Issues
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Cover image
Cover Image
Cover: Growth-arrested mammalian cells display reduced mitochondrial dynamics and a concomitant decrease in mitochondrial association with the endoplasmic reticulum. This de-tethering of these organelles ultimately causes reduced compartment-specific activity of mTORC1 complex, leading to polysomal retention and reduced export of miRNAs. The 3D rendering of mitochondrial structures from a proliferating HeLa cell (yet to reach growth arrest) shown here depicts the highly branched mitochondrial network in a gradient of dark pink to off-white according to individual strand lengths. The blue to green colour marks the degree of association of the mitochondria and endoplasmic reticulum at specific points. See article by S. Chatterjee et al. (jcs250241).
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RESEARCH HIGHLIGHTS
STICKY WICKETS
OBITUARY
FIRST PERSON
CELL SCIENTISTS TO WATCH
CELL SCIENCE AT A GLANCE
Tumour-directed microenvironment remodelling at a glance
Summary: An outline of the processes by which epithelial tumours regulate their tumour microenvironment, and how new insights into tumour–microenvironment interactions have led to ideas on targeting it as treatments.
REVIEWS
The journey of Ca2+ through the cell – pulsing through the network of ER membrane contact sites
Summary: Traveling through the ER, Ca2+ is transported towards membrane contact sites with mitochondria or endolysosomes, where it plays key roles in the regulation of essential organellar biology, which are reviewed here.
Notch in mechanotransduction – from molecular mechanosensitivity to tissue mechanostasis
Summary: This Review presents evidence that Notch signaling is directly and indirectly mechanosensitive, and discusses engineered and computational approaches to help unravel its complex dynamics.
RESEARCH ARTICLES
Sec71 separates Golgi stacks in Drosophila S2 cells
Summary: Golgi stacks are scattered in the cytoplasm of Drosophila cells. Sec71 is required for separating Golgi stacks, as its impairment, for example, through brefeldin A (BFA) treatment, produces Golgi aggregations termed BFA bodies.
Mitochondria control mTORC1 activity-linked compartmentalization of eIF4E to regulate extracellular export of microRNAs
Summary:Mitochondrial activity and tethering with the ER are linked to compartmentalization of the translation initiation factor eIF4E to the polysomes, which controls miRNA-mediated repression and miRNA export.
A novel mitosis-specific Cep215 domain interacts with Cep192 and phosphorylated Aurora A for organization of spindle poles
Summary: A mitosis-specific centrosome-targeting domain of Cep215 binds Cep192 and phosphorylated Aurora A to play a role in maintaining the structural integrity of spindle poles during mitosis.
Retromer retrieves the Wilson disease protein ATP7B from endolysosomes in a copper-dependent manner
Summary: The Wilson disease protein ATP7B utilizes lysosomal exocytosis to export excess copper in hepatocytes. The retromer complex retrieves ATP7B from endolysosomes and recycles it back to the trans-Golgi network.
Disrupting polycystin-2 EF hand Ca2+ affinity does not alter channel function or contribute to polycystic kidney disease
Summary: A refutation of a common hypothesis regarding Ca2+ control mechanisms of polycystin-2 – a primary cilia ion channel, the dysregulation of which causes autosomal dominant polycystic kidney disease.
EGFRvIII uses intrinsic and extrinsic mechanisms to reduce glioma adhesion and increase migration
Summary: Constitutively active and truncated EGFR transcriptionally represses integrins via a SHC–MEK signaling axis, and communicates with neighboring cells through TNFα to promote cooperative invasion.
TrkB deubiquitylation by USP8 regulates receptor levels and BDNF-dependent neuronal differentiation
Summary: USP8 interacts with and deubiquitylates TrkB neurotrophin receptors, regulating levels of both total and activated receptors and BDNF-dependent differentiation of hippocampal neurons.
CD301 mediates fusion in IL-4-driven multinucleated giant cell formation
Highlighted Article: CD301, a C-type lectin domain family 10 member, is driven by IL-4 and mediates macrophage fusion for the formation of multinucleated giant cells.
ESCRT recruitment by the S. cerevisiae inner nuclear membrane protein Heh1 is regulated by Hub1-mediated alternative splicing
Highlighted Article: Heh1-S, the inner nuclear membrane protein resulting from Hub1-mediated splicing of HEH1 pre-mRNA, contributes to nuclear envelope maintenance by preventing excessive recruitment of the ESCRT adaptor Chm7.
The budding yeast Start repressor Whi7 differs in regulation from Whi5, emerging as a major cell cycle brake in response to stress
Highlighted Article: Cells can use the interplay between functionally redundant but differentially regulated cell-cycle repressors in order to confer new repression capabilities and to respond to specific cellular conditions.
A piggybacking mechanism enables peroxisomal localization of the glyoxylate cycle enzyme Mdh2 in yeast
Highlighted Article: Yeast Mdh2 is dually localized to the cytosol and peroxisomes, and is targeted to peroxisomes via association with Mdh3 and a Pex5-dependent piggybacking mechanism.
Sequential peripheral enrichment of H2A.Zac and H3K9me2 during trophoblast differentiation in human embryonic stem cells
Highlighted Article: As early as 12 hours after embryonic stem cells begin differentiating to trophoblasts, acetylated H2A.Z becomes enriched at the nuclear periphery; we find that loss of H2A.Z acetylation is followed sequentially by enrichment of dimethylated H3K9.
TOOLS AND RESOURCES
Trackosome: a computational toolbox to study the spatiotemporal dynamics of centrosomes, nuclear envelope and cellular membrane
Summary: Development of a new image analysis toolbox called Trackosome and its use to study nuclear envelope oscillations during early mitosis and correlations between the trajectories of the centrosomes.
CORRECTION
Imaging Cell Architecture and Dynamics
We are still welcoming submissions for our upcoming Special Issue: Imaging Cell Architecture and Dynamics. This issue will be coordinated by two Guest Editors: Lucy Collinson (The Francis Crick Institute, UK) and Guillaume Jacquemet (University of Turku, Finland). Extended submission deadline: 29 March 2024.
Journal of Cell Science - more than just a journal
People who know JCS well will know that we're more than just a journal and that our community – the cell biology community – really is at the heart of everything we do. Read the full Editorial by Editor-in-Chief Michael Way and Executive Editor Seema Grewal.
2024 Journal Meeting 'Diversity and Evolution in Cell Biology'
Registration is open for our 2024 Journal Meeting Diversity and Evolution in Cell Biology, which aims to bring together evolutionary biologists and cell biologists investigating diverse aspects of cellular physiology. Submit your abstract by 5 April. Final registration deadline: 3 May 2024.
Workshop: Roles of Lipids in Nuclear Homeostasis and Genome Stability
Early-career researchers interested in the roles of nuclear lipids, apply now for one of the ten funded places at this Workshop, which will take place 14-17 October 2024. Application deadline: 19 April.
Reasons to submit to Journal of Cell Science
There are many benefits to publishing in Journal of Cell Science - read more about why you should choose JCS or visit our submission page now.