Intercalary regeneration in the amphibian limb and the rule of distal transformation.

The applicability to the amphibian limb of the rule of distal transformation, which states that tissue from any level can only become more distal, has been tested during intercalary regeneration following various types of shift-level transplantation. Following the grafting of distal blastemas to proximal levels, such that part of the presumptive pattern is missing, complete limbs nevertheless formed (Series I). That the intercalated tissue arose entirely from the stump was shown by exchanging blastemas between black and white animals. When the proximal stump was irradiated and its contribution eliminated, intercalary deletions were produced (Series II). This was not due to the inability of irradiated and normal tissue to communicate since irradiated distal blastemas grafted onto proximal stumps still stimulated intercalary regeneration (Series III). When proximal blastemas were grafted to distal levels intercalary regenerates were obtained in about 20% of the cases (Series IV) and under these circumstances the grafted blastema was the sole source of intercalated tissue. The precise structure of these intercalated elements was impossible to ascertain, but it is suggested that they might be of reversed polarity as found in insects. These results are dicussed in relation to similar experiments on the insect limb.

[1]  S. Strub Leg regeneration in insects. An experimental analysis in Drosophila and a new interpretation. , 1979, Developmental biology.

[2]  Interactions between irradiated and unirradiated tissues during supernumerary limb formation in the newt. , 1979, The Journal of experimental zoology.

[3]  M. Maden The regeneration of positional information in the amphibian limb. , 1977, Journal of theoretical biology.

[4]  Polarized inhibitory effects during regeneration in tubularia , 1957 .

[5]  S. Bryant,et al.  The interaction between the blastema and stump in the establishment of the anterior--posterior and proximal--distal organization of the limb regenerate. , 1975, Developmental biology.

[6]  V. French Leg regeneration in the cockroach, Blatella germanica. II. Regeneration from a non-congruent tibial graft/host junction. , 1976, Journal of embryology and experimental morphology.

[7]  D. Stocum Regulation after proximal or distal transposition of limb regeneration blastemas and determination of the proximal boundary of the regenerate. , 1975, Developmental biology.

[8]  B. Carlson,et al.  Morphogenetic interactions between rotated skin cuffs and underlying stump tissues in regenerating axolotl forelimbs. , 1974, Developmental biology.

[9]  D. Melton,et al.  Self-organizational capacity of distally transplanted limb regeneration blastemas in larval salamanders. , 1977, The Journal of experimental zoology.

[10]  M. Maden The role of irradiated tissue during pattern formation in the regenerating limb. , 1979, Journal of embryology and experimental morphology.

[11]  H. Bohn Regeneration of proximal tissues from a more distal amputation level in the insect leg (Blaberus craniifer, Blattaria). , 1976, Developmental biology.

[12]  Elmer G. Butler,et al.  Regeneration of the urodele forelimb after reversal of its proximo‐distal axis , 1955 .

[13]  Absence of distal to proximal intercalary regeneration in imaginal wing discs of Drosophila melanogaster. , 1979, Developmental biology.