Pl. Hertzler et al., MESENDODERM CELL AND ARCHENTERON FORMATION IN ISOLATED BLASTOMERES FROM THE SHRIMP SICYONIA-INGENTIS, Developmental biology, 164(2), 1994, pp. 333-344
The fate map of 2- and 4-cell-stage Sicyonia ingentis embryos was dete
rmined by microinjection of lysyl-rhodamine-dextran into single blasto
meres. Microinjected embryos were cultured to the limb bud stage, when
the body plan of the nauplius larva was evident, The animal blastomer
e, AB, gave rise to anterior ectoderm, while the vegetal blastomere, C
D, gave rise to posterior structures, including the invagination site
during gastrulation. The A blastomere gave rise to mirror-image patter
ns of dorsal-lateral ectoderm, while the B blastomere gave rise to ant
erior, ventral ectoderm. The C blastomere gave rise to posterior, dors
al-lateral ectoderm, complementary to the A pattern, as well as some n
aupliar mesoderm. The D blastomere gave rise to mesendoderm, naupliar
mesoderm, and some posterior ectoderm. To study the specification of t
he early blastomeres, they were microsurgically separated and cultured
in isolation. Two mesendoderm cells formed in 1/2 , 1/4, 1/8, and 1/1
6 blastomeres in embryos dissociated at the 2-, 4-, 8-, and 16-cell st
ages, respectively. CD and D blastomeres could be distinguished by the
ir larger size and gave rise to the mesendoderm cells. Archenteron for
mation and elongation of the embryo occurred in CD but not in AB isola
tes. Isolated blastomeres were recombined in various ways to determine
whether their state of commitment could be altered in different cellu
lar environments. Duplicated mesendoderm cells and archenterons formed
in CD + CD recombinations, while AB + AB recombinations formed blastu
lae but did not produce mesendoderm cells and did not invaginate. The
normal number of mesendoderm cells and a single archenteron formed in
D + AB recombinations, while C + AB recombinations remained as blastul
ae and did not form mesendoderm cells. The results suggest that the me
sendoderm cells are autonomously specified, possibly by cytoplasmic lo
calization at the vegetal pole. The mesendoderm may also function as a
signaling region to organize other developmental events. (C) 1994 Aca
demic Press, Inc.