NEUROTROPHIC CONTROL OF LIMB REGENERATION IN THE NEWT

1974 ◽  
Vol 228 (1 Trophic Funct) ◽  
pp. 308-321 ◽  
Author(s):  
Marcus Singer
Development ◽  
1978 ◽  
Vol 48 (1) ◽  
pp. 169-175
Author(s):  
M. Maden

It is shown here that amputated and denervated limbs of larval axolotls dedifferentiate and a proportion of the cells released undergo DNA synthesis and mitosis. When the limb is denervated prior to amputation fewer cells go through the cell cycle, implying the existence of a pool of trophic factor in the limb. Recent work has demonstrated that denervated blastemal cells accumulate in the G1 phase of the cycle. These results strongly argue against the theory that the trophic factor controls the G2 phase. Rather, it is proposed that this factor regulates either the total number of cells cycling or the rate at which they cycle by varying the length of the G1 phase.


2021 ◽  
Author(s):  
Kaylee M. Wells-Enright ◽  
Kristina Kelley ◽  
Mary Baumel ◽  
Warren A. Vieira ◽  
Catherine D. McCusker

AbstractThe mechanisms that regulate the sizing of the regenerating limb in tetrapods such as the Mexican axolotl are unknown. Upon the completion of the developmental stages of regeneration, when the regenerative organ known as the blastema completes patterning and differentiation, the limb regenerate is proportionally small in size. It then undergoes a phase of regeneration that we have called the “tiny-limb” stage, that is defined by rapid growth until the regenerate reaches the proportionally appropriate size. In the current study we have characterized this growth and have found that signaling from the limb nerves is required for its maintenance. Using the regenerative assay known as the Accessory Limb Model, we have found that the size of the limb can be positively and negatively manipulated by nerve abundance. We have additionally developed a new regenerative assay called the Neural Modified-ALM (NM-ALM), which decouples the source of the nerve from the regenerating host environment. Using the NM-ALM we discovered that non-neural extrinsic factors from differently sized host animals do not play a prominent role in determining the size of the regenerating limb. We have also discovered that the regulation of limb size is not autonomously regulated by the limb nerves. Together, these observations show that the limb nerves provide essential and instructive cues to regulate the final size of the regenerating limb.


2010 ◽  
Vol 344 (1) ◽  
pp. 518
Author(s):  
Michael P. Sarras ◽  
Ansgar Olsen ◽  
Robert Intine

1987 ◽  
Vol 65 (8) ◽  
pp. 739-749 ◽  
Author(s):  
Roy A. Tassava ◽  
David J. Goldhamer ◽  
Bruce L. Tomlinson

Data from pulse and continuous labeling with [3H]thymidine and from studies with monoclonal antibody WE3 have led to the modification of existing models and established concepts pertinent to understanding limb regeneration. Not all cells of the adult newt blastema are randomly distributed and actively progressing through the cell cycle. Instead, many cells are in a position that we have designated transient quiescence (TQ) and are not actively cycling. We postulate that cells regularly leave the TQ population and enter the actively cycling population and vice versa. The size of the TQ population may be at least partly determined by the quantity of limb innervation. Larval Ambystoma may have only a small or nonexisting TQ, thus accounting for their rapid rate of regeneration. Examination of reactivity of monoclonal antibody WE3 suggests that the early wound epithelium, which is derived from skin epidermis, is later replaced by cells from skin glands concomitant with blastema formation. WE3 provides a useful tool to further investigate the regenerate epithelium.


1944 ◽  
Vol 97 (1) ◽  
pp. 71-93 ◽  
Author(s):  
Natalie M. Gidge ◽  
S. Meryl Rose
Keyword(s):  

2005 ◽  
Vol 279 (1) ◽  
pp. 86-98 ◽  
Author(s):  
Vladimir Vinarsky ◽  
Donald L. Atkinson ◽  
Tamara J. Stevenson ◽  
Mark T. Keating ◽  
Shannon J. Odelberg

PLoS ONE ◽  
2012 ◽  
Vol 7 (9) ◽  
pp. e41804 ◽  
Author(s):  
Edna C. Holman ◽  
Leah J. Campbell ◽  
John Hines ◽  
Craig M. Crews

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