Apical constriction in morphogenesis: From actomyosin architecture to regulatory networks
Samara N Ranie1, Melanie D White2
1Institute for Molecular Bioscience, the University of Queensland, Brisbane, Australia.
Current Opinion in Cell Biology
|June 13, 2025
Summary
Apical constriction, a crucial process for tissue remodeling, involves dynamic actomyosin structures and complex regulation. Understanding these diverse mechanisms is key to comprehending developmental tissue shaping.
Area of Science:
- Cell Biology
- Developmental Biology
- Biophysics
Background:
- Apical constriction is vital for tissue remodeling during development and throughout life.
- Previously viewed as simple actomyosin ring contraction, it's now understood as a dynamic process with varied actomyosin architectures.
- Regulation spans multiple scales, from tissue mechanics to protein trafficking.
Purpose of the Study:
- To explore the diverse actomyosin architectures and regulatory pathways of apical constriction.
- To highlight the integration of variable actomyosin structures with emerging regulatory networks.
- To emphasize the role of in vivo live imaging in understanding these processes.
Main Methods:
- Review of current literature on apical constriction.
- Analysis of diverse actomyosin architectures across species and tissues.
- Investigation of regulatory mechanisms including cytoskeletal-junctional interactions and protein levels.
Main Results:
- Apical constriction exhibits diverse actomyosin architectures, challenging the uniform ring model.
- Regulation involves complex interactions at the cytoskeletal-junctional interface and protein trafficking.
- In vivo live imaging is advancing insights into regulatory networks.
Conclusions:
- Apical constriction is a dynamic process with variable actomyosin structures and complex regulation.
- Integrating diverse structural and regulatory pathways is crucial for understanding tissue development.
- Further research using advanced imaging will illuminate the coordination of actomyosin dynamics in morphogenesis.
Related Concept Videos
The Role of Actin and Myosin in Non-muscle Cells
3.4K
Actin and myosin or actomyosin filaments also play a significant role in cells other than those involved in muscle contraction (which occurs within the sarcomere of muscle cells). The mechanism of non-muscle cell contractile bundles was first observed in Dictyostelium and Acanthamoeba. In non-muscle cells, two bundles are commonly found: stress fibers and actomyosin adherence belts. These contractile bundles are smaller and less organized than the ones found in muscle cells. They are held...
3.4K
The Contractile Ring
6.3K
Contractile rings are composed of microfilaments and are responsible for separating the daughter cells during cytokinesis. Contractile ring assembly proceeds along with other cell cycle events; however, very few mechanistic details are known about the timing and coordination of the contractile rings with the cell cycle.
A small GTPase, RhoA, controls the function and assembly of the contractile ring. RhoA belongs to the Ras superfamily of proteins. The activation of formins by RhoA promotes...
A small GTPase, RhoA, controls the function and assembly of the contractile ring. RhoA belongs to the Ras superfamily of proteins. The activation of formins by RhoA promotes...
6.3K
Cell Motility through Blebbing
1.9K
Blebs are a type of membrane protrusion formed by the internal hydrostatic pressure of the cytoplasm. Blebs are observed in several cell types, including fibroblasts, immune cells, and single-celled organisms like the amoeba. The primary function of blebs is cell locomotion and apoptosis, but they are also found during necrosis and cell division. The life cycle of a bleb comprises an initiation phase followed by the expansion and retraction phases.
Blebbing Through the Matrix
In multicellular...
Blebbing Through the Matrix
In multicellular...
1.9K
Generation of Straight or Branched Actin Filaments
2.9K
The straight or branched structure formation of actin filaments is controlled by nucleating proteins such as the formins and Arp2/3 complex. Formin-mediated assembly results in straight filaments, whereas Arp2/3 protein complex-mediated assembly results in branched actin filaments.
Arp2/3 Complex
Arp2/3 complex is a seven-subunit complex consisting of two proteins similar to actin- Arp2 and Arp3, and five other subunits that help keep Arp2 and Arp3 inactive. When required, the complex is...
Arp2/3 Complex
Arp2/3 complex is a seven-subunit complex consisting of two proteins similar to actin- Arp2 and Arp3, and five other subunits that help keep Arp2 and Arp3 inactive. When required, the complex is...
2.9K
Mechanism of Lamellipodia Formation
2.5K
Cells migrating in response to external stimuli form lamellipodia, which are thin membrane protrusions supported by a mesh of linked, branched, or unbranched actin filaments. These actin filaments interact with myosin motor proteins, creating the dynamic actomyosin complex within the cytoskeleton. Contractility, or the ability to generate contractile stress, is inherent to the actomyosin complex. It helps cells detect the stiffness of the surrounding ECM and exert contractile force for...
2.5K
Actin and Myosin in Muscle Contraction
9.4K
Actin and myosin are contractile proteins that form the sarcomere found in skeletal muscle tissues for regulating muscle contraction. Actin, a globular contractile protein, interacts with myosin for muscle contraction. The skeletal tissue appears striped or striated under a microscope due to the repeated arrangement of contractile proteins actin and myosin along the length of myofibrils. Dark A bands and light I bands repeat along myofibrils, and the alignment of myofibrils in the cell causes...
9.4K


