Cellular dynamics underlying regeneration of appropriate segment number during axolotl tail regeneration. Issue 1 (December 2015)

• Record Type: Journal Article
• Authors: Vincent, Carr; Rost, Fabian; Masselink, Wouter; Brusch, Lutz; Tanaka, Elly
• Is Part Of: BMC developmental biology. Volume 15:Issue 1(2015)
• Page Start: 1
• Page End: 11
• Publication Date: 2015-12
• Subjects: Salamander -- Tail -- Regeneration -- Size control -- Cell cycle -- Myotome -- Segmentation; Developmental biology -- Periodicals; 571.8
• DOI: 10.1186/s12861-015-0098-1
• Languages: English
• ISSNs: 1471-213X

Abstract

Abstract Background Salamanders regenerate their tails after amputation anywhere along their length. How the system faithfully reconstitutes the original number of segments and length is not yet known. Methods To gain quantitative insight into how the system regenerates the appropriate length, we amputated tails at 4 or 16 myotomes post-cloaca and measured blastema size, cell cycle kinetics via cumulative Bromodeoxyuridine (BrdU) incorporation and the method of Nowakowski, and myotome differentiation rate. Results In early stages until day 15, blastema cells were all proliferative and divided at the same rate at both amputation levels. A larger blastema was formed in 4th versus 16th myotome amputations indicating a larger founding population. Myotome differentiation started at the same timepoint in the 4th and 16 th level blastemas. The rate of myotome formation was more rapid in 4th myotome blastemas so that by day 21 the residual blastema from the two amputation levels achieved equivalent size. At that time point, only a fraction of blastema cells remain in cycle, with the 4th myotome blastema harboring double the number of cycling cells as the 16th myotome blastema allowing it to grow faster and further reconstitute the larger number of missing myotomes. Conclusions These data suggest that there are two separable phases of blastema growth. The first is level-independent, with cells displaying unrestrained proliferation. In the second phase, the level-specific growth is revealed, where differing fractions of cells remain in the cell cycle over time.