact brain growth and structure. However, many neurological diseases lack obvious anatomical abnormalities, yet significantly impact neural network functions, raising the question of whether organoids possess sufficient neural network architecture and complexity to model these conditions. Here, we explore the network level functions of brain organoids using calcium sensor imaging and extracellular recording approaches that together reveal the existence of complex oscillatory network behaviors reminiscent of intact brain preparations. We further demonstrate strikingly abnormal epileptiform network activity in organoids derived from a Rett Syndrome patient despite only modest anatomical differences from isogenically matched controls, and rescue with an unconventional neuromodulatory drug Pifithrin-α. Together, these findings provide an essential foundation for the utilization of human brain organoids to study intact and disordered human brain network formation and illustrate their utility in therapeutic discovery.



Development ◽  
1997 ◽  
Vol 124 (20) ◽  
pp. 4143-4152 ◽  
Author(s):  
H. Kose ◽  
D. Rose ◽  
X. Zhu ◽  
A. Chiba

We demonstrate that the cell adhesion molecule Fasciclin III (FAS3) mediates synaptic target recognition through homophilic interaction. FAS3 is expressed by the RP3 motoneuron and its target muscles during synaptic target recognition. The RP3 growth cone can form synapses on muscles that ectopically express FAS3. This mistargeting is dependent on FAS3 expression in the motoneurons. In addition, when the FAS3-negative aCC and SNa motoneuron growth cones ectopically express FAS3, they gain the ability to recognize FAS3-expressing muscles as alternative targets. We propose that homophilic synaptic target recognition serves as a basic mechanism of neural network formation.



2005 ◽  
Vol 15 (1) ◽  
pp. 108-115 ◽  
Author(s):  
Anne Eichmann ◽  
Ferdinand Le Noble ◽  
Monica Autiero ◽  
Peter Carmeliet


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