A picket fence function for adherens junctions in epithelial cell polarity
Teresa Bonello1, Mario Aguilar-Aragon1, Alexander Tournier1
1ACRF Department of Cancer Biology and Therapeutics, The John Curtin School of Medical Research, The Australian National University, 131 Garran Rd, Acton, ACT 2601, Canberra, Australia.
This study explores how adherens junctions contribute to cell polarity in epithelial cells. Adherens junctions are known to help cells stick together and form contractile rings. The researchers found that when adherens junctions are disrupted, the boundaries between apical and basolateral domains become less defined. They used experiments and simulations to show that adherens junctions act as a 'picket fence' to restrict the spread of polarity determinants. This function is essential for maintaining domain size and cell shape. The study also suggests that adherens junctions can move in response to mechanical forces, allowing for spontaneous adjustments during tissue morphogenesis.
Area of Science:
- Cell biology of epithelial polarity
- Molecular mechanisms in developmental biology
Background:
Epithelial cells rely on precise apical-basolateral polarity to maintain tissue organization. Adherens junctions are known to mediate cell-cell adhesion and contractile ring formation. Prior research has shown that in Drosophila, apical polarity is defined by aPKC-Par6-Baz complexes, while basolateral regions are marked by Lgl/Dlg/Scrib. Neuroblasts, which lack adherens junctions, still display apical-basal polarization, raising questions about the role of adherens junctions in polarity. This gap motivated researchers to investigate whether adherens junctions are necessary for domain boundary formation. No prior work had resolved how polarity determinants interact with adherens junctions. Existing studies suggest that polarity determinants can segregate without adherens junctions. However, the absence of a clear boundary between apical and basolateral domains in neuroblasts indicates a possible role for adherens junctions in domain size control. This uncertainty drove the current investigation into the function of adherens junctions in epithelial polarity.
Purpose Of The Study:
The aim of this study was to determine whether adherens junctions contribute to apical-basal polarization in epithelial cells. Researchers sought to clarify whether adherens junctions function as a diffusion barrier for polarity determinants. The specific problem addressed was the lack of understanding about how adherens junctions influence domain boundary formation. The motivation for this work was to resolve whether adherens junctions are essential for maintaining sharp polarity boundaries. Prior research suggested that neuroblasts can polarize without adherens junctions, but domain size control was unclear. This study aimed to test whether adherens junctions provide a 'picket fence' barrier. The researchers also wanted to explore how polarity determinants interact with adherens junctions. By manipulating polarity determinants and simulating their behavior, the study aimed to uncover the role of adherens junctions in domain size regulation.
Main Methods:
The researchers used a combination of experimental and computational approaches to investigate adherens junction function. They disrupted adherens junctions in epithelial cells and observed the distribution of polarity determinants. Apical markers like aPKC and basolateral markers like Lgl were tracked using fluorescence imaging. Computer simulations were employed to model the diffusion of polarity determinants along the membrane. The levels of Par3/Baz and Lgl were manipulated to test their interactions with adherens junctions. The experiments focused on how polarity determinants segregate in the presence or absence of adherens junctions. Researchers also examined whether adherens junctions influence domain size and cell shape. The study combined live imaging with quantitative analysis to assess boundary sharpness and domain size.
Main Results:
Disruption of adherens junctions led to a loss of sharp boundaries between apical and basolateral domains. aPKC remained segregated from Lgl but overlapped with Dlg and Scrib, similar to neuroblasts. Domain size control was lost in the absence of adherens junctions, affecting cell shape. Manipulating apical Par3/Baz or basolateral Lgl levels confirmed the role of adherens junctions as a diffusion barrier. Computer simulations supported the idea that adherens junctions restrict the spread of polarity determinants. The results suggest that adherens junctions act as a 'picket fence' to maintain domain size. Movement of adherens junctions in response to mechanical forces allows for spontaneous adjustment of domain size. These findings indicate that adherens junctions are necessary for precise domain size control.
Conclusions:
The authors propose that adherens junctions function as a 'picket fence' diffusion barrier for polarity determinants. This role is essential for maintaining sharp boundaries between apical and basolateral domains. The study confirms that adherens junctions are necessary for domain size control in epithelial cells. In the absence of adherens junctions, polarity determinants overlap, leading to loss of domain size regulation. The findings suggest that adherens junctions are not required for initial segregation of polarity determinants. However, they are necessary for maintaining precise domain boundaries. The authors suggest that movement of adherens junctions allows for spontaneous adjustment during morphogenetic changes. These conclusions are based on experimental and computational evidence presented in the study.
Frequently Asked Questions
The study shows that adherens junctions act as a 'picket fence' diffusion barrier to maintain sharp boundaries between apical and basolateral domains.
Fluorescence imaging was used to track apical aPKC and basolateral Lgl/Dlg/Scrib in epithelial cells.
Domain size control ensures proper cell shape and tissue organization by maintaining sharp polarity boundaries.
Adherens junctions restrict the spread of polarity determinants along the membrane to enable precise domain size control.
Disruption of adherens junctions causes aPKC to overlap with Dlg and Scrib, leading to loss of domain size control.
Adherens junctions move in response to mechanical forces, allowing spontaneous adjustment of domain size as an emergent property.
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