Does the respiratory rate in sea urchin embryos increase during early development without proliferation of mitochondria?

During early development of the sea urchin, the respiratory rate, enhanced upon fertilization, is maintained up to hatching (pre‐hatching period) and then gradually increases to a maximum at the gastrula stage (post‐gastrula period). Except for a short duration after fertilization, respiration in embryos is strongly inhibited by CN− and antimycin A. During the whole span of early development, the amounts of proteins, cytochromes and the specific activities of cytochrome c oxidase and reduced nicotinamide adenine dinucleotide (NADH) cytochrome c reductase in mitochondria are practically the same as in unfertilized eggs. A marked augmentation of mitochondrial respiration after hatching probably occurs without net increase in whole mitochondrial intrinsic capacities. Carbonylcyanide p‐trifluoromethoxyphenylhydrazone (FCCP) or tetramethyl p‐phenylenediamine (TMPD) enhances the respiratory rate in the pre‐hatching period but hardly augments the respiration in the post‐gastrula period. In the presence of both FCCP and TMPD, the respiratory rate in the pre‐hatching period was as high as in the post‐gastrula period. Probably, electron transport in the mitochondrial respiratory chain is regulated by acceptor control and limitation of cytochrome c reduction in the pre‐hatching period and released from those regulations in the post‐gastrula period. Acceptor control of respiration is experimentally reproduced in isolated mitochondria by making adenine nucleotide levels as those levels in the pre‐hatching period.

[1]  A. Fujiwara,et al.  Does the low respiratory rate in unfertilized eggs result mainly from depression of the redox reaction catalyzed by flavoproteins? Analysis of the respiratory system by light‐induced release of CO‐mediated inhibition , 1996 .

[2]  B. Shapiro,et al.  The respiratory burst oxidase of fertilization. A physiological target for regulation by protein kinase C. , 1992, The Journal of biological chemistry.

[3]  H. Jacobs,et al.  Replication origins and pause sites in sea urchin mitochondrial DNA , 1992, Proceedings of the Royal Society of London. Series B: Biological Sciences.

[4]  M. Klingenberg Mechanism and evolution of the uncoupling protein of brown adipose tissue. , 1990, Trends in biochemical sciences.

[5]  T. Kawashima,et al.  Stimulation of Protein Synthesis in the Mitochondria of Sea Urchin Embryos before Gastrulation , 1988, Development, growth & differentiation.

[6]  S. Nemoto,et al.  Fertilization-induced change in the respiratory rate in eggs of several marine invertebrates , 1988 .

[7]  C. Scandella,et al.  Respiration capacity of mitochondria isolated from unfertilized and fertilized sea urchin eggs. , 1987, Experimental cell research.

[8]  G. Giudice The Sea Urchin Embryo: A Developmental Biological System , 1986 .

[9]  D. Epel,et al.  Characterization of a Ca2+-stimulated lipid peroxidizing system in the sea urchin egg. , 1985, Developmental biology.

[10]  D. Epel,et al.  Fertilization stimulates lipid peroxidation in the sea urchin egg. , 1985, Developmental biology.

[11]  A. Fujiwara,et al.  Effect of Several Redox Dyes on the Respiration of Unfertilized Eggs of Sea Urchin , 1984 .

[12]  M. Mita,et al.  Change in the levels of adenine nucleotides in sea urchin eggs and embryos during early development , 1984 .

[13]  A. Fujiwara,et al.  Stage Specific Effects on Sea Urchin Embryogenesis of Zn2+, Li+, several Inhibitors of cAMP‐Phosphodiesterase and Inhibitors of Protein Synthesis , 1983, Development, growth & differentiation.

[14]  B. Shapiro,et al.  Hydrogen peroxide production, chemiluminescence, and the respiratory burst of fertilization: interrelated events in early sea urchin development. , 1978, Proceedings of the National Academy of Sciences of the United States of America.

[15]  H. Bresch Mitochondrial profile densities and areas in different developmental stages of the sea urchin Sphaerechinus granularis. , 1978, Experimental cell research.

[16]  D. Epel,et al.  Does ADP regulate respiration following fertilization of sea urchin eggs? , 1969, Experimental cell research.

[17]  Eric H. Davidson,et al.  Gene activity in early development , 1968 .

[18]  L. Ernster,et al.  [5] Use of artificial electron acceptors for abbreviated phosphorylating electron transport: Flavin-cytochrome c , 1967 .

[19]  T. Yanagisawa,et al.  Acid-soluble nucleotides in the sea urchin egg. II. Uridine diphosphate sugars. , 1966, Embryologia.

[20]  H. Heldt,et al.  ENDOGENOUS ADP OF MITOCHONDRIA, AN EARLY PHOSPHATE ACCEPTOR OF OXIDATIVE PHOSPHORYLATION AS DISCLOSED BY KINETIC STUDIES WITH C14 LABELLED ADP AND ATP AND WITH ATRACTYLOSIDE. , 1965, Biochemical and biophysical research communications.

[21]  M. Sugiyama,et al.  POLAROGRAPHIC STUDIES OF OXYGEN UPTAKE OF SEA URCHIN EGGS , 1963 .

[22]  T. Hultin Acid-soluble nucleotides in the early development of Psammechinus miliaris. , 1957, Experimental cell research.

[23]  H. Mahler [120] DPNH cytochrome c reductase (animal) , 1955 .

[24]  O. H. Lowry,et al.  Protein measurement with the Folin phenol reagent. , 1951, The Journal of biological chemistry.

[25]  O. Warburg,et al.  Über die Oxydationen in lebenden Zellen nach Versuchen am Seeigelei , 1910 .

[26]  O. Warburg Beobachtungen über die Oxydationsprozesse im Seeigelei. , 1908 .