Click
here to close Hello! We notice that
you are using Internet Explorer, which is not supported by Echinobase
and may cause the site to display incorrectly. We suggest using a
current version of Chrome,
FireFox,
or Safari.
Acta Histochem
2008 Jan 01;1104:265-75. doi: 10.1016/j.acthis.2007.11.004.
Show Gene links
Show Anatomy links
Hyalin is a cell adhesion molecule involved in mediating archenteron-blastocoel roof attachment.
Carroll EJ
,
Hutchins-Carroll V
,
Coyle-Thompson C
,
Oppenheimer SB
.
???displayArticle.abstract???
The US National Institutes of Health has designated the sea urchin embryo as a model organism because around 25 discoveries in this system have led to insights into the physiology of higher organisms, including humans. Hyalin is a large glycoprotein in the hyaline layer of sea urchin embryos that functions to maintain general adhesive relationships in the developing embryo. It consists of the hyalin repeat domain that has been identified in organisms as diverse as bacteria, worms, flies, mice, sea urchins and humans. Here we show, using a polyclonal antibody raised against the 11.6 S species of hyalin, that it localizes at the tip of the archenteron and on the roof of the blastocoel exactly where these two structures bond in an adhesive interaction that has been of interest for over a century. In addition, the antibody blocks the interaction between the archenteron tip and blastocoel roof. These results, in addition to other recent findings from this laboratory that will be discussed, suggest that hyalin is involved in mediating this cellular interaction. This is the first demonstration that suggests that hyalin functions as a cell adhesion molecule in many organisms, including humans.
Alvarez,
Exogenous hyalin and sea urchin gastrulation, Part II: hyalin, an interspecies cell adhesion molecule.
2008, Pubmed,
Echinobase
Alvarez,
Exogenous hyalin and sea urchin gastrulation, Part II: hyalin, an interspecies cell adhesion molecule.
2008,
Pubmed
,
Echinobase
Callebaut,
HYR, an extracellular module involved in cellular adhesion and related to the immunoglobulin-like fold.
2000,
Pubmed
Cerra,
Lectin histochemistry of the hyaline layer around the larvae of Patiriella species (Asteroidea) with different developmental modes.
1999,
Pubmed
,
Echinobase
Citkowitz,
The hyaline layer: its isolation and role in echinoderm development.
1971,
Pubmed
,
Echinobase
Contreras,
Exogenous hyalin and sea urchin gastrulation. Part III: biological activity of hyalin isolated from Lytechinus pictus embryos.
2008,
Pubmed
,
Echinobase
Coyle-Thompson,
A novel approach to study adhesion mechanisms by isolation of the interacting system.
2005,
Pubmed
,
Echinobase
Davidson,
The sea urchin genome: where will it lead us?
2006,
Pubmed
,
Echinobase
Edelman,
CAMs and Igs: cell adhesion and the evolutionary origins of immunity.
1987,
Pubmed
Gray,
Resolution and characterization of a major protein of the sea urchin hyaline layer.
1986,
Pubmed
,
Echinobase
GUSTAFSON,
CELLULAR MECHANISMS IN THE MORPHOGENESIS OF THE SEA URCHIN EMBRYO. CELL CONTACTS WITHIN THE ECTODERM AND BETWEEN MESENCHYME AND ECTODERM CELLS.
1963,
Pubmed
,
Echinobase
Hardin,
Target recognition by the archenteron during sea urchin gastrulation.
1990,
Pubmed
,
Echinobase
Hardin,
Short-range cell-cell signals control ectodermal patterning in the oral region of the sea urchin embryo.
1997,
Pubmed
,
Echinobase
Hertzler,
alphaSU2, an epithelial integrin that binds laminin in the sea urchin embryo.
1999,
Pubmed
,
Echinobase
Hoodbhoy,
p62/p56 are cortical granule proteins that contribute to formation of the cortical granule envelope and play a role in mammalian preimplantation development.
2001,
Pubmed
,
Echinobase
Justice,
A calcium-insoluble 6.4 S protein derived from sea urchin cortical granule exudate.
1988,
Pubmed
,
Echinobase
Katow,
An RGDS peptide-binding receptor, FR-1R, localizes to the basal side of the ectoderm and to primary mesenchyme cells in sand dollar embryos.
2001,
Pubmed
,
Echinobase
Khurrum,
Carbohydrate involvement in cellular interactions in sea urchin gastrulation.
2004,
Pubmed
,
Echinobase
Latham,
A putative role for carbohydrates in sea urchin gastrulation.
1999,
Pubmed
,
Echinobase
Latham,
Accessing the embryo interior without microinjection.
1998,
Pubmed
,
Echinobase
McClay,
Regulative capacity of the archenteron during gastrulation in the sea urchin.
1996,
Pubmed
,
Echinobase
McClay,
Sea urchin hyalin: appearance and function in development.
1982,
Pubmed
,
Echinobase
Razinia,
Microplate assay for quantifying developmental morphologies: effects of exogenous hyalin on sea urchin gastrulation.
2007,
Pubmed
,
Echinobase
Sajadi,
Cyclodextrin, a probe for studying adhesive interactions.
2007,
Pubmed
,
Echinobase
Sodergren,
The genome of the sea urchin Strongylocentrotus purpuratus.
2006,
Pubmed
,
Echinobase
Vater,
Purification and characterization of a cortical secretory vesicle membrane fraction.
1989,
Pubmed
,
Echinobase
Wessel,
SFE1, a constituent of the fertilization envelope in the sea urchin is made by oocytes and contains low-density lipoprotein-receptor-like repeats.
2000,
Pubmed
,
Echinobase
Wessel,
A molecular analysis of hyalin--a substrate for cell adhesion in the hyaline layer of the sea urchin embryo.
1998,
Pubmed
,
Echinobase