Control of blastema cell proliferation by possible interplay of calcium and cyclic nucleotides during newt limb regeneration

1987 ◽  
Vol 35 (2) ◽  
pp. 94-99 ◽  
Author(s):  
Morton Globus ◽  
Swani Vethamany-Globus ◽  
Agnes Kesik
1987 ◽  
Vol 65 (8) ◽  
pp. 726-729 ◽  
Author(s):  
Richard A. Liversage

Various regulatory factors are required in epimorphic regeneration of an adult newt limb. These factors (namely, amputational injury, the wound and apical epithelium, nerves (mitogenic agents), hormones (the hormonal milieu), bioelectric fields, probably the immune system, and possibly cyclic nucleotides and heretofore unknown regulators) act in concert and contribute to the developing microenvironment of the regenerate in support of normal regrowth and differentiation.


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

2016 ◽  
Vol 129 (1) ◽  
pp. 276-280
Author(s):  
Kaoru Nomura ◽  
Yasushi Tanimoto ◽  
Fumio Hayashi ◽  
Erisa Harada ◽  
Xiao-Yuan Shan ◽  
...  

Development ◽  
1993 ◽  
Vol 117 (4) ◽  
pp. 1397-1407 ◽  
Author(s):  
H.G. Simon ◽  
C.J. Tabin

Adult urodele amphibians can regenerate their limbs and tail. Based on their roles in other developing systems, Hox genes are strong candidates for genes that play a role in regulating pattern formation during regeneration. There are four homologous clusters of Hox genes in vertebrate genomes. We isolated cDNA clones of two newt homeobox genes from homologous positions within two Hox clusters; Hox-4.5 and Hox-3.6. We used RNase protection on nonamputated (normal) and regenerating newt appendages and tissue to compare their transcriptional patterns. Both genes show increased expression upon amputation with similar kinetics. Hox-4.5 and Hox-3.6 transcription is limited to the mesenchymal cells in the regenerates and is not found in the epithelial tissue. In addition to regenerating appendages, both genes are transcriptionally active in adult kidney of the newt. Striking differences were found in the regulation of Hox-4.5 and Hox-3.6 when they were compared in unamputated limbs and in regenerating forelimbs versus regenerating hindlimbs. Hox-4.5 is expressed in the blastema of regenerating fore- and hindlimbs, but Hox-4.5 transcripts are not detectable in normal limbs. In contrast, Hox-3.6 transcripts are found exclusively in posterior appendages, but are present in normal as well as regenerating hindlimbs and tails. Hox-4.5 is also expressed at a higher level in proximal (mid-humerus) regenerates than in distal ones (mid-radius). When we proximalized the positional memory of a distal blastema with retinoic acid, we find that the early expression level of Hox-4.5 is also proximalized. When the expression of these genes is compared to the expression of two previously reported newt Hox genes, a consistent pattern emerges, which can be interpreted in terms of differential roles for the different Hox clusters in determining regenerative limb morphology.


1991 ◽  
Vol 148 (1) ◽  
pp. 219-232 ◽  
Author(s):  
Hiroaki Onda ◽  
Matthew L. Poulin ◽  
Roy A. Tassava ◽  
Ing-Ming Chiu

1915 ◽  
Vol 35 ◽  
pp. 78-94 ◽  
Author(s):  
J. Herbert Paul

Summary(1) Homarus vulgáris, Eupagurus bernhardus, and Carcinus mœnas all form limb-buds or papillæ in the process of limb regeneration. These are covered by a chitinous envelope, and the observations here recorded show that their outer form and size are adaptations to the requirements of the animal. That of the lobster is straight, that of the hermit crab curved, while the shore crab has a papilla which may be folded on itself three times inside the envelope.(2) Valvular action of the diaphragm at the breaking plane plays a greater part in the stopping of haemorrhage after self-amputation than clotting, and the dilatation of small vessels which pass beneath the epidermis detaches a layer of cells. This layer of epidermis proliferates from its free edges to form the new limb.(3) A new diaphragm is the first structure laid down, and differentiation takes place from the base outwards. Muscle arises at the growing tip from cells proliferated from the old epidermis (an ectodermal structure), and the nerve grows outwards from the torn end by cell proliferation.(4) Muscle-fibres are anatomically complete immediately before moulting. The fibrillæ are cross-striated and enclosed in a sarcolemma, but full functional activity does not come till several days after moulting, beginning with slow rhythmic movements. Sarcoplasm seems to be less plentiful than in the normal fibre.(5) When moulting occurs the papilla is at once expanded to several times its previous size by valvular action, and the epidermis, previously composed of several layers of cells, now thins to a single layer, as is seen in the normal limb.


2000 ◽  
Vol 218 (2) ◽  
pp. 125-136 ◽  
Author(s):  
Anoop Kumar ◽  
Cristiana P. Velloso ◽  
Yutaka Imokawa ◽  
Jeremy P. Brockes

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