scholarly journals Functional Regeneration of the Sensory Root via Axonal Invasion

Cell Reports ◽  
2020 ◽  
Vol 30 (1) ◽  
pp. 9-17.e3 ◽  
Author(s):  
Evan L. Nichols ◽  
Cody J. Smith
2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Yu Wang ◽  
Shanshan Jin ◽  
Dan Luo ◽  
Danqing He ◽  
Chunyan Shi ◽  
...  

AbstractTendon injuries disrupt the balance between stability and mobility, causing compromised functions and disabilities. The regeneration of mature, functional tendons remains a clinical challenge. Here, we perform transcriptional profiling of tendon developmental processes to show that the extracellular matrix-associated protein periostin (Postn) contributes to the maintenance of tendon stem/progenitor cell (TSPC) functions and promotes tendon regeneration. We show that recombinant periostin (rPOSTN) promotes the proliferation and stemness of TSPCs, and maintains the tenogenic potentials of TSPCs in vitro. We also find that rPOSTN protects TSPCs against functional impairment during long-term passage in vitro. For in vivo tendon formation, we construct a biomimetic parallel-aligned collagen scaffold to facilitate TSPC tenogenesis. Using a rat full-cut Achilles tendon defect model, we demonstrate that scaffolds loaded with rPOSTN promote endogenous TSPC recruitment, tendon regeneration and repair with native-like hierarchically organized collagen fibers. Moreover, newly regenerated tendons show recovery of mechanical properties and locomotion functions.


1985 ◽  
Vol 16 (2) ◽  
pp. 137-151 ◽  
Author(s):  
A. Don Murphy ◽  
David L. Barker ◽  
Jeanne F. Loring ◽  
S. B. Kater

Neuroscience ◽  
2014 ◽  
Vol 262 ◽  
pp. 40-52 ◽  
Author(s):  
M. Heidemann ◽  
J. Streit ◽  
A. Tscherter

eLife ◽  
2018 ◽  
Vol 7 ◽  
Author(s):  
Chen Ding ◽  
Marc Hammarlund

Functional axon regeneration requires regenerating neurons to restore appropriate synaptic connectivity and circuit function. To model this process, we developed an assay in Caenorhabditis elegans that links axon and synapse regeneration of a single neuron to recovery of behavior. After axon injury and regeneration of the DA9 neuron, synapses reform at their pre-injury location. However, these regenerated synapses often lack key molecular components. Further, synaptic vesicles accumulate in the dendrite in response to axon injury. Dendritic vesicle release results in information misrouting that suppresses behavioral recovery. Dendritic synapse formation depends on dynein and jnk-1. But even when information transfer is corrected, axonal synapses fail to adequately transmit information. Our study reveals unexpected plasticity during functional regeneration. Regeneration of the axon is not sufficient for the reformation of correct neuronal circuits after injury. Rather, synapse reformation and function are also key variables, and manipulation of circuit reformation improves behavioral recovery.


Life Sciences ◽  
2004 ◽  
Vol 74 (15) ◽  
pp. 1937-1943 ◽  
Author(s):  
Liang-Ming Lee ◽  
Ming-Chao Huang ◽  
Tien-Yow Chuang ◽  
Liang-Shong Lee ◽  
Henrich Cheng ◽  
...  

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