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Transmission electron microscopy (TEM) is a powerful tool that has been used for the visualization of biological materials since the 1940s. This technique permits the detailed observation of cellular organelles and other intracellular structures as well as infectious agents, like viruses. Important insights about the structure and function of the cell nucleus have been gleaned using TEM. Here we present a method for visualization of the nuclear envelope in cultured HeLa cells using TEM. The method covers cell culturing, fixation, embedding, sectioning, staining, and visualization. This approach is particularly useful to understand how the ultrastructure of the nuclear envelope is affected by cell culture conditions, genetic manipulations, and stress treatments.
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http://dx.doi.org/10.1007/978-1-0716-4714-1_3 | DOI Listing |
BMB Rep
September 2025
Department of Biochemistry and Molecular Biology, Ajou University School of Medicine, Suwon 16499; Department of Biomedical Sciences, The Graduate School of Ajou University, Suwon 16499; BK21 R&E Initiative for Advanced Precision Medicine, Ajou University School of Medicine, Suwon 16499, Korea.
Altered nuclear morphology, one of the characteristics of cancer cells, is often indicative of tumor prognosis. While reactive oxygen species (ROS) are known to induce nuclear morphology changes, mechanisms underlying these effects remain elusive, particularly regarding nuclear assembly. We hypothesized that mitotic cells might exhibit increased susceptibility to ROSinduced nuclear deformation due to the dynamic nature of nuclear envelope during mitosis, i.
View Article and Find Full Text PDFAnim Cells Syst (Seoul)
August 2025
Department of Integrated Biological Science, Pusan National University, Busan, South Korea.
Mammalian spermatozoa acquire fertilizing ability in response to environmental factors enriched in the female reproductive tract, a process called capacitation. During capacitation, sperm undergo physiological changes that are accompanied by functional regulation of sperm proteins. However, the mechanism by which capacitation orchestrates sperm protein functions to modulate physiological characteristics remains unclear.
View Article and Find Full Text PDFAlzheimers Dement
September 2025
Talisman Therapeutics, Babraham Research Campus, Cambridge, UK.
Introduction: Mutations in the MAPT gene that are causal for frontotemporal dementia (FTD) lead to mislocalization of tau protein to the neuronal cell body, changing microtubule dynamics to disrupt the nuclear envelope and nucleocytoplasmic transport.
Methods: We report a high content imaging-based phenotypic screen to identify novel small molecules that correct nuclear envelope defects in human neurons expressing the MAPT IVS10+16 mutation causal for FTD.
Results: Screening a 19,786-compound chemical diversity library, we identified > 100 compounds that corrected nuclear membrane defects in MAPT IVS10+16 neurons, with 23 demonstrating robust dose-dependent rescue.
J Theor Biol
August 2025
Department of Mathematics, Brandeis University, Waltham, MA, USA. Electronic address:
It has been observed that the growth of the nucleus and the cytoplasm is coordinated during cell growth, resulting in a nearly constant nuclear-to-cell volume ratio (N/C) throughout the cell cycle. Previous studies have shown that the N/C ratio is determined by the ratio between the number of proteins in the nucleus and the total number of proteins in the cell. These observations suggest the importance of the nucleocytoplasmic transport process in nuclear size by regulating protein concentrations in the nucleus and cytoplasm.
View Article and Find Full Text PDFAm J Obstet Gynecol
August 2025
State Key Laboratory of Reproductive Medicine and Offspring Health, Nanjing Medical University, Nanjing, China; Center of Reproduction and Genetics, The Affiliated Suzhou Hospital of Nanjing Medical University, Suzhou Municipal Hospital, Gusu School, Nanjing Medical University, Suzhou, China; Innova
Background: During mammalian oocyte meiosis, accurate chromosome segregation critically depends on precise regulation of kinetochore-microtubule (K-MT) attachments, a process monitored by the spindle assembly checkpoint (SAC). While CENP-F has been well characterized as a kinetochore-associated protein that stabilizes K-MT connections during mitosis, its functional mechanisms during meiosis remain poorly understood. In particular, there is still controversy over whether farnesylation modification governs localization and functionality of CENP-F.
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