Julia Eckert
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juliaeckert.bsky.social
Julia Eckert
@juliaeckert.bsky.social
@dfg.de Walter Benjamin Fellow & Postdoctoral Researcher @yap-lab.bsky.social | Co-organizer @epimechfc.bsky.social | Mechanobiology - Cell & Tissue Mechanics - Soft Matter Physics - Image Analysis

👉 https://julia-eckert.github.io
Excited to participate in the Scientific Art Contest at #CellMech2025.
October 2, 2025 at 1:55 PM
The last paper from my PhD is now online! 🥳

👉 pubs.aip.org/aip/rsi/arti...

We have designed a new device based on the elastic micropillar array assay to measure the detachment forces between spread cells.

@leidenphysics.bsky.social
September 5, 2025 at 1:11 PM
Now published in @natcomms.nature.com! 🥳

👉 rdcu.be/eATn3

We developed image analysis tools to capture the nematic orientation field of 3D tissue surfaces. Tested on epithelial aggregates, zebrafish hearts, myoblasts on spheres & micro-vessels, we combined soft matter physics with exp. biology.
August 15, 2025 at 12:13 PM
A fantastic week at the Mechanobiology Conference in Vietnam, filled with fascinating talks, fruitful discussions, and amazing people.

Huge thanks to the organizers and ICISE for making it all possible!
July 11, 2025 at 4:49 PM
Please check out this fantastic work by my friend Svetlana Jovanic 👇

'Resilience in zebrafish embryoids'
www.biorxiv.org/content/10.1...
June 20, 2025 at 10:27 PM
Our new review paper from @yap-lab.bsky.social is online - together with Virgile Viasnoff!

👉 'New directions in epithelial mechanoadaptation'

www.sciencedirect.com/science/arti...
May 25, 2025 at 2:42 AM
Started my first day as a Walter Benjamin Fellow! 🥳

Looking forward to study symmetry-breaking in morphogenesis using and connecting concepts from soft matter physics & cell/molecular biology @yap-lab.bsky.social. 👉 physics meets biology!

Big thanks to the @dfg.de for funding my research.
May 1, 2025 at 3:27 AM
Congratulations to Denni from our @yap-lab.bsky.social team and all authors on the new paper! 🥳

'Advecting scaffolds: Controlling the remodeling of actomyosin with anillin' 👇

journals.aps.org/pre/abstract...
February 10, 2025 at 8:18 AM
… F-actin signal anti-correlates with the mean curvature, H, in Region I & II for each developmental stage. Assuming F-actin represents surface tension, gamma, the results correlate with Laplace’s law (P ~ gamma*H) for constant pressure!

👉 Linking biological properties with physical interpretations
January 29, 2025 at 11:01 PM
The sarcomeric network composed of acto-myosin contracts the heart … it pumps. We used the same tangent planes and analyzed the fluorescent signal of F-actin …
(Directors: high intensity = red, low = blue)

👉 Spatio-temporal correlations
January 29, 2025 at 11:01 PM
By selecting data points, we can compare properties such as alignment of cells, i.e. local nematic order, between different regions (Region I: outer curvature, Region II: axes) in the heart & between different developmental stages (72, 120 hpf).

Region I: high alignment -> in direction of tension?
January 29, 2025 at 11:01 PM
Spheroids are simple systems with only convex curvature. What about more complex systems?

We teamed up with @tobyandrews.bsky.social & @rashmi-priya.bsky.social, and analyzed the ventricular myocardium of Zebrafish hearts ... and it works! 👇

(Directors: high alignment = red, misaligned = blue)
January 29, 2025 at 11:01 PM
As expected, our spherical aggregates have a total topological charge of +2.

We show that the number of defects correlates with the surface area, as previously reported in the theoretical literature, for example by Henkes et al, 2020.

👉 Experiment verifies theory
January 29, 2025 at 11:01 PM
Nematic directors (white rods) align with cell orientation & spheroid surface, highlighting a big difference compared to 2D intensity projections of multiple image planes.

Our method allows not only the generation of the orientation field, but also the calculation of nematic topological defects.
January 29, 2025 at 11:01 PM
Yes, but how?

We have developed an analysis pipeline that slices the outer layer of the cell system via tangent planes and analyzes the properties of these 2D-generated images. The center information, where the region is approximately flat, is then transferred back to the 3D surface.
Input: z-stack
January 29, 2025 at 11:01 PM
Thrilled to share our new preprint on detecting the nematic orientation field on surfaces of 3D multicellular systems!

www.biorxiv.org/content/10.1...

Huge thanks to all authors: @tobyandrews.bsky.social,Joe Pollard, @rashmi-priya.bsky.social, @yap-lab.bsky.social &Richard Morris

Any 3D systems?👇
January 29, 2025 at 11:01 PM
Nematic directors (white rods) align with cell orientation & spheroid surface, highlighting a big difference compared to 2D intensity projections of multiple image planes.

Our method allows not only the generation of the orientation field, but also the calculation of nematic topological defects.
January 29, 2025 at 10:52 PM
Interesting findings by Jacob Notbohm's group. Nematic defects may form as a result of spatially coordinated patterns in cell forces and motion.
👉 arxiv.org/abs/2501.04827
January 13, 2025 at 9:06 AM
The crossover length scale, in which the hexatic and nematic order are equally present, depends on cell-cell adhesion and correlates with the monolayer density.

www.nature.com/articles/s41...
November 16, 2024 at 11:49 PM
However, nematic symmetry requires elongated cells. Are they elongated? Not always, and most cells are hexagons, indicating hexatic (p=6) symmetry.

Indeed, hexatic symmetry is dominant at small (single cell) and nematic at large (tissue) length scales.

www.nature.com/articles/s41...
November 16, 2024 at 11:49 PM
Even in animals, the position of integer defects has been shown to correlate with the regeneration of the Hydra's head and foot, and is thought to control or drive morphogenesis.

www.nature.com/articles/s41...
November 16, 2024 at 11:49 PM
Integer defects (i.e. spirals: +1) can also generate local compressive stresses, which can lead to the formation of multicellular 3D protrusions.

www.nature.com/articles/s41...
November 16, 2024 at 11:49 PM
The direction of the +1/2 defect migration tells us whether cells can be collectively contractile (head->tail) or extensile (tail->head). This behavior arises from an interplay between intercellular (cell-cell) and intracellular (cell-matrix) forces.

www.nature.com/articles/s41...
November 16, 2024 at 11:49 PM
Comet-like (+1/2) and trefoil-like (-1/2) defects have been shown to be involved in various biological processes.

Cell assemblies of +1/2 defects are able to move, resulting in local compressive stresses in tissues that can cause cell extrusions.

www.nature.com/articles/nat...
November 16, 2024 at 11:49 PM
Also at smaller scales, cytoskeleton filaments, bacteria, and various cell types display polar (p=1) and nematic (p=2) symmetry.

This symmetry can be broken by topological defect, i.e. singularities of the aligned orientation field of cells in tissues.

www.sciencedirect.com/science/arti...
November 16, 2024 at 11:49 PM