Cells, Free Full-Text
Por um escritor misterioso
Last updated 16 junho 2024
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Twenty-five years ago, the first mammalian Transient Receptor Potential Canonical (TRPC) channel was cloned, opening the vast horizon of the TRPC field. Today, we know that there are seven TRPC channels (TRPC1–7). TRPCs exhibit the highest protein sequence similarity to the Drosophila melanogaster TRP channels. Similar to Drosophila TRPs, TRPCs are localized to the plasma membrane and are activated in a G-protein-coupled receptor-phospholipase C-dependent manner. TRPCs may also be stimulated in a store-operated manner, via receptor tyrosine kinases, or by lysophospholipids, hypoosmotic solutions, and mechanical stimuli. Activated TRPCs allow the influx of Ca2+ and monovalent alkali cations into the cytosol of cells, leading to cell depolarization and rising intracellular Ca2+ concentration. TRPCs are involved in the continually growing number of cell functions. Furthermore, mutations in the TRPC6 gene are associated with hereditary diseases, such as focal segmental glomerulosclerosis. The most important recent breakthrough in TRPC research was the solving of cryo-EM structures of TRPC3, TRPC4, TRPC5, and TRPC6. These structural data shed light on the molecular mechanisms underlying TRPCs’ functional properties and propelled the development of new modulators of the channels. This review provides a historical overview of the major advances in the TRPC field focusing on the role of gene knockouts and pharmacological tools.
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MitoQuicLy: A high-throughput method for quantifying cell-free DNA
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Postbiotics-parabiotics: the new horizons in microbial biotherapy
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Cells, Free Full-Text
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Cell-free DNA tissues of origin by methylation profiling reveals
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Anomalous Scaling of Gene Expression in Confined Cell-Free
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STEM CELLS: Vol 35, No 5
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Five-Year Outcomes for Refractory B-Cell Lymphomas with CAR T-Cell
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JCM, Free Full-Text
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Extracellular histones, cell-free DNA, or nucleosomes: differences
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An integrated in vivo/in vitro framework to enhance cell-free
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