Cell lineage analysis in ascidian embryos by intracellular injection of a tracer enzyme. I. Up to the eight-cell stage.

Cell lineages during development of ascidian embryos were analyzed by injection of horseradish peroxidase as a tracer enzyme into identified cells at the one-, two-, four-, and eight-cell stages of the ascidians, Halocynthia roretzi, Ciona intestinalis, and Ascidia ahodori. Identical results were obtained with eggs of the three different species examined. The first cleavage furrow coincided with the bilateral symmetry plane of the embryo. The second furrow did not always divided the embryo into anterior and posterior halves as each of the anterior and posterior cell pairs gave rise to different tissues according to their destinies, which became more definitive in the cell pairs at the eight-cell stage. Of the blastomeres constituting the eight-cell stage embryo, the a4.2 pair (the anterior animal blastomeres) differentiated into epidermis, brain, and presumably sense organ and palps. Every descendant cell of the b4.2 pair (the posterior animal blastomeres) has been thought to become epidermis; however, the horseradish peroxidase injection probe revealed that the b4.2 pair gave rise to not only epidermis but also muscle cells at the caudal tip region of the developing tailbud-stage embryos. The A4.1 pair (the anterior vegetal blastomeres) developed into endoderm, notochord, brain stem, spinal cord, and also muscle cells next the caudal tip muscle cells. From the B4.1 pair (the posterior vegetal blastomeres) originated muscle cells of the anterior and middle parts of the tail, mesenchyme, endoderm, endodermal strand, and also notochord at the caudal tip region. These results clearly demonstrate that muscle cells are derived not only from the B4.1 pair, as has hitherto been believed, but also from both the b4.2 and A4.1 pairs.

[1]  T. Kominami Establishment of embryonic axes in larvae of the starfish, Asterina pectinifera. , 1983, Journal of embryology and experimental morphology.

[2]  E. Conklin Scientific Books: The Organization and Cell-Lineage of the Ascidian Egg , 1905 .

[3]  J. Whittaker Segregation during ascidian embryogenesis of egg cytoplasmic information for tissue-specific enzyme development. , 1973, Proceedings of the National Academy of Sciences of the United States of America.

[4]  E. Wulf,et al.  Fluorescent phallotoxin, a tool for the visualization of cellular actin. , 1979, Proceedings of the National Academy of Sciences of the United States of America.

[5]  M. J. Katz COMPARATIVE ANATOMY OF THE TUNICATE TADPOLE, CIONA INTESTINALIS , 1983 .

[6]  N. Satoh,et al.  Autonomous muscle cell differentiation in partial ascidian embryos according to the newly verified cell lineages. , 1984, Developmental biology.

[7]  U J McMahan,et al.  The shapes of sensory and motor neurones and the distribution of their synapses in ganglia of the leech: a study using intracellular injection of horseradish peroxidase , 1976, Proceedings of the Royal Society of London. Series B. Biological Sciences.

[8]  S. Ikegami,et al.  On the 'clock' mechanism determining the time of tissue-specific enzyme development during ascidian embryogenesis. II. Evidence for association of the clock with the cycle of DNA replication. , 1981, Journal of embryology and experimental morphology.

[9]  J. Sulston,et al.  The embryonic cell lineage of the nematode Caenorhabditis elegans. , 1983, Developmental biology.

[10]  M. Jacobson,et al.  Clonal organization of the central nervous system of the frog. I. Clones stemming from individual blastomeres of the 16-cell and earlier stages. , 1979, Developmental biology.

[11]  M. Jacobson,et al.  Origin of the retina from both sides of the embryonic brain: a contribution to the problem of crossing at the optic chiasma. , 1978, Science.

[12]  R. Pedersen,et al.  Allocation of cells to inner cell mass and trophectoderm lineages in preimplantation mouse embryos. , 1982, Developmental biology.

[13]  P J Snow,et al.  Tracing axons and axon collaterals of spinal neurons using intracellular injection of horseradish peroxidase. , 1976, Science.

[14]  N. Satoh On the 'clock' mechanism determining the time of tissue-specific enzyme development during ascidian embryogenesis. I. Acetylcholinesterase development in cleavage-arrested embryos. , 1979, Journal of embryology and experimental morphology.

[15]  N. Gilula,et al.  Gap junctional communication in the preimplantation mouse embryo , 1979, Cell.

[16]  G. Stent,et al.  Cell lineage analysis by intracellular injection of a tracer enzyme. , 1978, Science.

[17]  N. Satoh Cellular morphology and architecture during early morphogenesis of the ascidian egg: an SEM study. , 1978, The Biological bulletin.

[18]  J. Whittaker Quantitative control of end products in the melanocyte lineage of the ascidian embryo. , 1979, Developmental biology.

[19]  J. Whittaker Cytoplasmic Determinants of Tissue Differentiation in the Ascidian Egg , 1979 .

[20]  M. Johnson,et al.  The nature of intercellular coupling within the preimplantation mouse embryo. , 1984, Journal of embryology and experimental morphology.

[21]  T. H. Meedel,et al.  Development of acetylchilinesterase during embryogenesis of the ascidian Ciona intestinalis. , 1979, The Journal of experimental zoology.

[22]  G. Reverberi Experimental embryology of marine and fresh-water invertebrates , 1971 .

[23]  M. Karnovsky,et al.  A "DIRECT-COLORING" THIOCHOLINE METHOD FOR CHOLINESTERASES , 1964, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[24]  C. Sardet,et al.  Tracing of cell lineage in embryonic development of Phallusia mammillata (Ascidia) by vital staining of mitochondria. , 1984, Developmental biology.

[25]  W. Castle The early embryology of ciona intestinalis, flemming (L.) , 1896 .

[26]  D. Weisblat,et al.  Stepwise commitment of blast cell fates during the positional specification of the O and P cell lines in the leech embryo. , 1984, Developmental biology.

[27]  J Kimble,et al.  Alterations in cell lineage following laser ablation of cells in the somatic gonad of Caenorhabditis elegans. , 1981, Developmental biology.

[28]  N. Satoh,et al.  A definite number of aphidicolin-sensitive cell-cyclic events are required for acetylcholinesterase development in the presumptive muscle cells of the ascidian embryos. , 2018, Journal of embryology and experimental morphology.

[29]  J. Whittaker Acetylcholinesterase development in extra cells caused by changing the distribution of myoplasm in ascidian embryos. , 1980, Journal of embryology and experimental morphology.

[30]  G. Stent,et al.  Embryonic cell lineages in the nervous system of the glossiphoniid leech Helobdella triserialis. , 1980, Developmental biology.

[31]  J. Adams,et al.  Technical considerations on the use of horseradish peroxidase as a neuronal marker , 1977, Neuroscience.

[32]  J. Whittaker Muscle lineage cytoplasm can change the developmental expression in epidermal lineage cells of ascidian embryos. , 1982, Developmental biology.

[33]  D. Weisblat,et al.  Developmental interdeterminacy in embryos of the leech Helobdella triserialis. , 1984, Developmental biology.

[34]  G. Freeman The role of cleavage in the localization of developmental potential in the ctenophore Mnemiopsis leidyi. , 1976, Developmental biology.

[35]  G. Ortolani,et al.  Autonomy of acetylcholinesterase differentiation in muscle lineage cells of ascidian embryos. , 1977, Developmental biology.

[36]  N. Dilly Studies on the Receptors in the Cerebral Vesicle of the Ascidian Tadpole, 2. The Ocellus , 1964 .

[37]  S. Miyazaki,et al.  Analysis of non‐linearity observed in the current—voltage relation of the tunicate embryo , 1974, The Journal of physiology.

[38]  J. Sulston,et al.  Regulation and cell autonomy during postembryonic development of Caenorhabditis elegans. , 1980, Developmental biology.

[39]  W. Jeffery PATTERN FORMATION BY OOPLASMIC SEGREGATION IN ASCIDIAN EGGS , 1984 .

[40]  G. Stent,et al.  Embryonic origins of cells in the leech Helobdella triserialis. , 1984, Developmental biology.

[41]  G. Materazzi,et al.  A study of the origin of the cells containing sulfated acid mucopolysaccharides in the cephalic portion of the larvae of Phallusia mamillata and Ascidia malaca , 1969 .

[42]  M. Shankland Positional determination of supernumerary blast cell death in the leech embryo , 1984, Nature.