Carbohydrate involvement in cellular interactions in sea urchin gastrulation

Acta Histochemica

Volumn 106, Issue 2, 2004, Pages 97-106

  Khurrum, Maria ^a   Hernandez, Astrid ^a   Eskalaei, Melika ^a   Badali, Oliver ^a   Coyle Thompson, Cathy ^a   Oppenheimer, Steven B ^a  

^a CALIFORNIA STATE UNIVERSITY   (United States)

Author keywords

Archenteron attachment; Disaggregation supernatant; Exogastrulation; Sea urchins; Sugars

Indexed keywords

CELLS; ENZYME KINETICS; GLUCOSE; LENSES; MOLECULAR BIOLOGY; OCEAN HABITATS; SODIUM COMPOUNDS; TRANSPARENCY;

ARCHENTERON ATTACHMENT; CELLULAR INTERACTIONS; DISAGGREGATION SUPERNATANT; EXOGASTRULATION; SEA URCHINS;

CARBOHYDRATES;

AGGLUTININ; ALPHA GLUCOSIDASE; ALPHA MANNOSIDASE; ALPHA METHYL MANNOSE; BETA AMYLASE; CARBOHYDRATE; CONCANAVALIN A; FUCOSE; MANNAN; MANNOSE; SELENATE; TUNICAMYCIN; UNCLASSIFIED DRUG; ENZYME INHIBITOR; GLYCOSIDASE; PROTEOGLYCAN;

ARTICLE; CELL AGGREGATION; CELL INTERACTION; CONTROLLED STUDY; DRUG BINDING; DRUG INHIBITION; EMBRYO DEVELOPMENT; GASTRULATION; NONHUMAN; PROTEOGLYCAN SYNTHESIS; SEA URCHIN; ANIMAL; ANIMAL EMBRYO; CELL ADHESION; CELL COMMUNICATION; CYTOLOGY; DRUG EFFECT; ENZYME ACTIVATION; GASTRULA; GENE EXPRESSION REGULATION; METABOLISM; PHYSIOLOGY; PRENATAL DEVELOPMENT;

ECHINOIDEA; LENS CULINARIS; LYTECHINUS PICTUS;

ANIMALS; CELL ADHESION; CELL COMMUNICATION; EMBRYO, NONMAMMALIAN; ENZYME ACTIVATION; ENZYME INHIBITORS; GASTRULA; GENE EXPRESSION REGULATION, DEVELOPMENTAL; GLYCOSIDE HYDROLASES; PROTEOGLYCANS; SEA URCHINS;

EID: 16644380388     PISSN: 00651281     EISSN: 16180372     Source Type: Journal    
DOI: 10.1016/j.acthis.2004.01.001     Document Type: Article

References (43)

1. Akasaka K, Amemiya S, Terayama H. Scanning electron microscopical study of the inside of sea urchin (Pseudocentrotus depressus): effects of aryl betaxyloside, tunicamycin, and deprivation of sulfate ions. Exp Cell Res 1980;129:1-13.
2. Ameye L, De Becker G, Killian C, Wilt F, Kemps R, Kuypers S, Dubois P. Proteins and saccharides of the sea urchin organic matrix of mineralization: characterization and localization in the spine skeleton. J Struct Biol 2001;134:56-66.
3. Contini A, Falugi C, Fasulo S. Developmental regulation of lectin-binding patterns in Paracentrotus lividus gonads, gametes, and early embryos. Acta Histochem 1992;92:179-89.
4. Dolo V, Forti C, Dell'Utri S, Ghersi G, Vittorelli ML. An acid extract from dissociation medium of sea urchin embryo induces mesenchyme differentiation. Cell Biol Int Rep 1992;16:517-32.
5. Ettensohn CA. Cell interactions and mesodermal cell fates in the sea urchin embryo. Development 1992; (Suppl):43-51.
6. Glabe CG, Grabel LB, Vacquier VD, Rosen SD. Carbohydrate specificity of sea urchin sperm binding: a cell surface lectin mediating sperm-egg adhesion. J Cell Biol 1982;94:123-8.
7. Hardin J. The role of secondary mesenchyme cells during sea urchin gastrulation studied by laser ablation. Development 1988;103:317-24.
8. Hardin JD. Archenteron elongation in the sea urchin embryo is a microtubule-independent process. Dev Biol 1987;121:253-62.
9. Haruguchi Y, Horu K, Suzuki G, Suyemitsu T, Ishihara K, Yamasu K. Genomic organization of the gene that encodes the precursor to EGF-related peptides, exogastrula- inducing peptides of the sea urchin Anthocidaris crassispina. Biochim Biophys Acta 2002;1574:311-20.
10. Hawkins RL, Fan J, Hille MB. Gastrulation in the sea urchin, Strongylocentrotus purpuratus, is disrupted by the small laminin peptides YIGSR and IKVAV. Cell Adhes Commun 1995;3:163-77.
11. Heifetz A, Lennarz WJ. Biosynthesis of N-glycosidically linked glycoproteins during gastrulation of sea urchin embryos. J Biol Chem 1979;254:6119-27.
12. Hoshi M. Exogastrulation induced by heavy water in sea urchin larvae. Cell Different 1979;8:431-5.
13. Humphreys T. Chemical dissolution and in vitro reconstruction of sponge cell adhesions. Dev Biol 1963;8: 27-47.
14. Khurrum MR, Weerasinghe GR, Soriano ES, Riman R, Badali O, Gipson S, Medina J, Alfaro J, Navarro VM, Harieg CB, Ngo L, Sakhakorn T, Kirzenbaum L, Khatibi D, Abedi K, Barajas M, Zem GC, Kirszenbaum A, Razi A, Oppenheimer SB. Analysis of surface properties of human cancer cells using derivatized agarose beads. Acta Histochem 2002;104:217-23.
15. Kinoshita S, Saiga H. The role of proteoglycans in the development of sea urchins. I: abnormal development of sea urchins caused by the disturbance of proteoglycan synthesis. Exp Cell Res 1979;123:229-36.
16. Kinoshita S, Yoshii K, Tonegawa Y. Specific binding of lectins with the nucleus of the sea urchin embryo and changes in the lectin affinity of the embryonic chromatin during the course of development. Exp Cell Res 1988;175:148-57.
17. Latham VH, Ducut JL, Rostamiani K, Chun HH, Lopez ME, Herrera S, Oppenheimer SB. A rapid lectin receptor-binding assay: comparative evaluation of sea urchin embryo cell surface lectin receptors. Acta Histochem 1995a;97:89-97.
18. Latham VH, Herrera S, Rostamiani K, Chun HH, Oppenheimer SB. Rapid identification of lectin receptors and their possible function in sea urchin cell systems. Acta Histochem 1995b;97:373-82.
19. Latham VH, Martinez AL, Cazares L, Hamburger H, Tully MJ, Oppenheimer SB. Accessing the embryo interior without microinjection. Acta Histochem 1998; 100:193-200.
20. Latham VH, Oppenheimer SB. A simple image analysis method for evaluating cell binding to derivatized beads. Acta Histochem 1999;101:263-70.
21. Latham VH, Tully MJ, Oppenheimer SB. A putative role for carbohydrates in sea urchin gastrulation. Acta Histochem 1999;101:293-303.
22. Martin EL, Consales C, Davidson EH, Arnone MI. Evidence for a mesodermal embryonic regulator of the sea urchin CyIIa gene. Dev Biol 2001;236:46-63.
23. McClay DR, Logan CY. Regulative capacity of the archenteron during gastrulation in the sea urchin. Development 1996;122:607-16.
24. McClay DR, Peterson RE, Range RC, Winter-Vann AM, Ferkowicz MJ. A micromere induction signal is activated by β-catenin and acts through Notch to initiate specification of secondary mesenchyme cells in the sea urchin embryo. Development 2000;127: 5113-22.
25. Moscona AA. Studies on cell aggregation and demonstration of materials with selective cell-binding activity. Proc Natl Acad Sci USA. 1962;49:742-7.
26. Navarro VM, Walker SL, Badali O, Abundis MI, Ngo L, Weerasinghe G, Barajas M, Zem G, Oppenheimer SB. Analysis of fixed and live cells using derivatized agarose beads. Acta Histochem 2002;104:99-106.
27. Neri A, Roberson M, Connolly D, Oppenheimer SB. Quantitative evaluation of concanavalin A receptor site distributions on the surface of specific populations of embryonic cells. Nature 1975;258:342-4.
28. Ngo L, Barajas M, Weerasinghe G, Zem G, Oppenheimer SB. A new histochemical approach for studying sperm cell surfaces. Acta Histochem 2003;105:21-8.
29. Oppenheimer SB, Carroll EJ. Introduction to embryonic development, 4th ed. Upper Saddle River, NJ, USA. Pearson Education: 2004. p. 138-142.
30. Oppenheimer SB, Meyer JT. Isolation of species-specific and stage-specific adhesion promoting component by disaggregation of intact sea urchin embryo cells. Exp Cell Res 1982;137:472-6.
31. Ozeki Y, Matsui T, Suzuki M, Titani K. Amino acid sequence and molecular characterization of a D-galactose-specific lectin purified from sea urchin (Anthocidaris crassispina) eggs. Biochemistry 1991;30:2391-4.
32. Ozeki Y, Yokota Y, Kato KH, Titani K, Matsui T. Developmental expression of D-galactose-binding lectin in sea urchin (Anthocidaris crassipina) eggs. Exp Cell Res 1995;216:318-24.
33. Pillai MC, Vines CA, Wikramanayake AH, Cherr GN. Polycyclic aromatic hydrocarbons disrupt axial development in sea urchin embryos through a beta-catenin dependent pathway. Toxicology 2003;186:93-108.
34. Roberson M, Neri A, Oppenheimer SB. Distribution of concanavalin A receptor sites on specific populations of embryonic cells. Science 1975;189:639-40.
35. Roberson M, Oppenheimer SB. Quantitative agglutination of specific populations of sea urchin embryo cells with concanavalin A. Exp Cell Res 1975;91:263-8.
36. Roque RL, Herrera S, Yeh TJ, Borisovlljevic TL, Brunick LA, Harritunians T, Addy C, Bada RA, Vaghefi H, Matsumoto S, Piccionelli G, Rodriguez L, Oppenheimer SB. Cell adhesion mechanisms: modeling using derivatized beads and sea urchin cell systems. Acta Histochem 1996;98:441-51.
37. Ruffins SW, Ettensohn CA. A fate map of the vegetal plate of the sea urchin (Lytechinus variegatus) mesenchyme blastula. Development 1996;122:253-63.
38. Schneider E, Nguyen N, Lennarz W. The effects of tunicamycin, an inhibitor of protein glycosylation, on embryonic development in the sea urchin embryo. J Biol Chem 1978;253:2348-55.
39. Sherwood DR, McClay DR. Lv Notch signaling mediates secondary mesenchyme specification in the sea urchin embryo. Development 1999;126:1703-13.
40. Sumitro SB, Sato H. The isotopic effects of D20 in developing sea urchin eggs. Cell Struct Funct 1989;14: 95-111.
41. Suzuki-Nishimura T, Nakagawa H, Uchida MK. D-galactose-specific sea urchin lectin sugar-specifically inhibited histamine release by Datura stramonium agglutinin: differences between sugar-specific effects of sea urchin lectin and those of D-galactose-or L-fucose-specific plant lectins. Jpn J Pharmacol 2001;85:443-52.
42. Tokuoka M, Setoguchi C, Kominami T. Specification and differentiation processes of secondary mesenchyme-derived cells in embryos of the sea urchin Hemicentrotus pulcherrimus. Dev Growth Differ 2002;44:239-50.
43. Yamasu K, Suzuki G, Horii K, Suyemitsu T. Transcriptional regulation of the gene for epidermal growth factor-like peptides in sea urchin embryos. Int J Dev Biol 2000;44:777-84.