The effects of retinoic acid on mitosis during tail and limb regeneration in the axolotl larva, Ambystoma mexicanum

1987 ◽  
Vol 196 (3) ◽  
pp. 169-175 ◽  
Author(s):  
Paul Pietsch
1999 ◽  
Vol 77 (11) ◽  
pp. 1835-1837 ◽  
Author(s):  
Steven R Scadding

While the effects of exogenous retinoids on amphibian limb regeneration have been studied extensively, the role of endogenous retinoids is not clear. Hence, I wished to investigate the role of endogenous retinoic acid during axolotl limb regeneration. Citral is a known inhibitor of retinoic acid synthesis. Thus, I treated regenerating limbs of the larval axolotl Ambystoma mexicanum with citral. The result of this inhibition of retinoic acid synthesis was that limb regeneration became extremely irregular and hypomorphic, with serious pattern defects, or was inhibited altogether. I conclude that endogenous retinoic acid plays an important role in pattern formation during limb regeneration.


1998 ◽  
Vol 76 (9) ◽  
pp. 1795-1796 ◽  
Author(s):  
Steven R Scadding ◽  
Andrew Burns

The purpose of this investigation was to determine whether there were any asymmetries in the vascularization of the limb-regeneration blastema in the axolotl, Ambystoma mexicanum, that might be related to pattern formation, and to determine if retinoic acid could modify the vascular patterns of the blastema. We used acrylic casts of the vascular system of the limbs to assess the pattern of vascularization. We observed a very regular symmetrical arrangement of capillaries in the limb-regeneration blastema that did not appear to be modified by doses of retinoic acid sufficient to modify the limb pattern.


1999 ◽  
Vol 77 (6) ◽  
pp. 902-909
Author(s):  
Leigh-Anne D Miller ◽  
Melissa L Farquhar ◽  
John S Greenwood ◽  
Steven R Scadding

Gap junctions are thought to play a role in pattern formation during limb development and regeneration by controlling the movement of small regulatory molecules between cells. An anteroposterior gradient of gap junctional communication that is higher posteriorly has been reported in the developing chick limb bud. In both the developing chick limb bud and the amphibian regenerating limb, an anteroposterior retinoic acid gradient is present, and this is also higher posteriorly. On the basis of these observations, we decided to examine the role of gap junctional communication in the regenerating amphibian limb. Gap junctions were observed in both the axolotl, Ambystoma mexicanum, limb regeneration blastema and cardiac tissue (as a positive control), using immunohistochemical labelling and laser scanning confocal microscopy. The scrape-loading/dye transfer technique for tracing the movement of a gap junction permeable dye, Lucifer yellow, showed that in blastemal epidermis there were nonuniform distributions of gap junctions in both the dorsoventral and anteroposterior axes of the blastema. Retinoic acid was found to increase gap junctional permeability in blastemal epidermis 48 h after injection and in blastemal mesenchyme 76 h after injection. The potential role of gap junctions during pattern formation in limb regeneration is discussed based on these results.


Development ◽  
1966 ◽  
Vol 16 (1) ◽  
pp. 143-158
Author(s):  
D. O. E. Gebhardt ◽  
J. Faber

During the last twenty-five years a number of authors have studied the influence of chemical substances on limb regeneration in amphibians. Examples of compounds which have been tested so far are: (1) the antimitotic agent, colchicine (Thornton, 1943); (2) the salt, beryllium nitrate (Thornton, 1949, 1950, 1951); (3) the carcinogens, dibenzanthracene and methylcholanthrene (Karczmar & Berg, 1952; Ruben & Balls, 1964); (4) the lathyrus factor, β- aminopropionitrile (Chang, Witschi & Ponseti, 1955); (5) the hormone, thyroxine (Hay, 1956); (6) atropine and other neuropharmacological drugs (Singer, Davis & Scheuing, 1960); (7) the metachromatic dye, toluidine blue (Csaba, Bierbauer & Törö, 1961); and (8) semicarbazide, an inhibitor of histamine formation (Deck & Shapiro, 1963). Most of these substances caused growth retardation as well as malformations of the limb regenerates. A number of other investigators have studied the effects of chemicals on the ontogenetic development of the amphibian limb.


2020 ◽  
Vol 164 ◽  
pp. 103651
Author(s):  
Annie Espinal-Centeno ◽  
Melissa Dipp-Álvarez ◽  
Carlos Saldaña ◽  
Laszlo Bako ◽  
Alfredo Cruz-Ramírez

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