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The Golgi complex is the central hub of the secretory pathway. In mammalian cells, it is formed by stacks of flattened cisternae organized in a continuous membrane system, the Golgi ribbon, located near the centrosome. During G2, the Golgi ribbon is disassembled into isolated stacks that, at the onset of mitosis, are further fragmented into small tubular-vesicular clusters that disperse throughout the cytoplasm. Here, we describe a set of methods to study the Golgi complex in different phases of the cell cycle, drawing attention to reproducing the mitotic Golgi fragmentation to gain knowledge and acquire the skills to study the mechanisms that regulate mitotic Golgi reorganization as well as its biological significance. The investigations based on these assays have been instrumental in understanding that Golgi disassembly is not only a consequence of mitosis but is also required for mitotic entry and cell division.
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http://dx.doi.org/10.1007/978-1-0716-2639-9_21 | DOI Listing |
Cancer Res
September 2025
The Catholic University of Korea College of Medicine, Seoul, Korea (South), Republic of.
Alterations in the structure of the Golgi apparatus play a pivotal role in cancer progression and invasion. A better understanding of how Golgi morphology regulates the metastatic potential of cancer cells could help identify potential treatment strategies. In this study, we investigated how specific structural variations in the Golgi, particularly fragmentation and condensation, influence the malignancy of gastric cancer using human cell lines, xenograft mouse models, and human patient tissue samples.
View Article and Find Full Text PDFChem Biol Interact
September 2025
Key Laboratory of Research on Clinical Molecular Diagnosis for High Incidence Diseases in Western Guangxi of Guangxi Higher Education Institutions, Reproductive Medicine of Guangxi Medical and Health Key Discipline Construction Project, Affiliated Hospital of Youjiang Medical University for National
Aluminum is a lightweight and corrosion-resistant metal element that is widely used in industries, construction, food, and pharmaceuticals, and it can adversely affect multiple organ systems including the nervous system, skeletal system, reproductive system, blood system, and immune system. In present study, we investigated the effects of aluminum exposure on mammalian embryo development. Our data demonstrate that aluminum exposure induces mouse early embryo development defects, including those at the zygotes and 2-cell stages, causing a decrease in general transcription activity.
View Article and Find Full Text PDFJ Appl Toxicol
September 2025
Department of Biology, Faculty of Science, Dicle University, Diyarbakır, Turkey.
Imidacloprid, a neonicotinoid pesticide widely used for controlling agricultural pests, is known to exert toxic effects on non-target aquatic organisms. This study aimed to investigate the toxicological impact of imidacloprid and the potential protective effect of an antioxidant, ascorbic acid, in the freshwater snail Melanopsis praemorsa. Eight experimental groups were established: two controls; three groups exposed to imidacloprid at concentrations of 4.
View Article and Find Full Text PDFDiabetes
September 2025
Fraternal Order of Eagles Diabetes Research Center, University of Iowa, Iowa City, IA.
Unlabelled: Type 1 diabetes (T1D) is caused by the selective autoimmune ablation of pancreatic β-cells. Emerging evidence reveals β-cell secretory dysfunction arises early in T1D development and may contribute to diseases etiology; however, the underlying mechanisms are not well understood. Our data reveal that proinflammatory cytokines elicit a complex change in the β-cell's Golgi structure and function.
View Article and Find Full Text PDFJ Lipid Res
September 2025
Keenan Centre for Biomedical Research, St. Michael's Hospital, Toronto, Canada; Department of Laboratory Medicine and Pathobiology, University of Toronto, Canada; Department of Biochemistry, University of Toronto, Canada; Department of Medicine and the Interdepartmental Division of Critical Care Med
Atherosclerosis begins with the subendothelial retention of low-density lipoproteins (LDL) from the circulation. While LDL transcytosis across the endothelium is mediated by SR-BI and ALK1 and is usually independent of LDLR, the intracellular mechanisms and route of LDL transcytosis remain unclear. Using total internal reflection fluorescence microscopy in LDLR-depleted human coronary artery endothelial cells (HCAECs), we found that LDL transcytosis can proceed both directly as well as indirectly from an intracellular compartment.
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