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Amel, A.

Publications and source records attributed to Amel, A..

2 recordsLinked to original sources

Matrigel inhibits elongation and drives endoderm differentiation in aggregates of mouse embryonic stem cells

Modelling peri-implantation mammalian development using the self-organising properties of stem cells is a rapidly growing field that has advanced our understanding of cell fate decisions occurring in the early embryo. Matrigel, a basement membrane matrix, is a critical substrate used in various protocols for its efficacy in promoting stem cell growth and self-organization. However, its role in driving stem cell lineage commitment, and whether this effect is driven by biochemical or physical cues is not being clearly defined. Here, we grow embryoid bodies in suspension, Matrigel, and agarose, an inert polysaccharide, to attempt to decouple the physical and biochemical roles of Matrigel and better understand how it drives stem cell differentiation. We show that stem cell aggregates in Matrigel are hindered in their ability to elongate compared to those grown in agarose or in suspension indicating that prohibitive role in self-organisation. Aggregates in Matrigel are also driven to differentiate into endoderm with ectoderm differentiation inhibited. Furthermore, these effects are not due to the physical presence of Matrigel as the same effects are not witnessed in aggregates grown in agarose. Our results thus indicate that Matrigel has a significant and complex effect on the differentiation and morphology of embryoid bodies.

developmental biology↗

Wnt and BMP signalling direct anterior/posterior differentiation in aggregates of mouse embryonic stem cells

Stem cell-based embryo models have allowed greater insight into peri-implantation mammalian developmental events that are otherwise difficult to manipulate due to the inaccessibility of the early embryo. The rapid development of this field has resulted in the precise roles of frequently used supplements such as N2, B27 and Chiron in driving stem cell lineage commitment not being clearly defined. Here, we investigate the effects of these supplements on embryoid bodies to better understand their roles in stem cell differentiation. We show that Wnt signalling has a posteriorising effect on stem cell aggregates and directs differentiation towards the mesoderm, as confirmed through the upregulation of posterior and mesodermal markers. N2 and B27 can mitigate these effects and up-regulate the expression of anterior markers. To control the Wnt gradient and the subsequent anterior vs. posterior fate, we make use of a BMP4 signalling centre and show that aggregates in these conditions express cephalic markers. These findings indicate that there is an intricate balance between various culture supplements and their ability to set up the anterior/posterior axis in stem cell embryo models. Summary StatementThe complex reagents used in stembryo protocols have unclear roles in stem cell differentiation in vitro requiring further investigation. This study examines their effects on embryoid bodies.

developmental biology↗