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1.
Front Cell Dev Biol ; 12: 1417242, 2024.
Article in English | MEDLINE | ID: mdl-38903534

ABSTRACT

Migrasomes are organelles produced by migrating cells that form on retraction fibers and are released during cell migration. Migrasomes are involved in physiological and pathological processes such as intercellular communication, cell homeostasis maintenance, signal transduction, disease occurrence and development, and cancer metastasis. In addition, methods and techniques for studying migrasomes are constantly evolving. Here, we review the discovery, formation process, regulation, and known functions of migrasomes, summarize the commonly used specific markers of migrasomes, and the methods for observing migrasomes. Meanwhile, this review also discusses the potential applications of migrasomes in physiological processes, disease diagnosis, treatment, and prognosis, and looks forward to their wider application in biomedicine. In addition, the study of migrasomes will also reveal a new perspective on the mechanism of intercellular communication and promote the further development of life science.

2.
Genomics ; 116(3): 110838, 2024 05.
Article in English | MEDLINE | ID: mdl-38537807

ABSTRACT

After epiphyseal fracture, the epiphyseal plate is prone to ischemia and hypoxia, leading to the formation of bone bridge and deformity. However, the exact mechanism controlling the bone bridge formation remains unclear. Notch/RBPJ signaling axis has been indicated to regulate angiogenesis and osteogenic differentiation. Our study aims to investigate the mechanism of bone bridge formation after epiphyseal plate injury, and to provide a theoretical basis for new therapeutic approaches to prevent the bone bridge formation. The expression of DLL4 and RBPJ was significantly up-regulated in HUVECs after ischemia and hypoxia treatment. Notch/RBPJ pathway positively regulated the osteogenic differentiation of BMSCs. HUVECs can induce osteogenic differentiation of BMSCs under ischemia and hypoxia. Notch/RBPJ pathway is involved in the regulation of the trans-epiphyseal bridge formation. Notch/RBPJ in HUVECs is associated with osteogenic differentiation of BMSCs and may participate in the regulation of the bone bridge formation across the epiphyseal plate.


Subject(s)
Cell Differentiation , Human Umbilical Vein Endothelial Cells , Immunoglobulin J Recombination Signal Sequence-Binding Protein , Neovascularization, Physiologic , Osteogenesis , Receptors, Notch , Signal Transduction , Humans , Human Umbilical Vein Endothelial Cells/metabolism , Receptors, Notch/metabolism , Receptors, Notch/genetics , Immunoglobulin J Recombination Signal Sequence-Binding Protein/metabolism , Immunoglobulin J Recombination Signal Sequence-Binding Protein/genetics , Cell Hypoxia , Mesenchymal Stem Cells/metabolism , Mesenchymal Stem Cells/cytology , Adaptor Proteins, Signal Transducing/metabolism , Adaptor Proteins, Signal Transducing/genetics , Cells, Cultured , Calcium-Binding Proteins/metabolism , Calcium-Binding Proteins/genetics , Angiogenesis
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