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Congress Abstracts - Society for Developmental Biology

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covering the surface by connections <strong>for</strong>med through protein interactions. At certain confocal sections of EB, instead of a round<br />

boundary, a polygonal boundary was observed even though the EB appeared round under conventional microscope. In these polygonal<br />

boundaries, β-catenin positive guarding epithelial cells were positioned on every corner of the polygon. In the inner portion of the EB,<br />

undifferentiated β-catenin positive cells express β-catenin in the nucleus. As the initially simple shape of EB becomes more and more<br />

intricate during development, we revealed that more β-catenin positive cells were also observed in this complex structure. Based on<br />

these results, we predicted β-catenin to play different roles while guarding epithelial cells or undifferentiated stem cells in the inner<br />

portion of EB in in vitro culture system. In this early differentiation process, phosphorylation of β-catenin may be a critical factor <strong>for</strong><br />

fate determination of the human stem cell.<br />

Program/Abstract # 410<br />

Organ-specific regulation of steroidogenesis by Hoxb9<br />

Gardiner, Jennifer (Institute of Cancer Research, UK)<br />

The gonads and adrenal cortex are derived from the same cell population, known as the adreno-gonadal primordium (AGP). The organ<br />

primordia separate from one another at around E11 in the mouse, and the testis and adrenal gland produce different steroidogenic<br />

enzymes from E13.5. Steroidogenesis is controlled by a master regulator transcription factor, steroidogenic factor 1 (Sf1). However,<br />

the genetic cues directing differential steroid production are currently poorly understood. Hox genes are well-documented regulators<br />

of embryonic patterning. Differential Hox gene expression was observed in the developing steroidogenic organs; Hoxb9 is expressed<br />

in the adrenal gland, Hoxd9 in the testis. In order to investigate the role of Hox genes in regulation of steroidogenesis, we have<br />

generated a transgenic mouse, named Sf1:Hoxb9, in which Hoxb9 is misexpressed under the control of Sf1. Sf1:Hoxb9 mice exhibit an<br />

increase in the number of ‘adrenal-like’ cells – those producing enzymes involved in adrenal steroidogenesis - in the developing testis<br />

from E13.5. We have investigated the cause of this phenotype, and further analysed the requirement <strong>for</strong> Hoxb9 in adrenal<br />

steroidogenesis in vitro.<br />

Program/Abstract # 411<br />

Cell fate mapping and specification of the coelomic lining epithelium in the avian embryo<br />

Arraf, Alaa; Yelin, Ronit; Schultheiss, Thomas M. (Technion-Israel Institute of Technology, Israel)<br />

Background: The coelomic lining epithelium of the embryo is composed of a single cell layer that invests the external surface of the<br />

viscera and the inner surface of the body wall. Studies indicate that the coelomic lining epithelium is an active tissue which<br />

participates in organogenesis of different significant organs including heart epicardium, liver, lung and gonads, but the full extent of<br />

the developmental potential of the coelomic lining is not known. Specification of the precise differential anatomical site in the anterioposterior<br />

axis, and the temporal sequence of the emergence of the lining cells are crucial <strong>for</strong> understanding of the molecular and<br />

cellular regulators that determines the coelomic lining cells` fate. Methods: We are using a cell tracking technique in which<br />

microinjection of the fluorescent vital DiI into the coelomic cavity of stage 12 avian embryo is analyzed after different time points of<br />

incubation. In addition we use histological methods, including in situ hybridization and immunohistochemistry to detect coexpression<br />

of DiI with specific markers of the candidate`s coelomic lining derived cells. Plastic sections of different stages embryos<br />

are used to study exact morphological development in the coelomic cavity region. Results: We have validated that coelomic injection<br />

of DiI at different stages, labels only the coelomic lining and not any of the underlying mesenchymal cells. We will present initial<br />

results regarding the cell fates of coelomic lining epithelium -derived cells and the timing of their departure from the coelomic lining.<br />

Program/Abstract # 412<br />

Scarb2a is essential <strong>for</strong> Notochord Development in Zebrafish<br />

Díaz Téllez, Abigail; Carrillo Rosas S.; Ramos Balderas J.; Zampedri C.; Maldonado E. (Universidad Nacional Autonoma de<br />

México, Mexico Distrito Federal, Mexico)<br />

Scarb2 is a membrane glycoprotein, whit two tran-membrane sites, 11 sites <strong>for</strong> N-glycosylation and a C-terminal di-leucine motif.<br />

Mutations in Scarb2 were described as a causing of Action Myclonus Renal Failure Syndrome (AMRF), which is characterized by<br />

progressive myoclonus epilepsy. Zebrafish has three copies of scarb2 (scarb2a, scarb2b and scab2c). Scarb2a insertional-mutant was<br />

obtained in a large-scale <strong>for</strong>ward genetic screening. This mutant is characterized by the presence of vesicular bodies in the brain at 1<br />

dpf and hypopigmentation at 2 dpf both phenotypes are restored at 3 dpf. However, since 1 dpf scarb2a mutant shows defects in the<br />

notochord <strong>for</strong>mation. There<strong>for</strong>e, we are using this mutant as model to gain better understanding in how Scarb2 works during<br />

notochord <strong>for</strong>mation. Through electronic microscopy, we have observed that vacuole notochord cells of scarb2a mutant are smalles.<br />

In situ hybridization revealed that scarb2a is expressed in the brain and in the notochord at early stages, also in the Scarb2a mutants<br />

there is a disordes in collagen II expression. Actually, experiments are ongoing to decipher if the defect in the notochord of scar2a<br />

Zebrafish mutant are cell autonomous or non-autonomous.<br />

Program/Abstract # 413<br />

<strong>Developmental</strong> hierarchy, cell fate regulation and carcinogenesis: a view from the Drosophila model<br />

Sinha, Pradip (Indian Institute of Technology Kanpur, India)<br />

Not all cells in a lineage hierarchy trans<strong>for</strong>m neoplastically when oncogenically targeted. <strong>Developmental</strong> disposition of a target cell,<br />

there<strong>for</strong>e, is a critical cancer determinant. A growing body of literature now shows that a majority of cancer cells of origin display<br />

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