Cited by 35Cell Adhesion Molecules ResearchDevelopmental Biology and Gene RegulationSkin and Cellular Biology Research

Expression patterns of nectins and afadin during epithelial remodeling in the mouse embryo

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Okabe, Noriko, Ozaki‐Kuroda, Kumi, Nakanishi, Hiroyuki, Shimizu, Kazuya, Takai, Yoshimi·2004·Developmental Dynamics

Abstract

Cell–cell adhesion plays key roles in tissue morphogenesis and organogenesis. Nectins are Ca 2+‐independent immunoglobulin‐like cell adhesion molecules connected to the actin cytoskeleton through afadin. Nectins play roles in a variety of cell–cell junctions in cooperation with or independently of cadherins. Here, we examined the cellular localization of nectins and afadin throughout primitive streak, neural plate, and early organogenesis stages of mouse development. Nectin and afadin localization coincided with a honeycomb‐shaped meshwork of actin filaments at adherens junctions of polarized epithelia, including neuroepithelium, epithelial somites, and facial primordia. As organogenesis progressed, nectin‐2 expression was maintained in general columnar epithelia, whereas nectin‐1 and ‐3 became highly concentrated at sites of neural morphogenesis. Moreover, nectin‐1 was highly expressed in keratinocytes of the skin, developing hair follicles, and epithelium of developing teeth. These results suggest that nectins and afadin are involved in dynamic epithelial remodeling during mouse development. Developmental Dynamics 230:174–186, 2004. © 2004 Wiley‐Liss, Inc.

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  • NECTIN signaling has a role in cell adhesion and skin morphogenesis.

    “given its role in cell adhesion and skin morphogenesis.56”

    From Single-cell transcriptomics of human-skin-equivalent organoids (2023) · cites this paper as [56]

    The Introduction describes the nectin–afadin system as a component of cell–cell adhesion and links nectin-1 mutations to abnormalities of skin, hair, and teeth. The Ectodermal Stratified Epithelia section reports nectin-1 expression in developing skin but says its role there remains elusive. The paper therefore supports a possible role in skin morphogenesis, not an established role for nectin signaling in that process. (LLM, conf=0.84)

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Research works printed but not linked: 2

  1. Hogan B, Beddington R, Costantini F, Lacy E. 1994. Manipulating the mouse embryo. New York: Cold Spring Harbor Laboratory Press. 497 p.
  2. Kaufman MH. 1992. The atlas of mouse development. San Diego: Academic Press. 525 p.

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Authors
Okabe, N., Ozaki‐Kuroda, K., Nakanishi, H., Shimizu, K., & Takai, Y.
Affiliations
The University of Osaka (JP)
Corresponding author
Takai, Yoshimi
Venue
Developmental Dynamics
Publisher
Wiley
Published
2004-03-31
Volume
230
Issue
1
Pages
174-186
ISSN
  • 1058-8388 (ISSN-L)
  • 1097-0177
OpenAlex
W2018716000
Cited by
35
References
3
Citations by year
2026: 1 · 2025: 1 · 2024: 1 · 2023: 1 · 2019: 1 · 2018: 1 · 2016: 4 · 2014: 3 · 2013: 1 · 2012: 1
FWCI
1.15
Type
journal article
Language
en
Open access
Locations
  • Developmental Dynamics (publishedVersion)
  • PubMed (publishedVersion)
  • Tokyo Tech Research Repository (Tokyo Institute of Technology) (submittedVersion)
Funders
RIKEN
Topics
  • Health Sciences › Medicine › Immunology and Allergy › Cell Adhesion Molecules Research
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Skin and Cellular Biology Research
Keywords
nectin, afadin, nectin-1, nectin-2, nectin-3, cell-cell adhesion, adherens junctions, epithelial remodeling, mouse embryo, neuronal morphogenesis, organogenesis, neuroepithelium, keratinocytes, hair follicle, actin cytoskeleton
MeSH terms
Nectins, Actins, Animals, Calcium, Cell Adhesion, Cytoskeleton, Epithelium, Immunoglobulins, Intercellular Junctions, Mice, Inbred ICR, Microfilament Proteins, Microscopy, Fluorescence, Myosins, Nucleic Acid Hybridization, RNA, Messenger, Time Factors, Tooth, Blotting, Western, Cell Adhesion Molecules, Kinesins, In Situ Hybridization, DNA, Complementary, Gene Expression Regulation, Developmental, Protein Isoforms, Adherens Junctions, Mice

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