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Posts by Ignasi Casanellas

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A series of spontaneously blinking dyes for super-resolution microscopy - Nature Methods A series of spontaneously blinking dyes in the far-red range facilitate single-molecule localization microscopy. These dyes vary in their blinking properties and can be matched to the applications and...

Out in @natmethods.nature.com: More dyes. They work. Quite well. And blink. Pick the one that fits your target, your technique, and your labeling density. With too many collaborators and institutes to list, but anchored at @hhmijanelia.bsky.social www.nature.com/articles/s41...

6 days ago 166 64 2 2
Fig. 1. Basic steps of cell migration. (a) Mesenchymal cell migration. Cells are attached to the extracellular matrix (ECM) via integrins and focal adhesions (FA). Actin polymerization at the leading edge extends filamentous actin (F-actin) protrusions inducing a front-rear polarization. New FA adhesions attach the protrusions to the ECM followed by F-actin rearward movement, known as actin retrograde flow. Disassembly of rear FA and myosin II contraction at the back of cell generate the pushing force to move the cell forward. (b) Amoeboid cell migration. Cells do not form adhesions with the ECM or other cells. Under confinement, amoeboid cells form membrane blebs, also known as pseudopodia, inducing a front-rear polarization. Actin retrograde flow is initiated by mechanical forces, such as confinement. Myosin II contraction at the back of cell generates the pushing force to move the cell forward.

Fig. 1. Basic steps of cell migration. (a) Mesenchymal cell migration. Cells are attached to the extracellular matrix (ECM) via integrins and focal adhesions (FA). Actin polymerization at the leading edge extends filamentous actin (F-actin) protrusions inducing a front-rear polarization. New FA adhesions attach the protrusions to the ECM followed by F-actin rearward movement, known as actin retrograde flow. Disassembly of rear FA and myosin II contraction at the back of cell generate the pushing force to move the cell forward. (b) Amoeboid cell migration. Cells do not form adhesions with the ECM or other cells. Under confinement, amoeboid cells form membrane blebs, also known as pseudopodia, inducing a front-rear polarization. Actin retrograde flow is initiated by mechanical forces, such as confinement. Myosin II contraction at the back of cell generates the pushing force to move the cell forward.

Fig. 2. MS ion channel families involved in cell migration. (a) Transient receptor potential channels (TRP). TRP channels form 6 transmembrane (TM) domains. TM 1-2 are represented in cyan, TM 3-4 in orange and TM 5-6 in magenta. The pore forming domain is formed between TM5 and TM6. Each subfamily of TRP channels contains unique domains in the cytoplasmic N- and C- termini. TRPC channels have three ankyrin repeats and a coiled-coil domain in the N-terminus. A TRP domain, which has gating functions, a calmodulin and IP3R binding domains are localized in the C-terminus. TRPV channels have six ankyrin repeats in the N-terminus. A TRP domain, a calmodulin and PIP2 binding domains are localized in the C-terminus. (b–b′) Piezo1 channels. (b) Each Piezo1 channel has at least 26 TM regions and up to 40 TM domains. The TM domains form three defined structures, known as blades. Each blade is colour coded in cyan, orange and magenta for easier representation. The carboy-terminal extracellular domain (CED) is located directly on top of the pore forming domain and is important for ion selectivity (Zhao et al., 2016). (b′) Due to its large size, a Piezo1 channel induces a small curvature to the plasma membrane, when force is applied the plasma membrane is stretched, thereby opening the Piezo1 channel.

Fig. 2. MS ion channel families involved in cell migration. (a) Transient receptor potential channels (TRP). TRP channels form 6 transmembrane (TM) domains. TM 1-2 are represented in cyan, TM 3-4 in orange and TM 5-6 in magenta. The pore forming domain is formed between TM5 and TM6. Each subfamily of TRP channels contains unique domains in the cytoplasmic N- and C- termini. TRPC channels have three ankyrin repeats and a coiled-coil domain in the N-terminus. A TRP domain, which has gating functions, a calmodulin and IP3R binding domains are localized in the C-terminus. TRPV channels have six ankyrin repeats in the N-terminus. A TRP domain, a calmodulin and PIP2 binding domains are localized in the C-terminus. (b–b′) Piezo1 channels. (b) Each Piezo1 channel has at least 26 TM regions and up to 40 TM domains. The TM domains form three defined structures, known as blades. Each blade is colour coded in cyan, orange and magenta for easier representation. The carboy-terminal extracellular domain (CED) is located directly on top of the pore forming domain and is important for ion selectivity (Zhao et al., 2016). (b′) Due to its large size, a Piezo1 channel induces a small curvature to the plasma membrane, when force is applied the plasma membrane is stretched, thereby opening the Piezo1 channel.

Fig. 3. Role of MS ion channels in cell migration. (a) Actin protrusions. MS ion channels can regulate the extension of actin-based protrusions through PI3K signalling. Ca2+ binding to PI3K leads to the activation of several Rac1-GEFs, including P-Rex1 and SWAP-70, Vav1, Sos1. Rac1-GEFs mediate the transition from inactive Rac1-GDP to Rac1-GTP, leading to actin polymerization and protrusion extension. (b) RhoA activation. The Ca2+ sensitive Pyk2 kinase is activated after MS ion channel opening. Pyk2 activates PDZ-RhoGEF which mediates the transition from inactive Rho-GDP to Rho-GTP, leading to Myosin II phosphorylation. Global Myosin II contraction leads to inhibition of cell migration. (c) Chemotaxis. The presence of a chemoattractant agent leads to re-localization of TRPC1 and TRPC6 MS ion channels to the direction of the chemoattractant signal. Localized Ca2+ can regulate actin remodelling via PI3K or induce Ca2+ flickers at the leading edge of the cell, promoting directional cell migration. (d) Focal adhesion (FA) disassembly. MS ion channels regulate FA disassembly via calpain, a Ca2+ dependant protease that mediates FA degradation. Restricted calpain activity at the rear of the cell mediates specific FA disassembly at the back of the cell, promoting cell migration. (e) Yap/Taz nuclear localization. Piezo1 activation is correlated with Yap translocation from the cytoplasm to the nucleus, leading to Yap mediated gene transcription. However, the biochemical signals downstream of Piezo1 have not been identified yet. Dashed line represents unknown signalling proteins.

Fig. 3. Role of MS ion channels in cell migration. (a) Actin protrusions. MS ion channels can regulate the extension of actin-based protrusions through PI3K signalling. Ca2+ binding to PI3K leads to the activation of several Rac1-GEFs, including P-Rex1 and SWAP-70, Vav1, Sos1. Rac1-GEFs mediate the transition from inactive Rac1-GDP to Rac1-GTP, leading to actin polymerization and protrusion extension. (b) RhoA activation. The Ca2+ sensitive Pyk2 kinase is activated after MS ion channel opening. Pyk2 activates PDZ-RhoGEF which mediates the transition from inactive Rho-GDP to Rho-GTP, leading to Myosin II phosphorylation. Global Myosin II contraction leads to inhibition of cell migration. (c) Chemotaxis. The presence of a chemoattractant agent leads to re-localization of TRPC1 and TRPC6 MS ion channels to the direction of the chemoattractant signal. Localized Ca2+ can regulate actin remodelling via PI3K or induce Ca2+ flickers at the leading edge of the cell, promoting directional cell migration. (d) Focal adhesion (FA) disassembly. MS ion channels regulate FA disassembly via calpain, a Ca2+ dependant protease that mediates FA degradation. Restricted calpain activity at the rear of the cell mediates specific FA disassembly at the back of the cell, promoting cell migration. (e) Yap/Taz nuclear localization. Piezo1 activation is correlated with Yap translocation from the cytoplasm to the nucleus, leading to Yap mediated gene transcription. However, the biochemical signals downstream of Piezo1 have not been identified yet. Dashed line represents unknown signalling proteins.

Many ion channels eg. TRP, Piezo are mechanically sensitive, meaning they can be activated/deactivated by mechanical stimuli such as membrane curvature or substrate stiffness. In this thorough review from the Mayor lab, they discuss how these channels regulate cell migration.
doi.org/10.1016/j.cd...

1 month ago 12 10 0 1
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Webster, S., Brynn, R., & Poole, K. (2025). Evaluating the roles of ion channels in cellular force sensing. Journal of cell science, 138(15), jcs264038. #EpithelialMechanicsReview
doi.org/10.1242/jcs....

1 month ago 3 1 0 0
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Permeability-driven pressure and cell proliferation control lumen morphogenesis in pancreatic organoids - Nature Cell Biology Using pancreatic organoids, Lee et al. show that the balance between epithelial tissue permeability-driven lumenal pressure and cell proliferation affects ductal morphogenesis.

☕Using #pancreatic #organoids, Lee et al. show that the balance between epithelial tissue permeability-driven lumenal pressure and cell proliferation affects ductal morphogenesis.
bit.ly/4qozmjG

2 months ago 10 6 0 0
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Early-bird deadline to join @jcellsci.bsky.social at their meeting on Imaging Cell Dynamics in Spain in May is Friday 16 January. Apply to attend at:
biologists.com/meetings/jcs...
#JCSimaging

3 months ago 19 8 0 4
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We wrote two reviews on cell migration, published today in Nature Methods.

They provides practical guidelines how to select a cell-migration assay and how to analyze cell-migration data

Review 1: nature.com/articles/s41...

Review 2: nature.com/articles/s41...

4 months ago 74 37 1 2
Lead a lab at Janelia

Janelia is hiring! "Invent new imaging methods, molecular tools, or protein chemistry approaches"

www.janelia.org/content/lead...

4 months ago 26 22 0 1

The bot doesn't know what Watson & Crick mean by "suggests", because the entire concept of formulating a hypothesis and doing any sort of thinking is not something a LLM can relate to.

5 months ago 32 2 0 0
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Intercellular propagation of ERK activation and ZO-1 localization to podosomes during collective cell migration.

Intercellular propagation of ERK activation and ZO-1 localization to podosomes during collective cell migration.

Translocation of ZO-1 from the apical side of the cells to the adhesive ring of podosomes.

Translocation of ZO-1 from the apical side of the cells to the adhesive ring of podosomes.

Cell-cell junction proteins like ZO-1 not only play a critical role in the mechanical interaction between cells, but also participate in the biochemical signalling to coordinate the cell sheet. Check out this review on collective cell migration here to learn more: doi.org/10.1016/j.cd...

5 months ago 13 9 0 1
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📣Announcing the 4th edition of the EMBL‑IBEC Conference on “Engineering Multicellular Systems”, taking place 11–13 March 2026 in Barcelona. Exploring organoids, mechanobiology, embryo models, organ-on-chip systems, multiomics and more. Abstracts open now!
events.ibecbarcelona.eu/embl-ibec-co...

5 months ago 66 41 0 2
Apply - Interfolio {{$ctrl.$state.data.pageTitle}} - Apply - Interfolio

During these uncertain times, I’m very happy to see that my institution, @scripps.edu has an open tenure-track Assistant Professor position. Any field in Chemistry or Biology is welcome. I’d especially love to see fellow neuroscientists apply. Please repost!

apply.interfolio.com/174756

6 months ago 130 94 2 5
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Neural Crest Migration Orchestrated by Molecular and Mechanical Signals The neural crest is a highly migratory multipotent cell population traveling large distances in the vertebrate embryo. Neural crest cells migrate collectively in subpopulations, ranging in size from s...

A new review from the @mayorlab.bsky.social on the chemical and physical cues regulating neural crest cells migration is out. Check it out!
www.annualreviews.org/content/jour...

6 months ago 7 3 0 0
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Fish keratocytes isolated from a fish scale crawling around. Technique: DIC microscopy. #CellBiology.
Another #NikonSmallWorldReject

6 months ago 53 9 2 1
Rainbow shading of a confocal micrograph of a developing mouse neural tube. The protein actin is stained and colored in rainbow to indicate depth in the section.

Rainbow shading of a confocal micrograph of a developing mouse neural tube. The protein actin is stained and colored in rainbow to indicate depth in the section.

Happy #FluorescenceFriday! This is a maximum intensity projection of depth shaded actin (🌈) in a section from an E9.5 🐭 neural tube (NT). 🔬 by postdoc @christinaadaly.bsky.social 👩‍🔬 🧪 Image shows the floor plate and lumen of the developing NT.

#SciArt #DevBio #DevNeuro

6 months ago 122 26 4 2
Video

We're now recruiting early career group leaders at the Crick to lead ambitious research programmes and explore bold scientific questions.

Hear our Director, Edith Heard, explain why the Crick is a unique place for curiosity-driven research.

Apply now ➡️ www.crick.ac.uk/careers-stud...

6 months ago 134 111 1 18

Perhaps one way to evaluate the quality of a research article is to assess its teachability.

Is the article clear about its identifying assumptions?

Does it lay out the results clearly?

Does it engage with its limitations transparently?

6 months ago 31 4 1 0
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The integrin odyssey – a journey full of fundamental discoveries Summary: This Perspective highlights the key discoveries in integrin research that laid the foundation for a successful field.

The integrin odyssey – a journey full of fundamental discoveries url: journals.biologists.com/jcs/article/...

Great to start the day while reading this #integrin odyssey.

6 months ago 3 1 0 0
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Cell Migration Seminars Cell Migration Seminars every Tuesday at 16:00 BST.

If anyone ever wants to brush up on a lot of cell migration concepts don't forget we have several wonderful scientists who have given talks previously in cell migration seminars. I find it so comforting to go look at old videos, maybe someone else who will do as well!!
youtube.com/@cellmigrati...

6 months ago 43 10 1 2
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PIEZO channels link mechanical forces to uterine contractions in parturition Mechanical forces are extensively involved in pregnancy and parturition, but their precise roles and mechanisms remain poorly understood. Here, we identify mechanically activated ion channels PIEZO1 a...

New preprint alert! The uterus expands ~500-fold in pregnancy, yet we know little about how pressures are sensed. Led by @yunxiao-dr.bsky.social, we show PIEZOs are required for contractions and birth in mice, with dual roles of PIEZO1 in muscle and PIEZO2 in neurons
www.biorxiv.org/content/10.1...

7 months ago 131 42 1 2
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How can we use cell shapes and geometry to study mechanics of tissues?

I'm @juliaeckert.bsky.social, and with this thread, I would like to show you the secrets of cells and tissues. Let’s connect biology with a little bit of physics. Don't be scared and get inspired 😀. #EpithelialMechanics

7 months ago 55 15 2 2
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We are excited to announce our new #partnership with the Mechanobiology Institute (MBI) in Singapore! 🇸🇬

This collaboration will combine MBI’s expertise on molecular, cell, and tissue mechanobiology with our research on spatiotemporal organization of living matter to understand how organisms form 🔬

7 months ago 20 3 0 0

A fascinating paper! I think in hindsight, us scientists are all expecting this to happen when we knockout something. But to actually characterise its effects and see it happening in real time is still eye opening. Watch out for Transcriptional Adaptation!

8 months ago 10 2 0 0
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AI Is a Mass-Delusion Event Three years in, one of AI’s enduring impacts is to make people feel like they’re losing it.

Hello. I wrote a nice long essay about AI and this very strange moment where we're constantly told we're living in the dawn of a strange new future but the only thing that's actually clear is that everyone feels pretty unmoored and uncertain. I hope you'll read it

8 months ago 4421 1418 150 301

I did enjoy S1 but found the first episode of S2 pretty underwhelming. I stopped it about two thirds through and am thinking of just tapping out. Does it get better soon (or do we just have different tastes)?

8 months ago 0 0 0 0
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Kids need freedom. Dangerous roads make it hard to grant it. Bigger cars, distracted drivers and worried parents mean fewer kids are roaming freely.

The number of children injured or killed by cars while walking or riding a bike has fallen steadily since the 1970s, but CDC researcher note that this decline is not because streets are safer, but because fewer kids are out and about in the first place.

8 months ago 3065 720 144 72
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My team has updated our free database of POSTDOC fellowships.

This database contains 286 entries. For each entry, we provide a link, short description, deadline, amount, and eligibility criteria.

Download this updated and expanded database here: research.jhu.edu/rdt/funding-...

8 months ago 186 127 4 1
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Mechanotransduction in the nucleus

Multiple TFs transmit mechanical forces into transcriptional regulation.

Nuclear shape, size, and chromatin abnormalities are common features of many diseases.

8 months ago 51 16 0 1

Out now! Our very first paper@crick.ac.uk, an impressive feat by @tobyandrews.bsky.social where we show how a developing heart grows and scales up its morphological complexity to keep beating...an excellent summary below ⬇️
www.cell.com/developmenta...

8 months ago 71 18 7 1
Brain Surfaces of 70 primate species

Brain Surfaces of 70 primate species

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To predict the behaviour of a primate, would you rather base your guess on a closely related species or one with a similar brain shape? We looked at brains & behaviours of 70 species, you’ll be surprised!

🧵Thread on our new preprint with @r3rt0.bsky.social , doi.org/10.1101/2025...

8 months ago 512 234 16 26
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Interested in nuclear #mechanobiology? Join us for the first ever FASEB Science Research Conference on the Mechanobiology of the Nucleus #MBNSRC.
Find more information and register at: events.faseb.org/event/Mechan...
Submit abstracts by August 31, 2025. Please share and see you in October!

9 months ago 54 18 1 3