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# Biology# Developmental Biology

Tissue Folding: The Art of Cell Shape

Discover how cells fold to form complex organ structures.

― 6 min read


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When you think about how your body forms, it’s a bit like origami. Instead of folding paper, our cells are folding in and out to create the complex shapes we see in organs. This process is called tissue folding, and it’s how flat cell layers turn into three-dimensional organ structures. Imagine a pancake transforming into a beautifully designed cake with layers-that’s what’s happening in cells!

The Start of Tissue Folding

So, how does this folding begin? Well, it all starts with a little boost in activity in a certain group of cells. These cells get motivated and change shape, sort of like when you decide to get up from the couch. If everything goes well, they fold perfectly, but if something goes wrong, we might end up with some defective shapes or even organs that don’t work properly. Just like a lopsided cake can mess up a birthday party, incorrect tissue folding can lead to developmental issues.

Why Timing and Precision Matter

Imagine trying to fold your bed sheets without any plan. You might end up with a crumpled mess! The same goes for cells when they fold. Each little movement needs to happen at the right time and in the right space. If one part of the cell folds at the wrong time, it might cause problems later on. This is why understanding how these mechanisms work can help in fields like tissue engineering, where scientists want to create new tissue for healing purposes.

The Different Faces of Tissue Folding

Tissue folding can happen on either the top (apical) or bottom (basal) sides of cells. Most of the attention has gone to the top side, where the cells pinch inwards due to forces from the inside, allowing the tissue to bend. Think of it like squeezing the middle of a balloon-when you push in the middle, the ends stick out. But scientists have found that the bottom side also folds a lot, although it's not as well understood yet.

The Drosophila Model

To figure out how this folding works, researchers have turned to the handy fruit fly, Drosophila. These little guys are great for studying how tissues fold because their wing discs-structures that eventually develop into wings-show a clear and well-organized way of folding. These discs are made up of two layers of cells and are connected to a supporting membrane underneath. When the flies develop, these discs undergo several folds, both on the top and bottom sides.

The Magic of Cell Movement

During the development phase of the Drosophila, certain regions of the wing disc are supposed to form key structures, like the wing blade and the base of the wing. But here’s the fun part: these cells don’t just sit still. Instead, they change their height and even detach from the supporting layer below! By shaping into a wedge, the cells create the necessary folds just in time for the fly’s metamorphosis-a transformation that’s a lot more interesting than your average caterpillar!

New Findings on Basal Folding

Most studies have focused on the top side of the cells, but recent work has shifted attention to what happens on the bottom side. When the influential acts like actomyosin networks and cell-ECM (extracellular matrix) adhesion are manipulated, surprising things happen. Lowering cell-ECM connection allows the cells to change shape, which is essential for folding at the bottom side.

The Dance of Integrins and Myosins

What’s fascinating in all this is the role of integrins-a type of protein that helps cells stick to their surroundings. Think of integrins as glue that keeps the cells in place. When the levels of integrins drop, the cells can start to wiggle and rearrange themselves more freely, which opens the door to folding. Meanwhile, myosin proteins are busy pulling on the cell’s insides, like a tug-of-war, helping the cells adjust their shape even further.

Watching the Changes in Real-Time

Using nifty techniques, researchers can watch these cells as they change shape. For example, they found that during the third larval stage, these wing margin cells, which will form the wing, become shorter and start to detach from their supporting layer. You could say they’re getting ready to stretch their wings!

Modeling the Folding Process

To better understand how all this works, scientists have created computer models that simulate what happens during tissue folding. These models can predict how changes in integrin levels and cell shape can lead to proper folding. It’s as if researchers are playing a video game where they control the cells’ movements to see if they can get them to fold correctly.

What Happens When Things Go Wrong?

Unfortunately, not everything goes according to plan. If integrin levels remain too high, or if the actomyosin doesn’t contract properly, the cells might not fold as they should. This can lead to misshapen organs and, in some cases, a complete failure of forming parts of the organism-kind of like a cake that doesn’t rise or one that’s burnt on the edges!

The Bigger Picture: Epithelial Folding Beyond Flies

Even though the Drosophila model is useful, it’s not the only case for studying tissue folding. Other organisms, like zebrafish and even humans, experience tissue folding in their development. Learning how these processes work can help scientists understand various developmental diseases and improve tissue engineering techniques-because who wouldn’t want to bake a perfect cake, or in this case, create perfect cells?

Why This Matters

Gaining insights into tissue folding can pave the way for advancements in medicine, especially in areas like regenerative medicine and tissue repair. If researchers can figure out how to better control tissue folding, they might be able to engineer new tissues or even organs, giving hope to those with injuries or conditions that affect their organs.

Conclusion: A World of Fascinating Cell Dynamics

The world of cells folding and shaping into complex forms is an amazing journey. From tiny fruit flies to larger organisms, tissue folding plays a crucial role in forming functional structures. And just like a cake, it’s all about timing, precision, and just the right ingredients. Whether you’re a budding scientist or just someone with a love for biology, there’s always more to learn about how life takes shape, quite literally!

Original Source

Title: Local weakening of cell-ECM adhesion triggers basal tissue folding via changes in cell shape, actomyosin organization and E-cad levels

Abstract: During embryogenesis, epithelial sheets sculpt organs by folding, either apically or basally, into complex 3D structures. Given the presence of actomyosin networks and cell adhesion sites on both sides of cells, a common machinery mediating apical and basal epithelial tissue folding has been proposed. However, little is known about the mechanisms regulating epithelial folding towards the basal side. Here, using the Drosophila wing imaginal disc and a multidisciplinary approach, combining genetic perturbations and computational modelling, we demonstrate opposing roles for cell-cell and cell-ECM adhesion systems during epithelial folding. Thus, while cadherin-mediated adhesion, linked to actomyosin network, regulates apical folding, a reduction on integrin-dependent adhesion, followed by changes in cell shape, organization of the basal actomyosin cytoskeleton and E-Cad levels, is necessary and sufficient to trigger basal folding. These results suggest that modulation of the cell mechanical landscape through the crosstalk between integrins and cadherins is essential for correct epithelial folding.

Authors: Andrea Valencia-Expósito, Nargess Khalilgharibi, Yanlan Mao, María D. Martín-Bermudo

Last Update: 2024-08-30 00:00:00

Language: English

Source URL: https://www.biorxiv.org/content/10.1101/2024.08.27.609853

Source PDF: https://www.biorxiv.org/content/10.1101/2024.08.27.609853.full.pdf

Licence: https://creativecommons.org/licenses/by/4.0/

Changes: This summary was created with assistance from AI and may have inaccuracies. For accurate information, please refer to the original source documents linked here.

Thank you to biorxiv for use of its open access interoperability.

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