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Force Generation, Transmission, and Integration during Cell and Tissue Morphogenesis
Abstract
Cell shape changes underlie a large set of biological processes ranging from cell division to cell motility. Stereotyped patterns of cell shape changes also determine tissue remodeling events such as extension or invagination. In vitro and cell culture systems have been essential to understanding the fundamental physical principles of subcellular mechanics. These are now complemented by studies in developing organisms that emphasize how cell and tissue morphogenesis emerge from the interplay between force-generating machines, such as actomyosin networks, and adhesive clusters that transmit tensile forces at the cell cortex and stabilize cell-cell and cell-substrate interfaces. Both force production and transmission are self-organizing phenomena whose adaptive features are essential during tissue morphogenesis. A new era is opening that emphasizes the similarities of and allows comparisons between distant dynamic biological phenomena because they rely on core machineries that control universal features of cytomechanics.
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“The mechanisms underlying junctional positioning and coupling to the contractile actomyosin network to provide tensile strength to the barrier have been mostly explored in simple epithelia in lower organisms or in cell culture32, 33.”
From E-cadherin integrates mechanotransduction and EGFR signaling to control junctional tissue polarization and tight junction positioning (2017) · cites this paper as [32]
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Metadata
- Authors
- Lecuit, T., Lenne, P.-F., & Munro, E.
- Affiliations
- Centre National de la Recherche Scientifique (FR)
- University of Chicago (US)
- Venue
- Annual Review of Cell and Developmental Biology
- Publisher
- Annual Reviews
- Published
- 2011-11-10
- Volume
- 27
- Issue
- 1
- Pages
- 157-184
- ISSN
- 1081-0706 (ISSN-L)
- 1530-8995
- OpenAlex
- W2121492835
- Cited by
- 621
- References
- 206
- Citations by year
- 2026: 36 · 2025: 39 · 2024: 45 · 2023: 44 · 2022: 43 · 2021: 49 · 2020: 45 · 2019: 47 · 2018: 44 · 2017: 46 · 2016: 41 · 2015: 42 · 2014: 41 · 2013: 39 · 2012: 17
- FWCI
- 2.73
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Annual Review of Cell and Developmental Biology (publishedVersion)
- PubMed (publishedVersion)
- HAL (submittedVersion)
- Funders
- Centre National de la Recherche Scientifique
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular Mechanics and Interactions
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Microtubule and mitosis dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Skin and Cellular Biology Research
- Keywords
- cell shape changes, tissue morphogenesis, force generation, force transmission, actomyosin network, cell adhesion, cell cortex, cell mechanics, tissue remodeling, cell motility, cell division, self-organization, cell-substrate interaction
- MeSH terms
- Animals, Biomechanical Phenomena, Cell Adhesion, Cell Movement, Cytoskeleton, Microfilament Proteins, Actin Cytoskeleton, Morphogenesis, Stress, Mechanical, Myosin Type II, Cell Shape, Actin-Related Protein 2-3 Complex
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
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