Cellular mechanisms of gastrulation: A combined experimental and modelling study

Lead Research Organisation: University of Dundee
Department Name: School of Life Sciences

Abstract

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Technical Summary

This study focuses on exploration of the cellular mechanisms that drive differentiation and movement of cells during gastrulation in the chick embryo, using a highly integrated experimental and mathematical modelling approach. The experimental approach will make extensive use of a newly developed membrane targeted GFP strain in combination with a newly build Digital Light Sheet Microscope (DSLM), which allows imaging of large parts of the embryo at enough (0.5um) resolution to distinguish important cellular events such as shape changes, protrusion formation for all cells in the embryo. The mathematical modelling will be performed using two kinds of models: continuous models represented by a system of coupled partial differential equations and an individual-cell based model, an extension of previous joint work on gastrulation.
Using these approaches we will study:
1. The chemical and mechanical interactions of cells in the epiblast and hypoblast and the influence of these interactions to the formation of primitive streak. We will focus on the role of ingression of epiblast cells to form hypoblast during streak formation. The analysis of these tissue interactions will require the further development of our experimental and modelling techniques to three-dimensional objects.
2. The formation of the primitive groove and the mechanism of ingression of mesendoderm epiblast cells. We expect that our experiments and simulations will identify the mechano-chemical signals, mechanisms and forces that result in the formation of primitive groove and of the cell flows of the epiblast towards the streak. We will explore the changes in adhesion dynamics of the cells during their ingression through the streak.
3. The mechano-chemical signals controlling the cellular flows of the mesenchyme cells during their collective migration to their targets and the feedback between signalling and movement and its resulting emergent properties important for tissue formation and morphogenesis.

Planned Impact

The research proposed is devoted to the investigation of the mechanisms governing gastrulation, a central process in the development of all higher animals. Findings made here will greatly increase our understanding of how cell-cell signalling directs cellular events, like differentiation, proliferation and migration, to build a complex 3 dimensional tissue structure. This is important for understanding development and the origin and cause of many congenital defects. Gastrulation is core material of many Life Sciences and Medical Text books. Provided the research proposed here will proceed as anticipated some of the findings made here are expected to become textbook material and therefore besides being relevant to the immediate academic circle carrying out this research it will affect many students of medical and life sciences.
The key processes of gastrulation such as directed collective migration, ingression and EMT (epithelial to mesenchymal transition) are also central to understanding other biological processes using similar cellular mechanisms processes such as wound healing, tissue repair and regeneration. Failure of proper control of these mechanisms is key to the development of autoimmune diseases and metastasis of cancer cells. Therefore findings made here will be of direct relevance to researchers in these areas. Finally, understanding the mechanisms by which cells organise themselves into tissues and discovering the signals that control their organisation are essential for the rational use of embryonic stem cells in regenerative medicine. It is by no means clear how suitably primed embryonic stem cells injected into organs (brain, heart) in the body, migrate to the right positions and organise themselves in the correct manner in the target tissues to repair defects in-situ. It is evident that the suucesful manipulation of stem cells will require understanding of the processes that we study here, namely directed cell migration, cell-cell interactions and interactions between behaviour and signalling. Therefore the research proposed here will in the longer term (5-10 years) undoubtedly have many practical applications in these increasingly important areas of medicine and healthcare, affecting researchers and practitioners working in the academic as well as in the commercial private sector.
Important interdisciplinary training will be provided to the PDRAs involved as well as associated PhD and master students. Dr Manli Chuai has worked 6 years as fully qualified doctor in China, completed a PhD in life sciences and now has gained expertise and experience in modelling. The modeller on the project will gain considerable experience in Life Sciences.
The research conducted generates many exquisite images both from the experiments and computer simulations. They have been and will be part of exhibitions in the local, national and international science museums.
The Life Sciences sector has an important economic impact in Dundee, contributing around 16% of the city's GDP. A range of activities and organisations in the city connect scientists with the public. In recognition of the economic and social impact of these interactions, the College of Life Sciences won the BBSRC "Excellence with Impact" Award in 2011. The University of Liverpool Maths Outreach Team runs activities in schools for pupils and students of all ages. These include the Liverpool Mathematical Societies FunMaths Roadshow, the Dragon Quiz, GCSE revision sessions and workshops. It also organises CPD events for both primary and secondary teachers, and a Pop-Maths Quiz and various competitions and Masterclasses for Year 6 to 13 pupils. The conducted research will be used in these activities as examples of the use of math in the analysis of real-life problems.
 
Title Reconstruction of distinct vertebrate gastrulation modes via modulation of key cell behaviors in the chick embryo 
Description Movie S1. Development of control embryo from stage HH1 to HH3+. The movie shows the development of a control embryo (left panel) and a zoom-in of the formation of the primitive streak (right panel). Inset side 650 µm. The time interval is 3 minutes., Movie S2. Strain rates and deformation grid of control embryo from stage HH1 to HH3+. The movie shows a bright field image (top panel) and strain rate tensor of the same embryo (bottom panel) Isotropic strain rate is colored blue (contraction) to red (expansion) scale bar 500 µm. The time interval is 3 minutes. Movie S3. Development of embryo treated with FGF signaling inhibitor LY287455. The movie shows a bright field image (top panel) and strain rate tensor of the same embryo (bottom panel). Isotropic strain rate is colored blue (contraction) to red (expansion) scale bar 500 µm. The time interval is 3 minutes. Movie S4. Formation of an ectopic circular primitive streak in FGF2 treated embryo. The movie shows the development of an FGF2-treated embryo (left panel) and a zoom-in of the formation of the ectopic circular primitive streak (right panel). Inset side 650 µm. The time interval is 3 minutes. Movie S5. Strain rates and deformation grid of embryo treated with FGF2. The movie shows a bright field image (top panel) and strain rate tensor of the same embryo (bottom panel) Isotropic strain rate colored blue (contraction) to red (expansion) scale bar 500 µm. The time interval is 3 minutes. Movie S6. Migration of mesoderm cells after addition of FGF2. Focusing deeper into the embryo shows that the mesoderm cells ingressing through the circular primitive streak migrate towards the center of the embryo. The time interval is 3 minutes. Movie S7. Formation of large invagination of the central epiblast in embryos treated with CHIR+LDN. The movie shows the development of a CHIR + LDN treated embryo (left panel) and a zoom-in of the formation of the large invagination in the central epiblast (right panel). Inset side 650 µm. The time interval is 3 minutes. Movie S8. Strain rates and deformation grid of embryo treated with CHIR+LDN. The movie shows a bright field image (top panel) and strain rate tensor of the same embryo (bottom panel) Isotropic strain rate colored blue (contraction) to red (expansion) scale bar 500 µm. The time interval is 3 minutes. Movie S9. Formation of an invaginating lip in an embryo treated with Axitinib. The movie shows the development of an Axitinib-treated embryo (left panel) and a zoom-in of the formation of the invaginating lip (right panel). Inset side 650 µm. The time interval is 3 minutes. Movie S10. Strain rates and deformation grid of embryo treated with Axitinib. The movie shows a bright field image (left panel) and strain rate tensor of the same embryo (right panel) Isotropic strain rate colored blue (contraction) to red (expansion) scale bar 500 µm. The time interval is 3 minutes. Movie S11. Comparison of the tip of streak formation in control embryo and embryo treated with 100 nM Axitinib. The time interval is 3 minutes. 
Type Of Art Film/Video/Animation 
Year Produced 2022 
URL https://discovery.dundee.ac.uk/en/datasets/reconstruction-of-distinct-vertebrate-gastrulation-modes-...
 
Description We have discovered new cellular mechanisms underlying streak formation and validated a chemotactic mechanisms guiding the migration of the mesendoderm cells after their ingression through the streak. We have switched almost exclusively to using the light sheet microscope for in vivo imaging, which delivers very high resolution images at a large scale. This microscope in combination with a novel chick strain expressing a GFP tagged membrane marker allows us to image all the epiblast cells in the embryo. We have so far characterised the cellular mechanisms that drive the formation of the primitive streak. We have shown that strek formation is driven by a combination of apical contraction of mesendoderm cells and directed intercalation of these cells. We have furthermore shown that both mechanism require the action of Myosin II. We are now performing a series of perturbation experiments to probe which are the key signalling pathways controlling myosin activity during streak formation. We have furthermore established methods to study the long term migration of mesendoderm cells in the light sheet microscope.
This will allow us to further characterise the signals that control mesendoderm migration. Finally we have established condition where we can isolate mesendoderm cells from the embryo and assess the chemotactic response in an in-vitro chemotaxis chamber. This allows us to study the detailed response (changes in cytoskeleton) of these cells to defined signal gradients. We have also shown that cells respond very strongly to an as yet uncharacterised factor detected via GPCR coupled receptors and we are now trying to further identify this novel factor.
In collaboration with our partner in Liver pool we have developed a vertex based model that allows us to investigate which behaviours ( cell division, ingression and intercalation) contribute to primitive streak formation. This work is still on going.
Exploitation Route The work will result in publications both in biology as well as in novel modeling approaches. This will be taken forward in publication as well as further research by us and others.
Sectors Pharmaceuticals and Medical Biotechnology,Other