Premium
Establishment of pigment cell lineage in embryos of the sea urchin, Hemicentrotus pulcherrimus
Author(s) -
Kominami Tetsuya
Publication year - 2000
Publication title -
development, growth and differentiation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.864
H-Index - 66
eISSN - 1440-169X
pISSN - 0012-1592
DOI - 10.1046/j.1440-169x.2000.00483.x
Subject(s) - hemicentrotus , biology , aphidicolin , sea urchin , microbiology and biotechnology , blastomere , embryo , pigment , chemistry , embryogenesis , cell , cell cycle , genetics , organic chemistry
In an attempt to estimate the number of pigment precursor cells in sea urchin embryos, DNA synthesis and cell divisions were blocked with aphidicolin from various stages of development. Interestingly, pigment cells differentiated on a normal time schedule, even if the embryos were treated from late cleavage stages on. In most of the embryos treated from 10 h on, 10–15 pigment cells differentiated. Thereafter, the number of pigment cells in the aphidicolin‐treated embryos further increased, as the initiation of the treatment was delayed. On the other hand, total cell volumes in the pigment lineage, calculated from the averaged number and diameter of differentiated pigment cells, were almost the same irrespective of the time of the initiation of aphidicolin treatment. This indicated that the increase in the number was caused by divisions of the pre‐existing cells in the pigment lineage. Thus, the founder cells that exclusively produce pigment cells could be identified. They are nine times‐cleaved blastomeres and specified by 10 h post‐fertilization. The obtained results also clarified the division schedule in the pigment lineage; the founder cells divide once (10th) until hatching, and divide once more (11th) by the end of gastrulation.