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  1. Article ; Online: Mechanical strengthening of cell-cell adhesion during mouse embryo compaction.

    de Plater, Ludmilla / Firmin, Julie / Maître, Jean-Léon

    Biophysical journal

    2024  

    Abstract: Compaction is the first morphogenetic movement of the eutherian mammals and involves a developmentally regulated adhesion process. Previous studies investigated cellular and mechanical aspects of compaction. During mouse and human compaction, cells ... ...

    Abstract Compaction is the first morphogenetic movement of the eutherian mammals and involves a developmentally regulated adhesion process. Previous studies investigated cellular and mechanical aspects of compaction. During mouse and human compaction, cells spread onto each other as a result of a contractility-mediated increase in surface tension pulling at the edges of their cell-cell contacts. However, how compaction may affect the mechanical stability of cell-cell contacts remains unknown. Here, we used a dual pipette aspiration assay on cell doublets to quantitatively analyze the mechanical stability of compacting mouse embryos. We measured increased mechanical stability of contacts with rupture forces growing from 40 to 70 nN, which was highly correlated with cell-cell contact expansion. Analyzing the dynamic molecular reorganization of cell-cell contacts, we find minimal recruitment of the cell-cell adhesion molecule Cdh1 (also known as E-cadherin) to contacts but we observe its reorganization into a peripheral adhesive ring. However, this reorganization is not associated with increased effective bond density, contrary to previous reports in other adhesive systems. Using genetics, we reduce the levels of Cdh1 or replace it with a chimeric adhesion molecule composed of the extracellular domain of Cdh1 and the intracellular domain of Cdh2 (also known as N-cadherin). We find that reducing the levels of Cdh1 impairs the mechanical stability of cell-cell contacts due to reduced contact growth, which nevertheless show higher effective bond density than wild-type contacts of similar size. On the other hand, chimeric adhesion molecules cannot form large or strong contacts indicating that the intracellular domain of Cdh2 is unable to reorganize contacts and/or is mechanically weaker than the one of Cdh1 in mouse embryos. Together, we find that mouse embryo compaction mechanically strengthens cell-cell adhesion via the expansion of Cdh1 adhesive rings that maintain pre-compaction levels of effective bond density.
    Language English
    Publishing date 2024-03-26
    Publishing country United States
    Document type Journal Article
    ZDB-ID 218078-9
    ISSN 1542-0086 ; 0006-3495
    ISSN (online) 1542-0086
    ISSN 0006-3495
    DOI 10.1016/j.bpj.2024.03.028
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Morphogenesis of the human preimplantation embryo: bringing mechanics to the clinics.

    Firmin, Julie / Maître, Jean-Léon

    Seminars in cell & developmental biology

    2021  Volume 120, Page(s) 22–31

    Abstract: During preimplantation development, the human embryo forms the blastocyst, the structure enabling uterine implantation. The blastocyst consists of an epithelial envelope, the trophectoderm, encompassing a fluid-filled lumen, the blastocoel, and a cluster ...

    Abstract During preimplantation development, the human embryo forms the blastocyst, the structure enabling uterine implantation. The blastocyst consists of an epithelial envelope, the trophectoderm, encompassing a fluid-filled lumen, the blastocoel, and a cluster of pluripotent stem cells, the inner cell mass. This specific architecture is crucial for the implantation and further development of the human embryo. Furthermore, the morphology of the human embryo is a prime determinant for clinicians to assess the implantation potential of in vitro fertilized human embryos, which constitutes a key aspect of assisted reproduction technology. Therefore, it is crucial to understand how the human embryo builds the blastocyst. As any material, the human embryo changes shape under the action of forces. Here, we review recent advances in our understanding of the mechanical forces shaping the blastocyst. We discuss the cellular processes responsible for generating morphogenetic forces that were studied mostly in the mouse and review the literature on human embryos to see which of them may be conserved. Based on the specific morphological defects commonly observed in clinics during human preimplantation development, we discuss how mechanical forces and their underlying cellular processes may be affected. Together, we propose that bringing tissue mechanics to the clinics will advance our understanding of human preimplantation development, as well as our ability to help infertile couples to have babies.
    MeSH term(s) Animals ; Blastocyst/physiology ; Humans ; Mice
    Language English
    Publishing date 2021-07-10
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 1312473-0
    ISSN 1096-3634 ; 1084-9521
    ISSN (online) 1096-3634
    ISSN 1084-9521
    DOI 10.1016/j.semcdb.2021.07.005
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Mechanics of blastocyst morphogenesis.

    Maître, Jean-Léon

    Biology of the cell

    2017  Volume 109, Issue 9, Page(s) 323–338

    Abstract: During pre-implantation development, the mammalian zygote transforms into the blastocyst, the structure that will implant the embryo in the maternal uterus. Consisting of a squamous epithelium enveloping a fluid-filled cavity and the inner cell mass, the ...

    Abstract During pre-implantation development, the mammalian zygote transforms into the blastocyst, the structure that will implant the embryo in the maternal uterus. Consisting of a squamous epithelium enveloping a fluid-filled cavity and the inner cell mass, the blastocyst is sculpted by a succession of morphogenetic events. These deformations result from the changes in the forces and mechanical properties of the tissue composing the embryo. Here, I review the recent studies, which, for the first time, informed us on the mechanics of blastocyst morphogenesis.
    Language English
    Publishing date 2017-09
    Publishing country England
    Document type Journal Article ; Review
    ZDB-ID 245745-3
    ISSN 1768-322X ; 0399-0311 ; 0248-4900
    ISSN (online) 1768-322X
    ISSN 0399-0311 ; 0248-4900
    DOI 10.1111/boc.201700029
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Mécanique de la formation de la masse cellulaire interne chez la souris.

    Maître, Jean-Léon

    Biologie aujourd'hui

    2017  Volume 211, Issue 2, Page(s) 137–148

    Abstract: During the very first days of mammalian development, the embryo forms a structure called the blastocyst. The blastocyst consists of two cell types: the trophectoderm (TE), which implants the embryo in the uterus and the inner cell mass (ICM), which gives ...

    Title translation Mechanics of inner cell mass formation.
    Abstract During the very first days of mammalian development, the embryo forms a structure called the blastocyst. The blastocyst consists of two cell types: the trophectoderm (TE), which implants the embryo in the uterus and the inner cell mass (ICM), which gives rise to all cells of the mammalian body. Previous works identified how cells differentiate according to their position within the embryo: TE for surface cells and ICM for internal cells. It is therefore essential to understand how cells acquire their position in the first place. During the formation of the blastocyst, cells distort and relocate as a consequence of forces that are generated by the cells themselves. Recently, several important studies have identified the forces and cellular mechanisms leading to the shaping of the ICM. Here, I describe how these studies led us to understand how contractile forces shape the mammalian embryo to position and differentiate the ICM.
    MeSH term(s) Animals ; Biomechanical Phenomena/physiology ; Blastocyst Inner Cell Mass/physiology ; Cell Differentiation ; Embryo, Mammalian ; Embryonic Development/physiology ; Female ; Humans ; Infant, Newborn ; Mice
    Language French
    Publishing date 2017-12-13
    Publishing country France
    Document type Journal Article ; Review
    ISSN 2105-0686
    ISSN (online) 2105-0686
    DOI 10.1051/jbio/2017021
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Multiscale morphogenesis of the mouse blastocyst by actomyosin contractility.

    Özgüç, Özge / Maître, Jean-Léon

    Current opinion in cell biology

    2020  Volume 66, Page(s) 123–129

    Abstract: During preimplantation development, the mouse embryo forms the blastocyst, which consists of a squamous epithelium enveloping a fluid-filled lumen and a cluster of pluripotent cells. The shaping of the blastocyst into its specific architecture is a ... ...

    Abstract During preimplantation development, the mouse embryo forms the blastocyst, which consists of a squamous epithelium enveloping a fluid-filled lumen and a cluster of pluripotent cells. The shaping of the blastocyst into its specific architecture is a prerequisite to implantation and further development of the embryo. Recent studies identified the central role of the actomyosin cortex in generating the forces driving the successive steps of blastocyst morphogenesis. As seen in other developing animals, actomyosin functions across spatial scales from the subcellular to the tissue levels. In addition, the slow development of the mouse embryo reveals that actomyosin contractility operates at multiple timescales with periodic cortical waves of contraction every ∼80 s and tissue remodeling over hours.
    MeSH term(s) Actin Cytoskeleton ; Actomyosin/metabolism ; Animals ; Blastocyst/cytology ; Embryonic Development ; Mice ; Models, Biological ; Morphogenesis
    Chemical Substances Actomyosin (9013-26-7)
    Language English
    Publishing date 2020-07-22
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 1026381-0
    ISSN 1879-0410 ; 0955-0674
    ISSN (online) 1879-0410
    ISSN 0955-0674
    DOI 10.1016/j.ceb.2020.05.002
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: A theoretical understanding of mammalian preimplantation development.

    Herrera-Delgado, Edgar / Maître, Jean-Léon

    Cells & development

    2021  Volume 168, Page(s) 203752

    Abstract: The blastocyst has long been a hallmark system of study in developmental biology due to its importance in mammalian development and clinical relevance for assisted reproductive technologies. In recent years, the blastocyst is emerging as a system of ... ...

    Abstract The blastocyst has long been a hallmark system of study in developmental biology due to its importance in mammalian development and clinical relevance for assisted reproductive technologies. In recent years, the blastocyst is emerging as a system of study for mathematical modelling. In this review, we compile, to our knowledge, all models describing preimplantation development. Coupled with experiments, these models have provided insight regarding the morphogenesis and cell-fate specification throughout preimplantation development. In the case of cell-fate specification, theoretical models have provided mechanisms explaining how proportion of cell types are established and maintained when confronted to perturbations. For cell-shape based models, they have described quantitatively how mechanical forces sculpt the blastocyst and even predicted how morphogenesis could be manipulated. As theoretical biology develops, we believe the next critical stage in modelling involves an integration of cell fate and mechanics to provide integrative models of development at distinct spatiotemporal scales. We discuss how, building on a balanced base of mechanical and chemical models, the preimplantation embryo will play a key role in integrating these two faces of the same coin.
    MeSH term(s) Animals ; Blastocyst/metabolism ; Cell Differentiation ; Embryonic Development ; Mammals ; Morphogenesis
    Language English
    Publishing date 2021-10-08
    Publishing country Netherlands
    Document type Journal Article ; Review ; Research Support, Non-U.S. Gov't
    ISSN 2667-2901
    ISSN (online) 2667-2901
    DOI 10.1016/j.cdev.2021.203752
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Stay hydrated: basolateral fluids shaping tissues.

    Schliffka, Markus Frederik / Maître, Jean-Léon

    Current opinion in genetics & development

    2019  Volume 57, Page(s) 70–77

    Abstract: During development, embryos perform a mesmerizing choreography, which is crucial for the correct shaping, positioning and function of all organs. The cellular properties powering animal morphogenesis have been the focus of much attention. In contrast, ... ...

    Abstract During development, embryos perform a mesmerizing choreography, which is crucial for the correct shaping, positioning and function of all organs. The cellular properties powering animal morphogenesis have been the focus of much attention. In contrast, much less consideration has been given to the invisible engine constituted by the intercellular fluid. Cells are immersed in fluid, of which the composition and physical properties have a considerable impact on development. In this review, we revisit recent studies from the perspective of the fluid, focusing on basolateral fluid compartments and taking the early mouse and zebrafish embryos as models. These examples illustrate how the hydration levels of tissues are spatio-temporally controlled and influence embryonic development.
    MeSH term(s) Animals ; Body Water/cytology ; Body Water/metabolism ; Embryonic Development/genetics ; Extracellular Fluid/cytology ; Extracellular Fluid/metabolism ; Mice ; Morphogenesis/genetics ; Zebrafish/genetics ; Zebrafish/growth & development
    Language English
    Publishing date 2019-08-21
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 1077312-5
    ISSN 1879-0380 ; 0959-437X
    ISSN (online) 1879-0380
    ISSN 0959-437X
    DOI 10.1016/j.gde.2019.06.015
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Un point de contrôle développemental synchronise la morphogenèse et la différenciation cellulaire dans l’embryon de mammifère.

    Dumortier, Julien G / Maître, Jean-Léon

    Medecine sciences : M/S

    2018  Volume 34, Issue 3, Page(s) 205–207

    Title translation A developmental checkpoint synchronizes morphogenesis and cellular differentiation in mammalian embryos.
    MeSH term(s) Amnion/embryology ; Animals ; Cell Cycle Checkpoints/genetics ; Cell Cycle Checkpoints/physiology ; Cell Differentiation/physiology ; Embryo, Mammalian/cytology ; Embryonic Development/physiology ; Female ; Genes, Developmental/physiology ; Genes, Switch/physiology ; Humans ; Mice ; Morphogenesis/physiology ; Pregnancy
    Language French
    Publishing date 2018-03-16
    Publishing country France
    Document type News
    ZDB-ID 632733-3
    ISSN 1958-5381 ; 0767-0974
    ISSN (online) 1958-5381
    ISSN 0767-0974
    DOI 10.1051/medsci/20183403005
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  9. Article ; Online: Cell fragmentation in mouse preimplantation embryos induced by ectopic activation of the polar body extrusion pathway.

    Pelzer, Diane / de Plater, Ludmilla / Bradbury, Peta / Eichmuller, Adrien / Bourdais, Anne / Halet, Guillaume / Maître, Jean-Léon

    The EMBO journal

    2023  Volume 42, Issue 17, Page(s) e114415

    Abstract: Cell fragmentation is commonly observed in human preimplantation embryos and is associated with poor prognosis during assisted reproductive technology (ART) procedures. However, the mechanisms leading to cell fragmentation remain largely unknown. Here, ... ...

    Abstract Cell fragmentation is commonly observed in human preimplantation embryos and is associated with poor prognosis during assisted reproductive technology (ART) procedures. However, the mechanisms leading to cell fragmentation remain largely unknown. Here, light sheet microscopy imaging of mouse embryos reveals that inefficient chromosome separation due to spindle defects, caused by dysfunctional molecular motors Myo1c or dynein, leads to fragmentation during mitosis. Extended exposure of the cell cortex to chromosomes locally triggers actomyosin contractility and pinches off cell fragments. This process is reminiscent of meiosis, during which small GTPase-mediated signals from chromosomes coordinate polar body extrusion (PBE) by actomyosin contraction. By interfering with the signals driving PBE, we find that this meiotic signaling pathway remains active during cleavage stages and is both required and sufficient to trigger fragmentation. Together, we find that fragmentation happens in mitosis after ectopic activation of actomyosin contractility by signals emanating from DNA, similar to those observed during meiosis. Our study uncovers the mechanisms underlying fragmentation in preimplantation embryos and, more generally, offers insight into the regulation of mitosis during the maternal-zygotic transition.
    MeSH term(s) Humans ; Animals ; Mice ; Polar Bodies/metabolism ; Actomyosin/metabolism ; Blastocyst ; Chromosomes ; Meiosis ; Oocytes/metabolism ; Spindle Apparatus/genetics ; Myosin Type I/genetics ; Myosin Type I/metabolism
    Chemical Substances Actomyosin (9013-26-7) ; Myo1c protein, mouse ; Myosin Type I (EC 3.6.1.-)
    Language English
    Publishing date 2023-07-10
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 586044-1
    ISSN 1460-2075 ; 0261-4189
    ISSN (online) 1460-2075
    ISSN 0261-4189
    DOI 10.15252/embj.2023114415
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Correction

    Markus Frederik Schliffka / Anna-Francesca Tortorelli / Özge Özgüç / Ludmilla de Plater / Oliver Polzer / Diane Pelzer / Jean-Léon Maître

    eLife, Vol

    Multiscale analysis of single and double maternal-zygotic Myh9 and Myh10 mutants during mouse preimplantation development

    2022  Volume 11

    Keywords Medicine ; R ; Science ; Q ; Biology (General) ; QH301-705.5
    Language English
    Publishing date 2022-03-01T00:00:00Z
    Publisher eLife Sciences Publications Ltd
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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