Cell-Cell Junctions in Adhesion, Signaling and Beyond—2nd Edition

A special issue of Life (ISSN 2075-1729). This special issue belongs to the section "Physiology and Pathology".

Deadline for manuscript submissions: closed (24 March 2024) | Viewed by 2707

Special Issue Editor

Centre for Immunobiology and Regenerative Medicine, Institute of Dentistry, Barts and The London, School of Medicine and Dentistry, Queen Mary University of London, London E1 4NS, UK
Interests: cell–cell junctions; desmosomes; cadherin signalling; mechanosensing; Hippo-YAP pathway; cell migration

Special Issue Information

Dear Colleagues,

The editors are grateful to the many researchers who contributed to the success of the first volume of this issue (https://www.mdpi.com/journal/life/special_issues/CCJ). We are very pleased to announce the second volume of our Special Issue “Cell–cell Junctions in Adhesion, Signaling and Beyond—2nd Edition".

Cell–cell junctions are dynamic adhesion complexes located on the plasma membrane between neighbouring cells that are essential in tissue morphogenesis, organ formation and collective cell migration in early embryonic development and tissue regeneration in adulthood. In principle, there are three distinct functional groups of cell junctions, i.e., tight junctions, gap junctions and anchoring junctions. Tight junctions are the key for the barrier function of the epithelial and endothelial cells, especially for the blood–brain barrier (BBB) in the endothelial cells of cerebral microvessels that provides a dynamic interface between the peripheral circulation and the central nervous system and restricts blood-borne substances from entering the brain. Tight junctions in stratified squamous epithelia are crucial for protection against all sorts of insults, microbial infection and water loss. In contrast, gap junctions allow cell communication that is vital in controlling homeostasis and responses to external stimuli in organisms. They are made by proteins that form many small channels on closely apposed plasma membranes to permit the transfer of ions and small molecules between cells. Anchoring junctions include adherens junctions and desmosomes that anchor the cytoskeletal filaments to the cell surface and confer strong cell–cell adhesion. Together with the cytoskeletal network, anchoring junctions provide the scaffolding necessary for the mechanical properties of cells, especially in complex tissues such as skin, mucous membranes and heart tissues that are subject to extensive stress daily. Collectively, these intercellular junctions crosstalk through protein–protein interactions and are coordinated in the regulation of diverse cellular processes. It has been increasingly appreciated that cell junctions are not merely protein complexes that mechanically join cells to each other, but rather function as the signalling hubs for cells, responding to both the external and internal stimuli and transmitting signals to the inside of cells that influence gene expression and cell activity to maintain tissue integrity and homeostasis. Recent studies have uncovered the previously unrecognised functions of adhesion molecules that act as stress sensors for signal transmission and transduction in controlling the higher-ordered network vital for cell fate decisions beyond cell cohesion. Given that cell–cell junctions have such a fundamentally important role in tissue generation and maintenance, it is not surprising that alterations and dysregulation of cell junctions contribute to a broad spectrum of inherited, infectious and auto-immune diseases, as well as cancers, that affect multiple organs of the body. For this Special Issue, we invite scientists actively working in the field to contribute original studies, reviews, and perspectives under the theme of cell–cell junctions in health and disease. We hope this issue will stimulate communication and advance our current knowledge in this fascinating and fast-growing field.

Dr. Hong Wan
Guest Editor

Manuscript Submission Information

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Keywords

  • cell–cell adhesion
  • tight junction
  • adherens junction
  • desmosome
  • gap junction
  • blood–brain barrier
  • cadherin signalling
  • inherited disease
  • auto-immune disease
  • cancer
  • infectious disease

Published Papers (1 paper)

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Review

20 pages, 1218 KiB  
Review
The Regulation of the Hippo Pathway by Intercellular Junction Proteins
by Usama Sharif Ahmad, Jutamas Uttagomol and Hong Wan
Life 2022, 12(11), 1792; https://doi.org/10.3390/life12111792 - 5 Nov 2022
Cited by 8 | Viewed by 2496
Abstract
The Hippo pathway is an evolutionarily conserved pathway that serves to promote cell death and differentiation while inhibiting cellular proliferation across species. The downstream effectors of this pathway, yes-associated protein (YAP) and transcriptional co-activator with PDZ-binding motif (TAZ), are considered vital in promoting [...] Read more.
The Hippo pathway is an evolutionarily conserved pathway that serves to promote cell death and differentiation while inhibiting cellular proliferation across species. The downstream effectors of this pathway, yes-associated protein (YAP) and transcriptional co-activator with PDZ-binding motif (TAZ), are considered vital in promoting the output of the Hippo pathway, with activation of upstream kinases negatively regulating YAP/TAZ activity. The upstream regulation of the Hippo pathway is not entirely understood on a molecular level. However, several studies have shown that numerous cellular and non-cellular mechanisms such as cell polarity, contact inhibition, soluble factors, mechanical forces, and metabolism can convey external stimuli to the intracellular kinase cascade, promoting the activation of key components of the Hippo pathway and therefore regulating the subcellular localisation and protein activity of YAP/TAZ. This review will summarise what we have learnt about the role of intercellular junction-associated proteins in the activation of this pathway, including adherens junctions and tight junctions, and in particular our latest findings about the desmosomal components, including desmoglein-3 (DSG3), in the regulation of YAP signalling, phosphorylation, and subcellular translocation. Full article
(This article belongs to the Special Issue Cell-Cell Junctions in Adhesion, Signaling and Beyond—2nd Edition)
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