Magdalena Zernicka-Goetz
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About
Magdalena Zernicka-Goetz is a Professor and Principal Investigator at the California Institute of Technology in the United States. Her research focuses on embryonic development, particularly in the areas of stem cell-derived embryo models and the mechanisms guiding axis formation during development. Recent publications include studies on the assembly of human and mouse embryo models and the application of AI to analyze variability in stem cell models.
Recent Grants
Grant: Close
Embryo architecture, potency and tissue interactions during mouse and human development
Open Date: 2019-09-01
Close Date: 2023-06-30
Grant: Close
Embryo architecture, potency and tissue interactions during mouse and human development
Open Date: 2018-04-01
Close Date: 2023-03-31
Grant: Close
Self-Organising Capacity of Stem Cells during Implantation and Early Post-implantation Development: Implications for Human Development
Open Date: 2016-01-01
Close Date: 2020-12-31
Grant: Close
Regulation and dynamics of progressive cell fate transitions and morphogenesis during development of the early mouse embryo.
Open Date: 2013-04-01
Close Date: 2018-06-30
Grant: Close
Zygote viability judged by image analysis.
Open Date: 2008-08-01
Close Date: 2011-12-31
Articles (10)
Year:
2025
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2025
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2025
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2025
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2023
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2023
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2023
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2023
Year:
2023
Individual cells within de novo polarising tubes and cavities must integrate their forming apical domains into a centralised apical membrane initiation site (AMIS). This is necessary to enable organised lumen formation within multi‐cellular tissue. Despite the well‐documented importance of cell division in localising the AMIS, we have found a division‐independent mechanism of AMIS localisation that relies instead on Cadherin‐mediated cell–cell adhesion. Our study of de novo polarising mouse embryonic stem cells (mESCs) cultured in 3D suggests that cell–cell adhesion localises apical proteins such as PAR‐6 to a centralised AMIS. Unexpectedly, we also found that mESC clusters lacking functional E‐cadherin still formed a lumen‐like cavity in the absence of AMIS localisation but did so at a later stage of development via a “closure” mechanism, instead of via hollowing. This work suggests that there are two, interrelated mechanisms of apical polarity localisation: cell adhesion and cell division. Alignment of these mechanisms in space allows for redundancy in the system and ensures the development of a coherent epithelial structure within a growing organ.
Year:
2022
Collaborators (3)
Ralf Mikut
Head of Research Area
Karlsruhe Institute of Technology
Clare E Buckley
-
Jay Shendure
Professor
University of Washington
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