Development and dynamics of cell polarity at a glance
Open accessAbstract
Cells exhibit morphological and molecular asymmetries that are broadly categorized as cell polarity. The cell polarity established in early embryos prefigures the macroscopic anatomical asymmetries characteristic of adult animals. For example, eggs and early embryos have polarized distributions of RNAs and proteins that generate global anterior/posterior and dorsal/ventral axes. The molecular programs that polarize embryos are subsequently reused in multiple contexts. Epithelial cells require apical/basal polarity to establish their barrier function. Migrating cells polarize in the direction of movement, creating distinct leading and trailing structures. Asymmetrically dividing stem cells partition different molecules between themselves and their daughter cells. Cell polarity can develop de novo, be maintained through rounds of cell division and be dynamically remodeled. In this Cell Science at a Glance review and poster, we describe molecular asymmetries that underlie cell polarity in several cellular contexts. We highlight multiple developmental systems that first establish cell/developmental polarity, and then maintain it. Our poster showcases repeated use of the Par, Scribble and Crumbs polarity complexes, which drive the development of cell polarity in many cell types and organisms. We then briefly discuss the diverse and dynamic changes in cell polarity that occur during cell migration, asymmetric cell division and in planar polarized tissues.
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Proper positioning of molecular machines underlies the global process of establishing cell polarity, epithelial apical-basal polarity being a cardinal example.
“The proper positioning of molecular machines underlies the global process of establishing cell polarity, epithelial apical–basal polarity being a cardinal example (reviewed in Campanale et al., 2017).”
From Scribble: A master scaffold in polarity, adhesion, synaptogenesis, and proliferation (2019) · cites this paper as Campanale et al., 2017
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References 123 · Cited by 198
- Authors
- Campanale, J. P., Sun, T. Y., & Montell, D. J.
- Affiliations
- University of California, Santa Barbara (US)
- Venue
- Journal of Cell Science
- Publisher
- The Company of Biologists
- Published
- 2017-04-01
- Volume
- 130
- Issue
- 7
- Pages
- 1201-1207
- ISSN
- 0021-9533 (ISSN-L)
- 1477-9137
- PMC
- PMC5399778
- OpenAlex
- W2599684899
- Cited by
- 198
- References
- 123
- Citations by year
- 2026: 15 · 2025: 13 · 2024: 15 · 2023: 20 · 2022: 21 · 2021: 31 · 2020: 24 · 2019: 20 · 2018: 22 · 2017: 15 · 2015: 1 · 2012: 1
- FWCI
- 2.07
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Journal of Cell Science (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- HighWire Press Open Archive (submittedVersion)
- Funders
- National Institutes of Health (GM46425-22)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular Mechanics and Interactions
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Hippo pathway signaling and YAP/TAZ
- Keywords
- cell polarity, embryonic axis formation, apical-basal polarity, epithelial barrier function, cell migration, asymmetric cell division, stem cell division, Par complex, Crumbs complex, planar cell polarity
- MeSH terms
- Animals, Cell Movement, Humans, Signal Transduction, Cell Polarity, Caenorhabditis elegans, Multiprotein Complexes, Asymmetric Cell Division
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