scholarly journals Angiogenesis is inhibitory for mammalian digit regeneration

Regeneration ◽  
2014 ◽  
Vol 1 (3) ◽  
pp. 33-46 ◽  
Author(s):  
Ling Yu ◽  
Mingquan Yan ◽  
Jennifer Simkin ◽  
Paulina D. Ketcham ◽  
Eric Leininger ◽  
...  
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Author(s):  
Tianyue Huang ◽  
Lingling Zuo ◽  
Katarzyna S. Walczyńska ◽  
Mengying Zhu ◽  
Yujun Liang


2010 ◽  
Vol 5 (2) ◽  
pp. 201-220 ◽  
Author(s):  
Gang Wang ◽  
Stephen F Badylak ◽  
Ellen Heber-Katz ◽  
Susan J Braunhut ◽  
Lorraine J Gudas


2021 ◽  
Vol 10 (1) ◽  
Author(s):  
Hanqian Xu ◽  
Hailin Zhang ◽  
Yanqing Fang ◽  
Huiran Yang ◽  
Ying Chen ◽  
...  

Abstract Background Expression of Mc4r in peripheral organs indicates it has broader roles in organ homeostasis and regeneration. However, the expression and function of Mc4r in the mouse limb and digit has not been fully investigated. Our previous work showed that Mc4r−/− mice fail to regenerate the digit, but whether activation of MC4R signaling could rescue digit regeneration, or stimulate proximal digit regeneration is not clear. Results We analyzed the expression dynamics of Mc4r in the embryonic and postnatal mouse limb and digit using the Mc4r-gfp mice. We found that Mc4r-GFP is mainly expressed in the limb nerves, and in the limb muscles that are undergoing secondary myogenesis. Expression of Mc4r-GFP in the adult mouse digit is restricted to the nail matrix. We also examined the effect of α-MSH on mouse digit regeneration. We found that administration of α-MSH in the Mc4r+/− mice rescue the delayed regeneration of distal digit tip. α-MSH could rescue distal digit regeneration in denervated hindlimbs. In addition, α-MSH could stimulate regeneration of the proximally amputated digit, which is non-regenerative. Conclusions Mc4r expression in the mouse limb and digit is closely related to nerve tissues, and α-MSH/MC4R signaling has a neurotrophic role in mouse digit tip regeneration.



2013 ◽  
Vol 27 (S1) ◽  
Author(s):  
Jennifer Simkin ◽  
Mimi Sammarco ◽  
Danielle Fassler ◽  
Alex Cammack ◽  
Ken Muneoka


Development ◽  
1978 ◽  
Vol 44 (1) ◽  
pp. 105-112
Author(s):  
A. R. Smith

Digit regeneration has been examined in Triturus cristatus. Because of their size, blastemas that form after digit amputation are relatively a lot more suitable for quantitative studies that involve for example the counting of cells in histological sections. They are also very useful for the study of some basic histological aspects of regeneration particularly cartilage formation. This has been looked at in regenerating digits, as there are only a maximum of three bones to regenerate and these lie in sequence, one after the other. It was seen that the cartilage is laid down as a solid rod by about 17 days post-amputation, and that by about 20 days, it starts to be split up into its three elements. An X-ray study of the growth of digit regeneration together with autoradiography experiments were also carried out as a comparison to studies already undertaken on larger more proximal blastemas. It was shown that in fact the behaviour of digit blastemas is very similar to those of a more proximal origin. This fact, together with the advantages of its size, make the digit a very strong candidate for the further study of regeneration.



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