Lithium-Induced respecification of pattern in Paramecium

The long-known teratogenic effects (dorsalisation) of lithium on amphibian embryos has recently raised renewed interest. As it is known that lithium blocks the polyphosphoinositide (PI) cycle, causing a depressed level of myo-inositol, and as injections of myo-inostiol have been shown to rescue the effects of Li+, it was postulated that Li+ causes a flattening of gradients of PI cycle activity underlying the developmental polarities. We have studied the effect of Li+ on the morphogenesis of the unicellular organism, Paramecium. We show (1) that exposure to 25 mM Li+ during division yields precise distorsions of the cortical pattern that can be explained by a uniformisation of surface growth i.e. partial suppression of the right/left and antero/posterior asymmetries and (2) that Li+ effects are rescued by injection of myo- inositol. These results suggest that spatially graded activity of the PI cycle (ensuring in turn a spatially graded distribution of secondary messengers directly involved in the morphogenetic processes) appeared early in evolution. © 1992 Wiley-Liss, Inc.

[1]  J. Beisson,et al.  Cortical morphogenesis in Paramecium: a transcellular wave of protein phosphorylation involved in ciliary rootlet disassembly. , 1991, Developmental biology.

[2]  D. Drubin Development of cell polarity in budding yeast , 1991, Cell.

[3]  H. Guyader,et al.  Duplication of cortical units on the cortex of paramecium: A model involving a Ca2+ wave* , 1991 .

[4]  A. Adoutte,et al.  Cortical alveoli of Paramecium: a vast submembranous calcium storage compartment , 1991, The Journal of cell biology.

[5]  T. Meyer Cell signalling by second messenger waves , 1991, Cell.

[6]  W. McGrew The importance of being alpha , 1990, Nature.

[7]  R. Bradshaw,et al.  Identification and initial characterization of an autocrine pheromone receptor in the protozoan ciliate Euplotes raikovi , 1990, The Journal of cell biology.

[8]  K. Kaji,et al.  Purification and identification of a growth factor produced by Paramecium tetraurelia. , 1990, Biochemical and biophysical research communications.

[9]  H. Guyader,et al.  Modelling of the duplication of cortical units along a kinety of Paramecium using reaction-diffusion equations , 1990 .

[10]  J. Beisson,et al.  Genetic approaches to ciliate pattern formation: from self-assembly to morphogenesis. , 1990, Trends in genetics : TIG.

[11]  Michael J. Berridge,et al.  Neural and developmental actions of lithium: A unifying hypothesis , 1989, Cell.

[12]  B. Livingston,et al.  Lithium evokes expression of vegetal-specific molecules in the animal blastomeres of sea urchin embryos. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[13]  P. V. van Haastert,et al.  Lithium ions induce prestalk-associated gene expression and inhibit prespore gene expression in Dictyostelium discoideum. , 1989, Journal of cell science.

[14]  W. Busa,et al.  Lithium-induced teratogenesis in frog embryos prevented by a polyphosphoinositide cycle intermediate or a diacylglycerol analog. , 1989, Developmental biology.

[15]  J. Beisson,et al.  Development of surface pattern during division in Paramecium. I. Mapping of duplication and reorganization of cortical cytoskeletal structures in the wild type , 1989 .

[16]  J. Beisson,et al.  A contractile cytoskeletal network of Paramecium: the infra ciliary lattice , 1988 .

[17]  J. Berger The Cell Cycle and Regulation of Cell Mass and Macronuclear DNA Content , 1988 .

[18]  A. Forer,et al.  The role of the phosphatidylinositol cycle in mitosis in sea urchin zygotes. Lithium inhibition is overcome by myo-inositol but not by other cyclitols or sugars. , 1987, Experimental cell research.

[19]  J. Beisson,et al.  Organization and dynamics of a cortical fibrous network of Paramecium: The outer lattice , 1987 .

[20]  M. Bornens,et al.  Myosin at the apical pole of ciliated epithelial cells as revealed by a monoclonal antibody , 1986, The Journal of cell biology.

[21]  T. Mustelin,et al.  myo‐Inositol reverses Li+‐induced inhibition of phosphoinositide turnover and ornithine decarboxylase induction during early lymphocyte activation , 1986, European journal of immunology.

[22]  J. Frankel Global patterning in single cells , 1982 .

[23]  M. Schliwa,et al.  Structural interaction of cytoskeletal components , 1981, The Journal of cell biology.

[24]  K J Aufderheide,et al.  Formation and positioning of surface-related structures in protozoa. , 1980, Microbiological reviews.

[25]  J. Knowles An improved microinjection technique in Paramecium aurelia. Transfer of mitochondria conferring erythromycin-resistance. , 1974, Experimental cell research.

[26]  R. Allen FINE STRUCTURE OF MEMBRANOUS AND MICROFIBRILLAR SYSTEMS IN THE CORTEX OF PARAMECIUM CAUDATUM , 1971, The Journal of cell biology.

[27]  T. M. Sonneborn DETERMINATION, DEVELOPMENT, AND INHERITANCE OF THE STRUCTURE OF THE CELL CORTEX* , 1970 .

[28]  V. Tartar Reactions of Stentor coeruleus to certain substances added to the medium. , 1957, Experimental cell research.